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Results: 1 to 20 of 690

1.

Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell lines.

Ebberink MS, Mooyer PA, Koster J, Dekker CJ, Eyskens FJ, Dionisi-Vici C, Clayton PT, Barth PG, Wanders RJ, Waterham HR.

Hum Mutat. 2009 Jan;30(1):93-8. doi: 10.1002/humu.20833.

PMID:
18712838
[PubMed - indexed for MEDLINE]
2.

An isoform of pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomes.

Braverman N, Dodt G, Gould SJ, Valle D.

Hum Mol Genet. 1998 Aug;7(8):1195-205.

PMID:
9668159
[PubMed - indexed for MEDLINE]
Free Article
4.

Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders.

Slawecki ML, Dodt G, Steinberg S, Moser AB, Moser HW, Gould SJ.

J Cell Sci. 1995 May;108 ( Pt 5):1817-29.

PMID:
7544797
[PubMed - indexed for MEDLINE]
Free Article
5.

Domain mapping of human PEX5 reveals functional and structural similarities to Saccharomyces cerevisiae Pex18p and Pex21p.

Dodt G, Warren D, Becker E, Rehling P, Gould SJ.

J Biol Chem. 2001 Nov 9;276(45):41769-81. Epub 2001 Sep 6.

PMID:
11546814
[PubMed - indexed for MEDLINE]
Free Article
6.

Rapid isolation and characterization of CHO mutants deficient in peroxisome biogenesis using the peroxisomal forms of fluorescent proteins.

Ito M, Ito R, Huang Y, Miura S, Imamura A, Suzuki Y, Shimozawa N.

Biochim Biophys Acta. 2000 Apr 17;1496(2-3):232-42.

PMID:
10771091
[PubMed - indexed for MEDLINE]
Free Article
7.

Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.

Matsumoto N, Tamura S, Furuki S, Miyata N, Moser A, Shimozawa N, Moser HW, Suzuki Y, Kondo N, Fujiki Y.

Am J Hum Genet. 2003 Aug;73(2):233-46. Epub 2003 Jul 8.

PMID:
12851857
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients.

Shimozawa N, Zhang Z, Suzuki Y, Imamura A, Tsukamoto T, Osumi T, Fujiki Y, Orii T, Barth PG, Wanders RJ, Kondo N.

Biochem Biophys Res Commun. 1999 Aug 27;262(2):504-8.

PMID:
10462504
[PubMed - indexed for MEDLINE]
9.

The Arabidopsis peroxisomal targeting signal type 2 receptor PEX7 is necessary for peroxisome function and dependent on PEX5.

Woodward AW, Bartel B.

Mol Biol Cell. 2005 Feb;16(2):573-83. Epub 2004 Nov 17.

PMID:
15548601
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants.

Otera H, Okumoto K, Tateishi K, Ikoma Y, Matsuda E, Nishimura M, Tsukamoto T, Osumi T, Ohashi K, Higuchi O, Fujiki Y.

Mol Cell Biol. 1998 Jan;18(1):388-99.

PMID:
9418886
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Isolation and characterization of novel phenotype CHO cell mutants defective in peroxisome assembly, using ICR191 as a potent mutagenic agent.

Ghaedi K, Fujiki Y.

Cell Biochem Funct. 2008 Aug;26(6):684-91. doi: 10.1002/cbf.1493.

PMID:
18543353
[PubMed - indexed for MEDLINE]
12.

A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import.

Akiyama N, Ghaedi K, Fujiki Y.

Biochem Biophys Res Commun. 2002 May 24;293(5):1523-9.

PMID:
12054689
[PubMed - indexed for MEDLINE]
13.

Temperature-sensitive phenotype of Chinese hamster ovary cells defective in PEX5 gene.

Ito R, Huang Y, Yao C, Shimozawa N, Suzuki Y, Kondo N, Imanaka T, Usuda N, Ito M.

Biochem Biophys Res Commun. 2001 Oct 26;288(2):321-7.

PMID:
11606046
[PubMed - indexed for MEDLINE]
14.

Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis.

Weller S, Cajigas I, Morrell J, Obie C, Steel G, Gould SJ, Valle D.

Am J Hum Genet. 2005 Jun;76(6):987-1007. Epub 2005 Apr 27.

PMID:
15858711
[PubMed - indexed for MEDLINE]
Free PMC Article
15.
16.

Metabolic control of peroxisome abundance.

Chang CC, South S, Warren D, Jones J, Moser AB, Moser HW, Gould SJ.

J Cell Sci. 1999 May;112 ( Pt 10):1579-90.

PMID:
10212151
[PubMed - indexed for MEDLINE]
Free Article
17.

Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor.

Purdue PE, Zhang JW, Skoneczny M, Lazarow PB.

Nat Genet. 1997 Apr;15(4):381-4.

PMID:
9090383
[PubMed - indexed for MEDLINE]
18.

Interaction defect of the medium isoform of PTS1-receptor Pex5p with PTS2-receptor Pex7p abrogates the PTS2 protein import into peroxisomes in mammals.

Honsho M, Hashiguchi Y, Ghaedi K, Fujiki Y.

J Biochem. 2011 Feb;149(2):203-10. doi: 10.1093/jb/mvq130. Epub 2010 Nov 2.

PMID:
21047816
[PubMed - indexed for MEDLINE]
19.

Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein.

Ghaedi K, Kawai A, Okumoto K, Tamura S, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y.

Exp Cell Res. 1999 May 1;248(2):489-97.

PMID:
10222140
[PubMed - indexed for MEDLINE]
20.

A missense mutation in the RING finger motif of PEX2 protein disturbs the import of peroxisome targeting signal 1 (PTS1)-containing protein but not the PTS2-containing protein.

Huang Y, Ito R, Miura S, Hashimoto T, Ito M.

Biochem Biophys Res Commun. 2000 Apr 21;270(3):717-21.

PMID:
10772890
[PubMed - indexed for MEDLINE]

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