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

P N Ray

Showing results (81-90 of 110) with videos related to

Pageof 11
Sort By:
The Journal of Biological Chemistry|October 25, 1990
Cloning and expression of rat histidase. Homology to two bacterial histidases and four phenylalanine ammonia-lyasesR G Taylor, M A Lambert, E Sexsmith, et al.
Muscle & Nerve|January 12, 1999
Dystrophin isoforms DP71 and DP427 have distinct roles in myogenic cellsP L Howard, G Y Dally, S D Ditta, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Immunogold labelling of dystrophin in human muscle, using an antibody to the last 17 amino acids of the C-terminusM J Cullen, J Walsh, L V Nicholson, et al.
American Journal of Medical Genetics|August 9, 1996
Tissue-specific methylation differences and cognitive function in fragile X premutation femalesD J Allingham-Hawkins, C A Brown, R Babul, et al.
American Journal of Human Genetics|August 1, 1992
Characterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosomeJ T Clarke, P J Wilson, C P Morris, et al.
British Medical Bulletin|July 1, 1989
Myogenic regulation of dystrophin gene expressionH J Klamut, E E Zubrzycka-Gaarn, D E Bulman, et al.
Cytogenetic and Genome Research|April 1, 2006
New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndromeA C Smith, T Rubin, C Shuman, et al.
Neurogenetics|June 5, 2013
Autosomal recessive hereditary spastic paraplegia-clinical and genetic characteristics of a well-defined cohortG Yoon, B Baskin, M Tarnopolsky, et al.
Gene|November 14, 1998
Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin geneJ C McNaughton, D J Cockburn, G Hughes, et al.
American Journal of Human Genetics|June 1, 1997
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy numberP E McAndrew, D W Parsons, L R Simard, et al.
Pageof 11

Showing results (81-90 of 110) with videos related to

Sort By:
Pageof 11
The Journal of Biological Chemistry|October 25, 1990
Cloning and expression of rat histidase. Homology to two bacterial histidases and four phenylalanine ammonia-lyasesR G Taylor, M A Lambert, E Sexsmith, et al.
Muscle & Nerve|January 12, 1999
Dystrophin isoforms DP71 and DP427 have distinct roles in myogenic cellsP L Howard, G Y Dally, S D Ditta, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Immunogold labelling of dystrophin in human muscle, using an antibody to the last 17 amino acids of the C-terminusM J Cullen, J Walsh, L V Nicholson, et al.
American Journal of Medical Genetics|August 9, 1996
Tissue-specific methylation differences and cognitive function in fragile X premutation femalesD J Allingham-Hawkins, C A Brown, R Babul, et al.
American Journal of Human Genetics|August 1, 1992
Characterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosomeJ T Clarke, P J Wilson, C P Morris, et al.
British Medical Bulletin|July 1, 1989
Myogenic regulation of dystrophin gene expressionH J Klamut, E E Zubrzycka-Gaarn, D E Bulman, et al.
Cytogenetic and Genome Research|April 1, 2006
New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndromeA C Smith, T Rubin, C Shuman, et al.
Neurogenetics|June 5, 2013
Autosomal recessive hereditary spastic paraplegia-clinical and genetic characteristics of a well-defined cohortG Yoon, B Baskin, M Tarnopolsky, et al.
Gene|November 14, 1998
Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin geneJ C McNaughton, D J Cockburn, G Hughes, et al.
American Journal of Human Genetics|June 1, 1997
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy numberP E McAndrew, D W Parsons, L R Simard, et al.
Pageof 11