Search research articles
Contact Us
Filters
Showing results (401-410 of 497) with videos related to
Page
of 50
Sort By:
Molecular and Cellular Biology
|
June 8, 2001
Identification of a peroxisomal ATP carrier required for medium-chain fatty acid beta-oxidation and normal peroxisome proliferation in Saccharomyces cerevisiae
C W van Roermund, R Drissen, M van Den Berg, et al.
Biochimica Et Biophysica Acta
|
July 26, 1991
Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblasts
J C Heikoop, M Van den Berg, A Strijland, et al.
European Journal of Pediatrics
|
November 1, 1990
Excessive urinary oxalate excretion after combined renal and hepatic transplantation for correction of hyperoxaluria type 1
H Ruder, G Otto, R B Schutgens, et al.
The EMBO Journal
|
August 1, 1996
The ABC transporter proteins Pat1 and Pat2 are required for import of long-chain fatty acids into peroxisomes of Saccharomyces cerevisiae
E H Hettema, C W van Roermund, B Distel, et al.
The Journal of Clinical Investigation
|
July 1, 1990
Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme
J C Heikoop, C W van Roermund, W W Just, et al.
Biochemical and Biophysical Research Communications
|
June 16, 1988
Direct demonstration that the deficient oxidation of very long chain fatty acids in X-linked adrenoleukodystrophy is due to an impaired ability of peroxisomes to activate very long chain fatty acids
R J Wanders, C W van Roermund, M J van Wijland, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
May 9, 2000
[Identification of the gene for hyper-IgD syndrome: a model of modern genetics]
J P Drenth, H R Waterham, W Kuis, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 6, 2001
Overview of common inherited metabolic diseases in a Southern Chinese population of Hong Kong
N L Tang, J Hui, L K Law, et al.
International Journal of Obesity (2005)
|
February 18, 2011
Preadipocytes of type 2 diabetes subjects display an intrinsic gene expression profile of decreased differentiation capacity
F H J van Tienen, C J H van der Kallen, P J Lindsey, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Molybdenum cofactor deficiency can mimic postanoxic encephalopathy
H D Bakker, N G Abeling, R ten Houten, et al.
Page
of 50
Search research articles
Search
Showing results (401-410 of 497) with videos related to
Sort By:
Page
of 50
Molecular and Cellular Biology
|
June 8, 2001
Identification of a peroxisomal ATP carrier required for medium-chain fatty acid beta-oxidation and normal peroxisome proliferation in Saccharomyces cerevisiae
C W van Roermund, R Drissen, M van Den Berg, et al.
Biochimica Et Biophysica Acta
|
July 26, 1991
Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblasts
J C Heikoop, M Van den Berg, A Strijland, et al.
European Journal of Pediatrics
|
November 1, 1990
Excessive urinary oxalate excretion after combined renal and hepatic transplantation for correction of hyperoxaluria type 1
H Ruder, G Otto, R B Schutgens, et al.
The EMBO Journal
|
August 1, 1996
The ABC transporter proteins Pat1 and Pat2 are required for import of long-chain fatty acids into peroxisomes of Saccharomyces cerevisiae
E H Hettema, C W van Roermund, B Distel, et al.
The Journal of Clinical Investigation
|
July 1, 1990
Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme
J C Heikoop, C W van Roermund, W W Just, et al.
Biochemical and Biophysical Research Communications
|
June 16, 1988
Direct demonstration that the deficient oxidation of very long chain fatty acids in X-linked adrenoleukodystrophy is due to an impaired ability of peroxisomes to activate very long chain fatty acids
R J Wanders, C W van Roermund, M J van Wijland, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
May 9, 2000
[Identification of the gene for hyper-IgD syndrome: a model of modern genetics]
J P Drenth, H R Waterham, W Kuis, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 6, 2001
Overview of common inherited metabolic diseases in a Southern Chinese population of Hong Kong
N L Tang, J Hui, L K Law, et al.
International Journal of Obesity (2005)
|
February 18, 2011
Preadipocytes of type 2 diabetes subjects display an intrinsic gene expression profile of decreased differentiation capacity
F H J van Tienen, C J H van der Kallen, P J Lindsey, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Molybdenum cofactor deficiency can mimic postanoxic encephalopathy
H D Bakker, N G Abeling, R ten Houten, et al.
Page
of 50