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W Moser

Showing results (391-400 of 466) with videos related to

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Pediatric Research|March 1, 1982
The prenatal diagnosis of adrenoleukodystrophy. Demonstration of increased hexacosanoic acid levels in cultured amniocytes and fetal adrenal glandH W Moser, A B Moser, J M Powers, et al.
Pediatric Neurology|May 1, 1986
Myopathy in an infant with a fatal peroxisomal disorderJ Wolff, W L Nyhan, H Powell, et al.
Osteoarthritis and Cartilage|August 7, 2012
Urinary CTX-II concentrations are elevated and associated with knee pain and function in subjects with ACL reconstructionT L Chmielewski, T N Trumble, A-M Joseph, et al.
Nature Genetics|December 17, 1997
Mutations in PEX1 are the most common cause of peroxisome biogenesis disordersB E Reuber, E Germain-Lee, C S Collins, et al.
European Journal of Pediatrics|April 1, 1989
A case of combined Farber and Sandhoff diseaseC Fusch, R Huenges, H W Moser, et al.
Molecular Genetics and Metabolism|December 14, 2004
Inhibition of peroxisomal functions due to oxidative imbalance induced by mistargeting of catalase to cytoplasm is restored by vitamin E treatment in skin fibroblasts from Zellweger syndrome-like patientsYasusada Kawada, Mushfiquddin Khan, Ashish K Sharma, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|May 8, 1999
A human-murine chimera model for in utero human hematopoietic stem cell transplantationW Leung, K Blakemore, R J Jones, et al.
Annals of Neurology|April 20, 2001
Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screeningL Bezman, A B Moser, G V Raymond, et al.
Journal of Nuclear Cardiology : Official Publication of the American Society of Nuclear Cardiology|August 9, 2005
Clinical utility of coronary calcium scoring after nonischemic myocardial perfusion imagingRandall C Thompson, A Iain McGhie, Kevin W Moser, et al.
Journal of Neuropathology and Experimental Neurology|December 2, 2005
Adreno-leukodystrophy: oxidative stress of mice and menJames M Powers, Zhengtong Pei, Ann K Heinzer, et al.
Pageof 47

Showing results (391-400 of 466) with videos related to

Sort By:
Pageof 47
Pediatric Research|March 1, 1982
The prenatal diagnosis of adrenoleukodystrophy. Demonstration of increased hexacosanoic acid levels in cultured amniocytes and fetal adrenal glandH W Moser, A B Moser, J M Powers, et al.
Pediatric Neurology|May 1, 1986
Myopathy in an infant with a fatal peroxisomal disorderJ Wolff, W L Nyhan, H Powell, et al.
Osteoarthritis and Cartilage|August 7, 2012
Urinary CTX-II concentrations are elevated and associated with knee pain and function in subjects with ACL reconstructionT L Chmielewski, T N Trumble, A-M Joseph, et al.
Nature Genetics|December 17, 1997
Mutations in PEX1 are the most common cause of peroxisome biogenesis disordersB E Reuber, E Germain-Lee, C S Collins, et al.
European Journal of Pediatrics|April 1, 1989
A case of combined Farber and Sandhoff diseaseC Fusch, R Huenges, H W Moser, et al.
Molecular Genetics and Metabolism|December 14, 2004
Inhibition of peroxisomal functions due to oxidative imbalance induced by mistargeting of catalase to cytoplasm is restored by vitamin E treatment in skin fibroblasts from Zellweger syndrome-like patientsYasusada Kawada, Mushfiquddin Khan, Ashish K Sharma, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|May 8, 1999
A human-murine chimera model for in utero human hematopoietic stem cell transplantationW Leung, K Blakemore, R J Jones, et al.
Annals of Neurology|April 20, 2001
Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screeningL Bezman, A B Moser, G V Raymond, et al.
Journal of Nuclear Cardiology : Official Publication of the American Society of Nuclear Cardiology|August 9, 2005
Clinical utility of coronary calcium scoring after nonischemic myocardial perfusion imagingRandall C Thompson, A Iain McGhie, Kevin W Moser, et al.
Journal of Neuropathology and Experimental Neurology|December 2, 2005
Adreno-leukodystrophy: oxidative stress of mice and menJames M Powers, Zhengtong Pei, Ann K Heinzer, et al.
Pageof 47