Seidman J - Search Results

1

Telomere shortening is a hallmark of genetic cardiomyopathies.

Chang ACY, Chang ACH, Kirillova A, Sasagawa K, Su W, Weber G, Lin J, Termglinchan V, Karakikes I, Seeger T, Dainis AM, Hinson JT, Seidman J, Seidman CE, Day JW, Ashley E, Wu JC, Blau HM. Chang ACY, et al. Among authors: seidman j, seidman ce. Proc Natl Acad Sci U S A. 2018 Sep 11;115(37):9276-9281. doi: 10.1073/pnas.1714538115. Epub 2018 Aug 27. Proc Natl Acad Sci U S A. 2018. PMID: 30150400 Free PMC article.

2

IL-12 is required for differentiation of pathogenic CD8+ T cell effectors that cause myocarditis.

Grabie N, Delfs MW, Westrich JR, Love VA, Stavrakis G, Ahmad F, Seidman CE, Seidman JG, Lichtman AH. Grabie N, et al. J Clin Invest. 2003 Mar;111(5):671-80. doi: 10.1172/JCI16867. J Clin Invest. 2003. PMID: 12618521 Free PMC article.

3

Rescue of cardiomyocyte dysfunction by phospholamban ablation does not prevent ventricular failure in genetic hypertrophy.

Song Q, Schmidt AG, Hahn HS, Carr AN, Frank B, Pater L, Gerst M, Young K, Hoit BD, McConnell BK, Haghighi K, Seidman CE, Seidman JG, Dorn GW 2nd, Kranias EG. Song Q, et al. J Clin Invest. 2003 Mar;111(6):859-67. doi: 10.1172/JCI16738. J Clin Invest. 2003. PMID: 12639992 Free PMC article.

4

A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia.

Jumlongras D, Lin JY, Chapra A, Seidman CE, Seidman JG, Maas RL, Olsen BR. Jumlongras D, et al. Hum Genet. 2004 Feb;114(3):242-9. doi: 10.1007/s00439-003-1066-6. Epub 2003 Dec 19. Hum Genet. 2004. PMID: 14689302

5

The T-Box transcription factor Tbx5 is required for the patterning and maturation of the murine cardiac conduction system.

Moskowitz IP, Pizard A, Patel VV, Bruneau BG, Kim JB, Kupershmidt S, Roden D, Berul CI, Seidman CE, Seidman JG. Moskowitz IP, et al. Development. 2004 Aug;131(16):4107-16. doi: 10.1242/dev.01265. Development. 2004. PMID: 15289437

6

Genetic causes of human heart failure.

Morita H, Seidman J, Seidman CE. Morita H, et al. Among authors: seidman j, seidman ce. J Clin Invest. 2005 Mar;115(3):518-26. doi: 10.1172/JCI24351. J Clin Invest. 2005. PMID: 15765133 Free PMC article. Review.

7

N488I mutation of the gamma2-subunit results in bidirectional changes in AMP-activated protein kinase activity.

Zou L, Shen M, Arad M, He H, Løfgren B, Ingwall JS, Seidman CE, Seidman JG, Tian R. Zou L, et al. Circ Res. 2005 Aug 19;97(4):323-8. doi: 10.1161/01.RES.0000179035.20319.c2. Epub 2005 Jul 28. Circ Res. 2005. PMID: 16051890

8

Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling.

Ingles J, Doolan A, Chiu C, Seidman J, Seidman C, Semsarian C. Ingles J, et al. Among authors: seidman j, seidman c. J Med Genet. 2005 Oct;42(10):e59. doi: 10.1136/jmg.2005.033886. J Med Genet. 2005. PMID: 16199542 Free PMC article.

9

Cardiac myosin-binding protein-C phosphorylation and cardiac function.

Sadayappan S, Gulick J, Osinska H, Martin LA, Hahn HS, Dorn GW 2nd, Klevitsky R, Seidman CE, Seidman JG, Robbins J. Sadayappan S, et al. Among authors: seidman jg, seidman ce. Circ Res. 2005 Nov 25;97(11):1156-63. doi: 10.1161/01.RES.0000190605.79013.4d. Epub 2005 Oct 13. Circ Res. 2005. PMID: 16224063 Free PMC article.

10

Cardiovascular genomics.

Sabatine MS, Seidman JG, Seidman CE. Sabatine MS, et al. Circulation. 2006 Mar 21;113(11):e450-5. doi: 10.1161/CIRCULATIONAHA.105.560151. Circulation. 2006. PMID: 16549641 No abstract available.

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