Literature DB >> 2595723

HLA linkage with familial vesicoureteral reflux and familial pelvi-ureteric junction obstruction.

P Mackintosh1, G Almarhoos, D A Heath.   

Abstract

The inheritance of HLA haplotypes has been looked at in a family with pelvi-ureteric junction obstruction (PUJO) and two families with vesicoureteric reflux (VUR). The data have been combined with those of other reported families and lod scores calculated for both these urinary tract anomalies. There seems no doubt that VUR is linked to HLA whilst the case for PUJO is equivocal.

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Year:  1989        PMID： 2595723     DOI： 10.1111/j.1399-0039.1989.tb01735.x

Source DB:  PubMed          Journal:  Tissue Antigens        ISSN： 0001-2815


  7 in total

1.  A genome-wide scan for genes involved in primary vesicoureteric reflux.

Authors:  H Kelly; C M Molony; J M Darlow; M E Pirker; A Yoneda; A J Green; P Puri; D E Barton
Journal:  J Med Genet       Date:  2007-07-27       Impact factor: 6.318

Review 2.  Genetic and developmental basis for urinary tract obstruction.

Authors:  Feng Chen
Journal:  Pediatr Nephrol       Date:  2008-12-16       Impact factor: 3.714

Review 3.  Vesicoureteric reflux and reflux nephropathy: from mouse models to childhood disease.

Authors:  Marie-Lyne Fillion; Christine L Watt; Indra R Gupta
Journal:  Pediatr Nephrol       Date:  2014-02-06       Impact factor: 3.714

4.  Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.

Authors:  S A Feather; S Malcolm; A S Woolf; V Wright; D Blaydon; C J Reid; F A Flinter; W Proesmans; K Devriendt; J Carter; P Warwicker; T H Goodship; J A Goodship
Journal:  Am J Hum Genet       Date:  2000-03-17       Impact factor: 11.025

5.  Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6p.

Authors:  L Izquierdo; M Porteous; P G Paramo; J M Connor
Journal:  Hum Genet       Date:  1992-07       Impact factor: 4.132

6.  Vesico-ureteric reflux: using mouse models to understand a common congenital urinary tract defect.

Authors:  Inga J Murawski; Christine L Watt; Indra R Gupta
Journal:  Pediatr Nephrol       Date:  2011-03-20       Impact factor: 3.714

7.  Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism.

Authors:  S H Pearce; D Trump; C Wooding; G M Besser; S L Chew; D B Grant; D A Heath; I A Hughes; C R Paterson; M P Whyte
Journal:  J Clin Invest       Date:  1995-12       Impact factor: 14.808
  7 in total

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