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peroxisome assembly factor-1
Known as:
PMP35
, peroxisomal membrane protein 35
National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Membrane Proteins
PEX2 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
1997
Review
1997
Molecular basis of zellweger syndrome, β-ketothiolase deficiency and mucopolysaccharidoses
T. Orii
The Japanese Journal of Human Genetics
1997
Corpus ID: 19328136
Summary1. A human peroxisome assembly factor-1 (PAF-1) complementary DNA has been cloned that restores the morphological and…
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1996
1996
Correction by Gene Expression of Biochemical Abnormalities in Fibroblasts from Zellweger Patients
N. Shimozawa
,
Yasuyuki Suzuki
,
+7 authors
T. Orii
Pediatric Research
1996
Corpus ID: 22439531
Zellweger syndrome is a prototype of peroxisomal biogenesis disorders and a fatal autosomal recessive disease with no effective…
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1994
1994
Restoration of peroxisome biogenesis in a peroxisome-deficient mammalian cell line by expression of either the 35 kDa or the 70 kDa peroxisomal membrane proteins
J. Gärtner
,
C. Obie
,
P. Watkins
,
D. Valle
Journal of Inherited Metabolic Disease
1994
Corpus ID: 11128917
Peroxisomes are single-membrane-bound organelles present in nearly all eukaryotic cells. Their size and number vary depending on…
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1994
1994
Genetic evidence supporting the role of peroxisome assembly factor (PAF)-1 in peroxisome biogenesis. Polymerase chain reaction detection of a missense mutation in PAF-1 of Chinese hamster ovary cells…
L. Allen
,
L. Hope
,
C. Raetz
,
R. Thieringer
Journal of Biological Chemistry
1994
Corpus ID: 29994775
The peroxisome/plasmalogen-deficient Chinese hamster ovary (CHO) mutant cell line ZR-78.1 contains a missense mutation in its…
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Review
1994
Review
1994
[Human peroxisome-deficient disorders and pathogenic gene].
Y. Fujiki
Rinshō shinkeigaku Clinical neurology
1994
Corpus ID: 20301448
Peroxisome is a model organelle to investigate the mechanism of protein translocation and organelle assembly. Human autosomal…
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Review
1993
Review
1993
[Clinical and molecular aspects of peroxisome-deficient disorders].
Y. Suzuki
,
N. Shimozawa
,
T. Orii
Nihon rinsho. Japanese journal of clinical…
1993
Corpus ID: 31894450
Peroxisome-deficient disorders including Zellweger syndrome (ZS), neonatal adrenoleukodystrophy (NALD) and infantile Refsum…
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Review
1993
Review
1993
[Molecular biology of peroxisome biogenesis].
Y. Fujiki
Nihon rinsho. Japanese journal of clinical…
1993
Corpus ID: 25947149
Molecular mechanisms of peroxisomal protein translocation and peroxisome assembly have been extensively studied these several…
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