Seidman JG - Search Results

1

Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.

Pollak MR, Brown EM, Chou YH, Hebert SC, Marx SJ, Steinmann B, Levi T, Seidman CE, Seidman JG. Pollak MR, et al. Among authors: seidman jg, seidman ce. Cell. 1993 Dec 31;75(7):1297-303. doi: 10.1016/0092-8674(93)90617-y. Cell. 1993. PMID: 7916660

2

The cloning of extracellular Ca(2+)-sensing receptors from parathyroid and kidney: molecular mechanisms of extracellular Ca(2+)-sensing.

Brown EM, Pollak M, Chou YH, Seidman CE, Seidman JG, Hebert SC. Brown EM, et al. Among authors: seidman jg, seidman ce. J Nutr. 1995 Jul;125(7 Suppl):1965S-1970S. doi: 10.1093/jn/125.suppl_7.1965S. J Nutr. 1995. PMID: 7602378 Review.

3

Mutations in the human Ca(2+)-sensing-receptor gene that cause familial hypocalciuric hypercalcemia.

Chou YH, Pollak MR, Brandi ML, Toss G, Arnqvist H, Atkinson AB, Papapoulos SE, Marx S, Brown EM, Seidman JG, et al. Chou YH, et al. Among authors: seidman jg. Am J Hum Genet. 1995 May;56(5):1075-9. Am J Hum Genet. 1995. PMID: 7726161 Free PMC article.

4

Calcium-ion-sensing cell-surface receptors.

Brown EM, Pollak M, Seidman CE, Seidman JG, Chou YH, Riccardi D, Hebert SC. Brown EM, et al. Among authors: seidman jg, seidman ce. N Engl J Med. 1995 Jul 27;333(4):234-40. doi: 10.1056/NEJM199507273330407. N Engl J Med. 1995. PMID: 7791841 Review. No abstract available.

5

Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation.

Pollak MR, Brown EM, Estep HL, McLaine PN, Kifor O, Park J, Hebert SC, Seidman CE, Seidman JG. Pollak MR, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1994 Nov;8(3):303-7. doi: 10.1038/ng1194-303. Nat Genet. 1994. PMID: 7874174

6

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.

Thierfelder L, Watkins H, MacRae C, Lamas R, McKenna W, Vosberg HP, Seidman JG, Seidman CE. Thierfelder L, et al. Among authors: seidman jg, seidman ce. Cell. 1994 Jun 3;77(5):701-12. doi: 10.1016/0092-8674(94)90054-x. Cell. 1994. PMID: 8205619

7

Cloning and functional characterization of extracellular Ca(2+)-sensing receptors from parathyroid and kidney.

Brown EM, Pollak M, Chou YH, Seidman CE, Seidman JG, Hebert SC. Brown EM, et al. Among authors: seidman jg, seidman ce. Bone. 1995 Aug;17(2 Suppl):7S-11S. doi: 10.1016/8756-3282(95)00199-n. Bone. 1995. PMID: 8579901 Review.

8

The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families.

Chou YH, Brown EM, Levi T, Crowe G, Atkinson AB, Arnqvist HJ, Toss G, Fuleihan GE, Seidman JG, Seidman CE. Chou YH, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1992 Jul;1(4):295-300. doi: 10.1038/ng0792-295. Nat Genet. 1992. PMID: 1302026

9

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.

Geisterfer-Lowrance AA, Kass S, Tanigawa G, Vosberg HP, McKenna W, Seidman CE, Seidman JG. Geisterfer-Lowrance AA, et al. Among authors: seidman jg, seidman ce. Cell. 1990 Sep 7;62(5):999-1006. doi: 10.1016/0092-8674(90)90274-i. Cell. 1990. PMID: 1975517

10

A molecular basis for familial hypertrophic cardiomyopathy: an alpha/beta cardiac myosin heavy chain hybrid gene.

Tanigawa G, Jarcho JA, Kass S, Solomon SD, Vosberg HP, Seidman JG, Seidman CE. Tanigawa G, et al. Among authors: seidman jg, seidman ce. Cell. 1990 Sep 7;62(5):991-8. doi: 10.1016/0092-8674(90)90273-h. Cell. 1990. PMID: 2144212

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