Seidman CE - Search Results

1

GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm.

Sharma A, Wasson LK, Willcox JA, Morton SU, Gorham JM, DeLaughter DM, Neyazi M, Schmid M, Agarwal R, Jang MY, Toepfer CN, Ward T, Kim Y, Pereira AC, DePalma SR, Tai A, Kim S, Conner D, Bernstein D, Gelb BD, Chung WK, Goldmuntz E, Porter G, Tristani-Firouzi M, Srivastava D, Seidman JG, Seidman CE; Pediatric Cardiac Genomics Consortium. Sharma A, et al. Among authors: seidman jg, seidman ce. Elife. 2020 Oct 15;9:e53278. doi: 10.7554/eLife.53278. Elife. 2020. PMID: 33054971 Free PMC article.

2

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

3

Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.

Watkins H, Thierfelder L, Hwang DS, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. J Clin Invest. 1992 Nov;90(5):1666-71. doi: 10.1172/JCI116038. J Clin Invest. 1992. PMID: 1430197 Free PMC article.

4

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.

Watkins H, Rosenzweig A, Hwang DS, Levi T, McKenna W, Seidman CE, Seidman JG. Watkins H, et al. Among authors: seidman jg, seidman ce. N Engl J Med. 1992 Apr 23;326(17):1108-14. doi: 10.1056/NEJM199204233261703. N Engl J Med. 1992. PMID: 1552912 Free article.

5

cis-dominance of rat atrial natriuretic factor gene regulatory sequences in transgenic mice.

Seidman CE, Schmidt EV, Seidman JG. Seidman CE, et al. Among authors: seidman jg. Can J Physiol Pharmacol. 1991 Oct;69(10):1486-92. doi: 10.1139/y91-223. Can J Physiol Pharmacol. 1991. PMID: 1723347

6

Mutations in cardiac myosin heavy chain genes cause familial hypertrophic cardiomyopathy.

Seidman CE, Seidman JG. Seidman CE, et al. Among authors: seidman jg. Mol Biol Med. 1991 Apr;8(2):159-66. Mol Biol Med. 1991. PMID: 1806760 Review.

7

Proximal regulatory domains of rat atrial natriuretic factor gene.

Rosenzweig A, Halazonetis TD, Seidman JG, Seidman CE. Rosenzweig A, et al. Among authors: seidman jg, seidman ce. Circulation. 1991 Sep;84(3):1256-65. doi: 10.1161/01.cir.84.3.1256. Circulation. 1991. PMID: 1832094

8

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

9

Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.

Solomon SD, Jarcho JA, McKenna W, Geisterfer-Lowrance A, Germain R, Salerni R, Seidman JG, Seidman CE. Solomon SD, et al. Among authors: seidman jg, seidman ce. J Clin Invest. 1990 Sep;86(3):993-9. doi: 10.1172/JCI114802. J Clin Invest. 1990. PMID: 1975599 Free PMC article.

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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