Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

L L Bachinski

Showing results (11-20 of 28) with videos related to

Pageof 3
Sort By:
Genomics|November 1, 1989
Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19L H Thompson, L L Bachinski, R L Stallings, et al.
Neurology|November 21, 2008
Premutation allele pool in myotonic dystrophy type 2L L Bachinski, T Czernuszewicz, L S Ramagli, et al.
American Journal of Human Genetics|June 1, 1990
A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locusK Johnson, P Shelbourne, J Davies, et al.
Circulation|February 1, 1993
Hypertrophic cardiomyopathy mutation is expressed in messenger RNA of skeletal as well as cardiac muscleQ T Yu, J Ifegwu, A J Marian, et al.
American Journal of Human Genetics|February 1, 1993
An informative panel of somatic cell hybrids for physical mapping on human chromosome 19qL L Bachinski, R Krahe, B F White, et al.
Circulation|July 12, 2001
Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophyS F Nagueh, L L Bachinski, D Meyer, et al.
Genomics|September 1, 1992
The CCAAT/enhancer binding protein (C/EBP alpha) gene (CEBPA) maps to human chromosome 19q13.1 and the related nuclear factor NF-IL6 (C/EBP beta) gene (CEBPB) maps to human chromosome 20q13.1L R Hendricks-Taylor, L L Bachinski, M J Siciliano, et al.
The New England Journal of Medicine|March 27, 1997
Identification of a genetic locus for familial atrial fibrillationR Brugada, T Tapscott, G Z Czernuszewicz, et al.
Circulation|December 22, 1998
Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23F Ahmad, D Li, A Karibe, et al.
Circulation|January 4, 2001
Hypertrophic cardiomyopathy caused by a novel alpha-tropomyosin mutation (V95A) is associated with mild cardiac phenotype, abnormal calcium binding to troponin, abnormal myosin cycling, and poor prognosisA Karibe, L S Tobacman, J Strand, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Genomics|November 1, 1989
Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19L H Thompson, L L Bachinski, R L Stallings, et al.
Neurology|November 21, 2008
Premutation allele pool in myotonic dystrophy type 2L L Bachinski, T Czernuszewicz, L S Ramagli, et al.
American Journal of Human Genetics|June 1, 1990
A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locusK Johnson, P Shelbourne, J Davies, et al.
Circulation|February 1, 1993
Hypertrophic cardiomyopathy mutation is expressed in messenger RNA of skeletal as well as cardiac muscleQ T Yu, J Ifegwu, A J Marian, et al.
American Journal of Human Genetics|February 1, 1993
An informative panel of somatic cell hybrids for physical mapping on human chromosome 19qL L Bachinski, R Krahe, B F White, et al.
Circulation|July 12, 2001
Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophyS F Nagueh, L L Bachinski, D Meyer, et al.
Genomics|September 1, 1992
The CCAAT/enhancer binding protein (C/EBP alpha) gene (CEBPA) maps to human chromosome 19q13.1 and the related nuclear factor NF-IL6 (C/EBP beta) gene (CEBPB) maps to human chromosome 20q13.1L R Hendricks-Taylor, L L Bachinski, M J Siciliano, et al.
The New England Journal of Medicine|March 27, 1997
Identification of a genetic locus for familial atrial fibrillationR Brugada, T Tapscott, G Z Czernuszewicz, et al.
Circulation|December 22, 1998
Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23F Ahmad, D Li, A Karibe, et al.
Circulation|January 4, 2001
Hypertrophic cardiomyopathy caused by a novel alpha-tropomyosin mutation (V95A) is associated with mild cardiac phenotype, abnormal calcium binding to troponin, abnormal myosin cycling, and poor prognosisA Karibe, L S Tobacman, J Strand, et al.
Pageof 3