U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from MedGen

Items: 7

1.
Isolation of peroxisome assembly mutants from Saccharomyces cerevisiae with different morphologies using a novel positive selection procedure
J Cell Biol. 1992 Oct 1; 119(1): 153–162. doi: 10.1083/jcb.119.1.153
PMCID:
PMC2289622
SummaryPDF–2.8M
2.
Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders
N. Shimozawa, A. Imamura, Z. Zhang, Y. Suzuki, T. Orii, T. Tsukamoto, T. Osumi, Y. Fujiki, R. Wanders, G. Besley, N. Kondo
J Med Genet. 1999 Oct; 36(10): 779–781. doi: 10.1136/jmg.36.10.779
PMCID:
PMC1734244
SummaryPDF–109K
3.
Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G
Ania C. Muntau, Peter U. Mayerhofer, Barbara C. Paton, Stefan Kammerer, Adelbert A. Roscher
Am J Hum Genet. 2000 Oct; 67(4): 967–975. Published online 2000 Aug 24. doi: 10.1086/303071
PMCID:
PMC1287898
AbstractArticlePDF–1.0M
4.
Disorders of Peroxisome Biogenesis Due to Mutations in PEX1: Phenotypes and PEX1 Protein Levels
Claudia Walter, Jeannette Gootjes, Petra A. Mooijer, Herma Portsteffen, Christina Klein, Hans R. Waterham, Peter G. Barth, Jörg T. Epplen, Wolf-H. Kunau, Ronald J. A. Wanders, Gabriele Dodt
Am J Hum Genet. 2001 Jul; 69(1): 35–48. Published online 2001 Jun 1. doi: 10.1086/321265
PMCID:
PMC1226046
AbstractArticlePDF–857K
5.
Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.
S Tamura, N Matsumoto, A Imamura, N Shimozawa, Y Suzuki, N Kondo, Y Fujiki
Biochem J. 2001 Jul 15; 357(Pt 2): 417–426. doi: 10.1042/0264-6021:3570417
PMCID:
PMC1221968
SummaryPDF–430K
6.
Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome-Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation
Naomi Matsumoto, Shigehiko Tamura, Satomi Furuki, Non Miyata, Ann Moser, Nobuyuki Shimozawa, Hugo W. Moser, Yasuyuki Suzuki, Naomi Kondo, Yukio Fujiki
Am J Hum Genet. 2003 Aug; 73(2): 233–246. Published online 2003 Jul 8. doi: 10.1086/377004
PMCID:
PMC1180364
AbstractArticlePDF–691K
7.
The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor.
T Yahraus, N Braverman, G Dodt, J E Kalish, J C Morrell, H W Moser, D Valle, S J Gould
EMBO J. 1996 Jun 17; 15(12): 2914–2923.
PMCID:
PMC450231
SummaryPage BrowsePDF–2.7M

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI > Literature > PubMed Central (PMC)
Support Center