Attach to Form 990 or Form 990-EZ.
Go to
www.irs.gov/Form990 for instructions and the latest information.
| (i) Name of supported organization | (ii) EIN | (iii) Type of organization (described on lines 1- 10 above (see instructions)) | (iv) Is the organization listed in your governing document? | (v) Amount of monetary support (see instructions) | (vi) Amount of other support (see instructions) | |
|---|---|---|---|---|---|---|
| Yes | No | |||||
|
Total |
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Calendar year (or fiscal year beginning in) ![]() |
(a) 2016 | (b) 2017 | (c) 2018 | (d) 2019 | (e) 2020 | (f) Total | |
|---|---|---|---|---|---|---|---|
| 1 | Gifts, grants, contributions, and membership fees received. (Do not include any "unusual grant.") .. | ||||||
| 2 | Tax revenues levied for the organization's benefit and either paid to or expended on its behalf.... | ||||||
| 3 | The value of services or facilities furnished by a governmental unit to the organization without charge.. | ||||||
| 4 | Total. Add lines 1 through 3 | ||||||
| 5 | The portion of total contributions by each person (other than a governmental unit or publicly supported organization) included on line 1 that exceeds 2% of the amount shown on line 11, column (f).. | ||||||
| 6 | Public support. Subtract line 5 from line 4. | ||||||
Calendar year
(or fiscal year beginning in) ![]() |
(a) 2016 | (b) 2017 | (c) 2018 | (d) 2019 | (e) 2020 | (f) Total | |
|---|---|---|---|---|---|---|---|
| 7 | Amounts from line 4.. | ||||||
| 8 | Gross income from interest, dividends, payments received on securities loans, rents, royalties and income from similar sources... | ||||||
| 9 | Net income from unrelated business activities, whether or not the business is regularly carried on.. | ||||||
| 10 | Other income. Do not include gain or loss from the sale of capital assets (Explain in Part VI.).. | ||||||
| 11 | Total support. Add lines 7 through 10 | ||||||
Calendar year (or fiscal year beginning in) ![]() |
(a) 2016 | (b) 2017 | (c) 2018 | (d) 2019 | (e) 2020 | (f) Total | |
|---|---|---|---|---|---|---|---|
| 1 | Gifts, grants, contributions, and membership fees received. (Do not include any "unusual grants.") . | ||||||
| 2 | Gross receipts from admissions, merchandise sold or services performed, or facilities furnished in any activity that is related to the organization's tax-exempt purpose | ||||||
| 3 | Gross receipts from activities that are not an unrelated trade or business under section 513 ..... | ||||||
| 4 | Tax revenues levied for the organization's benefit and either paid to or expended on its behalf... | ||||||
| 5 | The value of services or facilities furnished by a governmental unit to the organization without charge | ||||||
| 6 | Total. Add lines 1 through 5 | ||||||
| 7a | Amounts included on lines 1, 2, and 3 received from disqualified persons | ||||||
| b | Amounts included on lines 2 and 3 received from other than disqualified persons that exceed the greater of $5,000 or 1% of the amount on line 13 for the year. | ||||||
| c | Add lines 7a and 7b.. | ||||||
| 8 | Public support. (Subtract line 7c from line 6.) | ||||||
Calendar year (or fiscal year beginning in) ![]() |
(a) 2016 | (b) 2017 | (c) 2018 | (d) 2019 | (e) 2020 | (f) Total | |
|---|---|---|---|---|---|---|---|
| 9 | Amounts from line 6... | ||||||
| 10a | Gross income from interest, dividends, payments received on securities loans, rents, royalties and income from similar sources.. | ||||||
| b | Unrelated business taxable income (less section 511 taxes) from businesses acquired after June 30, 1975. | ||||||
| c | Add lines 10a and 10b. | ||||||
| 11 | Net income from unrelated business activities not included in line 10b, whether or not the business is regularly carried on. | ||||||
| 12 | Other income. Do not include gain or loss from the sale of capital assets (Explain in Part VI.) .. | ||||||
| 13 | Total support. (Add lines 9, 10c, 11, and 12.).. | ||||||
| Section A - Adjusted Net Income | (A) Prior Year |
(B) Current Year (optional) |
||||
| 1 | Net short-term capital gain | 1 | ||||
| 2 | Recoveries of prior-year distributions | 2 | ||||
| 3 | Other gross income (see instructions) | 3 | ||||
| 4 | Add lines 1 through 3 | 4 | ||||
| 5 | Depreciation and depletion | 5 | ||||
| 6 | Portion of operating expenses paid or incurred for production or collection of gross income or for management, conservation, or maintenance of property held for production of income (see instructions) | 6 | ||||
| 7 | Other expenses (see instructions) | 7 | ||||
| 8 | Adjusted Net Income (subtract lines 5, 6 and 7 from line 4) | 8 | ||||
| Section B - Minimum Asset Amount | (A) Prior Year |
(B) Current Year (optional) |
||||
| 1 | Aggregate fair market value of all non-exempt-use assets (see instructions for short tax year or assets held for part of year): | 1 | ||||
| a | Average monthly value of securities | 1a | ||||
| b | Average monthly cash balances | 1b | ||||
| c | Fair market value of other non-exempt-use assets | 1c | ||||
| d | Total (add lines 1a, 1b, and 1c) | 1d | ||||
| e |
Discount claimed for blockage or other factors (explain in detail in Part VI): |
|||||
| 2 | Acquisition indebtedness applicable to non-exempt use assets | 2 | ||||
| 3 | Subtract line 2 from line 1d | 3 | ||||
| 4 | Cash deemed held for exempt use. Enter 0.015 of line 3 (for greater amount, see instructions). | 4 | ||||
| 5 | Net value of non-exempt-use assets (subtract line 4 from line 3) | 5 | ||||
| 6 | Multiply line 5 by 0.035 | 6 | ||||
| 7 | Recoveries of prior-year distributions | 7 | ||||
| 8 | Minimum Asset Amount (add line 7 to line 6) | 8 | ||||
| Section C - Distributable Amount | Current Year | |||||
| 1 | Adjusted net income for prior year (from Section A, line 8, Column A) | 1 | ||||
| 2 | Enter 85% of line 1 | 2 | ||||
| 3 | Minimum asset amount for prior year (from Section B, line 8, Column A) | 3 | ||||
| 4 | Enter greater of line 2 or line 3 | 4 | ||||
| 5 | Income tax imposed in prior year | 5 | ||||
| 6 | Distributable Amount. Subtract line 5 from line 4, unless subject to emergency temporary reduction (see instructions) | 6 | ||||
| Section D - Distributions | Current Year | |
|---|---|---|
| 1 Amounts paid to supported organizations to accomplish exempt purposes | 1 | |
|
2
Amounts paid to perform activity that directly furthers exempt purposes of supported organizations, in excess of income from activity |
2 | |
| 3 Administrative expenses paid to accomplish exempt purposes of supported organizations | 3 | |
| 4 Amounts paid to acquire exempt-use assets | 4 | |
| 5 Qualified set-aside amounts (prior IRS approval required - provide details in Part VI) | 5 | |
| 6 Other distributions (describe in Part VI). See instructions | 6 | |
| 7Total annual distributions. Add lines 1 through 6. | 7 | |
|
8
Distributions to attentive supported organizations to which the organization is responsive (provide details in Part VI). See instructions |
8 | |
| 9 Distributable amount for 2020 from Section C, line 6 | 9 | |
| 10 Line 8 amount divided by Line 9 amount | 10 | |
| Section E - Distribution Allocations (see instructions) |
(i) Excess Distributions |
(ii) Underdistributions Pre-2020 |
(iii) Distributable Amount for 2020 |
|
|---|---|---|---|---|
| 1 Distributable amount for 2020 from Section C, line 6 | ||||
|
2
Underdistributions, if any, for years prior to 2019 (reasonable cause required-- explain in Part VI). See instructions. |
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| 3 Excess distributions carryover, if any, to 2020: | ||||
| a From 2015....... | ||||
| b From 2016....... | ||||
| c From 2017....... | ||||
| d From 2018....... | ||||
| e From 2019....... | ||||
| fTotal of lines 3a through e | ||||
| g Applied to underdistributions of prior years | ||||
| h Applied to 2020 distributable amount | ||||
|
i
Carryover from 2015 not applied (see instructions) |
||||
| j Remainder. Subtract lines 3g, 3h, and 3i from line 3f. | ||||
| 4Distributions for 2020 from Section D, line 7: | ||||
| $ | ||||
| a Applied to underdistributions of prior years | ||||
| b Applied to 2020 distributable amount | ||||
| c Remainder. Subtract lines 4a and 4b from line 4. | ||||
|
5
Remaining underdistributions for years prior to 2020, if any. Subtract lines 3g and 4a from line 2. If the amount is greater than zero, explain in Part VI. See instructions. |
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|
6
Remaining underdistributions for 2020. Subtract lines 3h and 4b from line 1. If the amount is greater than zero, explain in Part VI. See instructions. |
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|
7 Excess distributions carryover to 2021. Add lines 3j and 4c. |
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| 8 Breakdown of line 7: | ||||
| a Excess from 2016..... | ||||
| b Excess from 2017..... | ||||
| c Excess from 2018..... | ||||
| d Excess from 2019..... | ||||
| e Excess from 2020..... | ||||
| Facts And Circumstances Test |
|---|
| Return Reference | Explanation |
|---|---|
