Harvard Title
Professor of Medicine
Address
Brigham and Women's Hospital
Endocrine RFB 296
221 Longwood Ave
Boston MA 02115
Publications View
Tet3 CXXC domain and dioxygenase activity cooperatively regulate key genes for Xenopus eye and neural development.
Authors: Xu Y, Xu C, Kato A, Tempel W, Abreu JG, Bian C, Hu Y, Hu D, Zhao B, Cerovina T, Diao J, Wu F, He HH, Cui Q, Clark E, Ma C, Barbara A, Veenstra GJ, Xu G, Kaiser UB, Liu XS, Sugrue SP, He X, Min J, Kato Y, Shi YG.
Cell
View full abstract on Pubmed
Cell
View full abstract on Pubmed
Mutational analysis of TAC3 and TACR3 genes in patients with idiopathic central pubertal disorders.
Authors: Tusset C, Noel SD, Trarbach EB, Silveira LF, Jorge AA, Brito VN, Cukier P, Seminara SB, Mendonça BB, Kaiser UB, Latronico AC.
Arq Bras Endocrinol Metabol
View full abstract on Pubmed
Arq Bras Endocrinol Metabol
View full abstract on Pubmed
Single-cell analyses reveal that KISS1R-expressing cells undergo sustained kisspeptin-induced signaling that is dependent upon an influx of extracellular Ca2+.
Authors: Babwah AV, Pampillo M, Min L, Kaiser UB, Bhattacharya M.
Endocrinology
View full abstract on Pubmed
Endocrinology
View full abstract on Pubmed
Increased neurokinin B (Tac2) expression in the mouse arcuate nucleus is an early marker of pubertal onset with differential sensitivity to sex steroid-negative feedback than Kiss1.
Authors: Gill JC, Navarro VM, Kwong C, Noel SD, Martin C, Xu S, Clifton DK, Carroll RS, Steiner RA, Kaiser UB.
Endocrinology
View full abstract on Pubmed
Endocrinology
View full abstract on Pubmed
Hyperprolactinemia and infertility: new insights.
Loss of 5-hydroxymethylcytosine is an epigenetic hallmark of melanoma.
Authors: Lian CG, Xu Y, Ceol C, Wu F, Larson A, Dresser K, Xu W, Tan L, Hu Y, Zhan Q, Lee CW, Hu D, Lian BQ, Kleffel S, Yang Y, Neiswender J, Khorasani AJ, Fang R, Lezcano C, Duncan LM, Scolyer RA, Thompson JF, Kakavand H, Houvras Y, Zon LI, Mihm MC, Kaiser UB, Schatton T, Woda BA, Murphy GF, Shi YG.
Cell
View full abstract on Pubmed
Cell
View full abstract on Pubmed
When genetic load does not correlate with phenotypic spectrum: lessons from the GnRH receptor (GNRHR).
Authors: Gianetti E, Hall JE, Au MG, Kaiser UB, Quinton R, Stewart JA, Metzger DL, Pitteloud N, Mericq V, Merino PM, Levitsky LL, Izatt L, Lang-Muritano M, Fujimoto VY, Dluhy RG, Chase ML, Crowley WF, Plummer L, Seminara SB.
J Clin Endocrinol Metab
View full abstract on Pubmed
J Clin Endocrinol Metab
View full abstract on Pubmed
Evidence of the importance of the first intracellular loop of prokineticin receptor 2 in receptor function.
Authors: Abreu AP, Noel SD, Xu S, Carroll RS, Latronico AC, Kaiser UB.
Mol Endocrinol
View full abstract on Pubmed
Mol Endocrinol
View full abstract on Pubmed
GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1.
Authors: Chan YM, Broder-Fingert S, Paraschos S, Lapatto R, Au M, Hughes V, Bianco SD, Min L, Plummer L, Cerrato F, De Guillebon A, Wu IH, Wahab F, Dwyer A, Kirsch S, Quinton R, Cheetham T, Ozata M, Ten S, Chanoine JP, Pitteloud N, Martin KA, Schiffmann R, Van der Kamp HJ, Nader S, Hall JE, Kaiser UB, Seminara SB.
J Clin Endocrinol Metab
View full abstract on Pubmed
J Clin Endocrinol Metab
View full abstract on Pubmed
G protein-coupled receptors involved in GnRH regulation: molecular insights from human disease.