Peroxisome Biogenesis Disorders: Identification of a New Complementation Group Distinct from Peroxisome-Deficient CHO Mutants and Not Complemented by Human PEX 13-Reference-Cited by-同舟云学术

Peroxisome Biogenesis Disorders: Identification of a New Complementation Group Distinct from Peroxisome-Deficient CHO Mutants and Not Complemented by Human PEX 13

Published:1998-02 Issue:2 Volume:243 Page:368-371
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Shimozawa Nobuyuki,Suzuki Yasuyuki,Zhang Zhongyi,Imamura Atsushi,Tsukamoto Toshiro,Osumi Takashi,Tateishi Keita,Okumoto Kanji,Fujiki Yukio,Orii Tadao,Barth Peter G.,Wanders Ronald J.A.,Kondo Naomi

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference16 articles.

1. Biochemical abnormalities in rhizomelic chondrodysplasia punctata

2. Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.

3. Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

4. Peroxisomal assembly defects: Clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group

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2. Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders;Orphanet Journal of Rare Diseases;2022-07-19

3. Endoplasmic Reticulum-directed Pex3p Routes to Peroxisomes and Restores Peroxisome Formation in a Saccharomyces cerevisiae pex3Δ Strain;Journal of Biological Chemistry;2005-10

4. Late onset white matter disease in peroxisome biogenesis disorder;Neurology;2001-12-11

5. Peroxisomal alterations in aging and age-related disease;Interorganellar Signaling in Age-Related Disease;2001