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THE STOWERS INSTITUTE FOR MEDICAL RESEARCH PERFORMS MEDICAL RESEARCH IN THE PUBLIC INTEREST WITH THE GOAL OF EXPANDING OUR UNDERSTANDING OF FUNDAMENTAL PROCESSES IN LIVING CELLS AND IMPROVING LIFE'S QUALITY THROUGH INNOVATIVE APPROACHES TO THE CAUSES, TREATMENT, AND PREVENTION OF DISEASE. |
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SIMR'S ACCOMPLISHMENTS ARE DESCRIBED AT END OF SCHEDULE O. |
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JAMES E. STOWERS JR. AND VIRGINIA G. STOWERS, DIRECTORS OF SIMR, HAVE A FAMILY RELATIONSHIP. JAMES E. STOWERS JR., RICHARD W. BROWN, DAVID A. WELTE, DAVID M. CHAO, AND RODERICK L. STURGEON, ALL DIRECTORS OF SIMR, HAVE A BUSINESS RELATIONSHIP; THEY SERVE ON THE BOARD OF AMERICAN CENTURY COMPANIES, INC. ("ACCI") AS DESCRIBED IN RESPONSE TO SCHEDULE L, PART IV. RICHARD W. BROWN, WILLIAM B. NEAVES, DAVID M. CHAO, AND RODERICK L. STURGEON, DIRECTORS OF SIMR, HAVE A BUSINESS RELATIONSHIP; THEY ALL SERVE ON THE BOARD OF BIOMED VALLEY DISCOVERIES, INC., A RELATED PARTY AS DISCUSSED ON SCHEDULE R. |
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THE DATA AND INFORMATION NECESSARY TO PREPARE SIMR'S FORM 990 WAS COMPILED BY SIMR'S ACCOUNTING DEPARTMENT AND THEN REVIEWED BY OUR TAX ATTORNEY AT BRYAN CAVE, LLP. PRICEWATERHOUSECOOPERS ("PWC"), OUR EXTERNAL TAX PREPARERS, USE THIS INFORMATION TO PREPARE THE FORM 990. THE COMPLETED FORM 990, INCLUDING REQUIRED SCHEDULES, IS DISTRIBUTED IN ADVANCE TO ALL SEVEN OFFICERS OF SIMR FOR THEIR REVIEW AND COMMENTS BEFORE THE FORM 990 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. |
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SIMR HAS ADOPTED A "CONFLICTS OF INTEREST AND DIRECTOR INDEPENDENCE POLICY". EACH DIRECTOR, OFFICER, AND OTHER PERSON WHO IS 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 INSURE THAT IT ENGAGES ONLY IN ACTIVITIES THAT ARE CONSISTENT WITH ITS TAX-EXEMPT PURPOSE. |
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THE PROCESS FOR DETERMINING COMPENSATION OF SIMRS PRESIDENT AND CEO INCLUDED RETAINING THE SERVICES OF A NATIONALLY KNOWN COMPENSATION CONSULTANT TO PROVIDE DATA AND ANALYSIS TO DETERMINE COMPARABLE SALARY AND BENEFITS FOR SIMILARLY QUALIFIED PERSONS IN COMPARABLE POSITIONS AT SIMILARLY SITUATED ORGANIZATIONS. THE PROCESS WAS UNDERTAKEN IN 2009 AT THE TIME THE CURRENT CONTRACT WAS EXECUTED AND APPROVED BY THE GOVERNING BOARD AS DOCUMENTED IN THE OFFICIAL MINUTES. ANOTHER REVIEW PROCESS FOR THE PRESIDENT AND CEO WAS COMPLETED IN 2012. |
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SIMR'S GOVERNING DOCUMENTS, CONFLICT OF INTEREST POLICY, AND FINANCIAL STATEMENTS ARE AVAILABLE ON REQUEST. |
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OTHER CHANGES IN NET ASSETS INCLUDE THE FOLLOWING: ACTUARIAL LOSS ON ANNUITY (541,913) |
| FORM 990, PART III, LINE 4 |
2012 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, TWO CANCER SURVIVORS WHO HAVE DEDICATED THEIR FORTUNE TO SUPPORTING BASIC RESEARCH IN CELL AND MOLECULAR BIOLOGY THAT WILL PROVIDE LONG-TERM SOLUTIONS TO GENE-BASED 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. LIKE A GROWING NUMBER OF SCIENTISTS TODAY, INSTITUTE SCIENTISTS ARE CONVINCED THAT BY STUDYING THE BASIC BIOLOGY OF CELLS THEY WILL DISCOVER HOW GENES CAUSE MANY DISEASES, INCLUDING CANCER, BIRTH DEFECTS, AND DEMENTIA. BASIC RESEARCH CONDUCTED AT SIMR SHOULD POINT THE WAY TO THE DEVELOPMENT OF NEW PREVENTIONS, TREATMENTS, AND CURES FOR GENETIC DISEASES. |
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2012 NOTABLE RESEARCH RESULTS IN 2012, SIMR RESEARCH TEAMS MADE DISCOVERIES MERITING PUBLICATION IN LEADING PEER-REVIEWED SCIENTIFIC JOURNALS - 59 ORIGINAL RESEARCH PAPERS IN ALL. SIMR RESEARCH TEAMS ALSO PUBLISHED 29 REVIEWS, COMMENTARIES, BOOK CHAPTERS. SOME OF THE HIGHLIGHTS AMONG PAPERS PUBLISHED IN 2012 INCLUDE: THE BAUMANN LAB DISCOVERED HOW THE RNA TER1, A COMPONENT OF THE ENZYME TELOMERASE, IS SCULPTED TO FAVOR INTERACTIONS WITH ITS PROTEIN PARTNERS: TWO RING-LIKE PROTEINS SEQUENTIALLY SLIP INTO ONTO UNPROCESSED TER1 RNA AND HOLD IT WHILE IT IS CLIPPED TO THE OPTIMUM SIZE, FOLDED AND CAPPED. (PUBLISHED IN THE MARCH 26, 2012 ISSUE OF NATURE) THE CONAWAY LAB REVEALED HOW ATF6, A MASTER REGULATOR THAT TAKES CHARGES FOLLOWING A CELLULAR CRISIS TRIGGERED BY THE ACCUMULATION OF MISFOLDED PROTEINS, ACTIVATES ITS TARGET GENES. THE STUDY WAS SELECTED BY THE EDITORS OF THE JOURNAL OF BIOLOGICAL CHEMISTRY AS "PAPER OF THE WEEK." (PUBLISHED IN THE JUNE 29, 2012 ISSUE OF THE JOURNAL OF BIOLOGICAL CHEMISTRY) THE GERTON LAB DEVELOPED AN INNOVATIVE METHOD TO COUNT THE NUMBER OF FLUORESCENT MOLECULES IN A TIGHT CLUSTER AND THEN APPLIED THE NOVEL APPROACH TO SETTLE THE DEBATE OF HOW DNA TWISTS INTO THE CENTROMERE, A SPECIALIZED STRUCTURE THAT SITS AT THE CROSS POINT OF THE "X" USED TO REPRESENT DUPLICATED CHROMOSOMES. (PUBLISHED IN THE JULY 20, 2012 ISSUE OF CELL) THE LINHENG LI LAB IDENTIFIED AN IMPORTANT MOLECULAR CUE THAT KEEPS QUIESCENT MOUSE HEMATOPOIETIC (OR BLOOD-FORMING) STEM CELLS FROM PROLIFERATING WHEN THEIR SERVICES ARE NOT NEEDED. (PUBLISHED IN THE JULY 20, 2012 ISSUE OF CELL.) THE RONG LI LAB DISCOVERED THAT YEAST CELLS CAN LOOSEN THE REINS ON THEIR GENOME, READILY ACQUIRING OR LOSING WHOLE CHROMOSOMES TO ENABLE RAPID ADAPTION. (PUBLISHED IN THE JANUARY 29, 2012, ONLINE ISSUE OF NATURE.) THE SANCHEZ LAB