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Biochemical and Biophysical Research Communications
|
May 16, 1988
Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disorders
S Brul, E A Wiemer, A Westerveld, et al.
Rheumatology (Oxford, England)
|
May 24, 2001
Clinical and molecular variability in childhood periodic fever with hyperimmunoglobulinaemia D
J Frenkel, S M Houten, H R Waterham, et al.
Biochemical and Biophysical Research Communications
|
September 28, 1984
Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome
R J Wanders, M Kos, B Roest, et al.
Biochemical and Biophysical Research Communications
|
March 3, 1998
Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13
N Shimozawa, Y Suzuki, Z Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 16, 1998
Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency
E G van Grunsven, E van Berkel, L Ijlst, et al.
American Journal of Human Genetics
|
June 5, 2001
Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels
C Walter, J Gootjes, P A Mooijer, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 31, 1990
Rapid diagnosis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency via enzyme activity measurements in leukocytes or platelets using a simple spectrophotometric method
R J Wanders, P H Zoeters, R B Schutgens, et al.
European Journal of Clinical Investigation
|
October 1, 1987
Bile acids in peroxisomal disorders
J R Van Eldere, G G Parmentier, H J Eyssen, et al.
Annals of Human Genetics
|
June 28, 2001
Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith--Lemli--Opitz syndrome
P E Jira, R J Wanders, J A Smeitink, et al.
Biochimica Et Biophysica Acta
|
April 24, 1995
Altered kinetics of cytochrome c oxidase in a patient with severe mitochondrial encephalomyopathy
L G Nijtmans, P G Barth, C R Lincke, et al.
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Search research articles
Search
Showing results (451-460 of 497) with videos related to
Sort By:
Page
of 50
Biochemical and Biophysical Research Communications
|
May 16, 1988
Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disorders
S Brul, E A Wiemer, A Westerveld, et al.
Rheumatology (Oxford, England)
|
May 24, 2001
Clinical and molecular variability in childhood periodic fever with hyperimmunoglobulinaemia D
J Frenkel, S M Houten, H R Waterham, et al.
Biochemical and Biophysical Research Communications
|
September 28, 1984
Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome
R J Wanders, M Kos, B Roest, et al.
Biochemical and Biophysical Research Communications
|
March 3, 1998
Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13
N Shimozawa, Y Suzuki, Z Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 16, 1998
Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency
E G van Grunsven, E van Berkel, L Ijlst, et al.
American Journal of Human Genetics
|
June 5, 2001
Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels
C Walter, J Gootjes, P A Mooijer, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 31, 1990
Rapid diagnosis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency via enzyme activity measurements in leukocytes or platelets using a simple spectrophotometric method
R J Wanders, P H Zoeters, R B Schutgens, et al.
European Journal of Clinical Investigation
|
October 1, 1987
Bile acids in peroxisomal disorders
J R Van Eldere, G G Parmentier, H J Eyssen, et al.
Annals of Human Genetics
|
June 28, 2001
Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith--Lemli--Opitz syndrome
P E Jira, R J Wanders, J A Smeitink, et al.
Biochimica Et Biophysica Acta
|
April 24, 1995
Altered kinetics of cytochrome c oxidase in a patient with severe mitochondrial encephalomyopathy
L G Nijtmans, P G Barth, C R Lincke, et al.
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of 50