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F M Hisama

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

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Cancer Research|May 16, 2000
WRN or telomerase constructs reverse 4-nitroquinoline 1-oxide sensitivity in transformed Werner syndrome fibroblastsF M Hisama, Y H Chen, M S Meyn, et al.
American Journal of Medical Genetics|February 27, 2001
46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sistersF M Hisama, S Zemel, E M Cherniske, et al.
Seizure|December 26, 2001
GABA and the ornithine delta-aminotransferase gene in vigabatrin-associated visual field defectsF M Hisama, R H Mattson, H H Lee, et al.
American Journal of Medical Genetics|December 18, 1998
Renal tubular dysgenesis, absent nipples, and multiple malformations in three brothers: a new, lethal syndromeF M Hisama, M Reyes-Mugica, D S Wargowski, et al.
Genomics|August 1, 1996
A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21C E Yu, J Oshima, F M Hisama, et al.
Archives of Neurology|November 16, 2001
Clinical and molecular studies in a family with probable X-linked dominant Charcot-Marie-Tooth disease involving the central nervous systemF M Hisama, H H Lee, A Vashlishan, et al.
Molecular Syndromology|October 30, 2010
A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid FeaturesB Saha, D Lessel, F M Hisama, et al.
Genomics|October 29, 1998
Comparison of methods for identifying transcription units and transcription map of the Werner syndrome gene regionF M Hisama, J Oshima, C E Yu, et al.
Brain : a Journal of Neurology|June 17, 2005
Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neuronsS D Dib-Hajj, A M Rush, T R Cummins, et al.
Human Mutation|April 11, 2001
Human GABA(B) receptor 1 gene: eight novel sequence variantsF M Hisama, J R Gruen, J Choi, et al.
Pageof 1

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

Sort By:
Pageof 1
Cancer Research|May 16, 2000
WRN or telomerase constructs reverse 4-nitroquinoline 1-oxide sensitivity in transformed Werner syndrome fibroblastsF M Hisama, Y H Chen, M S Meyn, et al.
American Journal of Medical Genetics|February 27, 2001
46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sistersF M Hisama, S Zemel, E M Cherniske, et al.
Seizure|December 26, 2001
GABA and the ornithine delta-aminotransferase gene in vigabatrin-associated visual field defectsF M Hisama, R H Mattson, H H Lee, et al.
American Journal of Medical Genetics|December 18, 1998
Renal tubular dysgenesis, absent nipples, and multiple malformations in three brothers: a new, lethal syndromeF M Hisama, M Reyes-Mugica, D S Wargowski, et al.
Genomics|August 1, 1996
A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21C E Yu, J Oshima, F M Hisama, et al.
Archives of Neurology|November 16, 2001
Clinical and molecular studies in a family with probable X-linked dominant Charcot-Marie-Tooth disease involving the central nervous systemF M Hisama, H H Lee, A Vashlishan, et al.
Molecular Syndromology|October 30, 2010
A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid FeaturesB Saha, D Lessel, F M Hisama, et al.
Genomics|October 29, 1998
Comparison of methods for identifying transcription units and transcription map of the Werner syndrome gene regionF M Hisama, J Oshima, C E Yu, et al.
Brain : a Journal of Neurology|June 17, 2005
Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neuronsS D Dib-Hajj, A M Rush, T R Cummins, et al.
Human Mutation|April 11, 2001
Human GABA(B) receptor 1 gene: eight novel sequence variantsF M Hisama, J R Gruen, J Choi, et al.
Pageof 1