SUCCESSFULLY TRACKED STEM CELLS IN THE FLATWORM SCHMIDTEA MEDITERRANEA AND REVEALED THAT THE WORMS' STEM CELLS, KNOWN AS NEOBLASTS, MARCH OUT, MULTIPLY AND START REBUILDING TISSUES LOST TO AMPUTATION SETTLING THE CENTURY-OLD QUESTIONS WHETHER NEOBLASTS CAN ACTIVELY TRAVEL TOWARDS WOUNDS. (PUBLISHED IN THE OCTOBER 1, 2012, ISSUE OF DEVELOPMENT) THE SHILATIFARD LAB REVEALED THAT ONE WAY STEM CELLS ENSURE THAT THEY ARE READY TO ACTIVATE HIGHLY DIVERSE GENE EXPRESSION PROGRAMS AT A MOMENT'S NOTICE IS BY STATIONING A PROTEIN CALLED ELL3 AT STRETCHES OF DNA REQUIRED TO ACTIVATE A NEIGHBORING GENE, GENOMIC REGIONS KNOWN AS ENHANCERS. (PUBLISHED IN THE DECEMBER 27, 2012, ONLINE ISSUE OF CELL) THE TRAINOR LAB DISCOVERED A KEY MOLECULAR PLAYER REQUIRED FOR THE PROPER MIGRATION AND SURVIVAL OF NEURAL CREST CELLS. THESE CELLS GENERATE MOST OF THE CARTILAGE, BONE AND CONNECTIVE TISSUE IN THE HEAD AND FACE EXPLAINING THE FREQUENTLY OBSERVED LINK BETWEEN CRANIAL AND FACIAL MALFORMATIONS. (PUBLISHED IN THE OCT. 4, 2012, ISSUE OF PLOS GENETICS) THE YU LAB TRACED THE SIGNALS INDUCED BY INDIVIDUAL ODOR MOLECULES DEEP INTO THE BRAIN AND FOUND EVIDENCE THAT CHEMICALLY RELATED ODORANTS MAPPED ALL OVER THE OLFACTORY BULB, WHICH PROCESSES INCOMING OLFACTORY INFORMATION, AND NOT NEXT TO EACH OTHER AS BELIEVED PREVIOUSLY. (PUBLISHED IN THE MARCH 19, 2012, ISSUE OF THE PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES) THE ZEITLINGER LAB DISCOVERED A FUNDAMENTALLY NEW MECHANISM THAT ENSURES THAT THE CORRECT GENES IN EACH TISSUE ARE TURNED ON AND OFF IN PRECISELY THE RIGHT SEQUENCE DURING DEVELOPMENT. THE TEAM FOUND THAT THE PATTERN OF GENES WITH POISED POLYMERASE IN MUSCLE AND NERVE CELLS VARIED DEPENDING ON THE STAGE OF DEVELOPMENT AND NOT DEPENDING ON TISSUE TYPE AS EXPECTED. (PUBLISHED IN THE DECEMBER 27, 2012, ISSUE OF CELL REPORTS) |
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COMPREHENSIVE LIST OF 2012 ORIGINAL RESEARCH PAPERS; REVIEWS, COMMENTARIES AND BOOK CHAPTERS ORIGINAL RESEARCH PAPERS 1. BAILEY CM, MORRISON JA, KULESA PM. MELANOMA REVIVES AN EMBRYONIC MIGRATION PROGRAM TO PROMOTE PLASTICITY AND INVASION. PIGMENT CELL MELANOMA RES. 2012;25:573-583. 2. BARDET AF, HE Q, ZEITLINGER J, STARK A. A COMPUTATIONAL PIPELINE FOR COMPARATIVE CHIP-SEQ ANALYSES. NAT PROTOC. 2012;7:45-61. 3. BARLOW AJ, DIXON J, DIXON MJ, TRAINOR PA. BALANCING NEURAL CREST CELL INTRINSIC PROCESSES WITH THOSE OF THE MICROENVIRONMENT IN TCOF1 HAPLOINSUFFICIENT MICE ENABLES COMPLETE ENTERIC NERVOUS SYSTEM FORMATION. HUM MOL GENET. 2012;21:1782-1793. 4. BOCCHINFUSO DG, TAYLOR P, ROSS E, IGNATCHENKO A, IGNATCHENKO V, KISLINGER T, PEARSON BJ, MORAN MF. PROTEOMIC PROFILING OF THE PLANARIAN SCHMIDTEA MEDITERRANEA AND ITS MUCOUS REVEALS SIMILARITIES WITH HUMAN SECRETIONS AND THOSE PREDICTED FOR PARASITIC FLATWORMS. MOL CELL PROTEOMICS. 2012;11:681-691. 5. BOSE T, LEE KK, LU S, XU B, HARRIS B, SLAUGHTER B, UNRUH J, GARRETT A, MCDOWELL W, BOX A, LI H, PEAK A, RAMACHANDRAN S, SEIDEL C, GERTON JL. COHESIN PROTEINS PROMOTE RIBOSOMAL RNA PRODUCTION AND PROTEIN TRANSLATION IN YEAST AND HUMAN CELLS. PLOS GENET. 2012;8:E1002749. 6. CHEN S, LEWIS B, MORAN A, XIE T. CADHERIN-MEDIATED CELL ADHESION IS CRITICAL FOR THE CLOSING OF THE MOUSE OPTIC FISSURE. PLOS ONE. 2012;7:E51705. 7. CHEN S, LI H, ZUECKERT-GAUDENZ K, PAULSON A, GUO F, TRIMBLE R, PEAK A, SEIDEL C, DENG C, FURUTA Y, XIE T. DEFECTIVE FGF SIGNALING CAUSES COLOBOMA FORMATION AND DISRUPTS RETINAL NEUROGENESIS [PUBLISHED AHEAD OF PRINT NOVEMBER 14 2012]. CELL RES. 2012. 8. CHEN Z, MCCROSKY S, GUO W, LI H, GERTON JL. A GENETIC SCREEN TO DISCOVER PATHWAYS AFFECTING COHESIN FUNCTION IN SCHIZOSACCHAROMYCES POMBE IDENTIFIES CHROMATIN EFFECTORS. G3 (BETHESDA). 2012;2:1161-1168. 9. CHEN G, BRADFORD WD, SEIDEL CW, LI R. HSP90 STRESS POTENTIATES RAPID CELLULAR ADAPTATION THROUGH INDUCTION OF ANEUPLOIDY. NATURE. 2012;482:246-250. 10. COLLINS KA, CALLICOAT JG, LAKE CM, MCCLURKEN CM, KOHL KP, HAWLEY RS. A GERMLINE CLONE SCREEN ON THE X CHROMOSOME REVEALS NOVEL MEIOTIC MUTANTS IN DROSOPHILA MELANOGASTER. G3. 2012;2:1369-1377. 11. COSTESSI A, MAHROUR N, SHARMA V, STUNNENBERG R, STOEL MA, TIJCHON E, CONAWAY JW, CONAWAY RC, STUNNENBERG HG. THE HUMAN EKC/KEOPS COMPLEX IS RECRUITED TO CULLIN2 UBIQUITIN LIGASES BY THE HUMAN TUMOUR ANTIGEN PRAME. PLOS ONE. 2012;7:E42822. 12. D'ANGIOLELLA V, DONATO V, FORRESTER FM, JEONG Y-T, KUDO Y, PELLACANI C, SARAF A, FLORENS L, WASHBURN MP, PAGANO M. THE CYCLIN F-RIBONUCLEOTIDE REDUCTASE M2 AXIS CONTROLS GENOME INTEGRITY AND DNA REPAIR. CELL. 2012;149:1023-1034. 13. DAS A, SLAUGHTER BD, UNRUH JR, BRADFORD WD, ALEXANDER R, RUBINSTEIN B, LI R. FLIPPASE-MEDIATED PHOSPHOLIPID ASYMMETRY PROMOTES FAST CDC42 RECYCLING IN DYNAMIC MAINTENANCE OF CELL POLARITY. NAT CELL BIOL. 2012;14:304-310. 14. DENNIS JF, KUROSAKA H, IULIANELLA A, PACE J, THOMAS N, BECKHAM S, WILLIAMS T, TRAINOR PA. MUTATIONS IN HEDGEHOG ACYLTRANSFERASE (HHAT) PERTURB HEDGEHOG SIGNALING, RESULTING IN SEVERE ACRANIA-HOLOPROSENCEPHALY-AGNATHIA CRANIOFACIAL DEFECTS. PLOS GENET. 2012;8:E1002927. 15. FRIEDERICHS JM, GARDNER JM, SMOYER CJ, WHETSTINE CR, GOGOL M, SLAUGHTER BD, JASPERSEN SL. GENETIC ANALYSIS OF MPS3 SUN DOMAIN MUTANTS IN SACCHAROMYCES CEREVISIAE REVEALS AN INTERACTION WITH THE SUN-LIKE PROTEIN SLP1. G3 (BETHESDA). 2012;2:1703-1718. 