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Stem Cell Research & Therapy
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October 6, 2012
The gene expression profiles of induced pluripotent stem cells from individuals with childhood cerebral adrenoleukodystrophy are consistent with proposed mechanisms of pathogenesis
Xiao-Ming Wang, Wing Yan Yik, Peilin Zhang, et al.
Journal of Cellular Biochemistry
|
May 31, 2021
Drug discovery for X-linked adrenoleukodystrophy: An unbiased screen for compounds that lower very long-chain fatty acids
Ann B Moser, Yanqiu Liu, Xiaohai Shi, et al.
Gastroenterology
|
January 4, 2003
Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy
Kenneth D R Setchell, James E Heubi, Kevin E Bove, et al.
Journal of Veterinary Internal Medicine
|
October 27, 2006
Primary renal neoplasia of dogs
Jeffrey N Bryan, Carolyn J Henry, Susan E Turnquist, et al.
Lipids in Health and Disease
|
June 18, 2011
Human and great ape red blood cells differ in plasmalogen levels and composition
Ann B Moser, Steven J Steinberg, Paul A Watkins, et al.
Clinical Medicine Insights. Cardiology
|
May 26, 2015
Association of common variations on chromosome 4q25 and left atrial volume in patients with atrial fibrillation
Yuliya Mints, Hirad Yarmohammadi, Irfan M Khurram, et al.
Stem Cell Research & Therapy
|
August 31, 2015
Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities
Xiao-Ming Wang, Wing Yan Yik, Peilin Zhang, et al.
The Journal of Biological Chemistry
|
May 1, 2002
Participation of two members of the very long-chain acyl-CoA synthetase family in bile acid synthesis and recycling
Stephanie J Mihalik, Steven J Steinberg, Zhengtong Pei, et al.
Molecular Genetics and Metabolism
|
January 12, 2016
Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines
Nancy E Braverman, Gerald V Raymond, William B Rizzo, et al.
Molecular Genetics and Metabolism
|
May 9, 2009
Newborn screening for X-linked adrenoleukodystrophy (X-ALD): validation of a combined liquid chromatography-tandem mass spectrometric (LC-MS/MS) method
Walter C Hubbard, Ann B Moser, Anita C Liu, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Stem Cell Research & Therapy
|
October 6, 2012
The gene expression profiles of induced pluripotent stem cells from individuals with childhood cerebral adrenoleukodystrophy are consistent with proposed mechanisms of pathogenesis
Xiao-Ming Wang, Wing Yan Yik, Peilin Zhang, et al.
Journal of Cellular Biochemistry
|
May 31, 2021
Drug discovery for X-linked adrenoleukodystrophy: An unbiased screen for compounds that lower very long-chain fatty acids
Ann B Moser, Yanqiu Liu, Xiaohai Shi, et al.
Gastroenterology
|
January 4, 2003
Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy
Kenneth D R Setchell, James E Heubi, Kevin E Bove, et al.
Journal of Veterinary Internal Medicine
|
October 27, 2006
Primary renal neoplasia of dogs
Jeffrey N Bryan, Carolyn J Henry, Susan E Turnquist, et al.
Lipids in Health and Disease
|
June 18, 2011
Human and great ape red blood cells differ in plasmalogen levels and composition
Ann B Moser, Steven J Steinberg, Paul A Watkins, et al.
Clinical Medicine Insights. Cardiology
|
May 26, 2015
Association of common variations on chromosome 4q25 and left atrial volume in patients with atrial fibrillation
Yuliya Mints, Hirad Yarmohammadi, Irfan M Khurram, et al.
Stem Cell Research & Therapy
|
August 31, 2015
Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities
Xiao-Ming Wang, Wing Yan Yik, Peilin Zhang, et al.
The Journal of Biological Chemistry
|
May 1, 2002
Participation of two members of the very long-chain acyl-CoA synthetase family in bile acid synthesis and recycling
Stephanie J Mihalik, Steven J Steinberg, Zhengtong Pei, et al.
Molecular Genetics and Metabolism
|
January 12, 2016
Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines
Nancy E Braverman, Gerald V Raymond, William B Rizzo, et al.
Molecular Genetics and Metabolism
|
May 9, 2009
Newborn screening for X-linked adrenoleukodystrophy (X-ALD): validation of a combined liquid chromatography-tandem mass spectrometric (LC-MS/MS) method
Walter C Hubbard, Ann B Moser, Anita C Liu, et al.
Page
of 3