Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q24316346)
Watch
English
A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p
scientific article
In more languages
edit
Statements
instance of
scholarly article
0 references
title
A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p
(English)
0 references
author name string
S Tamura
series ordinal
1
0 references
N Shimozawa
series ordinal
2
0 references
Y Suzuki
series ordinal
3
0 references
T Tsukamoto
series ordinal
4
0 references
T Osumi
series ordinal
5
0 references
Y Fujiki
series ordinal
6
0 references
language of work or name
English
0 references
publication date
28 April 1998
0 references
published in
Biochemical and Biophysical Research Communications
0 references
volume
245
0 references
issue
3
0 references
page(s)
883-6
0 references
cites work
A 200-amino acid ATPase module in search of a basic function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular defects in genetic diseases of peroxisomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PEX12 encodes an integral membrane protein of peroxisomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisome assembly factor-2, a putative ATPase cloned by functional complementation on a peroxisome-deficient mammalian cell mutant
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role of the PAS1 gene of Pichia pastoris in peroxisome biogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A human gene responsible for Zellweger syndrome that affects peroxisome assembly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1006%2FBBRC.1998.8522
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1006/BBRC.1998.8522
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2639900
OpenCitations bibliographic resource ID
2639900
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2639900
PubMed publication ID
9588209
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit