Literature DB >> 6729952

Immunoglobulin (Gm) allotype frequencies in idiopathic membranous nephropathy and minimal change nephropathy.

A G Demaine, J S Cameron, D T Taube, R W Vaughan, K I Welsh.   

Abstract

40 Caucasoid patients with idiopathic membranous nephropathy (IMN) and 49 Caucasoid patients with minimal change nephropathy (MCN) were immunoglobulin allotyped for the Gm markers G1m (1, 2, 3) and G3m (5, 11, 21). Compared with normal controls the IMN group had a significantly decreased incidence of the G1m (3); G3m (5, 11) phenotype (P = less than 0.005). This decrease was accompanied by concommitant increase in both the G1m (1, 3); G3m (5, 11, 21) and the G1m (1, 2, 3); G3m (5, 11, 21) phenotypes. The result was most pronounced in IMN patients with deteriorating renal function. In contrast no significant differences were observed between the Gm phenotype frequencies of the MCN patients and controls.

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Year:  1984        PMID: 6729952     DOI: 10.1097/00007890-198405000-00017

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  4 in total

Review 1.  The immune system in minimal change nephrotic syndrome.

Authors:  H W Schnaper
Journal:  Pediatr Nephrol       Date:  1989-01       Impact factor: 3.714

Review 2.  Immunogenetics of glomerulonephritis.

Authors:  G A Müller; C A Müller
Journal:  Clin Investig       Date:  1993-10

3.  Immunoglobulin heavy chain switch region restriction fragment length polymorphisms are associated with renal disease.

Authors:  A G Demaine; D H Taube; R W Vaughan; L A Kerr; K I Welsh
Journal:  Clin Exp Immunol       Date:  1986-11       Impact factor: 4.330

4.  Association of membranous nephropathy with T-cell receptor constant beta chain and immunoglobulin heavy chain switch region polymorphisms.

Authors:  A G Demaine; R W Vaughan; D H Taube; K I Welsh
Journal:  Immunogenetics       Date:  1988       Impact factor: 2.846

  4 in total

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