Literature DB >> 7883989

Of mice and men: the mice were right.

V Bennett.   

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Year:  1995        PMID： 7883989      PMCID： PMC441420          DOI： 10.1172/JCI117797

Source DB:  PubMed          Journal:  J Clin Invest        ISSN： 0021-9738            Impact factor:   14.808


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  10 in total

Review 1.  The spectrin-based membrane skeleton and micron-scale organization of the plasma membrane.

Authors:  V Bennett; D M Gilligan
Journal:  Annu Rev Cell Biol       Date:  1993

2.  A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosis.

Authors:  P Jarolim; H L Rubin; V Brabec; J Palek
Journal:  J Clin Invest       Date:  1995-03       Impact factor: 14.808

3.  Deficient red-cell spectrin in severe, recessively inherited spherocytosis.

Authors:  P Agre; E P Orringer; V Bennett
Journal:  N Engl J Med       Date:  1982-05-13       Impact factor: 91.245

4.  Marked reduction of spectrinin hereditary spherocytosis in the common house mouse.

Authors:  A C Greenquist; S B Shohet; S E Bernstein
Journal:  Blood       Date:  1978-06       Impact factor: 22.113

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.  Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types.

Authors:  A B Bianchi; T Hara; V Ramesh; J Gao; A J Klein-Szanto; F Morin; A G Menon; J A Trofatter; J F Gusella; B R Seizinger
Journal:  Nat Genet       Date:  1994-02       Impact factor: 38.330

7.  Spectrin deficient inherited hemolytic anemias in the mouse: characterization by spectrin synthesis and mRNA activity in reticulocytes.

Authors:  D M Bodine; C S Birkenmeier; J E Barker
Journal:  Cell       Date:  1984-07       Impact factor: 41.582

8.  Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.

Authors:  P G Gallagher; S A Weed; W T Tse; L Benoit; J S Morrow; S L Marchesi; N Mohandas; B G Forget
Journal:  J Clin Invest       Date:  1995-03       Impact factor: 14.808

9.  Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice.

Authors:  L L Peters; C S Birkenmeier; R T Bronson; R A White; S E Lux; E Otto; V Bennett; A Higgins; J E Barker
Journal:  J Cell Biol       Date:  1991-09       Impact factor: 10.539

10.  Distinct ankyrin isoforms at neuron cell bodies and nodes of Ranvier resolved using erythrocyte ankyrin-deficient mice.

Authors:  E Kordeli; V Bennett
Journal:  J Cell Biol       Date:  1991-09       Impact factor: 10.539
  10 in total
  1 in total

1.  A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis.

Authors:  E Jennifer Edelman; Yelena Maksimova; Feride Duru; Cigdem Altay; Patrick G Gallagher
Journal:  Blood       Date:  2007-02-27       Impact factor: 22.113
  1 in total

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