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H P Vosberg

Showing results (51-60 of 58) with videos related to

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Journal of Muscle Research and Cell Motility|October 1, 1990
Expression of human beta-myosin heavy chain fragments in Escherichia coli; localization of actin interfaces on cardiac myosinP Eldin, M Le Cunff, K W Diederich, et al.
Journal of Molecular and Cellular Cardiology|September 1, 1994
Identification of a mutation near a functional site of the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathyC Dufour, E Dausse, L Fetler, et al.
Circulation Research|July 1, 1992
Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French familiesK Schwartz, J Beckmann, C Dufour, et al.
Heart (British Cardiac Society)|February 16, 2002
Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C geneJ R Ortlepp, H P Vosberg, S Reith, et al.
Journal of the American College of Cardiology|March 1, 1997
Clinical features of hypertrophic cardiomyopathy caused by mutation of a "hot spot" in the alpha-tropomyosin geneD A Coviello, B J Maron, P Spirito, et al.
Circulation|March 29, 2000
A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetranceJ A Moolman, S Reith, K Uhl, et al.
American Journal of Human Genetics|September 1, 1990
A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12S D Solomon, A A Geisterfer-Lowrance, H P Vosberg, et al.
Nature Genetics|December 1, 1995
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathyG Bonne, L Carrier, J Bercovici, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Journal of Muscle Research and Cell Motility|October 1, 1990
Expression of human beta-myosin heavy chain fragments in Escherichia coli; localization of actin interfaces on cardiac myosinP Eldin, M Le Cunff, K W Diederich, et al.
Journal of Molecular and Cellular Cardiology|September 1, 1994
Identification of a mutation near a functional site of the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathyC Dufour, E Dausse, L Fetler, et al.
Circulation Research|July 1, 1992
Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French familiesK Schwartz, J Beckmann, C Dufour, et al.
Heart (British Cardiac Society)|February 16, 2002
Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C geneJ R Ortlepp, H P Vosberg, S Reith, et al.
Journal of the American College of Cardiology|March 1, 1997
Clinical features of hypertrophic cardiomyopathy caused by mutation of a "hot spot" in the alpha-tropomyosin geneD A Coviello, B J Maron, P Spirito, et al.
Circulation|March 29, 2000
A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetranceJ A Moolman, S Reith, K Uhl, et al.
American Journal of Human Genetics|September 1, 1990
A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12S D Solomon, A A Geisterfer-Lowrance, H P Vosberg, et al.
Nature Genetics|December 1, 1995
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathyG Bonne, L Carrier, J Bercovici, et al.
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