16. GAERTNER B, JOHNSTON J, CHEN K, WALLASCHEK N, PAULSON A, GARRUSS AS, GAUDENZ K, DE KUMAR B, KRUMLAUF R, ZEITLINGER J. POISED RNA POLYMERASE II CHANGES OVER DEVELOPMENTAL TIME AND PREPARES GENES FOR FUTURE EXPRESSION. CELL REP. 2012;2:1670-1683. 17. GILMORE JM, SARDIU ME, VENKATESH S, STUTZMAN B, PEAK A, SEIDEL CW, WORKMAN JL, FLORENS L, WASHBURN MP. CHARACTERIZATION OF A HIGHLY CONSERVED HISTONE RELATED PROTEIN, YDL156W, AND ITS FUNCTIONAL ASSOCIATIONS USING QUANTITATIVE PROTEOMIC ANALYSES. MOL CELL PROTEOMICS. 2012;11:M111 011544. 18. GHOSH S, GARDNER JM, SMOYER CJ, FRIEDERICHS JM, UNRUH JR, SLAUGHTER BD, ALEXANDER R, CHISHOLM RD, LEE KK, WORKMAN JL, JASPERSEN SL. ACETYLATION OF THE SUN PROTEIN MPS3 BY ECO1 REGULATES ITS FUNCTION IN NUCLEAR ORGANIZATION. MOL BIOL CELL. 2012;23:2546-2559. 19. GOTTSCHALK AJ, TRIVEDI RD, CONAWAY JW, CONAWAY RC. ACTIVATION OF THE SNF2 FAMILY ATPASE ALC1 BY POLY(ADP-RIBOSE) IN A STABLE ALC1{MIDDLE DOT}PARP1{MIDDLE DOT}NUCLEOSOME INTERMEDIATE. J BIOL CHEM. 2012;287:43527-43532. 20. HERZ HM, MOHAN M, GARRUSS AS, LIANG K, TAKAHASHI YH, MICKEY K, VOETS O, VERRIJZER CP, SHILATIFARD A. ENHANCER-ASSOCIATED H3K4 MONOMETHYLATION BY TRITHORAX-RELATED, THE DROSOPHILA HOMOLOG OF MAMMALIAN MLL3/MLL4. GENES DEV. 2012;26:2604-2620. 21. HERZ HM, MOHAN M, GARRETT AS, MILLER C, CASTO D, ZHANG Y, SEIDEL C, HAUG JS, FLORENS L, WASHBURN MP, YAMAGUCHI M, SHIEKHATTAR R, SHILATIFARD A. POLYCOMB REPRESSIVE COMPLEX 2-DEPENDENT AND -INDEPENDENT FUNCTIONS OF JARID2 IN TRANSCRIPTIONAL REGULATION IN DROSOPHILA. MOL CELL BIOL. 2012;32:1683-1693. 22. KAIPA BR, SHAO H, SCHAFER G, TRNKEWITZ T, GROTH V, LIU J, BECK L, ABMAYR SM, ONEL SF. DOCK MEDIATES SCAR- AND WASP-DEPENDENT ACTIN POLYMERIZATION THROUGH INTERACTION WITH CELL ADHESION MOLECULES IN FOUNDER CELLS AND FUSION-COMPETENT MYOBLASTS [PUBLISHED AHEAD OF PRINT SEPTEMBER 19 2012]. J CELL SCI. 2012. 23. KANAKOUSAKI K, GIBSON MC. A DIFFERENTIAL REQUIREMENT FOR SUMOYLATION IN PROLIFERATING AND NON-PROLIFERATING CELLS DURING DROSOPHILA DEVELOPMENT. DEVELOPMENT. 2012;139:2751-2762. 24. KIM S, MA L, JENSEN KL, KIM MM, BOND CT, ADELMAN JP, YU CR. PARADOXICAL CONTRIBUTION OF SK3 AND GIRK CHANNELS TO THE ACTIVATION OF MOUSE VOMERONASAL ORGAN. NAT NEUROSCI. 2012;15:1236-1244. 25. KORFALI N, WILKIE GS, SWANSON SK, SRSEN V, DE LAS HERAS J, BATRAKOU DG, MALIK P, ZULEGER N, KERR AR, FLORENS L, SCHIRMER EC. THE NUCLEAR ENVELOPE PROTEOME DIFFERS NOTABLY BETWEEN TISSUES. NUCLEUS. 2012;3:552-564. 26. KUMAR S, SANDELL LL, TRAINOR PA, KOENTGEN F, DUESTER G. ALCOHOL AND ALDEHYDE DEHYDROGENASES: RETINOID METABOLIC EFFECTS IN MOUSE KNOCKOUT MODELS. BIOCHIM BIOPHYS ACTA. 2012;1821:198-205. 27. KURYAN BG, KIM J, TRAN NNH, LOMBARDO SR, VENKATESH S, WORKMAN JL, CAREY M. HISTONE DENSITY IS MAINTAINED DURING NUCLEOSOMAL TRANSCRIPTION MEDIATED BY RSC AND NAP1 IN VITRO. PNAS. 2012;109:1931-1936. 28. LABBE RM, IRIMIA M, CURRIE KW, LIN A, ZHU SJ, BROWN DD, ROSS EJ, VOISIN V, BADER GD, BLENCOWE BJ, PEARSON BJ. A COMPARATIVE TRANSCRIPTOMIC ANALYSIS REVEALS CONSERVED FEATURES OF STEM CELL PLURIPOTENCY IN PLANARIANS AND MAMMALS. STEM CELLS. 2012;30:1734-1745. 29. LEE JS, GARRETT A, YEN K, TAKAHASHI YH, JACKSON J, SEIDEL C, PUGH BF, SHILATIFARD A. LEE JS, GARRETT AS, YEN K, TAKAHASHI YH, HU D, JACKSON J, SEIDEL C, PUGH BF, SHILATIFARD A. CO-DEPENDENCY OF H2B MONOUBIQUITINATION AND NUCLEOSOME RE-ASSEMBLY ON CHD1. GENES DEV. 2012; 26:914-919. 30. LIN C-H, PAULSON A, ABMAYR SM, WORKMAN JL. HP1A TARGETS THE DROSOPHILA KDM4A DEMETHYLASE TO A SUBSET OF HETEROCHROMATIC GENES TO REGULATE H3K36ME3 LEVELS. PLOS ONE. 2012:E39758. |
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31. LUO Z, LIN C, GUEST E, GARRETT AS, MOHAGHEGH N, SWANSON S, MARSHALL S, FLORENS L, WASHBURN MP, SHILATIFARD A. THE SUPER ELONGATION COMPLEX FAMILY OF RNA POLYMERASE II ELONGATION FACTORS: GENE TARGET SPECIFICITY AND TRANSCRIPTIONAL OUTPUT. MOL CELL BIOL. 2012;32:2608-2617. 32. MA L, QIU Q, GRADWOHL S, SCOTT A, YU EQ, ALEXANDER R, WIEGRAEBE W, YU CR. DISTRIBUTED REPRESENTATION OF CHEMICAL FEATURES AND TUNOTOPIC ORGANIZATION OF GLOMERULI IN THE MOUSE OLFACTORY BULB. PROC NATL ACAD SCI U S A. 2012;109:5481-5486. 33. MAJUMDAR A, CESARIO WC, WHITE-GRINDLEY E, JIANG H, REN F, KHAN MR, LI L, CHOI EM, KANNAN K, GUO F, UNRUH J, SLAUGHTER B, SI K. CRITICAL ROLE OF AMYLOID-LIKE OLIGOMERS OF DROSOPHILA ORB2 IN THE PERSISTENCE OF MEMORY. CELL. 2012;148:515-529. 34. MCLENNAN R, DYSON L, PRATHER KW, MORRISON JA, BAKER RE, MAINI PK, KULESA PM. MULTISCALE MECHANISMS OF CELL MIGRATION DURING DEVELOPMENT: THEORY AND EXPERIMENT. DEVELOPMENT. 2012;139:2935-2944. 35. MILLER DE, HAWLEY RS. BISPHENOL A AND THE PRIMATE OVARY. PROC NATL ACAD SCI U S A. 2012;109:17315-17316. 36. MORRISON JA, BAILEY CM, KULESA PM. GENE PROFILING IN THE AVIAN EMBRYO USING LASER CAPTURE MICRODISSECTION AND RT-QPCR [PUBLISHED AHEAD OF PRINT DECEMBER 5 2012]. COLD SPRING HARB PROTOC. 2012. 37. PINTO IM, RUBINSTEIN B, KUCHARAVY A, UNRUH J, LI R. ACTIN DEPOLYMERIZATION DRIVES ACTOMYOSIN RING CONTRACTION DURING BUDDING YEAST CYTOKINESIS. DEV CELL. 2012;22:1247-1260. 38. RIDENOUR DA, MCKINNEY MC, BAILEY CM, KULESA PM. CYCLETRAK: A NOVEL SYSTEM FOR THE SEMI-AUTOMATED ANALYSIS OF CELL CYCLE DYNAMICS. DEV BIOL. 2012;365:189-195. 39. RUBINSTEIN B, SLAUGHTER BD, LI R. WEAKLY NONLINEAR ANALYSIS OF SYMMETRY BREAKING IN CELL POLARITY MODELS. PHYS BIOL. 2012;9:045006. 40. SAKAI D, DIXON J, DIXON MJ, TRAINOR PA. MAMMALIAN NEUROGENESIS REQUIRES TREACLE-PLK1 FOR PRECISE CONTROL OF SPINDLE ORIENTATION, MITOTIC PROGRESSION, AND MAINTENANCE OF NEURAL PROGENITOR CELLS. PLOS GENET. 