Metabolic and molecular basis of peroxisomal disorders: A review-Reference-Cited by-同舟云学术

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Metabolic and molecular basis of peroxisomal disorders: A review

Published:2004 Issue:4 Volume:126A Page:355-375
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Wanders Ronald J.A.

Publisher

Wiley

Subject

Genetics(clinical)

Reference105 articles.

1. The cerebro-hepato-renal (Zellweger) syndrome: Lamellar lipid profiles in adrenocortical, hepatic mesenchymal, astrocyte cells and increased levels of very long chain fatty acids and phytanic acid in the plasma

2. Neonatal adrenoleukodystrophy.

3. Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism

4. Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency.

5. Late onset white matter disease in peroxisome biogenesis disorder

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1. Peroxisomal tail-anchored proteins do not reach peroxisomes via ER, instead mitochondria can be involved;2023-05-23

2. Loss of pex5 sensitizes zebrafish to fasting due to deregulated mitochondria, mTOR, and autophagy;Cellular and Molecular Life Sciences;2023-02-23

3. Current Scenario of Clinical Diagnosis to Identify Inborn Errors of Metabolism with Precision Profiling for Expanded Screening in Infancy in a Resource-limited Setting;Current Pediatric Reviews;2023-02

4. Intramolecular autoinhibition of human PEX13 modulates peroxisomal import;2022-12-19

5. Identification of Genes Related to Squab Muscle Growth and Lipid Metabolism from Transcriptome Profiles of Breast Muscle and Liver in Domestic Pigeon (Columba livia);Animals;2022-04-20

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