AAAAAA

   
Results: 1-8 |
Results: 8
Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome
Authors: Ichida, F Tsubata, S Bowles, KR Haneda, N Uese, K Miyawaki, T Dreyer, WJ Messina, J Li, H Bowles, NE Towbin, JA
Citation: F. Ichida et al., Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome, CIRCULATION, 103(9), 2001, pp. 1256-1263
Construction of a high-resolution physical map of the chromosome 10q22-q23dilated cardiomyopathy locus and analysis of candidate genes
Authors: 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
Citation: Kr. Bowles et al., Construction of a high-resolution physical map of the chromosome 10q22-q23dilated cardiomyopathy locus and analysis of candidate genes, GENOMICS, 67(2), 2000, pp. 109-127
The "final common pathway" hypothesis and inherited cardiovascular disease- The role of cytoskeletal proteins in dilated cardiomyopathy
Authors: Bowles, NE Bowles, KR Towbin, JA
Citation: Ne. Bowles et al., The "final common pathway" hypothesis and inherited cardiovascular disease- The role of cytoskeletal proteins in dilated cardiomyopathy, HERZ, 25(3), 2000, pp. 168-175
Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy
Authors: Tsubata, S Bowles, KR Vatta, M Zintz, C Titus, J Muhonen, L Bowles, NE Towbin, JA
Citation: S. Tsubata et al., Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy, J CLIN INV, 106(5), 2000, pp. 655-662
Etiologies of cardiomyopathy and heart failure
Authors: Towbin, JA Bowles, KR Bowles, NE
Citation: Ja. Towbin et al., Etiologies of cardiomyopathy and heart failure, NAT MED, 5(3), 1999, pp. 266-267
Revised fine mapping of the human voltage-dependent anion channel loci by radiation hybrid analysis
Authors: Decker, WK Bowles, KR Schatte, EC Towbin, JA Craigen, WJ
Citation: Wk. Decker et al., Revised fine mapping of the human voltage-dependent anion channel loci by radiation hybrid analysis, MAMM GENOME, 10(10), 1999, pp. 1041-1042
Genomic characterization of the human peptidyl-prolyl-cis-trans-isomerase,mitochondrial precursor gene: assessment of its role in familial dilated cardiomyopathy
Authors: Bowles, KR Zintz, C Abraham, SE Brandon, L Bowles, NE Towbin, JA
Citation: Kr. Bowles et al., Genomic characterization of the human peptidyl-prolyl-cis-trans-isomerase,mitochondrial precursor gene: assessment of its role in familial dilated cardiomyopathy, HUM GENET, 105(6), 1999, pp. 582-586
Genomic organization and chromosomal localization of the human Coxsackievirus B-adenovirus receptor gene
Authors: Bowles, KR Gibson, J Wu, J Shaffer, LG Towbin, JA Bowles, NE
Citation: Kr. Bowles et al., Genomic organization and chromosomal localization of the human Coxsackievirus B-adenovirus receptor gene, HUM GENET, 105(4), 1999, pp. 354-359
Risultati: 1-8 |