Bowles KR - Search Results

1

The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathy.

Bowles NE, Bowles KR, Towbin JA. Bowles NE, et al. Among authors: bowles kr. Herz. 2000 May;25(3):168-75. doi: 10.1007/s000590050003. Herz. 2000. PMID: 10904835 Review.

2

Prospects for gene therapy for inherited cardiomyopathies.

Bowles NE, Bowles K, Towbin JA. Bowles NE, et al. Prog Pediatr Cardiol. 2000 Nov 4;12(1):133-145. doi: 10.1016/s1058-9813(00)00065-5. Prog Pediatr Cardiol. 2000. PMID: 11114553

3

Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis.

Mohapatra B, Jimenez S, Lin JH, Bowles KR, Coveler KJ, Marx JG, Chrisco MA, Murphy RT, Lurie PR, Schwartz RJ, Elliott PM, Vatta M, McKenna W, Towbin JA, Bowles NE. Mohapatra B, et al. Among authors: bowles kr, bowles ne. Mol Genet Metab. 2003 Sep-Oct;80(1-2):207-15. doi: 10.1016/s1096-7192(03)00142-2. Mol Genet Metab. 2003. PMID: 14567970

4

Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction.

Vatta M, Mohapatra B, Jimenez S, Sanchez X, Faulkner G, Perles Z, Sinagra G, Lin JH, Vu TM, Zhou Q, Bowles KR, Di Lenarda A, Schimmenti L, Fox M, Chrisco MA, Murphy RT, McKenna W, Elliott P, Bowles NE, Chen J, Valle G, Towbin JA. Vatta M, et al. Among authors: bowles kr, bowles ne. J Am Coll Cardiol. 2003 Dec 3;42(11):2014-27. doi: 10.1016/j.jacc.2003.10.021. J Am Coll Cardiol. 2003. PMID: 14662268 Free article.

5

Genetics of inherited cardiomyopathies.

Bowles KR, Bowles NE. Bowles KR, et al. Among authors: bowles ne. Expert Rev Cardiovasc Ther. 2004 Sep;2(5):683-97. doi: 10.1586/14779072.2.5.683. Expert Rev Cardiovasc Ther. 2004. PMID: 15350170 Review.

6

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

Bowles KR, Gajarski R, Porter P, Goytia V, Bachinski L, Roberts R, Pignatelli R, Towbin JA. Bowles KR, et al. J Clin Invest. 1996 Sep 15;98(6):1355-60. doi: 10.1172/JCI118922. J Clin Invest. 1996. PMID: 8823300 Free PMC article.

7

Genomic characterization of the human peptidyl-prolyl-cis-trans-isomerase, mitochondrial precursor gene: assessment of its role in familial dilated cardiomyopathy.

Bowles KR, Zintz C, Abraham SE, Brandon L, Bowles NE, Towbin JA. Bowles KR, et al. Among authors: bowles ne. Hum Genet. 1999 Dec;105(6):582-6. doi: 10.1007/s004399900173. Hum Genet. 1999. PMID: 10647893

8

Construction of a high-resolution physical map of the chromosome 10q22-q23 dilated cardiomyopathy locus and analysis of candidate genes.

Bowles KR, Abraham SE, Brugada R, Zintz C, Comeaux J, Sorajja D, Tsubata S, Li H, Brandon L, Gibbs RA, Scherer SE, Bowles NE, Towbin JA. Bowles KR, et al. Among authors: bowles ne. Genomics. 2000 Jul 15;67(2):109-27. doi: 10.1006/geno.2000.6242. Genomics. 2000. PMID: 10903836

9

Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy.

Tsubata S, Bowles KR, Vatta M, Zintz C, Titus J, Muhonen L, Bowles NE, Towbin JA. Tsubata S, et al. Among authors: bowles kr, bowles ne. J Clin Invest. 2000 Sep;106(5):655-62. doi: 10.1172/JCI9224. J Clin Invest. 2000. PMID: 10974018 Free PMC article.

10

Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction.

Chen R, Tsuji T, Ichida F, Bowles KR, Yu X, Watanabe S, Hirono K, Tsubata S, Hamamichi Y, Ohta J, Imai Y, Bowles NE, Miyawaki T, Towbin JA; Noncompaction study collaborators. Chen R, et al. Among authors: bowles kr, bowles ne. Mol Genet Metab. 2002 Dec;77(4):319-25. doi: 10.1016/s1096-7192(02)00195-6. Mol Genet Metab. 2002. PMID: 12468278

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