| PART I, LINE 4 | STOWERS INSTITUTE FOR MEDICAL RESEARCH ("SIMR") CONDUCTS MEDICAL RESEARCH IN CONJUNCTION WITH THE UNIVERSITY OF KANSAS (KU) AND ITS AFFILIATES, THE UNIVERSITY OF KANSAS HOSPITAL AUTHORITY AND THE UNIVERSITY OF KANSAS MEDICAL CENTER (KUMC), PURSUANT TO A WRITTEN MEMORANDUM OF UNDERSTANDING. KUMC IS THE ACADEMIC HEALTH SCIENCE CENTER OF THE LARGEST PUBLIC RESEARCH UNIVERSITY IN THE STATE OF KANSAS. KUMC OFFERS PROGRAMS AND SERVICES THAT FOCUS ON EDUCATION, RESEARCH, PATIENT CARE, AND COMMUNITY ENGAGEMENT. AS OF DECEMBER 31, 2020, FIVE KUMC STUDENTS HAVE RECEIVED MS DEGREES AND FORTY-SIX KUMC STUDENTS HAVE RECEIVED PHD DEGREES FOR THESIS WORK PERFORMED IN SIMR LABS. KUMC IS AFFILIATED WITH THE UNIVERSITY OF KANSAS HOSPITAL, A NONPROFIT INDEPENDENT HOSPITAL CO-LOCATED WITH THE MAIN KUMC CAMPUS IN KANSAS CITY, KS. IN 2020, TWENTY SIMR RESEARCH PROGRAM LEADERS WERE ADJUNCT FACULTY IN FOUR KUMC DEPARTMENTS. THESE APPOINTMENTS INCLUDED TWELVE FULL PROFESSORS, FOUR ASSOCIATE PROFESSORS, AND FOUR ASSISTANT PROFESSORS. IN 2020, FORTY-EIGHT OF SIMR'S FIFTY-NINE ORIGINAL RESEARCH PUBLICATIONS INCLUDED BOTH SIMR AND KUMC AFFILIATIONS. ABOUT A DOZEN KUMC STUDENTS PERFORMED PREDOCTORAL RESEARCH IN SIMR LABS IN 2020. SIMR IS ALSO A CONSORTIUM MEMBER OF THE UNIVERSITY OF KANSAS CANCER CENTER AT KUMC, A CANCER RESEARCH AND CARE PARTNERSHIP SPANNING TWO STATES AND INVOLVING COLLABORATION AMONG RESEARCHERS, PHYSICIANS, AND CANCER SUPPORT PROFESSIONALS IN BASIC, TRANSLATIONAL, AND CLINICAL RESEARCH AREAS. IN JUNE 2012, THE NIH'S NATIONAL CANCER INSTITUTE (NCI) NAMED THE UNIVERSITY OF KANSAS CANCER CENTER AN NCI-DESIGNATED CANCER CENTER. THE NCI CANCER CENTERS PROGRAM IS A PILLAR OF FEDERAL CANCER RESEARCH EFFORTS AND INTEGRAL TO THE NCI'S PROGRAMS FOR STUDYING, TREATING, AND PREVENTING CANCER. IN KUMC'S APPLICATION TO THE NCI CANCER CENTERS PROGRAM, $4 MILLION OF THE $48 MILLION IN GRANTS CITED IN THE APPLICATION WERE GRANTS THAT HAD BEEN AWARDED TO SIMR INVESTIGATORS. IN 2020, TWELVE SIMR RESEARCH PROGRAM LEADERS WERE MEMBERS OF THE UNIVERSITY OF KANSAS CANCER CENTER'S CANCER BIOLOGY RESEARCH PROGRAM, INCLUDING LINHENG LI, PHD, WHO SERVES AS CO-LEADER OF THE PROGRAM. IN 2020, SIMR RESEARCH PROGRAM LEADER LINHENG LI, PHD, CONTINUED A COLLABORATION WITH THE UNIVERSITY OF KANSAS CANCER CENTER AND CHILDREN'S MERCY HOSPITAL, KANSAS CITY, MO, TO INVESTIGATE APPROACHES TO TREAT LEUKEMIA. THIS RESEARCH FOCUSES ON TARGETING CANCER STEM CELLS TO HELP REDUCE THE RECURRENCE OF CANCER AFTER A PATIENT GOES INTO REMISSION. THE COLLABORATION BUILDS ON FOUNDATIONAL RESEARCH FROM THE LI LAB THAT HAS CHARACTERIZED CANCER STEM CELLS AT MOLECULAR AND CELLULAR LEVELS. THIS ONGOING RESEARCH COLLABORATION HAS GENERATED FINDINGS THAT HAVE BEEN REPORTED IN ORIGINAL RESEARCH PUBLICATIONS INCLUDING PERRY J ET AL, 2020. KUMC IS THE SPONSOR OF A RELATED CLINICAL RESEARCH STUDY, "LOW-DOSE DAUNORUBICIN IN PATIENTS WITH RELAPSED/REFRACTORY ACUTE LEUKEMIA," WHICH IS DESIGNED TO ASSESS THE FEASIBILITY AND TOLERABILITY OF ADMINISTERING A LOW DOSE OF THE DRUG TO PATIENTS WITH RELAPSED OR REFRACTORY ACUTE MYELOID LEUKEMIA (AML) OR ACUTE LYMPHOBLASTIC LEUKEMIA (ALL), AND TO OBTAIN PRELIMINARY DATA ON THE DRUG ENGAGING ITS TARGET. IN 2020, SIMR RESEARCH PROGRAM LEADER MICHAEL WASHBURN, PHD, CONTINUED A RESEARCH PROJECT IN COLLABORATION WITH ROY JENSEN, MD, DIRECTOR OF THE UNIVERSITY OF KANSAS CANCER CENTER. THE OVERALL AIM OF THIS RESEARCH EFFORT IS TO DETERMINE HOW CANCER THERAPEUTICS ACT ON PROTEIN NETWORKS IN CELLS AND TISSUES. JENSEN IS A WORLD-RENOWNED EXPERT ON BREAST CANCER AND HOLDS ADDITIONAL POSITIONS AS DIRECTOR, KANSAS MASONIC CANCER RESEARCH INSTITUTE, WILLIAM R. JEWELL DISTINGUISHED KANSAS MASONIC PROFESSOR, AND PROFESSOR OF PATHOLOGY AND LABORATORY MEDICINE, ANATOMY AND CELL BIOLOGY, CANCER BIOLOGY, AND MOLECULAR BIOSCIENCES AT KUMC. THE PROJECT AIMS TO FURTHER EXPLORE THE MECHANISM OF ACTION OF SUBEROYLANILIDE HYDROXAMIC ACID (SAHA), WHICH IS USED AS CHEMOTHERAPY FOR CERTAIN LYMPHOMAS AND IS BEING EVALUATED IN CLINICAL TRIALS FOR OTHER CANCERS. RECENT REPORTS SUGGEST THAT SAHA HAS ADDITIONAL EFFECTS THAT INVOLVE PROTEIN NETWORKS MORE BROADLY, THUS SUGGESTING OTHER POSSIBLE MECHANISMS OF ACTION. RESULTS FROM THIS JOINT RESEARCH EFFORT MAY ENABLE THE FUTURE DEVELOPMENT OF MORE SPECIFIC AND EFFECTIVE HUMAN THERAPEUTICS. THIS PROJECT IS SUPPORTED IN PART BY A NIH GRANT FROM THE NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES AND HAS GENERATED FINDINGS THAT HAVE BEEN REPORTED IN ORIGINAL RESEARCH PUBLICATIONS INCLUDING LEVY MJ ET AL, 2020, LIU ET AL, 2020, AND BANKS ET AL, 2020. IN 2020, SIMR SCIENTISTS ALSO COLLABORATED WITH RESEARCHERS AT EIGHTY-SEVEN NATIONAL AND SIXTY-FOUR INTERNATIONAL INSTITUTIONS INCLUDING DOZENS OF HOSPITALS, MEDICAL CENTERS, AND MEDICAL SCHOOLS. MANY OF THESE COLLABORATIONS RESULTED IN DISCOVERIES THAT MERITED PUBLICATION IN LEADING PEER-REVIEWED SCIENTIFIC JOURNALS AND/OR SUCCESSFULLY FUNDED GRANT AWARDS. SIMR PARTICIPATED IN COLLABORATIONS CONDUCTING RESEARCH IN CONJUNCTION WITH THE FOLLOWING US HOSPITALS, PURSUANT TO AN UNDERSTANDING TO MAINTAIN CONTINUING CLOSE COOPERATION IN THE ACTIVE CONDUCT OF MEDICAL RESEARCH IN 2020: INSTITUTION LOCATION BRIGHAM AND WOMEN'S HOSPITAL BOSTON, MA CHILDREN'S MERCY HOSPITAL KANSAS CITY, MO CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER CINCINNATI, OH DANA-FARBER CANCER INSTITUTE BOSTON, MA DUKE UNIVERSITY MEDICAL CENTER DURHAM, NC GEORGE WASHINGTON UNIVERSITY SCHOOL OF MEDICINE AND HEALTH SCIENCES WASHINGTON, DC HARVARD MEDICAL SCHOOL BOSTON, MA JOHNS HOPKINS SCHOOL OF MEDICINE BALTIMORE, MD LE BONHEUR CHILDREN'S HOSPITAL MEMPHIS, TN MEMORIAL SLOAN KETTERING CANCER CENTER NEW YORK, NY NEW YORK UNIVERSITY LANGONE MEDICAL CENTER NEW YORK, NY SEATTLE CHILDREN'S HOSPITAL SEATTLE, WA SHRINER'S HOSPITALS FOR CHILDREN - NORTHERN CALIFORNIA SACRAMENTO, CA ST. JUDE CHILDREN'S RESEARCH HOSPITAL NASHVILLE, TN STANFORD UNIVERSITY SCHOOL OF MEDICINE STANFORD, CA UNIVERSITY OF CALIFORNIA LOS ANGELES DAVID GEFFEN SCHOOL OF MEDICINE LOS ANGELES, CA UNIVERSITY OF CALIFORNIA SAN FRANCISCO SAN FRANCISCO, CA UNIVERSITY OF CINCINNATI MEDICAL CENTER CINCINNATI, OH UNIVERSITY OF COLORADO ANSCHUTZ MEDICAL CAMPUS AURORA, CO UNIVERSITY OF KANSAS CANCER CENTER KANSAS CITY, KS UNIVERSITY OF KANSAS MEDICAL CENTER KANSAS CITY, KS UNIVERSITY OF MISSOURI-KANSAS CITY SCHOOL OF MEDICINE KANSAS CITY, MO UNIVERSITY OF PENNSYLVANIA PERELMAN SCHOOL OF MEDICINE PHILADELPHIA, PA UNIVERSITY OF PITTSBURGH CANCER INSTITUTE PITTSBURGH, PA UNIVERSITY OF ROCHESTER MEDICAL CENTER ROCHESTER, NY UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER MEMPHIS, TN UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT HOUSTON HOUSTON, TX UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER HOUSTON, TX UNIVERSITY OF VERMONT CANCER CENTER BURLINGTON, VT UNIVERSITY OF VIRGINIA SCHOOL OF MEDICINE CHARLOTTESVILLE, VA UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE SEATTLE, WA UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH MADISON, WI VANDERBILT UNIVERSITY MEDICAL CENTER NASHVILLE, TN WASHINGTON UNIVERSITY SCHOOL OF MEDICINE IN ST. LOUIS ST.LOUIS, MO WEILL CORNELL SCHOOL OF MEDICINE NEW YORK, NY TO CARRY OUT THE RESEARCH DESCRIBED IN THE FOLLOWING EXAMPLES, SIMR AND HOSPITAL, MEDICAL CENTER, OR MEDICAL SCHOOL ENTERED INTO A COOPERATION AGREEMENT PURSUANT TO WHICH THEY AGREED TO ESTABLISH, DEVELOP, ADMINISTER, AND MAINTAIN CONTINUING CLOSE COOPERATION IN THE ACTIVE CONDUCT OF MEDICAL RESEARCH, INCLUDING THROUGH SPECIFIC COOPERATIVE EFFORTS IN THE AREAS OF RESEARCH, SHARING OF INFORMATION, PURSUANT OF JOINT GRANTS, INTERACTION OF STAFF, ADJUNCT/JOINT APPOINTMENTS, AND SHARING OF FACILITIES. TO ASSURE THE SUCCESS OF THEIR COOPERATIVE RELATIONSHIP, EACH AGREED TO ENGAGE IN EFFECTIVE, COORDINATED, AND ONGOING PLANNING, OVERSIGHT, AND COMMUNICATION, AND TO COMMIT THE NECESSARY RESOURCES, BOTH HUMAN AND MONETARY, TO SUPPORT, FACILITATE, AND PROMOTE THE COOPERATION. JOINT MEDICAL RESEARCH ON THE CHARACTERIZATION OF INTESTINAL STEM CELLS - THE LI LAB PERFORMED JOINT MEDICAL RESEARCH ON THE CHARACTERIZATION OF INTESTINAL STEM CELLS WITH COLLABORATORS AT CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER, DAVID GEFFEN SCHOOL OF MEDICINE AT UCLA, OREGON HEALTH AND SCIENCE UNIVERSITY SCHOOL OF MEDICINE, STANFORD UNIVERSITY SCHOOL OF MEDICINE, AND UNIVERSITY OF PITTSBURGH CANCER INSTITUTE. INTESTINAL DISEASES RANGING FROM CROHN'S DISEASE TO COLITIS TO CANCER MAY BENEFIT FROM INTESTINAL STEM CELL THERAPIES. THIS RESEARCH ADVANCES THE UNDERSTANDING OF THE BIOLOGY OF STEM CELLS THAT RESIDE IN THE INTESTINE AND EXPLORES HOW THEY CAN BE USED TO TREAT AND CURE INTESTINAL DISEASES. THIS RESEARCH COLLABORATION IS SUPPORTED IN PART BY A NIH GRANT AWARDED BY THE NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES AND HAS GENERATED FINDINGS PUBLISHED IN ORIGINAL RESEARCH PUBLICATIONS INCLUDING KARMAKAR S ET AL, 2020. JOINT MEDICAL RESEARCH ON EYE DEVELOPMENT AND FUNCTION - THE XIE LAB PERFORMED JOINT MEDI |
| Software ID: | |
| Software Version: |
Attach to Form 990 or 990-EZ.
