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Is there a third gene for autosomal dominant polycystic kidney disease?

作者信息

Paterson A D, Pei Y

出版信息

Kidney Int. 1998 Nov;54(5):1759-61. doi: 10.1046/j.1523-1755.1998.00166.x.

DOI:10.1046/j.1523-1755.1998.00166.x
PMID:9844156
Abstract
摘要

相似文献

1
Is there a third gene for autosomal dominant polycystic kidney disease?常染色体显性多囊肾病是否存在第三个基因？
Kidney Int. 1998 Nov;54(5):1759-61. doi: 10.1046/j.1523-1755.1998.00166.x.
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Somatic mutation as mechanism for cyst formation in autosomal dominant polycystic kidney disease.体细胞突变作为常染色体显性多囊肾病中囊肿形成的机制。
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Autosomal dominant polycystic kidney disease: modification of disease progression.常染色体显性多囊肾病：疾病进展的调控
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Genotypes of autosomal dominant polycystic kidney disease in Japanese.日本人常染色体显性多囊肾病的基因型
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Recurrent fetal loss associated with bilineal inheritance of type 1 autosomal dominant polycystic kidney disease.与常染色体显性遗传1型多囊肾病双系遗传相关的复发性胎儿丢失
Am J Kidney Dis. 2002 Jul;40(1):16-20. doi: 10.1053/ajkd.2002.33908.
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Transepithelial chloride secretion and cystogenesis in autosomal dominant polycystic kidney disease.常染色体显性遗传性多囊肾病中的跨上皮氯化物分泌与囊肿形成
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引用本文的文献

1
A Case of New Familiar Genetic Variant of Autosomal Dominant Polycystic Kidney Disease-2: A Case Study.常染色体显性多囊肾病2型新的家族性基因变异病例：一项病例研究
Front Pediatr. 2015 Oct 9;3:82. doi: 10.3389/fped.2015.00082. eCollection 2015.
2
Bilineal inheritance of type 1 autosomal dominant polycystic kidney disease (ADPKD) and recurrent fetal loss.1型常染色体显性多囊肾病（ADPKD）的双系遗传与复发性胎儿丢失。
NDT Plus. 2008 Oct;1(5):289-91. doi: 10.1093/ndtplus/sfn103. Epub 2008 Jul 11.
3
Polycystic liver disease: an overview of pathogenesis, clinical manifestations and management.
多囊肝病：发病机制、临床表现及管理概述
Orphanet J Rare Dis. 2014 May 1;9:69. doi: 10.1186/1750-1172-9-69.
4
Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families.对指定的PKD3家系进行重新分析，并未发现支持第三个常染色体显性多囊肾病（ADPKD）位点的证据。
Kidney Int. 2014 Feb;85(2):383-92. doi: 10.1038/ki.2013.227. Epub 2013 Jun 12.
5
Cystic kidney diseases: many ways to form a cyst.囊性肾病：多种途径形成囊肿。
Pediatr Nephrol. 2013 Jan;28(1):33-49. doi: 10.1007/s00467-012-2221-x. Epub 2012 Jun 27.
6
Diagnosis and screening of autosomal dominant polycystic kidney disease.常染色体显性遗传性多囊肾病的诊断与筛查。
Adv Chronic Kidney Dis. 2010 Mar;17(2):140-52. doi: 10.1053/j.ackd.2009.12.001.
7
Unified criteria for ultrasonographic diagnosis of ADPKD.常染色体显性多囊肾病超声诊断的统一标准。
J Am Soc Nephrol. 2009 Jan;20(1):205-12. doi: 10.1681/ASN.2008050507. Epub 2008 Oct 22.
8
Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney disease.常染色体显性多囊肾病中的双系疾病和反式杂合子
Am J Hum Genet. 2001 Feb;68(2):355-63. doi: 10.1086/318188. Epub 2001 Jan 10.
9
Identification of mutations in the repeated part of the autosomal dominant polycystic kidney disease type 1 gene, PKD1, by long-range PCR.通过长程聚合酶链反应鉴定1型常染色体显性多囊肾病基因PKD1重复部分的突变。
Am J Hum Genet. 1999 Jul;65(1):39-49. doi: 10.1086/302460.