There is a widely acknowledged national shortage of translationally trained young investigators, both Ph.D.s and M.D.s. To accomplish this goal, the Reproductive & Developmental Biology Training Program at the Massachusetts General Hospital selects strongly motivated candidates from a rich candidate pool; provides trainees with an intensive research experience in basic and/or clinical investigation; supports these efforts with a skilled and well-funded faculty engaged in important research questions; and complements this mentored research experience by a strong didactic experience in the underpinning sciences of genetics, reproductive and developmental biology and clinical investigation. Trainees are selected on the basis of prior academic and research accomplishments; a strong future commitment to an academic career; and a personal interview indicating their motivation and future potential as independent investigators. The PI (Dr. Crowley) is a Professor of Medicine at Harvard Medical School, Director of the Harvard Reproductive Endocrine Sciences Center, an established scientist and recognized mentor who governs in conjunction with Dr. Patricia Donahoe, a highly qualified senior scientist, who serves as Co-Director. The training faculty consists of active, well-funded scientists whose expertise lines the full spectrum of reproductive and developmental research from fundamental developmental biology to bench-to-bedside investigations. The training faculty has been expanded in this proposal to reflect and take appropriate advantage of the new tools and opportunities that are redefining translational research. Each trainee is closely supervised by an active yet individualized mentorship program overseen by a senior faculty member. An extensive and rigorous didactic program interlaces tightly with their strong, independent laboratory programs and compliments the trainees' 2-3 years of research experience (90%effort). The training period often involves additional years as junior faculty to ensure maximal competitiveness for subsequent independent support, the ultimate goal of this Training Program. Research facilities are spacious and fully equipped with recently modernized laboratory and clinical research space dedicated to the training faculty of this grant. The institutional environment is superb and the reinforcement from the Reproductive Endocrine Sciences Centers programs is substantial. This institutional training grant represents a critical stabilizing element in these programs and is a critical link that enables talented trainees to achieve subsequent independent careers in Reproduction and Developmental Biology. ? ? ?

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Institutional National Research Service Award (T32)
Project #
5T32HD007396-17
Application #
7496455
Study Section
Pediatrics Subcommittee (CHHD)
Program Officer
Taymans, Susan
Project Start
2007-05-01
Project End
2012-04-30
Budget Start
2008-05-01
Budget End
2009-04-30
Support Year
17
Fiscal Year
2008
Total Cost
$247,920
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
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Shaw, Natalie D; Brand, Harrison; Kupchinsky, Zachary A et al. (2017) SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. Nat Genet 49:238-248
Cox, Kimberly H (2016) A Bisphenol by Any Other Name... Endocrinology 157:449-51
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Cox, Kimberly H (2015) A Kiss and a PRomise. Endocrinology 156:3063-5
Brand, Harrison; Collins, Ryan L; Hanscom, Carrie et al. (2015) Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation. Am J Hum Genet 97:170-6
Miraoui, Hichem; Dwyer, Andrew A; Sykiotis, Gerasimos P et al. (2013) Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism. Am J Hum Genet 92:725-43
Chew, Sheena; Balasubramanian, Ravikumar; Chan, Wai-Man et al. (2013) A novel syndrome caused by the E410K amino acid substitution in the neuronal ?-tubulin isotype 3. Brain 136:522-35
Yang, Jasmine J; Caligioni, Claudia S; Chan, Yee-Ming et al. (2012) Uncovering novel reproductive defects in neurokinin B receptor null mice: closing the gap between mice and men. Endocrinology 153:1498-508

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