Go to www.irs.gov/Form990 for the latest information.
| Return Reference | Explanation |
|---|---|
| PART III, LINE 1: | THE STOWERS INSTITUTE FOR MEDICAL RESEARCH ("SIMR") PERFORMS MEDICAL RESEARCH IN THE PUBLIC INTEREST WITH THE GOAL OF EXPANDING THE UNDERSTANDING OF FUNDAMENTAL PROCESSES IN LIVING CELLS AND IMPROVING LIFE'S QUALITY THROUGH INNOVATIVE APPROACHES TO THE CAUSES, TREATMENT, AND PREVENTION OF DISEASE. PART III, LINE 4: SIMR'S ACCOMPLISHMENTS ARE DESCRIBED AT THE END OF SCHEDULE O. PART VI, LINE 2: VIRGINIA G. STOWERS, JONATHAN THOMAS, RICHARD W. BROWN, DAVID A. WELTE, DAVID M. CHAO, CHARLES GERMAN, ALBERZINE FREEMAN, AND ALEJANDRO SANCHEZ ALVARADO, ALL DIRECTORS OF SIMR, HAVE A BUSINESS RELATIONSHIP. JONATHAN THOMAS, RICHARD W. BROWN, DAVID A. WELTE, DAVID M. CHAO, CHARLES GERMAN, RODERICK L. STURGEON, AND ALBERZINE FREEMAN, DIRECTORS OF SIMR, AND BRENT KREIDER, OFFICER OF SIMR, HAVE A BUSINESS RELATIONSHIP. DAVID A. WELTE, RICHARD W. BROWN, CHARLES GERMAN, AND RODERICK L. STURGEON, DIRECTORS OF SIMR, AND BRENT KREIDER, OFFICER OF SIMR, HAVE A BUSINESS RELATIONSHIP. PART VI, LINE 11B: THE DATA AND INFORMATION NECESSARY TO PREPARE SIMR'S FORM 990 WAS COMPILED BY SIMR'S ACCOUNTING DEPARTMENT AND THEN REVIEWED BY THE INSTITUTE'S TAX ATTORNEY AT BRYAN CAVE LEIGHTON PAISNER, LLP. PRICEWATERHOUSECOOPERS ("PWC"), THE INSTITUTE'S EXTERNAL TAX PREPARERS, USED THIS INFORMATION TO PREPARE THE FORM 990. THE COMPLETED FORM 990, INCLUDING REQUIRED SCHEDULES, IS REVIEWED BY THE OFFICERS OF SIMR BEFORE IT IS FILED WITH THE IRS. AFTER THE PREPARATION AND REVIEW PROCESS DESCRIBED ABOVE, THE FORM 990, INCLUDING REQUIRED SCHEDULES, IS PROVIDED TO EACH VOTING MEMBER OF THE ORGANIZATION'S BOARD BEFORE IT IS FILED WITH THE IRS. PART VI, LINE 12C: SIMR HAS ADOPTED A "CONFLICTS OF INTEREST AND DIRECTOR INDEPENDENCE POLICY". EACH DIRECTOR, OFFICER, AND ALL OTHER PERSONS IN A POSITION TO EXERCISE SUBSTANTIAL INFLUENCE OVER DECISIONS OF SIMR ARE REQUIRED TO ANNUALLY COMPLETE AND SIGN A DISCLOSURE STATEMENT THAT IS PART OF THE POLICY. A COVERED PERSON MUST ALSO DISCLOSE THE EXISTENCE OF A POTENTIAL CONFLICT AND ALL MATERIAL FACTS TO THE GOVERNING BOARD AS SOON AS THE PERSON HAS KNOWLEDGE THAT A POTENTIAL CONFLICT MIGHT EXIST. SIMR CONDUCTS PERIODIC AND ADHOC REVIEWS OF TRANSACTIONS AND AGREEMENTS TO ENSURE THAT IT ENGAGES ONLY IN ACTIVITIES THAT ARE CONSISTENT WITH ITS TAX-EXEMPT PURPOSE. PART VI, LINE 15A: THE COMPENSATION FOR DAVID CHAO, THE PRESIDENT AND CEO OF SIMR THROUGH 10/10/2020, WAS ESTABLISHED PURSUANT TO THE PROCEDURES OF TREAS. REG. SECTION 53.4958-6, INCLUDING (1) REVIEW AND APPROVAL BY SIMR'S COMPENSATION COMMITTEE COMPRISED OF INDEPENDENT PERSONS, (2) RELYING ON COMPARABILITY DATA, INCLUDING DATA PREPARED BY A NATIONALLY KNOWN COMPENSATION CONSULTANT REGARDING COMPARABLE SALARY AND BENEFITS FOR SIMILARLY QUALIFIED PERSONS IN FUNCTIONALLY COMPARABLE POSITIONS AT SIMILARLY SITUATED ORGANIZATIONS, AND (3) CONTEMPORANEOUS DOCUMENTATION AND RECORD KEEPING OF THE DELIBERATION AND DECISIONS REGARDING THE COMPENSATION ARRANGEMENT. THIS PROCESS WAS LAST UNDERTAKEN IN 2020. PART VI, LINE 19: SIMR'S GOVERNING DOCUMENTS, CONFLICT OF INTEREST POLICY, AND FINANCIAL STATEMENTS ARE AVAILABLE UPON REQUEST. PART VII, SECTION A, COLUMN B: DAVID M. CHAO, OFFICER OF SIMR THROUGH 10/10/2020, PERFORMED SUPPORT SERVICES FOR ONE OR MORE OF THE RELATED ORGANIZATIONS DISCLOSED IN SCHEDULE R. THESE SERVICES WERE PERFORMED IN HIS ROLE AS A SIMR EMPLOYEE AND SIMR IS REIMBURSED BY THE RELATED ORGANIZATIONS. PART VII, SECTION B: SIMR RECEIVES INVESTMENT MANAGEMENT SERVICES FROM AMERICAN CENTURY INVESTMENTS ("ACI"). ACI IS A WHOLLY OWNED SUBSIDIARY OF AMERICAN CENTURY COMPANIES, INC. ("ACCI"). IN SELECTING ACI TO MANAGE ITS LIQUID INVESTMENTS, SIMR NOT ONLY CHOSE A HIGH QUALITY MUTUAL FUND COMPANY WITH AN OUTSTANDING TRACK RECORD, BUT ALSO PLACED ITS LIQUID INVESTMENTS IN A COMPANY IN WHICH IT OWNS STOCK AND RECEIVES DIVIDENDS. SIMR PAYS ACI THE SAME ADMINISTRATIVE FEES FOR THESE SERVICES AS ANY ARMS-LENGTH INVESTOR. THOSE INVESTMENT FEES FOR A SHARED INVESTMENT POOL ARE PAID BY ITS SUPPORTING ORGANIZATION, STOWERS RESOURCE MANAGEMENT. PART XI, LINE 9: OTHER CHANGES IN NET ASSETS INCLUDE THE FOLLOWING: CHANGE IN ANNUITY RECEIVABLE, NET ($208,120) |
| PART III, LINE 4A: | 2020 PROGRAM SERVICE ACCOMPLISHMENTS THE STOWERS INSTITUTE FOR MEDICAL RESEARCH ("SIMR") IS A PRIVATE, NONPROFIT MEDICAL RESEARCH ORGANIZATION. SIMR WAS FOUNDED IN 1994 BY JIM AND VIRGINIA STOWERS, WHO EACH SURVIVED A BOUT WITH CANCER AND SUBSEQUENTLY DEDICATED THEIR FORTUNE TO SUPPORTING BASIC RESEARCH IN CELL AND MOLECULAR BIOLOGY THAT WILL PROVIDE LONG-TERM SOLUTIONS TO HUMAN DISEASES. SIMR CONDUCTS BASIC BIOMEDICAL RESEARCH IN THE PUBLIC INTEREST THAT WILL ULTIMATELY PROVIDE A GREATER UNDERSTANDING OF THE GENES AND PROTEINS THAT CONTROL HOW CELLS IN OUR BODIES MULTIPLY, FORM TISSUES, AND DIE. STUDYING THE BASIC BIOLOGY OF CELLS ENABLES SCIENTISTS TO DISCOVER HOW GENES CAUSE MANY DISEASES, INCLUDING CANCER, BIRTH DEFECTS, AND DEMENTIA. HISTORY HAS SHOWN THAT BASIC MEDICAL RESEARCH IS OFTEN A KEY FIRST STEP IN THE DEVELOPMENT OF NEW TREATMENTS, CURES, AND PREVENTIONS FOR MANY HUMAN DISEASES. 2020 NOTABLE RESEARCH RESULTS IN 2020, SIMR RESEARCH TEAMS MADE DISCOVERIES MERITING PUBLICATION IN LEADING PEER-REVIEWED SCIENTIFIC JOURNALS - FIFTY-NINE ORIGINAL RESEARCH PAPERS IN ALL. SIMR RESEARCH TEAMS ALSO PRODUCED TWENTY-NINE OTHER PUBLICATIONS INCLUDING REVIEWS, COMMENTARIES, BOOK CHAPTERS, AND BOOKS. SOME OF THE HIGHLIGHTS AMONG THESE PAPERS AND OTHER ADVANCES INVOLVING STOWERS RESEARCH INCLUDE THE FOLLOWING: THE SI LAB CHARACTERIZED THE STRUCTURE OF A PROTEIN CALLED ORB2, WHICH IS NEEDED FOR LONG-TERM MEMORY FORMATION AND PERSISTENCE, AT ATOMIC-LEVEL RESOLUTION. PREVIOUS WORK BY THE SI LAB AND OTHERS HAD INDICATED THAT ORB2 MAY BE ABLE TO ADOPT THE SHAPE OF AN AMYLOID AS PART OF ITS NORMAL AND NECESSARY FUNCTION. HOWEVER, IT HAD NOT BEEN ESTABLISHED THAT ORB2 EXISTS IN THE BRAIN AS A BONA FIDE AMYLOID, AS ITS STRUCTURE WAS NOT PREVIOUSLY KNOWN. THE SI LAB PURIFIED ORB2 FROM ITS NATIVE SOURCE (THE BRAINS OF MILLIONS OF FRUIT FLIES) AND DEMONSTRATED THAT IT DOES INDEED EXIST AS A FUNCTIONAL AMYLOID WITHIN THE BRAIN. THIS STUDY MARKS THE FIRST TIME AN AMYLOID WITH A KNOWN BIOLOGICAL FUNCTION HAS EVER BEEN PURIFIED AND DESCRIBED STRUCTURALLY FROM THE BRAIN. THESE FINDINGS RAISE TWO INTERESTING POSSIBILITIES THAT WILL BE FURTHER PURSUED IN THE SI LAB-THE POSSIBILITY THAT SUCH A FUNCTIONING NEURONAL AMYLOID ALSO EXISTS IN HUMANS, AND THE POSSIBILITY THAT OTHER PROTEINS, KNOWN TO HAVE SPECIFIC FUNCTIONS, ARE