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L Carrier

Showing results (171-180 of 211) with videos related to

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Mutagenesis|March 1, 1989
CHO mutant UV61 removes (6-4) photoproducts but not cyclobutane dimersL H Thompson, D L Mitchell, J D Regan, et al.
Journal of Molecular and Cellular Cardiology|August 5, 1998
Genomic organisation, alternative splicing and polymorphisms of the human cardiac troponin T geneH Farza, P J Townsend, L Carrier, et al.
Journal of Medical Genetics|February 9, 2000
First description of germline mosaicism in familial hypertrophic cardiomyopathyJ F Forissier, P Richard, S Briault, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 16, 1998
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathyJ Flavigny, P Richard, R Isnard, et al.
Journal of Medical Genetics|October 4, 2002
Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experienceP Charron, D Héron, M Gargiulo, et al.
Journal of Molecular and Cellular Cardiology|July 20, 2000
Homozygotes for a R869G mutation in the beta -myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathyP Richard, P Charron, C Leclercq, et al.
Journal of Medical Genetics|July 29, 1999
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathyP Richard, R Isnard, L Carrier, et al.
Journal of Materials Chemistry. B|July 1, 2024
Cationic-motif-modified exosomes for mRNA delivery to retinal photoreceptorsHéctor A Millán Cotto, Tanvi Vinod Pathrikar, Bill Hakim, et al.
Circulation|July 1, 1997
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult populationP Charron, O Dubourg, M Desnos, et al.
European Heart Journal|October 29, 1998
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped childrenP Charron, O Dubourg, M Desnos, et al.
Pageof 22

Showing results (171-180 of 211) with videos related to

Sort By:
Pageof 22
Mutagenesis|March 1, 1989
CHO mutant UV61 removes (6-4) photoproducts but not cyclobutane dimersL H Thompson, D L Mitchell, J D Regan, et al.
Journal of Molecular and Cellular Cardiology|August 5, 1998
Genomic organisation, alternative splicing and polymorphisms of the human cardiac troponin T geneH Farza, P J Townsend, L Carrier, et al.
Journal of Medical Genetics|February 9, 2000
First description of germline mosaicism in familial hypertrophic cardiomyopathyJ F Forissier, P Richard, S Briault, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 16, 1998
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathyJ Flavigny, P Richard, R Isnard, et al.
Journal of Medical Genetics|October 4, 2002
Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experienceP Charron, D Héron, M Gargiulo, et al.
Journal of Molecular and Cellular Cardiology|July 20, 2000
Homozygotes for a R869G mutation in the beta -myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathyP Richard, P Charron, C Leclercq, et al.
Journal of Medical Genetics|July 29, 1999
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathyP Richard, R Isnard, L Carrier, et al.
Journal of Materials Chemistry. B|July 1, 2024
Cationic-motif-modified exosomes for mRNA delivery to retinal photoreceptorsHéctor A Millán Cotto, Tanvi Vinod Pathrikar, Bill Hakim, et al.
Circulation|July 1, 1997
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult populationP Charron, O Dubourg, M Desnos, et al.
European Heart Journal|October 29, 1998
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped childrenP Charron, O Dubourg, M Desnos, et al.
Pageof 22