Immunohistologic findings in Alport syndrome.

Suppr

超能文献

作者信息

Kashtan C E, Kleppel M M, Gubler M C

机构信息

Department of Pediatrics, University of Minnesota Medical School, Minneapolis, USA.

出版信息

Contrib Nephrol. 1996;117:142-53. doi: 10.1159/000424811.

DOI:10.1159/000424811

PMID:8801043

Abstract

摘要

相似文献

Immunohistologic findings in Alport syndrome.

Contrib Nephrol. 1996;117:142-53. doi: 10.1159/000424811.

Morphologic alterations and biochemical studies of the glomerular basement membrane in Alport syndrome.阿尔波特综合征肾小球基底膜的形态学改变及生化研究

Contrib Nephrol. 1990;80:41-6. doi: 10.1159/000418626.

[Molecular genetics of Alport syndrome].[奥尔波特综合征的分子遗传学]

Nihon Rinsho. 1992 Dec;50(12):3021-6.

Mutations in type IV collagen genes and Alport phenotypes.IV型胶原基因的突变与奥尔波特综合征表型

Contrib Nephrol. 1996;117:154-71. doi: 10.1159/000424812.

Alpha 5 COLIV chain distribution in glomerular basement membrane in a male with X-linked Alport syndrome and thin basement membrane.一名患有X连锁Alport综合征和薄基底膜的男性肾小球基底膜中α5（IV）链分布情况

Pediatr Nephrol. 2000 Dec;15(3-4):325.

Type IV collagen in normal and diseased glomerular basement membrane.正常和病变肾小球基底膜中的IV型胶原蛋白。

Adv Nephrol Necker Hosp. 1993;22:1-14.

Genetic, clinical, and morphologic heterogeneity in Alport's syndrome.奥尔波特综合征的遗传、临床和形态学异质性。

Adv Nephrol Necker Hosp. 1993;22:15-35.

Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution.常染色体隐性遗传性阿尔波特综合征：IV型胶原链分布的免疫组织化学研究

Kidney Int. 1995 Apr;47(4):1142-7. doi: 10.1038/ki.1995.163.

Distribution of familial nephritis antigen in normal tissue and renal basement membranes of patients with homozygous and heterozygous Alport familial nephritis. Relationship of familial nephritis and Goodpasture antigens to novel collagen chains and type IV collagen.家族性肾炎抗原在正常组织以及纯合子和杂合子Alport家族性肾炎患者肾基底膜中的分布。家族性肾炎和Goodpasture抗原与新型胶原链及IV型胶原的关系。

Lab Invest. 1989 Sep;61(3):278-89.

Comparison of alpha5(IV) collagen chain expression in skin with disease severity in women with X-linked Alport syndrome.X连锁遗传性Alport综合征女性患者皮肤中α5(IV)胶原链表达与疾病严重程度的比较。

J Am Soc Nephrol. 1998 Aug;9(8):1433-40. doi: 10.1681/ASN.V981433.

引用本文的文献

Type IV Collagen Variants in CKD: Performance of Computational Predictions for Identifying Pathogenic Variants.慢性肾脏病中的IV型胶原蛋白变体：识别致病变体的计算预测性能

Kidney Med. 2021 Feb 10;3(2):257-266. doi: 10.1016/j.xkme.2020.12.007. eCollection 2021 Mar-Apr.

Genetic diagnosis of Alport syndrome.奥尔波特综合征的基因诊断

Korean J Pediatr. 2019 May;62(5):164-165. doi: 10.3345/kjp.2018.07339. Epub 2019 Jan 3.

Alport Syndrome: De Novo Mutation in the COL4A5 Gene Converting Glycine 1205 to Valine.奥尔波特综合征：COL4A5基因发生从头突变，将甘氨酸1205转换为缬氨酸。

Clin Med Insights Pediatr. 2012 Jun 28;6:41-9. doi: 10.2147/CBF.S23366. Print 2012.

Diagnosis of Alport syndrome without biopsy?无需活检诊断Alport综合征？

Pediatr Nephrol. 2007 May;22(5):621-5. doi: 10.1007/s00467-006-0376-z. Epub 2006 Dec 2.

Stage-specific action of matrix metalloproteinases influences progressive hereditary kidney disease.基质金属蛋白酶的阶段特异性作用影响进行性遗传性肾病。

PLoS Med. 2006 Apr;3(4):e100. doi: 10.1371/journal.pmed.0030100. Epub 2006 Mar 7.

Glomerular expression of type IV collagen chains in normal and X-linked Alport syndrome kidneys.正常及X连锁遗传性肾炎肾脏中IV型胶原链的肾小球表达

Am J Pathol. 2000 Jun;156(6):1901-10. doi: 10.1016/S0002-9440(10)65063-8.

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。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验