CAPABLE OF ACHIEVING AMYLOID STATES TO ACHIEVE ALTERNATE FUNCTIONS. THIS WORK WAS PUBLISHED ONLINE MARCH 13, 2020, IN SCIENCE. THE WASHBURN LAB COMBINED SEVERAL PROTEOMICS TECHNOLOGIES TO STUDY PROTEIN NETWORKS AND OBTAIN DETAILED INFORMATION ABOUT THE SPATIAL ARRANGEMENT OF NEIGHBORING SURFACES WITHIN MULTI-PROTEIN COMPLEXES. IN PARTICULAR, THE RESEARCHERS FOCUSED ON SIN3/HDAC, A LARGE MULTI-PROTEIN COMPLEX THAT IS NORMALLY RESPONSIBLE FOR "TURNING OFF" A SPECIFIC SET OF GENES. WHEN ITS MAIN SCAFFOLD IS MUTATED, THE COMPLEX IS ALSO IMPLICATED IN CANCER BIOLOGY, AND IS TARGETED FOR TREATMENT OF MANY HUMAN CANCERS, INCLUDING TRIPLE NEGATIVE BREAST CANCER AND PANCREATIC CANCER. ALTHOUGH SIN3/HDAC HAS BEEN WELL STUDIED AND ITS COMPONENT SUBUNITS HAVE BEEN IDENTIFIED, GETTING A CLEAR PICTURE OF HOW THE SUBUNITS ASSEMBLE HAS BEEN DIFFICULT. THE RESEARCHERS COMBINED THREE EXISTING APPROACHES-AFFINITY TAG PROTEIN PURIFICATION, CHEMICAL CROSSLINKING WITH HIGH RESOLUTION MASS SPECTROMETRY, AND COMPUTATIONAL MOLECULAR MODELING WITH PROTEIN DOCKING-TO PINPOINT SPECIFIC SURFACES, WITHIN THE INTACT PROTEIN COMPLEX, THAT ARE IN VERY CLOSE PROXIMITY WITH EACH OTHER. IN TOTAL, THEY IDENTIFIED 66 INTER-PROTEIN CROSSLINKS (BETWEEN TWO DIFFERENT PROTEINS) AND 63 SELF-CROSSLINKS (WITHIN THE SAME PROTEIN) FOR 13 SIN3/HDAC SUBUNITS. MORE GENERALLY, USING THE COMBINED TECHNOLOGIES ALLOWS RESEARCHERS TO PINPOINT INTERACTING SURFACES IN VIRTUALLY ANY PROTEIN COMPLEX, OBTAINED FROM ANY SOURCE. THIS STUDY WAS PUBLISHED ONLINE APRIL 14, 2020, IN CELL REPORTS. THE LI LAB REPORTED A PROMISING NEW STRATEGY TO OVERCOME DRUG RESISTANCE IN LEUKEMIA, USING TARGETED DOSES OF THE WIDELY USED CHEMOTHERAPY DRUG DOXORUBICIN. THE FINDINGS WERE THE RESULT OF A DECADE-SPANNING COLLABORATIVE EFFORT AMONG RESEARCHERS AT THE STOWERS INSTITUTE FOR MEDICAL RESEARCH, CHILDREN'S MERCY KANSAS CITY, THE UNIVERSITY OF KANSAS CANCER CENTER, AND OTHER INSTITUTIONS, EVOLVING FROM STUDIES IN THE LI LAB. THE RESEARCHERS FOUND THAT LOW DOSES OF DOXORUBICIN, A STANDARD TREATMENT FOR SEVERAL TYPES OF CANCER INCLUDING LEUKEMIA, INHIBITS TWO MOLECULAR PATHWAYS-WNT/BETA-CATENIN AND PI3K/AKT-WHICH WORK CLOSELY TOGETHER TO PROMOTE TUMOR GROWTH AND RESISTANCE TO THERAPY. THE TEAM ALSO FOUND THAT LOW-DOSE BUT NOT HIGH-DOSE DOXORUBICIN ACTIVATED ANTICANCER IMMUNITY AGAINST THERAPY-RESISTANT LEUKEMIA STEM CELLS, AN UNEXPECTED AND NOVEL DISCOVERY. THE RESEARCH HOLDS PROMISE AS A MORE EFFECTIVE STRATEGY TO OVERCOME CANCER THERAPY RESISTANCE AND STIMULATE IMMUNITY THAT CAN BE USED IN COMBINATION WITH OTHER CANCER THERAPIES INCLUDING CHEMOTHERAPY, RADIATION, AND IMMUNOTHERAPY FOR PATIENTS WITH LEUKEMIA AND OTHER TYPES OF CANCER. LOW-DOSE DOXORUBICIN ALSO AVOIDS THE HARSH SIDE EFFECTS OF HIGH-DOSE DOXORUBICIN, POTENTIALLY OFFERING PATIENTS A BETTER QUALITY OF LIFE. THE FINDINGS WERE PUBLISHED ONLINE APRIL 20, 2020, IN NATURE CELL BIOLOGY. THE GERTON LAB DESCRIBED A DETAILED STUDY OF THE PLACENTAS OF MOUSE MODELS OF CORNELIA DE LANGE SYNDROME. PEOPLE WITH THIS RARE GENETIC DISORDER OFTEN HARBOR MUTATIONS IN COHESINS, RING-LIKE PROTEINS THAT HELP DNA ORGANIZE AND REPAIR ITSELF. THE RESEARCHERS DISCOVERED THAT THE CORNELIA DE LANGE MOUSE MODEL PLACENTAS ACCUMULATED DAMAGE TO THEIR DNA, ENTERED A PERMANENT GROWTH-ARRESTED STATE KNOWN AS SENESCENCE, AND CHURNED OUT PRO-INFLAMMATORY CYTOKINES THAT AFFECTED THE GROWTH OF THE EMBRYONIC MICE. THESE FINDINGS HAVE IMPORTANT IMPLICATIONS FOR UNDERSTANDING THE CRUCIAL ROLE THAT THE PLACENTA PLAYS IN MAMMALIAN DEVELOPMENT AND SUGGEST THAT TARGETING CYTOKINE SIGNALING MAY BE A WAY TO PROTECT THE HEALTH OF THE PLACENTA AND PROMOTE HEALTHY PREGNANCIES. THE STUDY WAS PUBLISHED ON JUNE 16, 2020, IN DEVELOPMENTAL CELL. THE BAZZINI LAB USED THE GENE-EDITING TOOL CRISPR TO TARGET GENE MESSAGES IN ANIMAL EMBRYOS TO GAIN A BETTER UNDERSTANDING OF THE GENETIC PROGRAMS THAT DIRECT EARLY STAGES OF VERTEBRATE DEVELOPMENT. THE RESEARCHERS AND THEIR COLLABORATORS SHOWED THAT THE TECHNOLOGY, CALLED CRISPR-CAS13, IS ABLE TO TARGET RNA-DNA'S CHEMICAL COUSIN THAT CARRIES MESSAGES NEEDED TO CONSTRUCT PROTEINS-IN ANIMAL EMBRYOS IN A SPECIFIC AND SYSTEMATIC MANNER, ALLOWING RESEARCHERS TO STUDY THE ROLE OF RNA IN THE EARLIEST HOURS OF DEVELOPMENT. THE RESEARCHERS SHOW THAT THE CRISPR-CAS13 METHOD IS EFFECTIVE IN ZEBRAFISH, KILLIFISH, MEDAKA, AND MOUSE EMBRYOS, AND THUS COULD BE USED TO EXPLORE EARLY DEVELOPMENTAL GENETIC PROGRAMS IN A BROAD RANGE OF ANIMAL SPECIES. THE STUDY WAS PUBLISHED ONLINE AUGUST 7, 2020, IN DEVELOPMENTAL CELL. |
| THE ZANDERS LAB UNCOVERED A STRATEGY THAT THE S. POMBE FISSION YEAST | GENOME CAN USE TO MINIMIZE SOME OF THE WORST EFFECTS CONFERRED BY PARASITIC GENE ELEMENTS KNOWN AS MEIOTIC DRIVERS. THE MEIOTIC DRIVERS ANALYZED IN THE STUDY HAVE THE ABILITY TO SHORT-CIRCUIT THE CONVENTIONAL LAW OF MENDELIAN SEGREGATION, WHICH USUALLY ENSURES THAT EACH GAMETE (REPRODUCTIVE CELL) RECEIVES ONE OF TWO COPIES OF EACH CHROMOSOME FROM THE PARENT CELL WITH EQUAL TRANSMISSION. MEIOTIC DRIVERS INSTEAD CAN "POISON" GAMETES THAT DO NOT CONTAIN THEIR GENETIC SEQUENCE, THEREBY SWINGING THE TRANSMISSION RATE IN THEIR FAVOR. AS A WAY OF ENABLING THE SURVIVAL OF SOME GAMETES THAT WOULD OTHERWISE DIE, THE S. POMBE GENOME CAN EMPLOY VARIANTS OF OTHER GENES TO CREATE A SITUATION THAT "PROTECTS" THEM, EVEN IF IT COMES AT A COST TO FITNESS. FOR EXAMPLE, A MUTATION IN REC12, A GENE RESPONSIBLE FOR PROPER CHROMOSOME SEGREGATION, LED TO GAMETES HAVING EXTRA CHROMOSOMES. WHILE EXTRA CHROMOSOMES ARE USUALLY UNDESIRABLE, IN THIS SCENARIO THEY ENABLED MORE GAMETES TO SURVIVE. THIS SURPRISING INSIGHT INTO MEIOTIC DRIVERS AND HOW THEY CAN BE SUPPRESSED COULD HELP RESEARCHERS BETTER UNDERSTAND THE FORCES THAT SHAPE THE EVOLUTION OF GAMETE FORMATION, AS WELL AS THOSE UNDERLYING HUMAN INFERTILITY. THIS RESEARCH WAS PUBLISHED ONLINE AUGUST 13, 2020, IN ELIFE. THE SNCHEZ ALVARADO LAB PUBLISHED A STUDY RELATED TO THE FUNDAMENTAL BIOLOGICAL QUESTION OF WHY SOME VERTEBRATE ANIMALS REGENERATE EXTENSIVELY WHILE OTHERS, SUCH AS MAMMALS, DO NOT. THE RESEARCHERS COMPARED THE REGENERATION PROCESS IN TWO SPECIES OF BONY FISH, ZEBRAFISH AND AFRICAN KILLIFISH, TO IDENTIFY SIMILARITIES AND DIFFERENCES IN THE GENOMIC RESPONSES UNDERLYING THE PROCESS. THE RESEARCHERS FOUND BOTH SPECIES-SPECIFIC AND EVOLUTIONARILY CONSERVED RESPONSES. THE CONSERVED RESPONSES REVEALED THE PRESENCE OF PARTICULAR DNA SEQUENCES CALLED REGENERATION-RESPONSIVE ENHANCERS (RRES) THAT ARE ALSO PRESENT IN MAMMALIAN GENOMES. SOME RRES APPEAR TO HAVE BEEN REPURPOSED DURING EVOLUTION, RESULTING IN A LOSS OF REGENERATIVE CAPACITY IN SOME SPECIES. THIS RESEARCH