Correction by Gene Expression of Biochemical Abnormalities in Fibroblasts from Zellweger Patients-Reference-Cited by-同舟云学术

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Correction by Gene Expression of Biochemical Abnormalities in Fibroblasts from Zellweger Patients

Published:1996-05 Issue:5 Volume:39 Page:812-815
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Shimozawa Nobuyuki,Suzuki Yasuyuki,Tomatsu Shunji,Tsukamoto Toshiro,Osumi Takashi,Fujiki Yukio,Kamijo Keiju,Hashimoto Takashi,Kondo Naomi,Orii Tadao

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells

2. Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant

3. Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes.

4. A Human Gene Responsible for Zellweger Syndrome That Affects Peroxisome Assembly

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The biogenesis protein PEX14 is an optimal marker for the identification and localization of peroxisomes in different cell types, tissues, and species in morphological studies;Histochemistry and Cell Biology;2013-08-20

2. Mammalian peroxisomal ABC transporters: from endogenous substrates to pathology and clinical significance;British Journal of Pharmacology;2011-11-15

3. Molekulare Ursachen von Störungen des hepatogastroenterologischen Systems bei Neugeborenen;Molekularmedizinische Grundlagen von fetalen und neonatalen Erkrankungen;2005

4. Accumulation of glycolipids in mutant Chinese hamster ovary cells (Z65) with defective peroxisomal assembly and comparison of the metabolic rate of glycosphingolipids between Z65 cells and wild-type CHO-K1 cells;Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids;1999-04

5. Genetic Basis of Peroxisome-Assembly Mutants of Humans, Chinese Hamster Ovary Cells, and Yeast: Identification of a New Complementation Group of Peroxisome-Biogenesis Disorders Apparently Lacking Peroxisomal-Membrane Ghosts;The American Journal of Human Genetics;1998-12

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