Jonathan G. Seidman, Ph.D.
Henrietta B. and Frederick H. Bugher Foundation Professor of Genetics, Harvard Medical School
Calcium-ion-sensing cell-surface receptors.
Authors: Authors: Brown EM, Pollak M, Seidman CE, Seidman JG, Chou YH, Riccardi D, Hebert SC.
N Engl J Med
View full abstract on Pubmed
N Engl J Med
View full abstract on Pubmed
The cloning of extracellular Ca(2+)-sensing receptors from parathyroid and kidney: molecular mechanisms of extracellular Ca(2+)-sensing.
Authors: Authors: Brown EM, Pollak M, Chou YH, Seidman CE, Seidman JG, Hebert SC.
J Nutr
View full abstract on Pubmed
J Nutr
View full abstract on Pubmed
A de novo mutation in alpha-tropomyosin that causes hypertrophic cardiomyopathy.
Authors: Authors: Watkins H, Anan R, Coviello DA, Spirito P, Seidman JG, Seidman CE.
Circulation
View full abstract on Pubmed
Circulation
View full abstract on Pubmed
Mutations in the human Ca(2+)-sensing-receptor gene that cause familial hypocalciuric hypercalcemia.
Authors: Authors: Chou YH, Pollak MR, Brandi ML, Toss G, Arnqvist H, Atkinson AB, Papapoulos SE, Marx S, Brown EM, Seidman JG, et al.
Am J Hum Genet
View full abstract on Pubmed
Am J Hum Genet
View full abstract on Pubmed
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy.
Authors: Authors: Watkins H, McKenna WJ, Thierfelder L, Suk HJ, Anan R, O'Donoghue A, Spirito P, Matsumori A, Moravec CS, Seidman JG, et al.
N Engl J Med
View full abstract on Pubmed
N Engl J Med
View full abstract on Pubmed
Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy.
A dinucleotide repeat polymorphism in the MYBPH gene.
Authors: Authors: Watkins H, MacRae CA, Fischman DA, Seidman JG, Seidman CE.
Hum Mol Genet
View full abstract on Pubmed
Hum Mol Genet
View full abstract on Pubmed
Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation.
Authors: Authors: Pollak MR, Brown EM, Estep HL, McLaine PN, Kifor O, Park J, Hebert SC, Seidman CE, Seidman JG.
Nat Genet
View full abstract on Pubmed
Nat Genet
View full abstract on Pubmed
Assignment of a locus for dominantly inherited venous malformations to chromosome 9p.
Authors: Authors: Boon LM, Mulliken JB, Vikkula M, Watkins H, Seidman J, Olsen BR, Warman ML.
Hum Mol Genet
View full abstract on Pubmed
Hum Mol Genet
View full abstract on Pubmed
T cell receptor (beta chain) transgenic mice have selective deficits in gamma delta T cell subpopulations.
Authors: Authors: Rimm IJ, Fruman DA, Abhyankar S, Sakamoto H, Orme IM, Milstone D, Seidman JG, Ferrara JL.
Transpl Immunol
View full abstract on Pubmed
Transpl Immunol
View full abstract on Pubmed