HELPS IDENTIFY MECHANISMS UNDERPINNING REGENERATIVE CAPACITY AND FURTHERS OUR UNDERSTANDING OF THE LONG-STANDING PROBLEM OF WHY SOME SPECIES CAN REGENERATE MISSING BODY PARTS AFTER AMPUTATION WHEREAS OTHERS CANNOT. THIS WORK WAS PUBLISHED ONLINE SEPTEMBER 4, 2020, IN SCIENCE. THE KRUMLAUF LAB IDENTIFIED TINY DIFFERENCES IN A KEY PROTEIN SEQUENCE THAT CAN HAVE AN IMPORTANT IMPACT ON HOW SPECIES EVOLVE. THE BREAKTHROUGH DISCOVERY SHEDS LIGHT ON THE EVOLUTION OF THE GENE REGULATORY NETWORKS THAT DRIVE DIVERSITY AMONG ORGANISMS. THE RESEARCHERS USED MODERN GENE EDITING TECHNOLOGIES TO REPLACE THE LABIAL HOX GENE IN THE FRUIT FLY WITH THE THREE RELATED GENES IN THE MOUSE-HOXA1, B1, AND D1. THEY FOUND REPLACING LABIAL FUNCTION WITH HOXA1 IN FRUIT FLIES RESTORES ITS ORIGINAL FUNCTION, BUT B1 AND D1 DO NOT, SUGGESTING THAT A1 RETAINS AN ANCESTRAL FUNCTION THAT HAS SURVIVED 600 MILLION YEARS OF EVOLUTION, WHILE B1 AND D1 HAVE DIVERGED. THE RESEARCHERS PINPOINTED A SIX AMINO ACID SEQUENCE CRITICAL FOR THE ANCESTRAL FUNCTION OF A1, WHICH IS IMPORTANT FOR MODULATING INTERACTIONS WITH OTHER PROTEINS. THE WORK PAVES THE WAY FOR ADDITIONAL STUDIES ON THE EVOLUTION OF PROTEIN ACTIVITY AS WELL AS FURTHER EXPLORATION INTO THE ROLE OF TOOLKIT GENES IN GENE DUPLICATION AND DIVERGENCE. THE STUDY WAS PUBLISHED ONLINE NOVEMBER 12, 2020, IN GENES AND DEVELOPMENT. COMPREHENSIVE LISTS OF 2020 ORIGINAL RESEARCH PAPERS, REVIEWS, COMMENTARIES, CHAPTERS, AND BOOKS |
| ORIGINAL RESEARCH PAPERS | 1. YEAST NUAK1 PHOSPHORYLATES HISTONE H3 THREONINE 11 IN LOW GLUCOSE STRESS BY THE COOPERATION OF AMPK AND CK2 SIGNALING. OH S, LEE J, SWANSON SK, FLORENS L, WASHBURN MP, WORKMAN JL. ELIFE. 2020;9:E64588 DOI: 64510.67554/ELIFE.64588. 2. THE PLASTICITY OF THE PYRUVATE DEHYDROGENASE COMPLEX CONFERS A LABILE STRUCTURE THAT IS ASSOCIATED WITH ITS CATALYTIC ACTIVITY. LEE J, OH S, BHATTACHARYA S, ZHANG Y, FLORENS L, WASHBURN MP, WORKMAN JL. PLOS ONE. 2020;15:E0243489. DOI: 10.1371/JOURNAL.PONE.0243489. 3. THE ROLE OF GENE DOSAGE IN BUDDING YEAST CENTROSOME SCALING AND SPONTANEOUS DIPLOIDIZATION. CHEN J, XIONG Z, MILLER DE, YU Z, MCCROSKEY S, BRADFORD WD, CAVANAUGH AM, JASPERSEN SL. PLOS GENET. 2020;16:E1008911. DOI: 1008910.1001371/JOURNAL.PGEN.1008911. 4. DRIVING INTEGRATIVE STRUCTURAL MODELING WITH SERIAL CAPTURE AFFINITY PURIFICATION. LIU X, ZHANG Y, WEN Z, HAO Y, BANKS CAS, LANGE JJ, SLAUGHTER BD, UNRUH JR, FLORENS L, ABMAYR SM, WORKMAN JL, WASHBURN MP. PROC NATL ACAD SCI U S A. 2020;117:31861-31870. 5. HIGH-THROUGHPUT IDENTIFICATION OF NUCLEAR ENVELOPE PROTEIN INTERACTIONS IN SCHIZOSACCHAROMYCES POMBE USING AN ARRAYED MEMBRANE YEAST-TWO HYBRID LIBRARY. VARBERG JM, GARDNER JM, MCCROSKEY S, SARAVANAN S, BRADFORD WD, JASPERSEN SL. G3 (BETHESDA). 2020. 6. SWR1-INDEPENDENT ASSOCIATION OF H2A.Z TO THE LINC COMPLEX PROMOTES MEIOTIC CHROMOSOME MOTION. GONZALEZ-ARRANZ S, GARDNER JM, YU Z, PATEL NJ, HELDRICH J, SANTOS B, CARBALLO JA, JASPERSEN SL, HOCHWAGEN A, SAN-SEGUNDO PA. FRONT CELL DEV BIOL. 2020;8:594092. 7. A SIX-AMINO-ACID MOTIF IS A MAJOR DETERMINANT IN FUNCTIONAL EVOLUTION OF HOX1 PROTEINS. SINGH NP, DE KUMAR B, PAULSON A, PARRISH ME, ZHANG Y, FLORENS L, CONAWAY JW, SI K, KRUMLAUF R. [PUBLISHED AHEAD OF PRINT NOVEMBER 14 2020]. GENES DEV. 2020. 8. IDENTIFICATION AND CHARACTERIZATION OF BREAKPOINTS AND MUTATIONS ON DROSOPHILA MELANOGASTER BALANCER CHROMOSOMES. MILLER DE, KAHSAI L, BUDDIKA K, DIXON MJ, KIM BY, CALVI BR, SOKOL NS, HAWLEY RS, COOK KR. G3(BETHESDA). 2020;10:4271-4285. 9. WTF4 MEIOTIC DRIVER UTILIZES CONTROLLED PROTEIN AGGREGATION TO GENERATE SELECTIVE CELL DEATH. NUCKOLLS NL, MOK AC, LANGE JJ, YI K, KANDOLA TS, HUNN AM, MCCROSKEY S, SNYDER JL, BRAVO NUNEZ MA, MCCLAIN M, MCKINNEY SA, WOOD C, HALFMANN R, ZANDERS SE. ELIFE. 2020;9:E55694. DOI: 55610.57554/ELIFE.55694. 10. THE MEDIATOR SUBUNIT, MED23 IS REQUIRED FOR EMBRYONIC SURVIVAL AND REGULATION OF CANONICAL WNT SIGNALING DURING CRANIAL GANGLIA DEVELOPMENT. DASH S, BHATT S, SANDELL L, SEIDEL C, AHN Y, KRUMLAUF R, TRAINOR P. FRONT PHYSIOL. 2020;11:531933. DOI: 531910.533389/FPHYS.532020.531933. 11. GENETIC BACKGROUND IMPACTS THE TIMING OF SYNAPTONEMAL COMPLEX BREAKDOWN IN DROSOPHILA MELANOGASTER. WESLEY ER, HAWLEY RS, BILLMYRE KK. [PUBLISHED AHEAD OF PRINT OCTOBER 18 2020]. CHROMOSOMA. 2020. 12. 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HU CK, WANG W, BRIND'AMOUR J, SINGH PP, REEVES GA, LORINCZ MC, SNCHEZ ALVARADO A, BRUNET A. SCIENCE. 2020;367:870-874. 50. SUPER-RESOLUTION MICROSCOPY-BASED BIMOLECULAR FLUORESCENCE COMPLEMENTATION TO STUDY PROTEIN COMPLEX ASSEMBLY AND CO-LOCALIZATION. CHEN J, YU Z, UNRUH JR, SLAUGHTER BD, JASPERSEN SL. BIO-PROTOCOL. 2020;10:E3524. DOI: 3510.21769/BIOPROTOC.23524. 51. DROSOPHILA YBX1 HOMOLOG YPS PROMOTES OVARIAN GERM LINE STEM CELL DEVELOPMENT BY PREFERENTIALLY RECOGNIZING 5-METHYLCYTOSINE RNAS. ZOU F, TU R, DUAN B, YANG Z, PING Z, SONG X, CHEN S, PRICE A, LI H, SCOTT A, PERERA A, LI S, XIE T. PROC NATL ACAD SCI U S A. 2020;117:3603-3609. 52. DRAMATICALLY DIVERSE SCHIZOSACCHAROMYCES POMBE WTF MEIOTIC DRIVERS ALL DISPLAY HIGH GAMETE-KILLING EFFICIENCY. BRAVO NUNEZ MA, SABBARINI IM, EICKBUSH MT, LIANG Y, LANGE JJ, KENT AM, ZANDERS SE. PLOS GENET. 2020;16:E1008350. DOI: 1008310.1001371/JOURNAL.PGEN.1008350. 53. COMPARATIVE TRANSCRIPTOME ANALYSIS OF WILD AND LAB POPULATIONS OF ASTYANAX MEXICANUS UNCOVERS DIFFERENTIAL EFFECTS OF ENVIRONMENT AND MORPHOTYPE ON GENE EXPRESSION. KRISHNAN J, PERSONS JL, PEUSS R, HASSAN H, KENZIOR A, XIONG S, OLSEN L, MALDONADO E, KOWALKO JE, ROHNER N. [PUBLISHED AHEAD OF PRINT FEBRUARY 6 2020]. J EXP ZOOL B MOL DEV EVOL. 2020. 54. SYNAPTONEMAL COMPLEX-DEFICIENT DROSOPHILA MELANOGASTER FEMALES EXHIBIT RARE DSB REPAIR EVENTS, RECURRENT COPY-NUMBER VARIATION, AND AN INCREASED RATE OF DE NOVO TRANSPOSABLE ELEMENT MOVEMENT. MILLER DE. G3 (BETHESDA). 2020;10:525-537. 55. THE CHROMATIN BOUND PROTEOME OF THE HUMAN MALARIA PARASITE. BATUGEDARA G, LU XM, SARAF A, SARDIU ME, CORT A, ABEL S, PRUDHOMME J, WASHBURN MP, FLORENS L, BUNNIK EM, LE ROCH KG. MICROB GENOM. 2020;6:E000327. DOI: 000310.001099/MGEN.000320.000327. 56. STRIPAK DIRECTS PP2A ACTIVITY TOWARD MAP4K4 TO PROMOTE ONCOGENIC TRANSFORMATION. 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| REVIEWS, COMMENTARIES, CHAPTERS, AND BOOKS | 1. INTRODUCTION TO THE SPECIAL ISSUE - CAVEFISH - ADAPTATION TO THE DARK. KOWALKO JE, FRANZ-ODENDAAL TA, ROHNER N. J EXP ZOO PT B MOL DEV EVOL. 2020;334:393-396./ 2. SEVEN MYTHS OF HOW TRANSCRIPTION FACTORS READ THE CIS-REGULATORY CODE. ZEITLINGER J. CURR OPIN SYST BIOL. 2020;23:22-31. 