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G M MARTIN

Showing results (231-240 of 253) with videos related to

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Clinical Genetics|May 13, 2014
Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinismC Saint-Martin, Q Zhou, G M Martin, et al.
Free Radical Biology & Medicine|October 18, 2000
Levels of DNA damage are unaltered in mice overexpressing human catalase in nucleiS E Schriner, C E Ogburn, A C Smith, et al.
Annals of the New York Academy of Sciences|September 24, 1993
Transgenic animal models for Alzheimer's diseaseK Fukuchi, C E Ogburn, A C Smith, et al.
Molecular Biology of the Cell|August 6, 1999
The Werner syndrome protein is involved in RNA polymerase II transcriptionA S Balajee, A Machwe, A May, et al.
Genomics|September 1, 1994
Integrated mapping analysis of the Werner syndrome region of chromosome 8J Oshima, C E Yu, M Boehnke, et al.
American Journal of Human Genetics|February 1, 1997
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative GroupC E Yu, J Oshima, E M Wijsman, et al.
American Journal of Human Genetics|September 1, 1991
APP717, APP693, and PRIP gene mutations are rare in Alzheimer diseaseG D Schellenberg, L Anderson, S O'dahl, et al.
Human Pathology|May 1, 1977
Carcinogenesis testing and the pathologistR E Anderson, E S Benson, D Korn, et al.
Pediatric Radiology|March 8, 2005
Merosin-deficient congenital muscular dystrophy (CMD): a study of 25 Brazilian patients using MRIClaudia C Leite, Leandro T Lucato, Maria G M Martin, et al.
Clinical Neurology and Neurosurgery|July 4, 2012
Semantic strategy training increases memory performance and brain activity in patients with prefrontal cortex lesionsEliane C Miotto, Cary R Savage, Jonathan J Evans, et al.
Pageof 26

Showing results (231-240 of 253) with videos related to

Sort By:
Pageof 26
Clinical Genetics|May 13, 2014
Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinismC Saint-Martin, Q Zhou, G M Martin, et al.
Free Radical Biology & Medicine|October 18, 2000
Levels of DNA damage are unaltered in mice overexpressing human catalase in nucleiS E Schriner, C E Ogburn, A C Smith, et al.
Annals of the New York Academy of Sciences|September 24, 1993
Transgenic animal models for Alzheimer's diseaseK Fukuchi, C E Ogburn, A C Smith, et al.
Molecular Biology of the Cell|August 6, 1999
The Werner syndrome protein is involved in RNA polymerase II transcriptionA S Balajee, A Machwe, A May, et al.
Genomics|September 1, 1994
Integrated mapping analysis of the Werner syndrome region of chromosome 8J Oshima, C E Yu, M Boehnke, et al.
American Journal of Human Genetics|February 1, 1997
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative GroupC E Yu, J Oshima, E M Wijsman, et al.
American Journal of Human Genetics|September 1, 1991
APP717, APP693, and PRIP gene mutations are rare in Alzheimer diseaseG D Schellenberg, L Anderson, S O'dahl, et al.
Human Pathology|May 1, 1977
Carcinogenesis testing and the pathologistR E Anderson, E S Benson, D Korn, et al.
Pediatric Radiology|March 8, 2005
Merosin-deficient congenital muscular dystrophy (CMD): a study of 25 Brazilian patients using MRIClaudia C Leite, Leandro T Lucato, Maria G M Martin, et al.
Clinical Neurology and Neurosurgery|July 4, 2012
Semantic strategy training increases memory performance and brain activity in patients with prefrontal cortex lesionsEliane C Miotto, Cary R Savage, Jonathan J Evans, et al.
Pageof 26