Schwartz K - Search Results

1

COOH-terminal truncated human cardiac MyBP-C alters myosin filament organization.

Sébillon P, Bonne G, Flavigny J, Venin S, Rouche A, Fiszman M, Vikstrom K, Leinwand L, Carrier L, Schwartz K. Sébillon P, et al. Among authors: schwartz k. C R Acad Sci III. 2001 Mar;324(3):251-60. doi: 10.1016/s0764-4469(00)01292-0. C R Acad Sci III. 2001. PMID: 11291312

2

Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy.

Carrier L, Bonne G, Bährend E, Yu B, Richard P, Niel F, Hainque B, Cruaud C, Gary F, Labeit S, Bouhour JB, Dubourg O, Desnos M, Hagège AA, Trent RJ, Komajda M, Fiszman M, Schwartz K. Carrier L, et al. Among authors: schwartz k. Circ Res. 1997 Mar;80(3):427-34. Circ Res. 1997. PMID: 9048664

3

COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes.

Flavigny J, Souchet M, Sébillon P, Berrebi-Bertrand I, Hainque B, Mallet A, Bril A, Schwartz K, Carrier L. Flavigny J, et al. Among authors: schwartz k. J Mol Biol. 1999 Nov 26;294(2):443-56. doi: 10.1006/jmbi.1999.3276. J Mol Biol. 1999. PMID: 10610770

4

Biomolecular interactions between human recombinant beta-MyHC and cMyBP-Cs implicated in familial hypertrophic cardiomyopathy.

Flavigny J, Robert P, Camelin JC, Schwartz K, Carrier L, Berrebi-Bertrand I. Flavigny J, et al. Among authors: schwartz k. Cardiovasc Res. 2003 Nov 1;60(2):388-96. doi: 10.1016/j.cardiores.2003.07.001. Cardiovasc Res. 2003. PMID: 14613868

5

Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice.

Carrier L, Knöll R, Vignier N, Keller DI, Bausero P, Prudhon B, Isnard R, Ambroisine ML, Fiszman M, Ross J Jr, Schwartz K, Chien KR. Carrier L, et al. Among authors: schwartz k. Cardiovasc Res. 2004 Aug 1;63(2):293-304. doi: 10.1016/j.cardiores.2004.04.009. Cardiovasc Res. 2004. PMID: 15249187

6

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy.

Bonne G, Carrier L, Bercovici J, Cruaud C, Richard P, Hainque B, Gautel M, Labeit S, James M, Beckmann J, Weissenbach J, Vosberg HP, Fiszman M, Komajda M, Schwartz K. Bonne G, et al. Among authors: schwartz k. Nat Genet. 1995 Dec;11(4):438-40. doi: 10.1038/ng1295-438. Nat Genet. 1995. PMID: 7493026

7

Exclusion of genes coding for proteins of the cytoskeleton and the extracellular matrix in familial hypertrophic cardiomyopathy using a candidate gene approach.

Dufour C, Carrier L, Hengstenberg C, Bercovici J, Dausse E, Weissenbach J, Dubourg O, Komajda M, Schwartz K, Beckmann JS. Dufour C, et al. Among authors: schwartz k. C R Acad Sci III. 1993;316(5):474-81. C R Acad Sci III. 1993. PMID: 8221230

8

Cardiac myosin binding protein C gene is specifically expressed in heart during murine and human development.

Fougerousse F, Delezoide AL, Fiszman MY, Schwartz K, Beckmann JS, Carrier L. Fougerousse F, et al. Among authors: schwartz k. Circ Res. 1998 Jan 9-23;82(1):130-3. doi: 10.1161/01.res.82.1.130. Circ Res. 1998. PMID: 9440712

9

The sarco(endo)plasmic reticulum Ca(2+)-ATPase gene is regulated at the transcriptional level during compensated left ventricular hypertrophy in the rat.

Ribadeau Dumas A, Wisnewsky C, Boheler KR, Ter Keurs H, Fiszman MY, Schwartz K. Ribadeau Dumas A, et al. Among authors: schwartz k. C R Acad Sci III. 1997 Dec;320(12):963-9. doi: 10.1016/s0764-4469(97)82469-9. C R Acad Sci III. 1997. PMID: 9587474

10

Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene.

Charron P, Dubourg O, Desnos M, Bennaceur M, Carrier L, Camproux AC, Isnard R, Hagege A, Langlard JM, Bonne G, Richard P, Hainque B, Bouhour JB, Schwartz K, Komajda M. Charron P, et al. Among authors: schwartz k. Circulation. 1998 Jun 9;97(22):2230-6. doi: 10.1161/01.cir.97.22.2230. Circulation. 1998. PMID: 9631872

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