2012;8:E1002566. 41. SANDELL LL, LYNN ML, INMAN KE, MCDOWELL W, TRAINOR PA. RDH10 OXIDATION OF VITAMIN A IS A CRITICAL CONTROL STEP IN SYNTHESIS OF RETINOIC ACID DURING MOUSE EMBRYOGENESIS. PLOS ONE. 2012;7:E30698. 42. SELA D, CHEN L, MARTIN-BROWN S, WASHBURN MP, FLORENS L, CONAWAY JW, CONAWAY RC. ENDOPLASMIC RETICULUM STRESS-RESPONSIVE TRANSCRIPTION FACTOR ATF6ALPHA DIRECTS RECRUITMENT OF THE MEDIATOR OF RNA POLYMERASE II TRANSCRIPTION AND MULTIPLE HISTONE ACETYLTRANSFERASE COMPLEXES. J BIOL CHEM. 2012;287:23035-23045. 43. SHIVARAJU M, UNRUH JR, SLAUGHTER BD, MATTINGLY M, BERMAN J, GERTON JL. CELL-CYCLE-COUPLED STRUCTURAL OSCILLATION OF CENTROMERIC NUCLEOSOMES IN YEAST. CELL. 2012;150:304-316. 44. SMITH KT, SARDIU ME, MARTIN-BROWN SA, SEIDEL C, MUSHEGIAN A, EGIDY R, FLORENS L, WASHBURN MP, WORKMAN JL. HUMAN FAMILY WITH SEQUENCE SIMILARITY 60 MEMBER A (FAM60A) PROTEIN: A NEW SUBUNIT OF THE SIN3 DEACETYLASE COMPLEX. MOL CELL PROTEOMICS. 2012;11:1815-1828. 45. SMOLLE M, VENKATESH S, GOGOL MM, LI H, ZHANG Y, FLORENS L, WASHBURN MP, WORKMAN JL. CHROMATIN REMODELERS ISW1 AND CHD1 MAINTAIN CHROMATIN STRUCTURE DURING TRANSCRIPTION BY PREVENTING HISTONE EXCHANGE. NAT STUCT MOL BIOL. 2012;19:884-892. 46. STEINBERG XP, HEPP MI, FERNANDEZ GARCIA Y, SUGANUMA T, SWANSON SK, WASHBURN M, WORKMAN JL, GUTIERREZ JL. HUMAN CCAAT/ENHANCER-BINDING PROTEIN BETA INTERACTS WITH CHROMATIN REMODELING COMPLEXES OF THE IMITATION SWITCH SUBFAMILY. BIOCHEMISTRY. 2012. 47. SUGANUMA T, MUSHEGIAN A, SWANSON SK, FLORENS L, WASHBURN MP, WORKMAN JL. A METAZOAN ATAC ACETYLTRANSFERASE SUBUNIT THAT REGULATES MAP KINASE SIGNALING IS RELATED TO AN ANCIENT MOLYBDOPTERIN SYNTHASE COMPONENT. MOL CELL PROTEOMICS. 2012. 48. SUGIMURA R, HE XC, VENKATRAMAN A, ARAI F, BOX A, SEMERAD C, HAUG JS, PENG L, ZHONG XB, SUDA T, LI L. NONCANONICAL WNT SIGNALING MAINTAINS HEMATOPOIETIC STEM CELLS IN THE NICHE. CELL. 2012;150:351-365. 49. SURANENI P, RUBINSTEIN B, UNRUH JR, DURNIN M, HANEIN D, LI R. THE ARP2/3 COMPLEX IS REQUIRED FOR LAMELLIPODIA EXTENSION AND DIRECTIONAL FIBROBLAST CELL MIGRATION. J CELL BIOL. 2012;197:239-251. 50. TAKEO S, SWANSON SK, NANDANAN K, NAKAI Y, AIGAKI T, WASHBURN MP, FLORENS L, HAWLEY RS. SHAGGY/GLYCOGEN SYNTHASE KINASE 3BETA AND PHOSPHORYLATION OF SARAH/REGULATOR OF CALCINEURIN ARE ESSENTIAL FOR COMPLETION OF DROSOPHILA FEMALE MEIOSIS. PROC NATL ACAD SCI U S A. 2012;109:6382-6389. 51. TANG W, KANNAN R, BLANCHETTE M, BAUMANN P. TELOMERASE RNA BIOGENESIS INVOLVES SEQUENTIAL BINDING BY SM AND LSM COMPLEXES. NATURE. 2012;484:260-264. 52. TU KC, PEARSON BJ, SANCHEZ ALVARADO A. TORC1 IS REQUIRED TO BALANCE CELL PROLIFERATION AND CELL DEATH IN PLANARIANS. DEV BIOL. 2012;365:458-469. 53. VENKATESH S, SMOLLE M, LI H, GOGOL MM, SAINT M, KUMAR S, NATARAJAN K, WORKMAN JL. SET2 METHYLATION OF HISTONE H3 LYSINE36 SUPPRESSES HISTONE EXCHANGE ON TRANSCRIBED GENES. NATURE 2012;489:452-455. 54. WANG L, GUO H, REYES N, LEE S, BORTZ E, GUO F, SUN R, TONG L, DENG H. DISTINCT DOMAINS IN ORF52 TEGUMENT PROTEIN MEDIATE ESSENTIAL FUNCTIONS IN MURINE GAMMAHERPESVIRUS 68 VIRION TEGUMENTATION AND SECONDARY ENVELOPMENT. J VIROL. 2012;86:1348-1357. 55. WYNN ML, KULESA PM, SCHNELL S. COMPUTATIONAL MODELLING OF CELL CHAIN MIGRATION REVEALS MECHANISMS THAT SUSTAIN FOLLOW-THE-LEADER BEHAVIOUR. J R SOC INTERFACE. 2012;9:1576-1588. 56. XU XP, ROUILLER I, SLAUGHTER BD, EGILE C, KIM E, UNRUH JR, FAN X, POLLARD TD, LI R, HANEIN D, VOLKMANN N. THREE-DIMENSIONAL RECONSTRUCTIONS OF ARP2/3 COMPLEX WITH BOUND NUCLEATION PROMOTING FACTORS. EMBO J. 2012;31:236-247. 57. YANG H, ZHANG Y, VALLANDINGHAM J, LI H, FLORENS L, MAK HY. THE RDE-10/RDE-11 COMPLEX TRIGGERS RNAI-INDUCED MRNA DEGRADATION BY ASSOCIATION WITH TARGET MRNA IN C. ELEGANS. GENES DEV. 2012;26:846-856. 58. ZHAO M, ROSS JT, ITKIN T, PERRY JM, VENKATRAMAN A, HAUG JS, HEMBREE MJ, DENG CX, LAPIDOT T, HE XC, LI L. FGF SIGNALING FACILITATES POST-INJURY RECOVERY OF MOUSE HEMATOPOIETIC SYSTEM. BLOOD. 2012;120:1831-1842. 59. ZHU J, PAVELKA N, BRADFORD WD, RANCATI G, LI R. KARYOTYPIC DETERMINANTS OF CHROMOSOME INSTABILITY IN ANEUPLOID BUDDING YEAST. PLOS GENET. 2012;8:E1002719. |
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REVIEWS, COMMENTARIES OR CHAPTERS 1. ABMAYR SM, PAVLATH GK. MYOBLAST FUSION: LESSONS FROM FLIES AND MICE. DEVELOPMENT. 2012;139:641-656. 2. ABMAYR SM, WORKMAN JL. HOLDING ON THROUGH DNA REPLICATION: HISTONE MODIFICATION OR MODIFIER? CELL. 2012;150:875-877. 3. ACHILLEOS A, TRAINOR PA. NEURAL CREST STEM CELLS: DISCOVERY, PROPERTIES AND POTENTIAL FOR THERAPY. CELL RES. 2012;22:288-304. 4. ALVARADO SA. Q&A: WHAT IS REGENERATION, AND WHY LOOK TO PLANARIANS FOR ANSWERS? BMC BIOLOGY. 2012;10:88. 5. BANKS CA, KONG SE, WASHBURN MP. AFFINITY PURIFICATION OF PROTEIN COMPLEXES FOR ANALYSIS BY MULTIDIMENSIONAL PROTEIN IDENTIFICATION TECHNOLOGY. PROTEIN EXPR PURIF. 2012;86:105-119. 6. BOX AC, PARK J, SEMERAD CL, KONNESKY J, HAUG JS. COST ACCOUNTING METHOD FOR CYTOMETRY FACILITIES. CYTOMETRY A. 2012;81:439-444. 7. CHEN G, RUBINSTEIN B, LI R. WHOLE CHROMOSOME ANEUPLOIDY: BIG MUTATIONS DRIVE ADAPTATION BY PHENOTYPIC LEAP. BIOESSAYS. 2012;34:893-900. 8. CONAWAY JW. INTRODUCTION TO THEME "CHROMATIN, EPIGENETICS, AND TRANSCRIPTION". ANNU REV BIOCHEM. 2012;81:61-64. 9. DUTTA A, WORKMAN JL. NUCLEOSOME POSITIONING: MULTIPLE MECHANISMS TOWARD A UNIFYING GOAL. MOL CELL. 2012;48:1-2. 