Literature DB >> 2675425

Hereditary disorders of the red cell membrane skeleton.

K A Davies, S E Lux.   

Abstract

The hereditary hemolytic anemias include a heterogeneous class of disorders caused by defects in the proteins that constitute the membrane skeleton of the red blood cell. The combination of classical and molecular genetics together with clinical findings is rapidly improving our understanding of the basis of these defects.

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Year:  1989        PMID： 2675425     DOI： 10.1016/0168-9525(89)90086-3

Source DB:  PubMed          Journal:  Trends Genet        ISSN： 0168-9525            Impact factor:   11.639


  11 in total

1.  Inherited haemolytic anaemia created by insertional inactivation of the alpha-spectrin gene.

Authors:  G Grimber; C Galand; M Garbarz; M G Mattei; C Cavard; A Zider; P Blanchet; P Boivin; P Briand; D Dhermy
Journal:  Transgenic Res       Date:  1992-11       Impact factor: 2.788

2.  Changing patterns in cytoskeletal mRNA expression and protein synthesis during murine erythropoiesis in vivo.

Authors:  L L Peters; R A White; C S Birkenmeier; M L Bloom; S E Lux; J E Barker
Journal:  Proc Natl Acad Sci U S A       Date:  1992-07-01       Impact factor: 11.205

3.  Stomatocytosis as a presenting symptom of myelodysplasia.

Authors:  K Konstantopoulos; G Vassilopoulos; S Adamides; M Alexandrakis; J Zervas
Journal:  Med Oncol Tumor Pharmacother       Date:  1992

Review 4.  Current problems in haematology. 2: Hereditary spherocytosis.

Authors:  J C Smedley; A J Bellingham
Journal:  J Clin Pathol       Date:  1991-06       Impact factor: 3.411

5.  Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13.

Authors:  L L Lien; F M Boyce; P Kleyn; L M Brzustowicz; J Menninger; D C Ward; T C Gilliam; L M Kunkel
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-01       Impact factor: 11.205

6.  Ankyrin and beta-spectrin accumulate independently of alpha-spectrin in Drosophila.

Authors:  R R Dubreuil; J Yu
Journal:  Proc Natl Acad Sci U S A       Date:  1994-10-25       Impact factor: 11.205

7.  An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells.

Authors:  J G Conboy; J A Chasis; R Winardi; G Tchernia; Y W Kan; N Mohandas
Journal:  J Clin Invest       Date:  1993-01       Impact factor: 14.808

8.  A beta-spectrin isoform from Drosophila (beta H) is similar in size to vertebrate dystrophin.

Authors:  R R Dubreuil; T J Byers; C T Stewart; D P Kiehart
Journal:  J Cell Biol       Date:  1990-11       Impact factor: 10.539

9.  Spectrin redistributes to the cytosol and is phosphorylated during mitosis in cultured cells.

Authors:  V M Fowler; E J Adam
Journal:  J Cell Biol       Date:  1992-12       Impact factor: 10.539

10.  Cell shape and interaction defects in alpha-spectrin mutants of Drosophila melanogaster.

Authors:  J K Lee; R S Coyne; R R Dubreuil; L S Goldstein; D Branton
Journal:  J Cell Biol       Date:  1993-12       Impact factor: 10.539
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