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Arthur L Beaudet

Showing results (71-80 of 190) with videos related to

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The Journal of Clinical Investigation|August 7, 2012
Aneuploidy as a mechanism for stress-induced liver adaptationAndrew W Duncan, Amy E Hanlon Newell, Weimin Bi, et al.
European Journal of Human Genetics : EJHG|November 3, 2011
Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypesSoo-Jeong Kim, Jennifer L Miller, Paul J Kuipers, et al.
BMC Genomics|January 30, 2008
Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint regionYong-Hui Jiang, Kekio Wauki, Qian Liu, et al.
Annals of Neurology|March 24, 2005
Creatine metabolism in combined methylmalonic aciduria and homocystinuriaOlaf A Bodamer, Trilochan Sahoo, Arthur L Beaudet, et al.
The American Journal of Pathology|February 1, 2005
Receptor-mediated tobacco toxicity: regulation of gene expression through alpha3beta2 nicotinic receptor in oral epithelial cellsJuan Arredondo, Alexander I Chernyavsky, Lisa M Marubio, et al.
American Journal of Medical Genetics. Part A|May 7, 2015
Improvement of regressive autism symptoms in a child with TMLHE deficiency following carnitine supplementationMark N Ziats, Mathew S Comeaux, Yaping Yang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 30, 2002
Involvement of the alpha3 subunit in central nicotinic binding populationsPaul Whiteaker, Cyrus G Peterson, Wei Xu, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 9, 2005
Lifelong elimination of hyperbilirubinemia in the Gunn rat with a single injection of helper-dependent adenoviral vectorGabriele Toietta, Viraj P Mane, Wilma S Norona, et al.
American Journal of Medical Genetics. Part A|September 11, 2015
Corrigendum to "Improvement of regressive autism symptoms in a child with TMLHE deficiency following carnitine supplementation"Mark N Ziats, Matthew S Comeaux, Yaping Yang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
Microarray analysis for constitutional cytogenetic abnormalitiesLisa G Shaffer, Arthur L Beaudet, Arthur R Brothman, et al.
Pageof 19

Showing results (71-80 of 190) with videos related to

Sort By:
Pageof 19
The Journal of Clinical Investigation|August 7, 2012
Aneuploidy as a mechanism for stress-induced liver adaptationAndrew W Duncan, Amy E Hanlon Newell, Weimin Bi, et al.
European Journal of Human Genetics : EJHG|November 3, 2011
Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypesSoo-Jeong Kim, Jennifer L Miller, Paul J Kuipers, et al.
BMC Genomics|January 30, 2008
Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint regionYong-Hui Jiang, Kekio Wauki, Qian Liu, et al.
Annals of Neurology|March 24, 2005
Creatine metabolism in combined methylmalonic aciduria and homocystinuriaOlaf A Bodamer, Trilochan Sahoo, Arthur L Beaudet, et al.
The American Journal of Pathology|February 1, 2005
Receptor-mediated tobacco toxicity: regulation of gene expression through alpha3beta2 nicotinic receptor in oral epithelial cellsJuan Arredondo, Alexander I Chernyavsky, Lisa M Marubio, et al.
American Journal of Medical Genetics. Part A|May 7, 2015
Improvement of regressive autism symptoms in a child with TMLHE deficiency following carnitine supplementationMark N Ziats, Mathew S Comeaux, Yaping Yang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 30, 2002
Involvement of the alpha3 subunit in central nicotinic binding populationsPaul Whiteaker, Cyrus G Peterson, Wei Xu, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 9, 2005
Lifelong elimination of hyperbilirubinemia in the Gunn rat with a single injection of helper-dependent adenoviral vectorGabriele Toietta, Viraj P Mane, Wilma S Norona, et al.
American Journal of Medical Genetics. Part A|September 11, 2015
Corrigendum to "Improvement of regressive autism symptoms in a child with TMLHE deficiency following carnitine supplementation"Mark N Ziats, Matthew S Comeaux, Yaping Yang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
Microarray analysis for constitutional cytogenetic abnormalitiesLisa G Shaffer, Arthur L Beaudet, Arthur R Brothman, et al.
Pageof 19