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W Moser

Showing results (341-350 of 466) with videos related to

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Neurochemical Research|October 11, 2002
Anti-ganglioside antibodies bind with enhanced affinity to gangliosides containing very long chain fatty acidsYumi Tagawa, Wouter Laroy, Leonardo Nimrichter, et al.
Journal of Neuroimmunology|September 1, 1995
Tumor necrosis factor-alpha and X-linked adrenoleukodystrophyM C McGuinness, D E Griffin, G V Raymond, et al.
Nature Genetics|February 1, 1995
Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disordersG Dodt, N Braverman, C Wong, et al.
The Journal of Orthopaedic and Sports Physical Therapy|June 22, 2005
Current concepts in the recognition and treatment of superior labral (SLAP) lesionsKevin E Wilk, Michael M Reinold, Jeffrey R Dugas, et al.
Sports Health|September 28, 2012
Factors associated with function after anterior cruciate ligament reconstructionTrevor A Lentz, Susan M Tillman, Peter A Indelicato, et al.
The Johns Hopkins Medical Journal|December 1, 1982
Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acidsF R Brown, A J McAdams, J W Cummins, et al.
Biochemical and Biophysical Research Communications|December 4, 1996
Phytanoyl-CoA hydroxylase is present in human liver, located in peroxisomes, and deficient in Zellweger syndrome: direct, unequivocal evidence for the new, revised pathway of phytanic acid alpha-oxidation in humansG A Jansen, S J Mihalik, P A Watkins, et al.
Neurology|March 27, 2002
Proton MR spectroscopic imaging predicts lesion progression on MRI in X-linked adrenoleukodystrophyF S Eichler, P B Barker, C Cox, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Peroxisomal integral membrane proteins in livers of patients with Zellweger syndrome, infantile Refsum's disease and X-linked adrenoleukodystrophyG M Small, M J Santos, T Imanaka, et al.
Microbial Cell Factories|March 18, 2017
Implications of evolutionary engineering for growth and recombinant protein production in methanol-based growth media in the yeast Pichia pastorisJosef W Moser, Roland Prielhofer, Samuel M Gerner, et al.
Pageof 47

Showing results (341-350 of 466) with videos related to

Sort By:
Pageof 47
Neurochemical Research|October 11, 2002
Anti-ganglioside antibodies bind with enhanced affinity to gangliosides containing very long chain fatty acidsYumi Tagawa, Wouter Laroy, Leonardo Nimrichter, et al.
Journal of Neuroimmunology|September 1, 1995
Tumor necrosis factor-alpha and X-linked adrenoleukodystrophyM C McGuinness, D E Griffin, G V Raymond, et al.
Nature Genetics|February 1, 1995
Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disordersG Dodt, N Braverman, C Wong, et al.
The Journal of Orthopaedic and Sports Physical Therapy|June 22, 2005
Current concepts in the recognition and treatment of superior labral (SLAP) lesionsKevin E Wilk, Michael M Reinold, Jeffrey R Dugas, et al.
Sports Health|September 28, 2012
Factors associated with function after anterior cruciate ligament reconstructionTrevor A Lentz, Susan M Tillman, Peter A Indelicato, et al.
The Johns Hopkins Medical Journal|December 1, 1982
Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acidsF R Brown, A J McAdams, J W Cummins, et al.
Biochemical and Biophysical Research Communications|December 4, 1996
Phytanoyl-CoA hydroxylase is present in human liver, located in peroxisomes, and deficient in Zellweger syndrome: direct, unequivocal evidence for the new, revised pathway of phytanic acid alpha-oxidation in humansG A Jansen, S J Mihalik, P A Watkins, et al.
Neurology|March 27, 2002
Proton MR spectroscopic imaging predicts lesion progression on MRI in X-linked adrenoleukodystrophyF S Eichler, P B Barker, C Cox, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Peroxisomal integral membrane proteins in livers of patients with Zellweger syndrome, infantile Refsum's disease and X-linked adrenoleukodystrophyG M Small, M J Santos, T Imanaka, et al.
Microbial Cell Factories|March 18, 2017
Implications of evolutionary engineering for growth and recombinant protein production in methanol-based growth media in the yeast Pichia pastorisJosef W Moser, Roland Prielhofer, Samuel M Gerner, et al.
Pageof 47