Literature DB >> 18263974

"Treasure your exceptions": recent advances in molecular genetics of glomerular disease.

Andrzej Ciechanowicz1, Andrzej Brodkiewicz, Agnieszka Bińczak-Kuleta, Miłosz Parczewski, Stanłisaw Czekalski.   

Abstract

The glomerular filtration barrier consists of endothelial cells, the glomerular basement membrane, and podocytes. The membrane is a highly crosslinked macromolecular meshwork composed of specific extracellular matrix proteins. The adjacent foot processes of podocytes are bridged along their basolateral surfaces by a slit diaphragm (a porous filter structure of nephrin molecules). Recent discoveries of mutations in the range of genes encoding proteins involved in the structure or function of the glomerular filtration barrier have provided new insights into mechanisms of glomerular diseases. In this review, we summarize recent progress in the elucidation of the genetic basis of some glomerulopathies in humans.

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Year:  2008        PMID: 18263974     DOI: 10.1007/BF03195253

Source DB:  PubMed          Journal:  J Appl Genet        ISSN: 1234-1983            Impact factor:   3.240


  27 in total

1.  Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites.

Authors:  S Bolk; E G Puffenberger; J Hudson; D H Morton; A Chakravarti
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

Review 2.  Unraveling the mechanisms of glomerular ultrafiltration: nephrin, a key component of the slit diaphragm.

Authors:  K Tryggvason
Journal:  J Am Soc Nephrol       Date:  1999-11       Impact factor: 10.121

Review 3.  Molecular basis of glomerular permselectivity.

Authors:  K Tryggvason; J Wartiovaara
Journal:  Curr Opin Nephrol Hypertens       Date:  2001-07       Impact factor: 2.894

4.  Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis.

Authors:  J M Kaplan; S H Kim; K N North; H Rennke; L A Correia; H Q Tong; B J Mathis; J C Rodríguez-Pérez; P G Allen; A H Beggs; M R Pollak
Journal:  Nat Genet       Date:  2000-03       Impact factor: 38.330

Review 5.  Diagnosis and management of kidney involvement in Fabry disease.

Authors:  David G Warnock; Michael L West
Journal:  Adv Chronic Kidney Dis       Date:  2006-04       Impact factor: 3.620

6.  NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome.

Authors:  N Boute; O Gribouval; S Roselli; F Benessy; H Lee; A Fuchshuber; K Dahan; M C Gubler; P Niaudet; C Antignac
Journal:  Nat Genet       Date:  2000-04       Impact factor: 38.330

7.  Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.

Authors:  O Beltcheva; P Martin; U Lenkkeri; K Tryggvason
Journal:  Hum Mutat       Date:  2001-05       Impact factor: 4.878

Review 8.  Congenital nephrotic syndromes.

Authors:  J Khoshnoodi; K Tryggvason
Journal:  Curr Opin Genet Dev       Date:  2001-06       Impact factor: 5.578

Review 9.  Familial hematurias: what we know and what we don't.

Authors:  Clifford E Kashtan
Journal:  Pediatr Nephrol       Date:  2005-04-27       Impact factor: 3.714

10.  Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome.

Authors:  M Kestilä; U Lenkkeri; M Männikkö; J Lamerdin; P McCready; H Putaala; V Ruotsalainen; T Morita; M Nissinen; R Herva; C E Kashtan; L Peltonen; C Holmberg; A Olsen; K Tryggvason
Journal:  Mol Cell       Date:  1998-03       Impact factor: 17.970

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  1 in total

Review 1.  Glomerular diseases: genetic causes and future therapeutics.

Authors:  Chih-Kang Chiang; Reiko Inagi
Journal:  Nat Rev Nephrol       Date:  2010-07-20       Impact factor: 28.314

  1 in total

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