Showing results (161-170 of 1,684) with videos related to

Sort By:
Pageof 169
Human Molecular Genetics|September 26, 2000
Myotubularin, a phosphatase deficient in myotubular myopathy, acts on phosphatidylinositol 3-kinase and phosphatidylinositol 3-phosphate pathwayF Blondeau, J Laporte, S Bodin, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|March 1, 1993
Comparison of monoclonal antibody methods and a ribosomal ribonucleic acid probe test for Neisseria gonorrhoeae culture confirmationW M Janda, L M Wilcoski, K L Mandel, et al.
Optics Letters|September 11, 2009
Chaos in a good-cavity single-mode dye laser due to turbulent dye flowT H Chyba, E C Gage, R Ghosh, et al.
Cell|July 1, 1978
Organization of coding and intervening sequences in the chicken ovalbumin split geneJ L Mandel, R Breathnach, P Gerlinger, et al.
Annals of Emergency Medicine|May 1, 1995
CPR knowledge, self-efficacy, and anticipated anxiety as functions of infant/child CPR trainingJ S Schlessel, H A Rappa, M Lesser, et al.
Neuromuscular Disorders : NMD|May 1, 1994
Expression of a recombinant dystrophin in mdx mice using adenovirus vectorH S Alameddine, B Quantin, A Cartaud, et al.
Journal of Clinical & Laboratory Immunology|January 1, 1990
Monoclonal antibodies to chick renal calcium regulating hemeproteins. Biochemical and immunohistochemical interactions with mitochondrial 25-hydroxyvitamin D3 hydroxylasesM L Mandel, B Moorthy, S J Swartz, et al.
The Journal of Clinical Investigation|August 1, 1994
Identification of mutations in the putative ATP-binding domain of the adrenoleukodystrophy geneP Fanen, S Guidoux, C O Sarde, et al.
American Journal of Human Genetics|January 1, 1990
The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15A Hanauer, M Chery, R Fujita, et al.
Journal of Medical Genetics|April 16, 1998
Extensive germinal mosaicism in a family with X linked myotubular myopathy simulates genetic heterogeneityM C Vincent, C Guiraud-Chaumeil, J Laporte, et al.
Pageof 169