Seidman CE - Search Results

1

Spatiotemporal Multi-Omics Mapping Generates a Molecular Atlas of the Aortic Valve and Reveals Networks Driving Disease.

Schlotter F, Halu A, Goto S, Blaser MC, Body SC, Lee LH, Higashi H, DeLaughter DM, Hutcheson JD, Vyas P, Pham T, Rogers MA, Sharma A, Seidman CE, Loscalzo J, Seidman JG, Aikawa M, Singh SA, Aikawa E. Schlotter F, et al. Among authors: seidman jg, seidman ce. Circulation. 2018 Jul 24;138(4):377-393. doi: 10.1161/CIRCULATIONAHA.117.032291. Circulation. 2018. PMID: 29588317 Free PMC article.

2

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.

3

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.

4

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

5

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.

6

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

7

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

8

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.

9

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

10

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1.

Jarcho JA, McKenna W, Pare JA, Solomon SD, Holcombe RF, Dickie S, Levi T, Donis-Keller H, Seidman JG, Seidman CE. Jarcho JA, et al. Among authors: seidman jg, seidman ce. N Engl J Med. 1989 Nov 16;321(20):1372-8. doi: 10.1056/NEJM198911163212005. N Engl J Med. 1989. PMID: 2811944

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