10. ELLIOTT SA, SANCHEZ ALVARADO A. THE HISTORY AND ENDURING CONTRIBUTIONS OF PLANARIANS TO THE STUDY OF ANIMAL REGENERATION. WIRES DEV BIOL. 2012:2012. DOI: 2010.1002/WDEV.2082. 11. GERTON JL. TRANSLATIONAL MECHANISMS AT WORK IN THE COHESINOPATHIES. NUCLEUS. 2012;3:520-525. GIBSON WT, GIBSON MC. GROWING CELLS PUSH BACK UNDER PRESSURE. CELL. 2012;149:259-261. 12. GUEDELHOEFER IV OC, SANCHEZ ALVARADO A. PLANARIAN IMMOBILIZATION, PARTIAL IRRADIATION, AND TISSUE TRANSPLANTATION. J VIS EXP. 2012;66:E4015. 13. HARALALKA S, CARTWRIGHT HN, ABMAYR SM. RECENT ADVANCES IN IMAGING EMBRYONIC MYOBLAST FUSION IN DROSOPHILA. METHODS. 2012;56:55-62. 14. HAWLEY RS, RUEDI EA. THE OTHER LIFE OF ARTICLES. GENETICS. 2012;191:1029. 15. JASPERSEN SL, GHOSH S. NUCLEAR ENVELOPE INSERTION OF SPINDLE POLE BODIES AND NUCLEAR PORE COMPLEXES. NUCLEUS. 2012;3:226-236. 16. KAPLAN KB, LI R. A PRESCRIPTION FOR 'STRESS' - THE ROLE OF HSP90 IN GENOME STABILITY AND CELLULAR ADAPTATION. TRENDS CELL BIOL. 2012;22:576-583. 17. LAKE CM, HAWLEY RS. THE MOLECULAR CONTROL OF MEIOTIC CHROMOSOMAL BEHAVIOR: EVENTS IN EARLY MEIOTIC PROPHASE IN DROSOPHILA OOCYTES. ANNU REV PHYSIOL. 2012;74:425-451. 18. LUO Z, LIN C, SHILATIFARD A. THE SUPER ELONGATION COMPLEX (SEC) FAMILY IN TRANSCRIPTIONAL CONTROL. NAT REV MOL CELL BIOL. 2012;13:543-547. 19. MAK HY. LIPID DROPLETS AS FAT STORAGE ORGANELLES IN CAENORHABDITIS ELEGANS: THEMATIC REVIEW SERIES: LIPID DROPLET SYNTHESIS AND METABOLISM: FROM YEAST TO MAN. J LIPID RES. 2012;53:28-33. 20. MOHAN M, HERZ HM, SHILATIFARD A. SNAPSHOT: HISTONE LYSINE METHYLASE COMPLEXES. CELL. 2012;149:498-498.E491. 21. MUSHEGIAN A, GUREVICH VV, GUREVICH EV. THE ORIGIN AND EVOLUTION OF G PROTEIN-COUPLED RECEPTOR KINASES. PLOS ONE. 2012;7:E33806. 22. NEAVES W. THE ROOTS OF RESEARCH MISCONDUCT. NATURE. 2012;488:121-122. 23. NOLTE C, AHN Y, KRUMLAUF R. EVOLUTIONARY DEVELOPMENTAL BIOLOGY: HOX GENE EVOLUTION. ELS ENCYCLOPEDIA OF LIFE SCIENCES: JOHN WILEY & SONS, INC.; 2012. 24. PERRY JM, LI L. TO BE OR NOT TO BE A STEM CELL: DISSECTION OF CELLULAR AND MOLECULAR COMPONENTS OF HAEMATOPOIETIC STEM CELL NICHES. EMBO J. 2012;31:1060-1061. 25. SANCHEZ ALVARADO A. CELLULAR HYPERPROLIFERATION AND CANCER AS EVOLUTIONARY VARIABLES. CURR BIOL. 2012;22:R772-778. 26. SHILATIFARD A. THE COMPASS FAMILY OF HISTONE H3K4 METHYLASES: MECHANISMS OF REGULATION IN DEVELOPMENT AND DISEASE PATHOGENESIS. ANNU REV BIOCHEM. 2012;81:65-95. 27. SMITH KT, WORKMAN JL. CHROMATIN PROTEINS: KEY RESPONDERS TO STRESS. PLOS BIOL. 2012;10:E1001371. 28. SUGANUMA T, WORKMAN JL. MAP KINASES AND HISTONE MODIFICATION. J MOL CELL BIOL. 2012;4:348-350. 29. WEAKE VM, WORKMAN JL. SAGA FUNCTION IN TISSUE-SPECIFIC GENE EXPRESSION. TRENDS CELL BIOL. YI K, LI R. ACTIN CYTOSKELETON IN CELL POLARITY AND ASYMMETRIC DIVISION DURING MOUSE OOCYTE MATURATION. CYTOSKELETON (HOBOKEN). 2012;69:727-737. |
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COMPETITIVE RESEARCH GRANT FUNDING & RESEARCH AWARDS & DISTINCTIONS THE ABILITY OF STOWERS INSTITUTE SCIENTISTS TO RECEIVE INCREASING NUMBERS OF COMPETITIVELY AWARDED RESEARCH GRANTS ATTESTS TO THE HIGH LEVEL OF RESEARCH PRODUCTIVITY PRESENT AT THE INSTITUTE. DURING 2012, STOWERS SCIENTISTS WORKED WITH THE SUPPORT OF 24 GRANTS AND FELLOWSHIPS FROM THE NATIONAL INSTITUTES OF HEALTH, FOUR GRANTS AND FELLOWSHIPS FROM THE AMERICAN CANCER SOCIETY, ONE FELLOWSHIP FROM THE LEUKEMIA AND LYMPHOMA SOCIETY, ONE FELLOWSHIP FROM THE AMERICAN HEART ASSOCIATION, ONE FELLOWSHIP FROM THE AMERICAN ASSOCIATION OF ANATOMISTS, ONE FELLOWSHIP FROM THE LIFE SCIENCES RESEARCH FOUNDATION, ONE FELLOWSHIP FROM THE DAMON RUNYON CANCER RESEARCH FOUNDATION, ONE FELLOWSHIP FROM THE JAPAN SOCIETY FOR THE PROMOTION OF SCIENCE, ONE AWARD FROM THE ELLISON MEDICAL FOUNDATION, ONE GRANT FROM THE GREATER KANSAS CITY COMMUNITY FOUNDATION, ONE HUDSON PRIZE FROM THE M.R. AND EVELYN HUDSON FOUNDATION, TWO AWARDS FROM THE UNIVERSITY OF KANSAS CANCER CENTER, ONE GRANT FROM THE HEARING HEALTH FOUNDATION, AND TWO INVESTIGATOR AWARDS FROM THE HOWARD HUGHES MEDICAL INSTITUTE. WITH NEW AND RECURRING GRANT SUPPORT, THE INSTITUTE IS RECEIVING MORE THAN $8 MILLION A YEAR IN RESEARCH FUNDING TO SUPPLEMENT THE INCOME FROM ITS ENDOWMENTS. TESTIFYING TO THE HIGH LEVEL OF ACHIEVEMENT TAKING PLACE AT THE INSTITUTE ARE THE AWARDS AND HONORS INSTITUTE SCIENTISTS RECEIVED IN 2012: - ANNITA ACHILLEOS, PH.D., POSTDOCTORAL RESEARCH ASSOCIATE IN THE TRAINOR LAB, RECEIVED A FELLOWSHIP FROM THE AMERICAN ASSOCIATION OF ANATOMISTS, EFFECTIVE IN JANUARY. - LAURENCE FLORENS, PH.D., HEAD, PROTEOMICS, RECEIVED A SUB-AWARD FROM A NATIONAL INSTITUTES OF HEALTH GRANT AWARDED TO THE UNIVERSITY OF INDIANA, EFFECTIVE IN DECEMBER. - ERIN GUEST, MD, VISITING SCIENTIST IN THE SHILATIFARD LAB, RECEIVED A GRANT FROM THE UNIVERSITY OF KANSAS CANCER CENTER EFFECTIVE IN MAY. - LINHENG LI, PH.D., INVESTIGATOR, RECEIVED A NATIONAL INSTITUTES OF HEALTH GRANT, EFFECTIVE IN SEPTEMBER AND A GRANT FROM THE UNIVERSITY OF KANSAS CANCER CENTER EFFECTIVE IN DECEMBER. - TATJANA PIOTROWSKI, PH.D., ASSOCIATE INVESTIGATOR, RECEIVED A GRANT FROM THE HEARING HEALTH FOUNDATION EFFECTIVE IN MAY. - TAMARA POTAPOVA, PH.D., POSTDOCTORAL RESEARCH ASSOCIATE IN THE RONG LI LAB, RECEIVED A FELLOWSHIP FROM THE AMERICAN CANCER SOCIETY, EFFECTIVE IN JULY. - ALI SHILATIFARD, PH.D., INVESTIGATOR, RECEIVED A NATIONAL INSTITUTES OF HEALTH GRANT, EFFECTIVE IN SEPTEMBER. - JERRY WORKMAN, PH.D., INVESTIGATOR, AND SUSAN