Literature DB >> 8520725

Adrenoleukodystrophy: molecular genetics, pathology, and Lorenzo's oil.

H W Moser1, J M Powers, K D Smith.   

Abstract

Knowledge about adrenoleukodystrophy (ALD), a disorder which was described first in 1923, has increased greatly during recent years. The principal biochemical abnormality, the presumed enzyme defect, and the gene defect, have been defined. A dietary therapy has been proposed and attracted world-wide attention through a motion picture. Nevertheless, many questions remain and cannot be answered without a more fundamental understanding of pathology and pathogenesis. This article will provide a review of the history, clinical features, pathology, biochemistry, and the gene defect, and then appraise current efforts to clarify pathogenesis and develop therapeutic approaches.

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Year:  1995        PMID: 8520725     DOI: 10.1111/j.1750-3639.1995.tb00602.x

Source DB:  PubMed          Journal:  Brain Pathol        ISSN: 1015-6305            Impact factor:   6.508


  2 in total

Review 1.  The Key Role of Peroxisomes in Follicular Growth, Oocyte Maturation, Ovulation, and Steroid Biosynthesis.

Authors:  Shan Wang; HaoXuan Yang; YongLun Fu; XiaoMing Teng; ChiChiu Wang; WenMing Xu
Journal:  Oxid Med Cell Longev       Date:  2022-02-03       Impact factor: 6.543

2.  Histone deacetylase inhibitor upregulates peroxisomal fatty acid oxidation and inhibits apoptotic cell death in abcd1-deficient glial cells.

Authors:  Jaspreet Singh; Mushfiquddin Khan; Aurora Pujol; Mauhamad Baarine; Inderjit Singh
Journal:  PLoS One       Date:  2013-07-26       Impact factor: 3.240

  2 in total

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