Literature DB >> 2961992

Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis.

T L Coetzer1, J Lawler, S C Liu, J T Prchal, R J Gualtieri, M C Brain, J V Dacie, J Palek.   

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Year:  1988        PMID： 2961992     DOI： 10.1056/NEJM198801283180407

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  18 in total

1.  cDNA sequence for human erythrocyte ankyrin.

Authors:  S Lambert; H Yu; J T Prchal; J Lawler; P Ruff; D Speicher; M C Cheung; Y W Kan; J Palek
Journal:  Proc Natl Acad Sci U S A       Date:  1990-03       Impact factor: 11.205

Review 2.  The spectrin skeleton: from red cells to brain.

Authors:  V Bennett; S Lambert
Journal:  J Clin Invest       Date:  1991-05       Impact factor: 14.808

3.  Prevalence of increased osmotic fragility of erythrocytes in German blood donors: screening using a modified glycerol lysis test.

Authors:  S W Eber; A Pekrun; A Neufeldt; W Schröter
Journal:  Ann Hematol       Date:  1992-02       Impact factor: 3.673

4.  Molecular basis of spectrin deficiency in beta spectrin Durham. A deletion within beta spectrin adjacent to the ankyrin-binding site precludes spectrin attachment to the membrane in hereditary spherocytosis.

Authors:  H Hassoun; J N Vassiliadis; J Murray; S J Yi; M Hanspal; R E Ware; S S Winter; S S Chiou; J Palek
Journal:  J Clin Invest       Date:  1995-12       Impact factor: 14.808

5.  Ankyrin and the hemolytic anemia mutation, nb, map to mouse chromosome 8: presence of the nb allele is associated with a truncated erythrocyte ankyrin.

Authors:  R A White; C S Birkenmeier; S E Lux; J E Barker
Journal:  Proc Natl Acad Sci U S A       Date:  1990-04       Impact factor: 11.205

6.  Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.

Authors:  P G Gallagher; M J Petruzzi; S A Weed; Z Zhang; S L Marchesi; N Mohandas; J S Morrow; B G Forget
Journal:  J Clin Invest       Date:  1997-01-15       Impact factor: 14.808

7.  An 11-amino acid beta-hairpin loop in the cytoplasmic domain of band 3 is responsible for ankyrin binding in mouse erythrocytes.

Authors:  Marko Stefanovic; Nicholas O Markham; Erin M Parry; Lisa J Garrett-Beal; Amanda P Cline; Patrick G Gallagher; Philip S Low; David M Bodine
Journal:  Proc Natl Acad Sci U S A       Date:  2007-08-22       Impact factor: 11.205

8.  Combined ankyrin and spectrin deficiency in hereditary spherocytosis.

Authors:  A Pekrun; S W Eber; A Kuhlmey; W Schröter
Journal:  Ann Hematol       Date:  1993-08       Impact factor: 3.673

9.  Identification of contact sites between ankyrin and band 3 in the human erythrocyte membrane.

Authors:  Jesse L Grey; Gayani C Kodippili; Katya Simon; Philip S Low
Journal:  Biochemistry       Date:  2012-08-14       Impact factor: 3.162

10.  Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis.

Authors:  J A Chasis; P Agre; N Mohandas
Journal:  J Clin Invest       Date:  1988-08       Impact factor: 14.808
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