ABMAYR, PH.D., ASSOCIATE INVESTIGATOR, RECEIVED A NATIONAL INSTITUTES OF HEALTH GRANT, EFFECTIVE IN MAY. - JULIA ZEITLINGER, PH.D., ASSOCIATE INVESTIGATOR, RECEIVED THE 2012 HUDSON PRIZE FROM THE M.R. AND EVELYN HUDSON FOUNDATION, EFFECTIVE IN JULY. COOPERATION AGREEMENTS AND COLLABORATIONS THE STOWERS INSTITUTE CONTINUED COLLABORATIONS IN 2012 WITH HOSPITALS IN KANSAS CITY (CHILDREN'S MERCY, AND ST. LUKE'S) AND BOSTON (BRIGHAM AND WOMEN'S HOSPITAL) AND ADDED NEW COLLABORATIONS IN MEMPHIS (ST. JUDE'S CHILDRENS HOSPITAL) AND TORONTO (HOSPITAL FOR SICK CHILDREN). THE INSTITUTE ALSO COLLABORATES WITH THE UNIVERSITY OF MISSOURI AT KANSAS CITY; THE UNIVERSITY OF MISSOURI MEDICAL CENTER; THE UNIVERSITY OF KANSAS MEDICAL CENTER; THE UNIVERSITY OF KANSAS MEDICAL SCHOOL; DAVID GEFFEN SCHOOL OF MEDICINE AT UCLA; THE ERASMUS UNIVERSITY MEDICAL CENTER; THE HOWARD HUGHES MEDICAL INSTITUTE; HARVARD UNIVERSITY; HARVARD MEDICAL SCHOOL; THE INDIANA UNIVERSITY SCHOOL OF MEDICINE; THE NEW YORK UNIVERSITY SCHOOL OF MEDICINE; ST. LOUIS UNIVERSITY SCHOOL OF MEDICINE; STANFORD UNIVERSITY AND THE STANFORD UNIVERSITY SCHOOL OF MEDICINE; THE UNIVERSITY OF CALIFORNIA, DAVIS, LOS ANGELES, SAN DIEGO, AND SAN FRANCISCO; THE UNIVERSITY OF COLORADO SCHOOL OF MEDICINE; THE UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL; THE UNIVERSITY OF MICHIGAN MEDICAL SCHOOL; THE UNIVERSITY OF NEBRASKA MEDICAL CENTER; UNIVERSITY OF NORTH DAKOTA SCHOOL OF MEDICINE & HEALTH SCIENCES; THE UNIVERSITY OF PENNSYLVANIA SCHOOL OF MEDICINE; THE UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE; THE UNIVERSITY OF TEXAS M.D. ANDERSON CANCER CENTER; THE UNIVERSITY OF VIRGINIA MEDICAL SCHOOL; UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER; UNIVERSITY OF UTAH SCHOOL OF MEDICINE; VANDERBILT UNIVERSITY SCHOOL OF MEDICINE AND WASHINGTON UNIVERSITY IN ST. LOUIS SCHOOL OF MEDICINE, MOST OF WHICH ARE ASSOCIATED WITH TEACHING AND RESEARCH HOSPITALS. IN TOTAL, STOWERS RESEARCHERS SUCCESSFULLY COLLABORATED WITH COLLEAGUES AT 82 NATIONAL AND 58 INTERNATIONAL UNIVERSITIES AND RESEARCH INSTITUTES. IN ADDITION TO THE INSTITUTIONS LISTED ABOVE, COLLABORATORS INCLUDE: AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH, SINGAPORE; BCM CENTER FOR CELL AND GENE THERAPY; BIOZENTRUM UNIVERSITY OF BASEL; BROWN UNIVERSITY; BURNHAM INSTITUTE FOR MEDICAL RESEARCH; CALIFORNIA INSTITUTE OF TECHNOLOGY; CARNEGIE INSTITUTION OF WASHINGTON; N MEDICAL COLLEGE, VELLORE; CNRS CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE; COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK; COLUMBIA UNIVERSITY, COLLEGE OF PHYSICIANS AND SURGEONS; CSIC - INSTITUTO DE PARASITOLOGIA Y BIOMEDICINA LOPEZ NEYRA IPBLN; DALHOUSIE UNIVERSITY; DANA-FARBER CANCER INSTITUTE; DARTMOUTH MEDICAL SCHOOL; ECOLE POLYTECHNIQUE; EMORY UNIVERSITY; EUROPEAN MOLECULAR BIOLOGY LABORATORY HEIDELBERG; EXPERIMENTAL THERAPEUTICS AND TRANSLATIONAL RESEARCH ONCOLOGY; FUDAN UNIVERSITY; GIFU UNIVERSITY SCHOOL OF MEDICINE; GRADUATE UNIVERSITY OF CHINESE ACADEMY OF SCIENCES; HARVARD SCHOOL OF PUBLIC HEALTH; HELSINGIN YLIOPISTO; HOKKAIDO UNIVERSITY SCHOOL OF MEDICINE; ICAHN MEDICAL INSTITUTE; IDEXX LABORATORIES; INDIANA UNIVERSITY; INSERM; INSTITUTE OF BIOPHYSICS CHINESE ACADEMY OF SCIENCES; INSTITUTE OF MEDICAL BIOLOGY, SINGAPORE; IRB BARCELONA - INSTITUTE FOR RESEARCH IN BIOMEDICINE; JAWAHARLAL NEHRU UNIVERSITY; KANSAS STATE UNIVERSITY AT MANHATTAN; KEENE STATE COLLEGE; KEIO UNIVERSITY; KOCHI MEDICAL SCHOOL; KOREA ADVANCED INSTITUTE OF SCIENCE & TECHNOLOGY; KYOTO INSTITUTE OF TECHNOLOGY; LA JOLLA INSTITUTE FOR ALLERGY AND IMMUNOLOGY; LSU HEALTH SCIENCES CENTER - SHREVEPORT; MANCHESTER ACADEMIC HEALTH SCIENCE CENTRE; MCGILL UNIVERSITY; MEDICAL RESEARCH COUNCIL; MERRIMACK PHARMACEUTICALS, INC; MRC MAMMALIAN GENETICS UNIT; MRC NATIONAL INSTITUTE FOR MEDICAL RESEARCH; MSM PROTEIN TECHNOLOGIES; NARA INSTITUTE OF SCIENCE AND TECHNOLOGY; NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES; NATIONAL UNIVERSITY OF SINGAPORE; NIJMEGEN CENTRE FOR MOLECULAR LIFE SCIENCES - NCMLS; NORTHWESTERN UNIVERSITY; ONTARIO CANCER INSTITUTE; ONTARIO INSTITUTE FOR CANCER RESEARCH; OPEN UNIVERSITY; ; OREGON HEALTH AND SCIENCE UNIVERSITY; OZGENE PTY. LTD.; PENNSYLVANIA STATE UNIVERSITY; PROMEGA CORPORATION; RESEARCH INSTITUTE OF MOLECULAR PATHOLOGY, VIENNA; ROCKHURST UNIVERSITY; ROYAL VETERINARY COLLEGE UNIVERSITY OF LONDON; SANFORD-BURNHAM MEDICAL RESEARCH INSTITUTE; SICHUAN UNIVERSITY; SIR WILLIAM DUNN SCHOOL OF PATHOLOGY; TECHNION - ISRAEL INSTITUTE OF TECHNOLOGY; THE COLLEGE OF WILLIAM AND MARY; THE UCLA SCHOOL OF DENTISTRY; THE UNIVERSITY OF BRITISH COLUMBIA; THE UNIVERSITY OF CALIFORNIA, SANTA BARBARA; THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL; THE WISTAR INSTITUTE; TOKYO MEDICAL AND DENTAL UNIVERSITY; TOKYO METROPOLITAN UNIVERSITY; ULSAN UNIVERSITY; UNIVERSITT FREIBURG IM BREISGAU; UNIVERSIT DE SHERBROOKE; UNIVERSITY OF ALABAMA AT BIRMINGHAM; UNIVERSITY OF BATH; UNIVERSITY OF CINCINNATI; UNIVERSITY OF COLORADO HEALTH SCIENCES CENTER; UNIVERSITY OF CONCEPCION - CHILE; UNIVERSITY OF EDINBURGH; UNIVERSITY OF GLASGOW; UNIVERSITY OF KENTUCKY COLLEGE OF MEDICINE; UNIVERSITY OF LOUISVILLE; UNIVERSITY OF LOUISVILLE HEALTH SCIENCES CENTER; UNIVERSITY OF MANCHESTER; UNIVERSITY OF MIAMI; UNIVERSITY OF MICHIGAN; UNIVERSITY OF NEW ORLEANS; UNIVERSITY OF OKLAHOMA; UNIVERSITY OF OXFORD; UNIVERSITY OF PENNSYLVANIA; UNIVERSITY OF PENNSYLVANIA, SCHOOL OF MEDICINE; UNIVERSITY OF PITTSBURGH; UNIVERSITY OF TOKUSHIMA; UNIVERSITY OF TORONTO; UNIVERSITY OF TSUKUBA; UNIVERSITY OF WISCONSIN MADISON; UNIVERSITY OF WYOMING; VANDERBILT UNIVERSITY; VIRGINIA COMMONWEALTH UNIVERSITY; WEIZMANN INSTITUTE OF SCIENCE ISRAEL; YALE UNIVERSITY; YONSEI UNIVERSITY. |