3. RESISTANCE TO NATURAL AND SYNTHETIC GENE DRIVE SYSTEMS. PRICE TAR, WINDBICHLER N, UNCKLESS RL, SUTTER A, RUNGE JN, ROSS PA, POMIANKOWSKI A, NUCKOLLS NL, MONTCHAMP-MOREAU C, MIDEO N, MARTIN OY, MANSER A, LEGROS M, LARRACUENTE AM, HOLMAN L, GODWIN J, GEMMELL N, COURRET C, BUCHMAN A, BARRETT LG, LINDHOLM AK. J EVOL BIOL. 2020;33:1345-1360. 4. ANATOMY OF THE FUNGAL MICROTUBULE ORGANIZING CENTER, THE SPINDLE POLE BODY. JASPERSEN SL. ANATOMY OF THE FUNGAL MICROTUBULE ORGANIZING CENTER, THE SPINDLE POLE BODY. CURR OPIN STRUCT BIOL. 2020;66:22-31. 5. THE SAGA CHROMATIN-MODIFYING COMPLEX: THE SUM OF ITS PARTS IS GREATER THAN THEWHOLE. SOFFERS JHM, WORKMAN JL. GENES DEV. 2020;34:1287-1303. 6. IMPLICATIONS OF THE ORB2 AMYLOID STRUCTURE IN HUNTINGTON'S DISEASE. HERVAS R, MURZIN AG, SI K. INT J MOL SCI. 2020;21:E6910. DOI: 6910.3390/IJMS21186910. 7. TO BEAD OR NOT TO BEAD? THAT IS THE QUESTION WITH CROSS-LINKING MASS SPECTROMETRY. FLORENS L, HAO Y, ZHANG Y, WEN Z, BANKS CAS, WASHBURN MP. J BIOMOL TECH : JBT. 2020;31:S24. 8. ALTERNATIVE SYNAPTONEMAL COMPLEX STRUCTURES: TOO MUCH OF A GOOD THING?. HUGHES SE, HAWLEY RS. [PUBLISHED AHEAD OF PRINT AUGUST 13 2020]. TRENDS GENET. 2020. 9. IN THE SPOTLIGHT-EARLY CAREER RESEARCHER. ROHNER N. J EXP ZOOL PT B MOL DEV EVOL. 2020;334:387-388. 10. THE SOCIETY FOR CRANIOFACIAL GENETICS AND DEVELOPMENTAL BIOLOGY 42ND ANNUAL MEETING. EISENHOFFER GT, JR., CLOUTHIER D, COX T, SAINT-JEANNET JP, TANEYHILL LA, TRAINOR PA, MOODY SA. AM J MED GENET A. 2020;182:1555-1561. 11. A HOX GENE REGULATORY NETWORK FOR HINDBRAIN SEGMENTATION. PARKER HJ, KRUMLAUF R. CURR TOP DEV BIOL. 2020;139:169-203. 12. OVERCOMING RESISTANCE TO IMMUNOTHERAPY BY TEACHING OLD DRUGS NEW TRICKS. PERRY JM, LI L. MOL CELL ONCOL. 2020;7:E1801088. DOI:10.1080/23723556.2020.1801088. 13. A REVIEW ON HISTOTECHNOLOGY PRACTICES IN COVID-19 PATHOLOGY INVESTIGATIONS. MALLOY S, WANG Y.[PUBLISHED ONLINE AHEAD OF PRINT JULY 2020]. J HISTOTECHNOL. 2020;1-6. DOI:10.1080/01478885.2020.1779484. 14. NEW AND IMPROVED TOOLS FOR THE OMICS CREW. FLORENS, L., DONG, M.-Q., LABAER, J. J PROTEOME RES 2020;19:2525-2528. DOI:10.1021/ACS.JPROTEOME.0C00328. 15. SAGA STRUCTURES PROVIDE MECHANISTIC MODELS FOR GENE ACTIVATION. SOFFERS JHM, POPOVA VV, WORKMAN JLW. TRENDS BIOCHEM SCI. 2020;45:547-549. 16. MEIOTIC DRIVE. SRINIVASA AN, ZANDERS SE. MEIOTIC DRIVE. CURR BIOL. 2020;30:R627-R629. 17. THE DEVELOPMENT, PATTERNING AND EVOLUTION OF NEURAL CREST CELL DIFFERENTIATION INTO CARTILAGE AND BONE. DASH S, TRAINOR P. [PUBLISHED ONLINE AHEAD OF PRINT MAY 14 2020]. BONE. 2020;115409. DOI:10.1016/J.BONE.2020.115409. 18. IDENTIFYING VITAMIN A SIGNALING BY VISUALIZING GENE AND PROTEIN ACTIVITY, AND BY QUANTIFICATION OF VITAMIN A METABOLITES. SHANNON SR, YU J, DEFNET AE, BONGFELDT D, MOISE AR, KANE MA, TRAINOR PA. METHODS ENZYMOL. 2020;637:367-418. 19. GENERATION AND ISOLATION OF RECOMBINANT RETINOID OXIDOREDUCTASE COMPLEX. ADAMS MK, BELYAEVA OV, KEDISHVILI NY. METHODS ENZYMOL. 2020;637:77-93. 20. A REVIEW OF THE SCIENTIFIC RIGOR, REPRODUCIBILITY, AND TRANSPARENCY STUDIES CONDUCTED BY THE ABRF RESEARCH GROUPS. MISCHE SM, FISHER NC, MEYN SM, SOL-CHURCH K, HEGSTAD-DAVIES RL, WEIS-GARCIA F, ADAMS M, ASHTON JM, DELVENTHAL KM, DRAGON JA, HOLMES L, JAGTAP P, KUBOW KE, MASON CE, PALMBLAD M, SEARLE BC, TURCK CW, KNUDTSON KL. JBT. 2020;31:11-26. 21. MEIOSIS: LOCATION, LOCATION, LOCATION, HOW CROSSOVERS ENSURE SEGREGATION. HUGHES, S. E., HAWLEY, R. S. CURR BIOL. 2020 APR 6;30(7):R311-R313 22. AN INTERDISCIPLINARY APPROACH TO INVESTIGATE COLLECTIVE CELL MIGRATION IN NEURAL CREST. GINIUNAITE R, MCLENNAN R, MCKINNEY MC, BAKER RE, KULESA PM, MAINI PK. DEV DYN. 2020;249:270-280. 23. ATLAS OF THE HUMAN INTESTINE. HE XC, LI L. ATLAS OF THE HUMAN INTESTINE. J EXP MED. 2020;217:E20191997. DOI:20191910.20191084/JEM.20191997. 24. WHEN HISTONES ARE UNDER GLUCOSE STARVATION. LEE J, OH S, ABMAYR SM, WORKMAN JL. J BIOSCI. 2020;45:E17. 25. INTESTINAL EPITHELIAL REGENERATION: ACTIVE VERSUS RESERVE STEM CELLS AND PLASTICITY MECHANISMS. KARMAKAR S, DENG L, HE XC, LI L. AM J PHYSIOL GASTROINTEST LIVER PHYSIOL. 2020;318:G796-G802. 26. MODELLING COLLECTIVE CELL MIGRATION: NEURAL CREST AS A MODEL PARADIGM. GINIUNAITE R, BAKER RE, KULESA PM, MAINI PK. J MATH BIOL. 2020;80:481-04. 27. EXPORT AND TRANSPORTATION OF ZEBRAFISH. BARTON CL, BAUMANN DP, COX JD. IN: SC CARTNER, JS EISEN, SC FARMER, KJ GUILLEMIN, ML KENT, AND GE SANDERS, EDS. THE ZEBRAFISH IN BIOMEDICAL RESEARCH : BIOLOGY, HUSBANDRY, DISEASE, AND RESEARCH APPLICATIONS. ACADEMIC PRESS; 2020:443-450. 28. UNCEASINGLY SEARCHING FOR ANSWERS - AN INTERVIEW WITH CLAUDIO STERN. SNCHEZ-ALVARADO A. INT J DEV BIOL. 2021;65:131-136. EPUB 2020. 29. DARK WORLD RISES: THE EMERGENCE OF CAVEFISH AS A MODEL FOR THE STUDY OF EVOLUTION, DEVELOPMENT, BEHAVIOR, AND DISEASE. MCGAUGH SE, KOWALKO JE, DUBOUE E, LEWIS P, FRANZ-ODENDAAL TA, ROHNER N, GROSS JB, KEENE AC. J EXP ZOOL B MOL DEV EVOL. 2020 NOV;334(7-8):397-404. DOI: 10.1002/JEZ.B.22978. EPUB 2020 JUL 7. COMPETITIVE RESEARCH GRANT FUNDING & RESEARCH AWARDS & DISTINCTIONS THE ABILITY OF SIMR SCIENTISTS TO RECEIVE COMPETITIVELY AWARDED RESEARCH FUNDING ATTESTS TO THE HIGH LEVEL OF RESEARCH PRODUCTIVITY PRESENT AT SIMR. DURING 2020, SIMR SCIENTISTS WORKED WITH THE SUPPORT OF THIRTY-NINE GRANTS AND FELLOWSHIPS FROM THE NATIONAL INSTITUTES OF HEALTH, THREE GRANTS FROM THE NATIONAL SCIENCE FOUNDATION, ONE GRANT FROM THE MARCH OF DIMES, ONE GRANT FROM THE GREATER KANSAS CITY COMMUNITY FOUNDATION, ONE FELLOWSHIP FROM THE JANE COFFIN CHILDS MEMORIAL FUND, ONE AWARD FROM THE SEARLE SCHOLARS PROGRAM, ONE AWARD FROM THE PEW CHARITABLE TRUSTS, ONE AWARD FROM THE UNIVERSITY OF KANSAS ENDOWMENT ASSOCIATION, ONE GRANT FROM THE EDWARD MALLINCKRODT JR. FOUNDATION, ONE GRANT FROM THE JUVENILE DIABETES RESEARCH FOUNDATION, ONE GRANT FROM THE AMERICAN CANCER SOCIETY, ONE GRANT FROM THE SOCIETY FOR DEVELOPMENTAL BIOLOGY, ONE FROM THE ST. BALDRICK'S FOUNDATION AND ONE INVESTIGATOR AWARD FROM THE HOWARD HUGHES MEDICAL INSTITUTE. SUPPORT FROM NEW AND CONTINUING AWARDS TO SIMR TOTALED MORE THAN $6.7 MILLION IN 2020 TO SUPPLEMENT INCOME FROM ITS ENDOWMENTS. TESTIFYING TO THE HIGH LEVEL OF ACHIEVEMENT TAKING PLACE AT SIMR ARE THE AWARDS AND HONORS SIMR MEMBERS RECEIVED IN 2020: 1. JOAN CONAWAY, PHD, WAS ELECTED TO THE NATIONAL ACADEMY OF SCIENCES. 2. NICOLAS ROHNER, PHD, WAS AWARDED A FIVE-YEAR NIH DIRECTOR'S NEW INNOVATOR AWARD. HE ALSO RECEIVED A ONE-TIME SUBCONTRACT GRANT FROM BIONEXUS KC. 3. SARAH ZANDERS, PHD, WAS NAMED ONE OF SCIENCE NEWS' 2020 SN 10: SCIENTISTS TO WATCH. 4. KAUSIK SI RECEIVED A FIVE-YEAR NIH GRANT FROM THE NATIONAL INSTITUTE ON AGING AND AN NIH GRANT RENEWAL PROVIDING FIVE MORE YEARS OF FUNDING FROM THE NATIONAL INSTITUTE OF MENTAL HEALTH. 