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Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes.

作者信息

Simon D B, Lifton R P

机构信息

Howard Hughes Medical Institute, Department of Medicine, Boyer Center for Molecular Medicine, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

出版信息

Curr Opin Cell Biol. 1998 Aug;10(4):450-4. doi: 10.1016/s0955-0674(98)80057-4.

DOI:10.1016/s0955-0674(98)80057-4
PMID:9719864
Abstract

The successful merging of modern molecular genetics with basic renal physiology is exemplified by the recent description of the molecular basis of two classic diseases of clinical nephrology; Bartter's and Gitelman's syndromes of inherited hypokalemic alkalosis. Mutations in four different genes have been identified, each of which causes hypokalemic alkalosis, salt wasting and hypotension. These genetic studies have greatly advanced our understanding of renal physiology.

摘要

相似文献

1
Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes.
Curr Opin Cell Biol. 1998 Aug;10(4):450-4. doi: 10.1016/s0955-0674(98)80057-4.
2
Ion transporter mutations in Gitelman's and Bartter's syndromes.吉特曼综合征和巴特综合征中的离子转运体突变。
Curr Opin Nephrol Hypertens. 1998 Jan;7(1):43-7. doi: 10.1097/00041552-199801000-00008.
3
"The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes".
Am J Physiol. 1996 Nov;271(5 Pt 2):F957-9. doi: 10.1152/ajprenal.1996.271.5.F957.
4
The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes.遗传性低钾性碱中毒的分子基础:巴特综合征和吉特曼综合征。
Am J Physiol. 1996 Nov;271(5 Pt 2):F961-6. doi: 10.1152/ajprenal.1996.271.5.F961.
5
Mutations in renal ion transporters cause Gitelman's and Bartter's syndromes of inherited hypokalemic alkalosis.肾脏离子转运体的突变会导致吉特曼综合征和巴特综合征这两种遗传性低钾性碱中毒。
Adv Nephrol Necker Hosp. 1997;27:343-59.
6
Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2.巴特综合征,即伴有高钙尿症的低钾性碱中毒,由钠-钾-2氯协同转运蛋白NKCC2的突变引起。
Nat Genet. 1996 Jun;13(2):183-8. doi: 10.1038/ng0696-183.
7
Molecular pathophysiology of Bartter's and Gitelman's syndromes.巴特综合征和吉特曼综合征的分子病理生理学
World J Pediatr. 2015 May;11(2):113-25. doi: 10.1007/s12519-015-0016-4. Epub 2015 Mar 9.
8
Bartter's and Gitelman's syndromes: from gene to clinic.巴特综合征和吉特曼综合征:从基因到临床
Nephron Physiol. 2004;96(3):p65-78. doi: 10.1159/000076752.
9
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.吉特曼综合征(Bartter综合征的变异型),即遗传性低钾性碱中毒,由噻嗪类敏感型钠氯共转运体的突变引起。
Nat Genet. 1996 Jan;12(1):24-30. doi: 10.1038/ng0196-24.
10
Miscellaneous non-inflammatory musculoskeletal conditions. Bartter's and Gitelman's diseases.杂类非炎性肌肉骨骼疾病。巴特氏症候群和吉特曼氏症候群。
Best Pract Res Clin Rheumatol. 2011 Oct;25(5):637-48. doi: 10.1016/j.berh.2011.10.013.

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