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INDEPENDENT RESEARCH PROGRAM LEADERS LABORATORIES INDIVIDUAL SCIENTISTS AT THE STOWERS INSTITUTE SPECIALIZE IN THE STUDY OF ONE OR MORE PARTICULAR GENES, EACH OF WHICH MAY CAUSE OR HAVE INFLUENCE IN VARIOUS KINDS OF DISEASE. A COMPREHENSIVE LIST OF RESEARCH LEADERS FOLLOWS: - ROBERT KRUMLAUF, PH.D., SCIENTIFIC DIRECTOR AND INVESTIGATOR, JOINED THE STOWERS INSTITUTE 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. DR. KRUMLAUF RECEIVED A PH.D. 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 MODEL SYSTEMS - SUSAN ABMAYR, PH.D., ASSOCIATE INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2003 FROM THE PENNSYLVANIA STATE UNIVERSITY WHERE SHE SERVED AS ASSOCIATE PROFESSOR OF MOLECULAR GENETICS. SHE EARNED A PH.D. IN BIOCHEMISTRY AND MOLECULAR BIOLOGY FROM THE ROCKEFELLER UNIVERSITY AND COMPLETED POSTDOCTORAL TRAINING IN THE DEPARTMENT OF BIOCHEMISTRY AND MOLECULAR BIOLOGY AT HARVARD UNIVERSITY UNDER THE DIRECTION OF PROFESSOR TOM MANIATIS. RESEARCH FOCUS: MOLECULAR GENETICS OF CELL FATE SPECIFICATION AND DIFFERENTIATION IN DROSOPHILA, USING THE EMBRYONIC DEVELOPMENT OF THE MUSCULATURE AS A MODEL SYSTEM - PETER BAUMANN, PH.D., INVESTIGATOR AND HOWARD HUGHES MEDICAL INSTITUTE EARLY CAREER SCIENTIST, JOINED THE STOWERS INSTITUTE IN 2002 AFTER COMPLETING A HOWARD HUGHES MEDICAL INSTITUTE POSTDOCTORAL FELLOWSHIP IN THE LABORATORY OF DR. THOMAS R. CECH AT THE UNIVERSITY OF COLORADO-BOULDER. DR. BAUMANN RECEIVED A PH.D. IN BIOCHEMISTRY FROM THE IMPERIAL CANCER RESEARCH FUND AND UNIVERSITY COLLEGE, LONDON. RESEARCH FOCUS: FUNCTIONAL ANALYSIS OF TELOMERES AND THEIR ROLES IN CELLULAR IMMORTALITY AND CANCER - MARCO BLANCHETTE, PH.D., ASSISTANT INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2006 FROM A POSTDOCTORAL POSITION WITH DR. DONALD C. RIO AT THE UNIVERSITY OF CALIFORNIA-BERKELEY WHERE HE WAS RECIPIENT OF A HUMAN FRONTIER LONG-TERM FELLOWSHIP. DR. BLANCHETTE RECEIVED A PH.D. DEGREE IN MICROBIOLOGY FROM THE UNIVERSIT DE SHERBROOKE, CANADA. RESEARCH FOCUS: FUNCTIONAL GENOMIC ANALYSIS OF THE MECHANISMS CONTROLLING ALTERNATIVE PRE-MRNA SPLICING - JOAN CONAWAY, PH.D., INVESTIGATOR, JOINED THE STOWERS INSTITUTE 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. DR. 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 - RONALD CONAWAY, PH.D., INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2001 FROM THE OKLAHOMA MEDICAL RESEARCH FOUNDATION WHERE HE WAS HOLDER OF THE CHAPMAN CHAIR IN MEDICAL RESEARCH. DR. CONAWAY RECEIVED HIS PH.D. IN BIOCHEMISTRY FROM STANFORD UNIVERSITY SCHOOL OF MEDICINE. RESEARCH FOCUS: ANALYSIS OF THE MOLECULAR MECHANISM AND REGULATION OF GENE TRANSCRIPTION - JENNIFER GERTON, PH.D., ASSOCIATE INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2002 FROM A POSTDOCTORAL FELLOWSHIP IN THE LABORATORY OF DR. JOSEPH DERISI IN THE DEPARTMENT OF BIOCHEMISTRY AND BIOPHYSICS AT THE UNIVERSITY OF CALIFORNIA-SAN FRANCISCO. DR. GERTON RECEIVED A PH.D. IN MICROBIOLOGY AND IMMUNOLOGY FROM STANFORD UNIVERSITY. RESEARCH FOCUS: GENOMIC AND GENETIC ANALYSIS OF CHROMOSOME SEGREGATION AND CHROMOSOME DYNAMICS - MATTHEW GIBSON, PH.D., ASSOCIATE INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2006 FROM A JANE COFFIN CHILDS MEMORIAL FUND POSTDOCTORAL FELLOWSHIP WITH DR. NORBERT PERRIMON AT HARVARD MEDICAL SCHOOL. DR. GIBSON RECEIVED A PH.D. IN ZOOLOGY FROM THE UNIVERSITY OF WASHINGTON. RESEARCH FOCUS: GENETIC ANALYSIS OF MECHANISMS CONTROLLING SIGNAL TRANSDUCTION, CELL PROLIFERATION, AND EPITHELIAL MORPHOGENESIS DURING DROSOPHILA DEVELOPMENT - R. SCOTT HAWLEY, PH.D., INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2001 FROM THE UNIVERSITY OF CALIFORNIA-DAVIS WHERE HE WAS A PROFESSOR OF GENETICS IN THE MOLECULAR AND CELLULAR BIOLOGY SECTION. DR. HAWLEY EARNED A PH.D. IN GENETICS FROM THE UNIVERSITY 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 - SUE JASPERSEN, PH.D., ASSOCIATE INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2005 FROM THE LABORATORY OF DR. MARK WINEY 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. DR. JASPERSEN HOLDS A PH.D. IN BIOCHEMISTRY FROM THE UNIVERSITY OF CALIFORNIA-SAN FRANCISCO. RESEARCH FOCUS: INNER NUCLEAR MEMBRANE PROTEIN LOCALIZATION AND ROLE IN CHROMOSOME POSITIONING AND SEGREGATION - LINHENG LI, PH.D., INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2000 FROM THE UNIVERSITY OF WASHINGTON MEDICAL CENTER WHERE HE HELD A FACULTY APPOINTMENT AFTER COMPLETING POSTDOCTORAL TRAINING IN THE LABORATORY DIRECTED BY DR. LEROY HOOD. DR. LI EARNED HIS PH.D. IN MOLECULAR AND CELLULAR BIOLOGY FROM NEW YORK UNIVERSITY MEDICAL SCHOOL UNDER THE MENTORING OF DR. EDWARD ZIFF. 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 - RONG LI, PH.D., INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2005 FROM THE DEPARTMENT OF CELL BIOLOGY AT HARVARD MEDICAL SCHOOL WHERE SHE SERVED AS AN ASSOCIATE PROFESSOR. SHE EARNED A PH.D. IN CELL BIOLOGY AT THE UNIVERSITY OF CALIFORNIA-SAN FRANCISCO WITH DR. ANDREW MURRAY AND HELD A DAMON RUNYON-WALTER WINCHELL CANCER RESEARCH FELLOWSHIP AS A POSTDOCTORAL ASSOCIATE WITH DR. DAVID DRUBIN AT THE UNIVERSITY OF CALIFORNIA-BERKELEY. RESEARCH FOCUS: MECHANISM OF CELL POLARIZATION AND CELL MOTILITY, GENOME DYNAMICS AND CELLULAR EVOLVABILITY, AND EPITHELIAL TISSUE MORPHOGENESIS - HO YI MAK, PH.D., ASSISTANT INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2006 FROM A HUMAN FRONTIER SCIENCE PROGRAM POSTDOCTORAL FELLOWSHIP IN THE LABORATORY OF DR. GARY RUVKUN AT HARVARD MEDICAL SCHOOL. DR. MAK RECEIVED A PH.D. IN MOLECULAR PATHOLOGY FROM THE IMPERIAL CANCER RESEARCH FUND AND UNIVERSITY COLLEGE, LONDON. RESEARCH FOCUS: ANALYSIS OF MOLECULAR PATHWAYS THAT REGULATE CELLULAR FAT STORAGE IN RESPONSE TO NUTRIENT AVAILABILITY AND LIPID METABOLISM |