5. RON YU, PHD, WAS AWARDED A ONE-YEAR SUPPLEMENT FOR HIS NIH GRANT FROM THE NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS. 6. ARIEL BAZZINI, PHD, RECEIVED A FIVE-YEAR GRANT FROM THE NIH NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES. 7. RANDAL HALFMANN, PHD, WAS AWARDED A THREE-YEAR RESEARCH SCHOLAR GRANT FROM THE AMERICAN CANCER SOCIETY. 8. PAUL KULESA, PHD, RECEIVED A ONE-YEAR GRANT FROM THE ST. BALDRICK'S FOUNDATION. 9. YONGFU WANG, PHD, HEAD OF HISTOLOGY, WAS AWARDED THE LEICA LEADERSHIP IN MANAGEMENT AWARD FROM THE NATIONAL SOCIETY FOR HISTOTECHNOLOGY. 10. KATIE BILLMYRE, PHD, A POSTDOCTORAL RESEARCHER IN THE HAWLEY LAB, WAS AWARDED A FIVE-YEAR NIH PATHWAY TO INDEPENDENCE FELLOWSHIP AND A ONE-TIME DELILL NASSER AWARD FOR PROFESSIONAL DEVELOPMENT FROM THE GENETICS SOCIETY OF AMERICA. 11. SOMA DASH, PHD, A POSTDOCTORAL RESEARCHER IN THE TRAINOR LAB, WAS RECOGNIZED WITH A ONE-TIME FELLOWSHIP FROM THE AMERICAN ASSOCIATION FOR ANATOMY. 12. JEREMY SANDLER, PHD, A POSTDOCTORAL RESEARCHER IN THE PIOTROWSKI LAB, WAS AWARDED A ONE-YEAR GRANT FROM THE NIH NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS. 13. NATASHA SHYLO HYSON, PHD, A POSTDOCTORAL RESEARCHER IN THE TRAINOR LAB, WAS AWARDED A ONE-TIME EMERGING RESEARCH ORGANISMS GRANT FROM THE SOCIETY OF DEVELOPMENTAL BIOLOGY. |
| 14. QIUSHUANG WU, A PREDOCTORAL RESEARCHER OF THE GRADUATE SCHOOL OF THE | STOWERS INSTITUTE IN THE BAZZINI LAB, RECEIVED A SIX-YEAR NIH PREDOCTORAL TO POSTDOCTORAL FELLOW TRANSITION AWARD. 15. ALEJANDRO RODRIGUEZ GAMA, A PREDOCTORAL RESEARCHER OF THE GRADUATE SCHOOL OF THE STOWERS INSTITUTE IN THE HALFMANN LAB, RECEIVED A SIX-YEAR NIH PREDOCTORAL TO POSTDOCTORAL FELLOW TRANSITION AWARD. 16. ALEXANDRIA COCKRELL, A PREDOCTORAL RESEARCHER FROM THE UNIVERSITY OF KANSAS MEDICAL CENTER IN THE GERTON LAB, RECEIVED A ONE-YEAR NIH GRANT FROM THE NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES. INDEPENDENT RESEARCH PROGRAM LEADERS LABORATORIES INDIVIDUAL SCIENTISTS AT THE SIMR SPECIALIZE IN THE STUDY OF ONE OR MORE PARTICULAR GENES, PROTEINS, OR OTHER MOLECULES, EACH OF WHICH MAY CAUSE OR INFLUENCE VARIOUS KINDS OF DISEASE. A COMPREHENSIVE LIST OF RESEARCH LEADERS FOLLOWS: 1. ALEJANDRO SNCHEZ ALVARADO, PHD, EXECUTIVE DIRECTOR AND CHIEF SCIENTIFIC OFFICER, INVESTIGATOR, AND HOWARD HUGHES MEDICAL INSTITUTE INVESTIGATOR, JOINED SIMR IN 2011 FROM THE UNIVERSITY OF UTAH'S SCHOOL OF MEDICINE, WHERE HE HELD THE H.A. & EDNA BENNING PROFESSORSHIP OF EUROBIOLOGY AND ANATOMY. HE RECEIVED A BS IN MOLECULAR BIOLOGY AND CHEMISTRY FROM VANDERBILT UNIVERSITY IN NASHVILLE, TENNESSEE, AND A PHD IN PHARMACOLOGY AND CELL BIOPHYSICS FROM THE UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE IN CINCINNATI, OHIO. RESEARCH FOCUS: THE MOLECULAR AND CELLULAR MECHANISMS UNDERPINNING ANIMAL REGENERATION USING THE PLANARIAN SCHMIDTEA MEDITERRANEA AND OTHER RESEARCH ORGANISMS. 2. ARIEL BAZZINI, PHD, ASSISTANT INVESTIGATOR, JOINED SIMR IN 2016 FROM THE LAB OF ANTONIO J. GIRALDEZ, PHD, IN THE DEPARTMENT OF GENETICS AT YALE UNIVERSITY, WHERE HE COMPLETED A POSTDOCTORAL FELLOWSHIP. BAZZINI RECEIVED HIS PHD IN MOLECULAR BIOLOGY AT THE UNIVERSITY OF BUENOS AIRES, ARGENTINA. FOR HIS DOCTORAL DISSERTATION, HE STUDIED PLANT GENETICS AT THE INSTITUTE OF BIOTECHNOLOGY IN ARGENTINA'S NATIONAL INSTITUTE OF AGRICULTURAL TECHNOLOGY (INTA). RESEARCH FOCUS: THE REGULATION OF GENE EXPRESSION IN VERTEBRATES. 3. JOAN CONAWAY, PHD, INVESTIGATOR, JOINED SIMR IN 2001 FROM THE OKLAHOMA MEDICAL RESEARCH FOUNDATION WHERE SHE WAS AN ASSOCIATE INVESTIGATOR OF THE HOWARD HUGHES MEDICAL INSTITUTE AND INTERIM HEAD OF THE PROGRAM IN MOLECULAR AND CELL BIOLOGY. CONAWAY RECEIVED HER DOCTORATE IN CELL BIOLOGY FROM STANFORD UNIVERSITY SCHOOL OF MEDICINE. RESEARCH FOCUS: ANALYSIS OF THE MOLECULAR MECHANISM AND REGULATION OF GENE TRANSCRIPTION. 4. RONALD CONAWAY, PHD, INVESTIGATOR, JOINED SIMR IN 2001 FROM THE OKLAHOMA MEDICAL RESEARCH FOUNDATION WHERE HE WAS HOLDER OF THE CHAPMAN CHAIR IN MEDICAL RESEARCH. CONAWAY RECEIVED HIS PHD IN BIOCHEMISTRY FROM STANFORD UNIVERSITY SCHOOL OF MEDICINE. RESEARCH FOCUS: ANALYSIS OF THE MOLECULAR MECHANISM AND REGULATION OF GENE TRANSCRIPTION. 5. JENNIFER GERTON, PHD, INVESTIGATOR, JOINED SIMR IN 2002 FROM A POSTDOCTORAL FELLOWSHIP IN THE LABORATORY OF JOSEPH DERISI, PHD, IN THE DEPARTMENT OF BIOCHEMISTRY AND BIOPHYSICS AT THE UNIVERSITY OF CALIFORNIA-SAN FRANCISCO. GERTON RECEIVED A PHD IN MICROBIOLOGY AND IMMUNOLOGY FROM STANFORD UNIVERSITY. RESEARCH FOCUS: GENOMIC AND GENETIC ANALYSIS OF CHROMOSOME SEGREGATION AND CHROMOSOME DYNAMICS. 6. MATTHEW GIBSON, PHD, INVESTIGATOR AND DEAN OF THE GRADUATE SCHOOL, JOINED SIMR IN 2006 FROM A JANE COFFIN CHILDS MEMORIAL FUND POSTDOCTORAL FELLOWSHIP WITH NORBERT PERRIMON, PHD, AT HARVARD MEDICAL SCHOOL. GIBSON RECEIVED A PHD IN ZOOLOGY FROM THE UNIVERSITY OF WASHINGTON. RESEARCH FOCUS: GENETIC ANALYSIS OF MECHANISMS CONTROLLINGSIGNAL TRANSDUCTION, CELL PROLIFERATION, AND EPITHELIAL MORPHOGENESIS DURING DROSOPHILA DEVELOPMENT. 7. RANDAL HALFMANN, PHD, ASSOCIATE INVESTIGATOR, JOINED SIMR IN 2015 FROM THE UNIVERSITY OF TEXAS (UT) SOUTHWESTERN MEDICAL CENTER. HE RECEIVED A PHD IN BIOLOGY FROM THE MASSACHUSETTS INSTITUTE OF TECHNOLOGY, WHERE HE WAS A NATIONAL SCIENCE FOUNDATION PREDOCTORAL FELLOW. AFTER COMPLETING HIS GRADUATE STUDIES, HALFMANN OBTAINED AN INDEPENDENT POSITION AT UT SOUTHWESTERN MEDICAL CENTER WHERE HE WAS A SARA AND FRANK MCKNIGHT FELLOW AND RECEIVED A DIRECTOR'S EARLY INDEPENDENCE AWARD FROM THE NATIONAL INSTITUTES OF HEALTH. RESEARCH FOCUS: CELLULAR AND EVOLUTIONARY IMPLICATIONS OF PROTEIN SELF-ASSEMBLY USING GENETIC, BIOCHEMICAL, AND CELL-BIOLOGICAL APPROACHES. 8. R. SCOTT HAWLEY, PHD, INVESTIGATOR AND DEAN EMERITUS OF THE GRADUATE SCHOOL, JOINED SIMR IN 2001 FROM THE UNIVERSITY OF CALIFORNIA-DAVIS WHERE HE WAS A PROFESSOR OF GENETICS IN THE MOLECULAR AND CELLULAR BIOLOGY SECTION. HAWLEY EARNED A PHD IN GENETICS FROM THE UNIVERSIT OF WASHINGTON AND COMPLETED POSTDOCTORAL TRAINING AS A HELEN HAY WHITNEY FELLOW AT THE INSTITUTE FOR CANCER RESEARCH IN PHILADELPHIA. RESEARCH FOCUS: INVESTIGATION OF MECHANISMS THAT INFLUENCE HOW CHROMOSOMES PAIR AND SEGREGATE DURING MEIOSIS USING DROSOPHILA AS AN EXPERIMENTAL SYSTEM. 9. SUE JASPERSEN, PHD, ASSOCIATE INVESTIGATOR, JOINED SIMR IN 2005 FRO THE LABORATORY OF MARK WINEY, PHD, AT THE UNIVERSITY OF COLORADO-BOULDER WHERE SHE WAS A KECK FOUNDATION FELLOW, A HELEN HAY WHITNEY FELLOW, AND THE RECIPIENT OF A LEUKEMIA & LYMPHOMA SOCIETY CAREER DEVELOPMENT AWARD. JASPERSEN HOLDS A PHD IN BIOCHEMISTRY FROM THE UNIVERSITY OF CALIFORNIA-SAN FRANCISCO. RESEARCH FOCUS: INNER NUCLEAR MEMBRANE PROTEIN LOCALIZATION AND ROLE IN CHROMOSOME POSITIONING AND SEGREGATION. 