Literature DB >> 2765409

Hereditary stomatocytosis: consistent association with an integral membrane protein deficiency.

S W Eber1, W M Lande, T A Iarocci, W C Mentzer, P Höhn, J S Wiley, W Schröter.   

Abstract

We studied the RBC membrane proteins of four patients, including a mother and daughter, with hereditary stomatocytosis. One- and two-dimensional gel electrophoresis revealed that a 28 kDa integral protein, present in normal RBC membranes, was absent in all four patients. This abnormality, reported once previously (Lande et al, 1982), appears to be a characteristic feature of hereditary stomatocytosis, and may be related to the underlying permeability defect in this disorder.

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Year:  1989        PMID: 2765409     DOI: 10.1111/j.1365-2141.1989.tb07731.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  4 in total

1.  A family showing recessively inherited multisystem pathology with aberrant splicing of the erythrocyte Band 7.2b ('stomatin') gene.

Authors:  A C Argent; M C Chetty; B Fricke; Y Bertrand; N Philippe; S Khogali; M von Düring; J Delaunay; G W Stewart
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

2.  Erythrocyte adducin: a structural regulator of the red blood cell membrane.

Authors:  T Franco; P S Low
Journal:  Transfus Clin Biol       Date:  2010-07-23       Impact factor: 1.406

Review 3.  Temperature effects on cation transport in hereditary stomatocytosis and allied disorders.

Authors:  S E Coles; G W Stewart
Journal:  Int J Exp Pathol       Date:  1999-10       Impact factor: 1.925

4.  Mechanosensitive Pannexin 1 Activity Is Modulated by Stomatin in Human Red Blood Cells.

Authors:  Sarah Rougé; Sandrine Genetet; Maria Florencia Leal Denis; Michael Dussiot; Pablo Julio Schwarzbaum; Mariano Anibal Ostuni; Isabelle Mouro-Chanteloup
Journal:  Int J Mol Sci       Date:  2022-08-20       Impact factor: 6.208

  4 in total

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