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- TATJANA PIOTROWSKI, PH.D. ASSOCIATE INVESTIGATOR, JOINED THE STOWERS INSTITUTE 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 TBINGEN, GERMANY, AND HER DOCTORATE DEGREE FROM THE MAX PLANCK INSTITUTE FOR DEVELOPMENTAL BIOLOGY IN TBINGEN. RESEARCH FOCUS: COLLECTIVE CELL MIGRATION, CELL TYPE SPECIFICATION AND STEM CELL BIOLOGY IN ZEBRAFISH AS A MODEL SYSTEM. - ALEJANDRO SNCHEZ ALVARADO, PH.D., INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2011 FROM THE UNIVERSITY OF UTAH'S SCHOOL OF MEDICINE, WHERE HE HELD THE H.A & EDNA BENNING PROFESSORSHIP OF NEUROBIOLOGY AND ANATOMY. HE RECEIVED A B.S. IN MOLECULAR BIOLOGY AND CHEMISTRY FROM VANDERBILT UNIVERSITY IN NASHVILLE, TENN., AND A PH.D. 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 AS A MODEL SYSTEM - ALI SHILATIFARD, PH.D., INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2007 FROM THE SAINT LOUIS UNIVERSITY SCHOOL OF MEDICINE WHERE HE WAS A PROFESSOR OF BIOCHEMISTRY AND ASSOCIATE DIRECTOR FOR BASIC SCIENCES AT THE SAINT LOUIS UNIVERSITY CANCER CENTER. DR. SHILATIFARD EARNED A PH.D. IN BIOCHEMISTRY FROM THE UNIVERSITY OF GEORGIA AND THE UNIVERSITY OF OKLAHOMA SCHOOL OF MEDICINE AND COMPLETED POSTDOCTORAL TRAINING AS A JANE COFFIN CHILDS FELLOW AT THE OKLAHOMA MEDICAL RESEARCH FOUNDATION. RESEARCH FOCUS: MOLECULAR PATHWAY OF LEUKEMOGENESIS - KAUSIK SI, PH.D., ASSOCIATE INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2005 FROM THE LABORATORY OF DR. ERIC KANDEL AT COLUMBIA UNIVERSITY CENTER FOR NEUROBIOLOGY AND BEHAVIOR WHERE HE WAS A JANE COFFIN CHILDS FELLOW AND A FRANCIS GOELET FELLOW IN NEUROSCIENCE. DR. SI EARNED A PH.D. IN MOLECULAR BIOLOGY FROM THE ALBERT EINSTEIN COLLEGE OF MEDICINE. RESEARCH FOCUS: ROLE OF SYNAPTIC PROTEIN SYNTHESIS IN INFORMATION ACQUISITION AND MEMORY STORAGE - PAUL TRAINOR, PH.D., INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2001 FROM A RESEARCH POSITION AT THE NATIONAL INSTITUTE FOR MEDICAL RESEARCH AT MILL HILL, LONDON, WHERE HE COMPLETED POSTDOCTORAL TRAINING. DR. TRAINOR HAS A PH.D. 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 - JERRY WORKMAN, PH.D., INVESTIGATOR, JOINED THE STOWERS INSTITUTE 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. DR. WORKMAN EARNED A PH.D. IN CELL AND MOLECULAR BIOLOGY FROM THE UNIVERSITY OF MICHIGAN AND COMPLETED POSTDOCTORAL TRAINING AT THE ROCKEFELLER UNIVERSITY WITH DR. BOB ROEDER. RESEARCH FOCUS: STUDY OF THE PROTEIN COMPLEXES THAT MODIFY CHROMATIN - TING XIE, PH.D., INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2000 AFTER COMPLETING A HOWARD HUGHES MEDICAL INSTITUTE POSTDOCTORAL FELLOWSHIP IN THE LABORATORY OF DR. ALLAN C. SPRADLING AT THE CARNEGIE INSTITUTION OF WASHINGTON. DR. XIE RECEIVED HIS PH.D. 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 - C. RON YU, PH.D., ASSISTANT INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2005 FROM THE LABORATORY OF DR. RICHARD AXEL 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. DR. YU EARNED HIS PH.D. 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 - JULIA ZEITLINGER, PH.D., ASSISTANT INVESTIGATOR, JOINED THE STOWERS INSTITUTE IN 2007 FROM THE LAB OF DR. RICHARD YOUNG 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. DR. ZEITLINGER EARNED A PH.D. 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 - PAUL KULESA, PH.D., DIRECTOR OF IMAGING, JOINED THE STOWERS INSTITUTE IN 2002 AFTER COMPLETING A BURROUGHS WELLCOME FUND POSTDOCTORAL FELLOWSHIP IN THE LABORATORY OF DR. SCOTT E. FRASER AT THE CALIFORNIA INSTITUTE OF TECHNOLOGY. DR. KULESA RECEIVED A PH.D. IN APPLIED MATHEMATICS UNDER DR. J.D. MURRAY AT THE UNIVERSITY OF WASHINGTON. RESEARCH FOCUS: CELL MIGRATION IN DEVELOPMENT AND CANCER - ARCADY MUSHEGIAN, PH.D., DIRECTOR OF BIOINFORMATICS RESEARCH, JOINED THE STOWERS INSTITUTE IN 2001 FROM AKKADIX CORPORATION IN SAN DIEGO WHERE HE LED THE BIOINFORMATICS PROGRAM. DR. MUSHEGIAN EARNED A DOCTORATE IN MOLECULAR BIOLOGY AT MOSCOW STATE UNIVERSITY AND RECEIVED TRAINING AT THE UNIVERSITY OF KENTUCKY, UNIVERSITY OF WASHINGTON, AND WITH DR. EUGENE KOONIN AT THE NATIONAL CENTER FOR BIOTECHNOLOGY INFORMATION AT THE U.S. NATIONAL INSTITUTES OF HEALTH. RESEARCH FOCUS: COMPUTATIONAL ANALYSIS OF GENES AND PROTEINS MICHAEL WASHBURN, PH.D., DIRECTOR OF PROTEOMICS, JOINED THE STOWERS INSTITUTE IN 2003 FROM THE TORREY MESA RESEARCH INSTITUTE IN SAN DIEGO WHERE HE WAS A SENIOR STAFF SCIENTIST IN PROTEOMICS. HE EARNED A PH.D. IN BIOCHEMISTRY AND ENVIRONMENTAL TOXICOLOGY FROM MICHIGAN STATE UNIVERSITY BEFORE COMPLETING A POSTDOCTORAL FELLOWSHIP WITH PROFESSOR JOHN YATES, III IN THE DEPARTMENT OF MOLECULAR BIOTECHNOLOGY AT THE UNIVERSITY OF WASHINGTON. RESEARCH FOCUS: QUANTITATIVE PROTEOMICS AND PROTEIN COMPLEX DYNAMICS |