Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux
about
Mutations in HPSE2 cause urofacial syndromeLower urinary tract development and diseaseVesicoureteral reflux and other urinary tract malformations in mice compound heterozygous for Pax2 and Emx2Primary, nonsyndromic vesicoureteric reflux and nephropathy in sibling pairs: a United Kingdom cohort for a DNA bank.Renal malformations associated with mutations of developmental genes: messages from the clinic.Association of ACE I/D gene polymorphism with vesicoureteral reflux susceptibility in children: a meta-analysis.Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients.Urinary tract effects of HPSE2 mutations.Congenital anomalies of the kidney and urinary tract: a genetic disorder?New congenital anomalies of the kidney and urinary tract and outcomes in Robo2 mutant mice with the inserted piggyBac transposon.Genetics of Vesicoureteral Reflux.Genetic contribution and associated pathophysiology in end-stage renal diseaseA new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development.Estimation of the relationship between the polymorphisms of selected genes: ACE, AGTR1, TGFβ1 and GNB3 with the occurrence of primary vesicoureteral reflux.Genetics of congenital anomalies of the kidney and urinary tract.Genetic susceptibility to renal scar formation after urinary tract infection: a systematic review and meta-analysis of candidate gene polymorphisms.Genetics of innate immunity and UTI susceptibility.A single-center cohort of Canadian children with VUR reveals renal phenotypes important for genetic studies.Renin-angiotensin system in ureteric bud branching morphogenesis: implications for kidney disease.Relevance of current guidelines in the management of VUR.Vesicoureteric reflux and reflux nephropathy: from mouse models to childhood disease.Genetic, environmental, and epigenetic factors involved in CAKUT.Identification of ethnically specific genetic variations in pan-asian ethnos.Genetics of vesicoureteral reflux.Genetics of kidney development: pathogenesis of renal anomalies.Genome gender diversity in affected sib-pairs with familial vesico-ureteric reflux identified by single nucleotide polymorphism linkage analysis.Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux.ROBO2 gene variants in children with primary nonsyndromic vesicoureteral reflux with or without renal hypoplasia/dysplasia.
P2860
Q24631978-2801CBDD-D0AF-4C59-BBAA-80EDB0487405Q27000375-D2246934-33FD-4A09-BA0E-87F1F5D5C836Q28478740-01D25C64-9D07-4BE8-B73B-0E3F036B543BQ33453529-A136DF5D-6CBA-46E0-AB08-CCFBAAA1D083Q34117987-1D2F52CD-C4BE-44F4-8A0C-FC8087430CADQ34186867-4D9BE7E5-D81E-4CC0-8D50-A2F1D3B92862Q34256093-9084BEC8-F5B8-4596-B065-A8C0F452097CQ35228493-B02B18EC-24C3-4B01-8689-6C488AF014FFQ35997775-2E2AD9F4-986A-46F5-8552-FF2D3F5ECC8BQ36086539-72D51ABD-4E0D-4F3F-A04B-8A9F53DE5E7EQ36658504-7417A2D6-340C-42F1-8A71-C039CD36D940Q36925161-708861B1-131D-4156-B085-4AA5456FE0C9Q37535775-3A6F4673-F2AE-451E-B2E6-F4ECF40F9C58Q37660514-3146DEDC-E376-4774-ABA2-AD9B0CEDB055Q37783542-6C398200-C505-4D3D-9410-8C2C28725A96Q37813488-2A9CAE85-778F-4BF3-BA60-5DCDC0BB9DB7Q37900471-BDB67BD4-1938-434D-830A-7BD04E558679Q38093100-54579107-7B70-43C8-8435-E10D91F1E658Q38141834-DE853701-3ED7-43A4-ACAA-3648A296109AQ38175300-32D2C9AF-594E-42F2-A098-4984F500508FQ38185597-3A869496-7E8F-4873-9917-6CE9D97F51A4Q38568437-3A1049C1-AA09-4F9B-AA26-AE5E333AC807Q38815008-15CC1720-2D3A-4836-A513-2008721650ACQ39485603-3C65C905-AF5D-466E-B050-678D14C216CAQ41238162-C8F76E17-338D-4D73-9B88-B28CF7B46B2DQ44770698-3EC12235-6452-4EEF-8E9A-204FB91AEC3DQ45138496-2A70A12C-B814-45E8-8AD1-DDE1409E4D51Q53979458-5C57FF60-BF3B-4A24-8C77-16588AC75C73
P2860
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux
@ast
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux
@en
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux.
@nl
type
label
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux
@ast
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux
@en
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux.
@nl
prefLabel
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux
@ast
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux
@en
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux.
@nl
P2093
P2860
P356
P1476
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux
@en
P2093
Aisling Stewart
Ambrose M Gullett
Heather J Cordell
Judith A Goodship
Pimphen Charoen
Rajko B Kenda
Rebecca Darlay
Sally A Feather
Sue Malcolm
Timothy H J Goodship
P2860
P304
P356
10.1681/ASN.2009060624
P577
2009-12-03T00:00:00Z