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本文引用的文献

1
The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3.1型口面指综合征（OFD1）是多囊肾病及相关畸形的病因之一，定位于Xp22.2-Xp22.3。
Hum Mol Genet. 1997 Jul;6(7):1163-7. doi: 10.1093/hmg/6.7.1163.
2
Expression of hepatocyte growth factor/scatter factor and its receptor, MET, suggests roles in human embryonic organogenesis.肝细胞生长因子/扩散因子及其受体MET的表达表明其在人类胚胎器官发生中发挥作用。
Pediatr Res. 1997 May;41(5):657-65. doi: 10.1203/00006450-199705000-00010.
3
Roles of growth factors in renal development.生长因子在肾脏发育中的作用。
Curr Opin Nephrol Hypertens. 1997 Jan;6(1):10-4. doi: 10.1097/00041552-199701000-00003.
4
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family.果蝇无眼基因的人类同源基因是鳃-耳-肾（BOR）综合征的基础，并鉴定出一个新的基因家族。
Nat Genet. 1997 Feb;15(2):157-64. doi: 10.1038/ng0297-157.
5
Insulin-like growth factor (IGF) and IGF binding protein gene expression in multicystic renal dysplasia.胰岛素样生长因子（IGF）及IGF结合蛋白基因在多囊性肾发育不良中的表达
J Am Soc Nephrol. 1997 Jan;8(1):85-94. doi: 10.1681/ASN.V8185.
6
The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney.小鼠Pax2(1Neu)突变与肾-眼裂综合征家族中的一种人类PAX2突变相同，会导致脑、耳、眼和肾的发育缺陷。
Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):13870-5. doi: 10.1073/pnas.93.24.13870.
7
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.范可尼贫血主要基因FAA的cDNA的表达克隆
Nat Genet. 1996 Nov;14(3):320-3. doi: 10.1038/ng1196-320.
8
Growth factors and apoptosis in neonatal ureteral obstruction.新生儿输尿管梗阻中的生长因子与细胞凋亡
J Am Soc Nephrol. 1996 Aug;7(8):1098-105. doi: 10.1681/ASN.V781098.
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Vesicoureteric reflux: all in the genes? Report of a meeting of physicians at the Hospital for Sick Children, Great Ormond Street, London.
Lancet. 1996 Sep 14;348(9029):725-8.
10
Deregulation of cell survival in cystic and dysplastic renal development.囊性和发育异常性肾发育中细胞存活的失调。
Kidney Int. 1996 Jan;49(1):135-46. doi: 10.1038/ki.1996.18.

Multiple causes of human kidney malformations.

作者信息

Woolf A S

机构信息

Nephrourology Unit, University College Hospital Medical School, London.

出版信息

Arch Dis Child. 1997 Dec;77(6):471-3. doi: 10.1136/adc.77.6.471.

DOI:10.1136/adc.77.6.471
PMID:9496175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1717414/
Abstract
摘要