Adrenoleukodystrophy, cerebrohepatorenal syndrome (Zellweger syndrome), and peroxisomes. - Suppr | 超能文献

Adrenoleukodystrophy, cerebrohepatorenal syndrome (Zellweger syndrome), and peroxisomes.

作者信息

Applegarth D A, Dimmick J E

出版信息

Pediatr Pathol. 1985;3(2-4):377-8. doi: 10.3109/15513818509078797.

DOI:10.3109/15513818509078797

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

Adrenoleukodystrophy, cerebrohepatorenal syndrome (Zellweger syndrome), and peroxisomes.

Pediatr Pathol. 1985;3(2-4):377-8. doi: 10.3109/15513818509078797.

2

Peroxisomal matrix enzymes in Zellweger syndrome: activity and subcellular localization in liver.齐-韦二氏综合征中的过氧化物酶体基质酶：肝脏中的活性及亚细胞定位

J Inherit Metab Dis. 1985;8 Suppl 2:151-2. doi: 10.1007/BF01811504.

3

Medium- and long-chain dicarboxylic aciduria in patients with Zellweger syndrome and neonatal adrenoleukodystrophy.泽尔韦格综合征和新生儿肾上腺脑白质营养不良患者的中长链二羧酸尿症

Pediatr Res. 1986 Jan;20(1):62-6. doi: 10.1203/00006450-198601000-00018.

4

Hepatic peroxisomes in adrenoleukodystrophy and related syndromes: cytochemical and morphometric data.肾上腺脑白质营养不良及相关综合征中的肝脏过氧化物酶体：细胞化学和形态计量学数据。

Virchows Arch A Pathol Anat Histopathol. 1988;413(4):275-85. doi: 10.1007/BF00783019.

5

Peroxisomal disorders. A review of a recently recognized group of clinical entities.

Clin Pediatr (Phila). 1987 Oct;26(10):497-504. doi: 10.1177/000992288702601001.

6

Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disorders.过氧化物酶体疾病患者肝脏过氧化物酶体和线粒体的病理学

Virchows Arch A Pathol Anat Histopathol. 1990;416(3):255-64. doi: 10.1007/BF01678985.

7

Ocular histopathologic and biochemical studies of the cerebrohepatorenal syndrome (Zellweger's syndrome) and its relationship to neonatal adrenoleukodystrophy.脑肝肾综合征（泽尔韦格综合征）的眼部组织病理学和生化研究及其与新生儿肾上腺脑白质营养不良的关系。

Am J Ophthalmol. 1983 Oct;96(4):488-501. doi: 10.1016/s0002-9394(14)77913-9.

8

Adrenoleukodystrophy and Zellweger syndrome.

Prog Clin Biol Res. 1990;321:511-35.

9

Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophies.新生儿期发病的和X连锁肾上腺脑白质营养不良中的过氧化物酶体缺陷。

Science. 1985 Jan 4;227(4682):67-70. doi: 10.1126/science.3964959.

10

Cerebrohepatorenal syndrome of Zellweger: a peroxisomal deficiency disorder. Case report and review.泽尔韦格脑肝肾综合征：一种过氧化物酶体缺乏症。病例报告及文献复习。

Isr J Med Sci. 1988 Jun;24(6):319-24.

引用本文的文献

1

Transforming Growth Factor-β1 Regulates Peroxisomal Genes/Proteins via Smad Signaling in Idiopathic Pulmonary Fibrosis Fibroblasts and Transgenic Mouse Models.转化生长因子-β1 通过 Smad 信号通路调节特发性肺纤维化成纤维细胞和转基因小鼠模型中的过氧化物酶体基因/蛋白。

Am J Pathol. 2023 Mar;193(3):259-274. doi: 10.1016/j.ajpath.2022.11.006. Epub 2022 Dec 12.

2

A defect in the peroxisomal biogenesis in germ cells induces a spermatogenic arrest at the round spermatid stage in mice.在生殖细胞中过氧化物酶体生物发生的缺陷会导致小鼠精原细胞停滞在圆形精子细胞阶段。

Sci Rep. 2019 Jul 2;9(1):9553. doi: 10.1038/s41598-019-45991-6.