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PMID: 647119 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

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

Blood ·Vol. 51 ·No. 6 ·1978-06-00 ·Pages 1149-55

Greenquist AC, Shohet SB, Bernstein SE

Abstract

In contrast to the disease in humans, hereditary spherocytosis in the common house mouse produces an extreme spherocytosis. The cells show a broad distribution in size ranging from microcytic to macrocytic. Of particular interest is the finding of a substantial reduction in the major membrane polypeptide called spectrin, supporting a critical role for this protein in the control of erythrocyte shape and membrane stability.

MeSH Terms
Animals Electrophoresis, Polyacrylamide Gel Erythrocyte Membrane Membrane Proteins/deficiency Mice Peptides Spectrin/deficiency Spherocytes Spherocytosis, Hereditary/blood,genetics
Chemicals
Membrane Proteins Peptides Spectrin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Greenquist A C
Shohet S B
Bernstein S E
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
1978-06-00
Pages
1149-55
Language
English
Region
United States
NLM ID
7603509
Subset
IM
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