2号染色体上多囊肾病的可能位点。 - Suppr

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超能文献

Possible locus for polycystic kidney disease on chromosome 2.

作者信息

Nørby S, Schwartz M

出版信息

Lancet. 1990 Aug 4;336(8710):323-4. doi: 10.1016/0140-6736(90)91870-g.

DOI:10.1016/0140-6736(90)91870-g

PMID:1974020

Abstract

摘要

相似文献

Possible locus for polycystic kidney disease on chromosome 2.2号染色体上多囊肾病的可能位点。

Lancet. 1990 Aug 4;336(8710):323-4. doi: 10.1016/0140-6736(90)91870-g.

Adult polycystic kidney disease and linked RFLPs at the alpha globin locus: a genetic study in the South Wales population.成人多囊肾病与α珠蛋白基因座连锁的限制性片段长度多态性：南威尔士人群的一项遗传学研究

J Med Genet. 1987 Aug;24(8):466-73. doi: 10.1136/jmg.24.8.466.

Linkage analysis excludes the involvement of the canine PKD2 homologue in bull terrier polycystic kidney disease.连锁分析排除了犬类PKD2同源物与牛头梗多囊肾病的关联。

Anim Genet. 2006 Oct;37(5):527-8. doi: 10.1111/j.1365-2052.2006.01517.x.

Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1.将160厘摩的1号染色体区域排除常染色体显性遗传性多囊肾病II型（ADPKD2）。

J Med Genet. 1990 Nov;27(11):697-700. doi: 10.1136/jmg.27.11.697.

Recombination or heterogeneity: is there a second locus for adult polycystic kidney disease?重组或异质性：成人多囊肾病是否存在第二个基因座？

J Med Genet. 1990 Jul;27(7):413-7. doi: 10.1136/jmg.27.7.413.

Gene defect in polycystic kidney disease.多囊肾病中的基因缺陷。

Exp Nephrol. 1995 Sep-Oct;3(5):267-9.

Rapid detection of polymorphism near gene for adult polycystic kidney disease.成人多囊肾病基因附近多态性的快速检测

Lancet. 1990 May 5;335(8697):1102-3. doi: 10.1016/0140-6736(90)92680-g.

[Genetic aspects of adult polycystic kidney disease].

Tanpakushitsu Kakusan Koso. 1988 Apr;33(5):1030-2.

The molecular genetics of autosomal dominant polycystic kidney disease.常染色体显性多囊肾病的分子遗传学

Semin Nephrol. 1989 Jun;9(2):122-34.

[Autosomal dominant polycystic kidney and genetic markers of chromosome 16].[常染色体显性多囊肾与16号染色体的遗传标记]

Nephrologie. 1990;11(2):79-82.

引用本文的文献

Autosomal dominant polycystic kidney disease: recent advances in pathogenesis and potential therapies.常染色体显性多囊肾病：发病机制和潜在治疗方法的最新进展。

Clin Exp Nephrol. 2013 Jun;17(3):317-26. doi: 10.1007/s10157-012-0741-0. Epub 2012 Nov 29.

Polycystic kidney disease: pathogenesis and potential therapies.多囊肾病：发病机制与潜在治疗方法

Biochim Biophys Acta. 2011 Oct;1812(10):1337-43. doi: 10.1016/j.bbadis.2010.11.014. Epub 2010 Dec 10.

Identification of the human CYS1 gene and candidate gene analysis in Boichis disease.

Pediatr Nephrol. 2003 Jun;18(6):498-505. doi: 10.1007/s00467-003-1141-1. Epub 2003 May 6.

A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2).常染色体显性多囊肾病（PKD2）第二个基因中的一系列突变。

Am J Hum Genet. 1997 Sep;61(3):547-55. doi: 10.1086/515497.

Icelandic families with autosomal dominant polycystic kidney disease: families unlinked to chromosome 16p13.3 revealed by linkage analysis.患有常染色体显性多囊肾病的冰岛家庭：连锁分析显示与16号染色体p13.3区域不连锁的家庭。

Hum Genet. 1993 Jul;91(6):609-13. doi: 10.1007/BF00205089.

Molecular genetic diagnosis of autosomal dominant polycystic kidney disease in a newborn with bilateral cystic kidneys detected prenatally and multiple skeletal malformations.一名产前检测出双侧肾囊肿且伴有多处骨骼畸形的新生儿常染色体显性多囊肾病的分子遗传学诊断

J Med Genet. 1993 May;30(5):419-22. doi: 10.1136/jmg.30.5.419.

Autosomal recessive polycystic kidney disease does not map to the second gene locus for autosomal dominant polycystic kidney disease on chromosome 4.常染色体隐性多囊肾病并不定位于4号染色体上常染色体显性多囊肾病的第二个基因位点。

Hum Genet. 1994 Jun;93(6):697-8. doi: 10.1007/BF00201574.

Estimating locus heterogeneity in autosomal dominant polycystic kidney disease (ADPKD) in the Spanish population.评估西班牙人群常染色体显性多囊肾病（ADPKD）中的基因座异质性。

J Med Genet. 1993 Nov;30(11):910-3. doi: 10.1136/jmg.30.11.910.

Adult polycystic kidney disease in a kindred of West Indian origin exhibits linkage with the 3'HVR probe on chromosome 16.起源于西印度群岛的一个家族中的成人多囊肾病与16号染色体上的3'HVR探针存在连锁关系。

J Med Genet. 1991 May;28(5):334-6. doi: 10.1136/jmg.28.5.334.

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