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L L Bachinski

Showing results (1-10 of 28) with videos related to

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Molecular Medicine Today|September 1, 1996
Familial hypertrophic cardiomyopathy: diagnostic and therapeutic implications of recent genetic studiesL L Bachinski, R Roberts
Cardiology Clinics|January 19, 1999
New theories. Causes of dilated cardiomyopathyL L Bachinski, R Roberts
Genomics|June 21, 2001
Genomic organization and isoform-specific tissue expression of human NAPOR (CUGBP2) as a candidate gene for familial arrhythmogenic right ventricular dysplasiaD Li, L L Bachinski, R Roberts
Gene|October 31, 2000
Human protein tyrosine phosphatase-like gene: expression profile, genomic structure, and mutation analysis in families with ARVDD Li, O Gonzalez, L L Bachinski, et al.
Annals of Neurology|March 11, 1999
Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsyT Matsuura, M Achari, M Khajavi, et al.
Molecular and Cellular Probes|February 1, 1997
Polymorphic trinucleotide repeat in the MEF2A gene at 15q26 is not expanded in familial cardiomyopathiesL L Bachinski, A Abchee, J B Durand, et al.
Genomics|February 13, 2001
Identification and characterization of a novel gene (C4orf5) located on human chromosome 4q with specific expression in cardiac and skeletal muscleF Ahmad, O Gonzalez, L Ramagli, et al.
American Journal of Human Genetics|August 1, 1988
Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repairR L Stallings, E Olson, A W Strauss, et al.
Neuropathology and Applied Neurobiology|July 5, 2012
Altered expression and splicing of Ca(2+) metabolism genes in myotonic dystrophies DM1 and DM2A Vihola, M Sirito, L L Bachinski, et al.
Biochemical and Biophysical Research Communications|July 25, 2000
Molecular cloning, expression analysis, and chromosome mapping of WDR6, a novel human WD-repeat geneD Li, P Burch, O Gonzalez, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Molecular Medicine Today|September 1, 1996
Familial hypertrophic cardiomyopathy: diagnostic and therapeutic implications of recent genetic studiesL L Bachinski, R Roberts
Cardiology Clinics|January 19, 1999
New theories. Causes of dilated cardiomyopathyL L Bachinski, R Roberts
Genomics|June 21, 2001
Genomic organization and isoform-specific tissue expression of human NAPOR (CUGBP2) as a candidate gene for familial arrhythmogenic right ventricular dysplasiaD Li, L L Bachinski, R Roberts
Gene|October 31, 2000
Human protein tyrosine phosphatase-like gene: expression profile, genomic structure, and mutation analysis in families with ARVDD Li, O Gonzalez, L L Bachinski, et al.
Annals of Neurology|March 11, 1999
Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsyT Matsuura, M Achari, M Khajavi, et al.
Molecular and Cellular Probes|February 1, 1997
Polymorphic trinucleotide repeat in the MEF2A gene at 15q26 is not expanded in familial cardiomyopathiesL L Bachinski, A Abchee, J B Durand, et al.
Genomics|February 13, 2001
Identification and characterization of a novel gene (C4orf5) located on human chromosome 4q with specific expression in cardiac and skeletal muscleF Ahmad, O Gonzalez, L Ramagli, et al.
American Journal of Human Genetics|August 1, 1988
Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repairR L Stallings, E Olson, A W Strauss, et al.
Neuropathology and Applied Neurobiology|July 5, 2012
Altered expression and splicing of Ca(2+) metabolism genes in myotonic dystrophies DM1 and DM2A Vihola, M Sirito, L L Bachinski, et al.
Biochemical and Biophysical Research Communications|July 25, 2000
Molecular cloning, expression analysis, and chromosome mapping of WDR6, a novel human WD-repeat geneD Li, P Burch, O Gonzalez, et al.
Pageof 3