Unravelling the pathogenesis of cystic kidney diseases.
作者信息
Woolf A S, Winyard P J
机构信息
Unit of Medicine, Institute of Child Health, London.
出版信息
Arch Dis Child. 1995 Feb;72(2):103-5. doi: 10.1136/adc.72.2.103.
Abstract
摘要
相似文献
1
Unravelling the pathogenesis of cystic kidney diseases.揭示多囊肾病的发病机制。
Arch Dis Child. 1995 Feb;72(2):103-5. doi: 10.1136/adc.72.2.103.
2
Heritable cystic disorders of the kidney. The mythology of polycystic disease.遗传性肾脏囊性疾病。多囊肾病的传奇故事。
Pediatr Clin North Am. 1971 May;18(2):435-44. doi: 10.1016/s0031-3955(16)32560-3.
3
Toxic metabolic defect in polycystic disease of kidney. Evidence from microscope studies.
Lancet. 1970 Mar 14;1(7646):547-50. doi: 10.1016/s0140-6736(70)90773-7.
4
Multicystic dysplasia of the kidney.
Clin Pediatr (Phila). 1995 Jan;34(1):32-40. doi: 10.1177/000992289503400106.
5
Cystic kidney disease.囊性肾病
Indian Pediatr. 1996 Feb;33(2):134-40.
6
Cystic diseases of the kidney in children.儿童肾囊性疾病
Adv Pediatr. 1984;31:371-404.
7
Cystic disease of the kidneys. Autopsy report and family study.
Acta Pathol Microbiol Scand. 1965;64(4):459-69. doi: 10.1111/apm.1965.64.4.459.
8
[Connatal cystic kidneys].先天性多囊肾
Padiatr Grenzgeb. 1985;24(3):221-7.
9
[Recent advances in molecular pathogenesis and treatment of polycystic kidney disease].[多囊肾病分子发病机制与治疗的最新进展]
Rev Med Chir Soc Med Nat Iasi. 2008 Jan-Mar;112(1):11-20.
10
The enigma of familial polycystic kidneys.家族性多囊肾之谜。
N Engl J Med. 1969 Oct 30;281(18):1013-4. doi: 10.1056/NEJM196910302811810.
引用本文的文献
1
The sea urchin sperm receptor for egg jelly is a modular protein with extensive homology to the human polycystic kidney disease protein, PKD1.海胆卵胶膜的精子受体是一种模块化蛋白质，与人类多囊肾病蛋白PKD1具有广泛的同源性。
J Cell Biol. 1996 May;133(4):809-17. doi: 10.1083/jcb.133.4.809.
本文引用的文献
1
Identification of the von Hippel-Lindau disease tumor suppressor gene.冯·希佩尔-林道病肿瘤抑制基因的鉴定。
Science. 1993 May 28;260(5112):1317-20. doi: 10.1126/science.8493574.
2
Bcl-2-deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair.Bcl-2基因缺陷型小鼠表现出暴发性淋巴细胞凋亡、多囊肾和毛发色素减退。
Cell. 1993 Oct 22;75(2):229-40. doi: 10.1016/0092-8674(93)80065-m.
3
WT-1 is required for early kidney development.WT-1是早期肾脏发育所必需的。
Cell. 1993 Aug 27;74(4):679-91. doi: 10.1016/0092-8674(93)90515-r.
4
Unilateral renal agenesis may result from in utero regression of multicystic renal dysplasia.单侧肾发育不全可能由子宫内多囊性肾发育异常的退化引起。
J Urol. 1993 Aug;150(2 Pt 2):793-4. doi: 10.1016/s0022-5347(17)35615-x.
5
Association of cyclosporin A with acquired cystic kidney disease of the native kidneys in renal transplant recipients.
Kidney Int. 1993 Sep;44(3):613-6. doi: 10.1038/ki.1993.288.
6
Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice.与导致小鼠隐性多囊肾病的突变相关的候选基因。
Science. 1994 May 27;264(5163):1329-33. doi: 10.1126/science.8191288.
7
Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret.缺乏酪氨酸激酶受体Ret的小鼠的肾脏和肠神经系统缺陷。
Nature. 1994 Jan 27;367(6461):380-3. doi: 10.1038/367380a0.
8
Large-scale normal cell death in the developing rat kidney and its reduction by epidermal growth factor.发育中大鼠肾脏的大规模正常细胞死亡及其被表皮生长因子的减少。
Development. 1993 Jul;118(3):777-84. doi: 10.1242/dev.118.3.777.
9
Branching out with the ureteric bud.
Exp Nephrol. 1994 Jul-Aug;2(4):211-9.
10
Outcome of antenatally detected cystic dysplastic kidney disease.产前检测出的多囊性发育不良性肾病的结局
Arch Dis Child. 1994 Jun;70(6):520-2. doi: 10.1136/adc.70.6.520.
Zotero 插件