10. ROBERT KRUMLAUF, PHD, SCIENTIFIC DIRECTOR EMERITUS AND INVESTIGATOR, JOINED THE SIMR IN 2000 FROM ENGLAND'S NATIONAL INSTITUTE FOR MEDICAL RESEARCH, THE RIDGEWAY, MILL HILL, LONDON, WHERE HE WAS HEAD OF THE DIVISION OF DEVELOPMENTAL NEUROBIOLOGY. KRUMLAUF RECEIVED A PHD IN DEVELOPMENTAL BIOLOGY FROM OHIO STATE UNIVERSITY. RESEARCH FOCUS: ANALYSIS OF MOLECULAR PATHWAYS THAT REGULATE HOW THE MAMMALIAN HEAD, BRAIN AND NERVOUS SYSTEM ARE BUILT, USING A VARIETY OF VERTEBRATE RESEARCH ORGANISMS. 11. LINHENG LI, PHD, INVESTIGATOR, JOINED SIMR IN 2000 FROM THE UNIVERSITY OF WASHINGTON MEDICAL CENTER WHERE HE HELD A FACULTY APPOINTMENT AFTER COMPLETING POSTDOCTORAL TRAINING IN THE LABORATORY DIRECTED BY LEROY HOOD, MD, PHD. LI EARNED HIS PHD IN MOLECULAR AND CELLULAR BIOLOGY FROM NEW YORK UNIVERSITY MEDICAL SCHOOL UNDER THE MENTORING OF EDWARD ZIFF, PHD. RESEARCH FOCUS: INVESTIGATION OF MOLECULAR AND GENETIC PATHWAYS CONTROLLING ADULT STEM CELL DEVELOPMENT IN THE HEMATOPOIETIC AND INTESTINAL SYSTEMS USING TRANSGENIC AND GENE TARGETING ANIMAL MODEL APPROACHES. 12. TATJANA PIOTROWSKI, PHD, INVESTIGATOR, JOINED SIMR IN 2011 FROM THE UNIVERSITY OF UTAH'S SCHOOL OF MEDICINE, WHERE SHE WAS AN ASSOCIATE PROFESSOR IN THE DEPARTMENT OF NEUROBIOLOGY AND ANATOMY. SHE RECEIVED HER MASTER'S DEGREE FROM THE UNIVERSITY OF TUBINGEN, GERMANY, AND HER DOCTORATE DEGREE FROM THE MAX PLANCK INSTITUTE FOR DEVELOPMENTAL BIOLOGY IN TUBINGEN. RESEARCH FOCUS: COLLECTIVE CELL MIGRATION, CELL TYPE SPECIFICATION, AND STEM CELL BIOLOGY IN ZEBRAFISH AS A RESEARCH SYSTEM. 13. NICOLAS ROHNER, PHD, ASSOCIATE INVESTIGATOR, JOINED SIMR IN 2015 FROM HARVARD MEDICAL SCHOOL, WHERE HE WAS A POSTDOCTORAL FELLOW IN THE LABORATORY OF CLIFF TABIN, PHD. ROHNER EARNED A PHD IN BIOLOGY FROM THE MAX PLANCK INSTITUTE FOR DEVELOPMENTAL BIOLOGY IN TUBINGEN, GERMANY. RESEARCH FOCUS: GENETIC MECHANISMS AND MUTATIONS THAT UNDERLIE THE ANIMAL KINGDOM'S TREMENDOUS DIVERSITY IN MORPHOLOGY, PHYSIOLOGY, AND BEHAVIOR. 14. KAUSIK SI, PHD, ASSOCIATE SCIENTIFIC DIRECTOR AND INVESTIGATOR, JOINED SIMR IN 2005 FROM THE LABORATORY OF ERIC KANDEL, MD, AT COLUMBIA UNIVERSITY CENTER FOR NEUROBIOLOGY AND BEHAVIOR WHERE HE WAS A JANE COFFIN CHILDS FELLOW AND A FRANCIS GOELET FELLOW IN NEUROSCIENCE. SI EARNED A PHD IN MOLECULAR BIOLOGY FROM THE ALBERT EINSTEIN COLLEGE OF MEDICINE. RESEARCH FOCUS: ROLE OF SYNAPTIC PROTEIN SYNTHESIS IN INFORMATION ACQUISITION AND MEMORY STORAGE. 15. PAUL TRAINOR, PHD, INVESTIGATOR, JOINED SIMR IN 2001 FROM A RESEARCH POSITION AT THE NATIONAL INSTITUTE FOR MEDICAL RESEARCH AT MILL HILL, LONDON, WHERE HE COMPLETED POSTDOCTORAL TRAINING. TRAINOR HAS A PHD IN DEVELOPMENTAL BIOLOGY FROM CHILDREN'S MEDICAL RESEARCH INSTITUTE AT THE UNIVERSITY OF SYDNEY, AUSTRALIA. RESEARCH FOCUS: INVESTIGATION OF THE INTERACTIONS BETWEEN DISTINCT TISSUES IN THE BODY AND THEIR REGULATION DURING NORMAL DEVELOPMENT TO REVEAL PATHWAYS THAT REGULATE NORMAL CRANIAL AND FACIAL DEVELOPMENT. 16. JERRY WORKMAN, PHD, INVESTIGATOR, JOINED SIMR IN 2003 FROM THE PENNSYLVANIA STATE UNIVERSITY WHERE HE HELD THE PAUL BERG PROFESSORSHIP OF BIOCHEMISTRY AND WAS AN ASSOCIATE INVESTIGATOR OF THE HOWARD HUGHES MEDICAL INSTITUTE. WORKMAN EARNED A PHD IN CELL AND MOLECULAR BIOLOGY FROM THE UNIVERSITY OF MICHIGAN AND COMPLETED POSTDOCTORAL TRAINING AT THE ROCKEFELLER UNIVERSITY WITH BOB ROEDER,PHD. RESEARCH FOCUS: STUDY OF THE PROTEIN COMPLEXES THAT MODIFY CHROMATIN. |
| 17. TING XIE, PHD, INVESTIGATOR, JOINED SIMR IN 2000 AFTER COMPLETING A | HOWARD HUGHES MEDICAL INSTITUTE POSTDOCTORAL FELLOWSHIP IN THE LABORATORY OF ALLAN C. SPRADLING, PHD, AT THE CARNEGIE INSTITUTION OF WASHINGTON. XIE RECEIVED HIS PHD FROM THE JOINT GRADUATE PROGRAM IN MOLECULAR BIOLOGY AND BIOCHEMISTRY OF RUTGERS UNIVERSITY AND THE UNIVERSITY OF MEDICINE AND DENTISTRY OF NEW JERSEY. RESEARCH FOCUS: GENETIC AND MOLECULAR ANALYSIS OF STEM CELLS AND GERM CELL DEVELOPMENT IN DROSOPHILA AND MOUSE. 18. C. RON YU, PHD, INVESTIGATOR, JOINED SIMR IN 2005 FROM THE LABORATORY OF RICHARD AXEL, MD, AT COLUMBIA UNIVERSITY CENTER FOR NEUROBIOLOGY AND BEHAVIOR WHERE HE HELD A NATIONAL INSTITUTES OF HEALTH MENTORED RESEARCH SCIENTIST AWARD FROM THE NATIONAL INSTITUTE OF MENTAL HEALTH. YU EARNED HIS PHD IN MOLECULAR, CELLULAR, AND BIOPHYSICAL STUDIES AT COLUMBIA UNIVERSITY. RESEARCH FOCUS: HOW OLFACTORY SENSORY INFORMATION IS DETECTED, INTEGRATED, AND PROCESSED IN THE BRAIN TO INFLUENCE SPECIFIC INNATE BEHAVIORS. 19. SARAH ZANDERS, PHD, ASSISTANT INVESTIGATOR AND VICE DEAN OF THE GRADUATE SCHOOL, JOINED SIMR IN 2016 AFTER COMPLETION OF HER POSTDOCTORAL TRAINING IN BASIC SCIENCES AT THE FRED HUTCHINSON CANCER RESEARCH CENTER (FHCRC) WITH SUPPORT FROM A PATHWAY TO INDEPENDENCE AWARD FROM THE NATIONAL INSTITUTES OF HEALTH. FHCRC FACULTY MEMBERS HARMIT S. MALIK, PHD, AND GERRY SMITH, PHD, ADVISED HER RESEARCH ON FERTILITY, GENOME EVOLUTION, AND THE ORIGIN OF NEW SPECIES. ZANDERS RECEIVED HER PHD IN GENETICS AND DEVELOPMENT FROM CORNELL UNIVERSITY. RESEARCH FOCUS: THE EFFECTS OF GENETIC CONFLICTS CAUSED BY SELFISH GENES THAT ARE EMBEDDED IN EUKARYOTIC GENOMES. 20. JULIA ZEITLINGER, PHD, INVESTIGATOR, JOINED SIMR IN 2007 FROM THE LAB OF RICHARD YOUNG, PHD, AT THE WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH AT MASSACHUSETTS INSTITUTE OF TECHNOLOGY WHERE SHE WAS THE RECIPIENT OF A LONG-TERM POSTDOCTORAL FELLOWSHIP FROM THE HUMAN FRONTIER SCIENCE PROGRAM. ZEITLINGER EARNED A PHD IN MOLECULAR BIOLOGY FROM THE EUROPEAN MOLECULAR BIOLOGY LABORATORY IN HEIDELBERG, GERMANY. RESEARCH FOCUS: ANALYSIS OF THE GENE REGULATORY NETWORKS UNDERLYING CELLULAR DIFFERENTIATION. TECHNOLOGY CENTERS 1. PAUL KULESA, PHD, DIRECTOR OF IMAGING, JOINED SIMR IN 2002 AFTER COMPLETING A BURROUGHS WELLCOME FUND POSTDOCTORAL FELLOWSHIP IN THE LABORATORY OF SCOTT E. FRASER, PHD, AT THE CALIFORNIA INSTITUTE OF TECHNOLOGY. KULESA RECEIVED A PHD IN APPLIED MATHEMATICS UNDER J.D. MURRAY, PHD, AT THE UNIVERSITY OF WASHINGTON. RESEARCH FOCUS: CELL MIGRATION IN DEVELOPMENT AND CANCER. 2. MICHAEL WASHBURN, PHD, DIRECTOR OF PROTEOMICS, JOINED SIMR IN 2003 FROM THE TORREY MESA RESEARCH INSTITUTE IN SAN DIEGO WHERE HE WAS A SENIOR STAFF SCIENTIST IN PROTEOMICS. HE EARNED A PHD IN BIOCHEMISTRY AND ENVIRONMENTAL TOXICOLOGY FROM MICHIGAN STATE UNIVERSITY BEFORE COMPLETING A POSTDOCTORAL FELLOWSHIP WITH JOHN YATES III, PHD, IN THE DEPARTMENT OF MOLECULAR BIOTECHNOLOGY AT THE UNIVERSITY OF WASHINGTON. RESEARCH FOCUS: QUANTITATIVE PROTEOMICS AND PROTEIN COMPLEX DYNAMICS. |
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