Hereditary elliptocytosis associated with spectrin Le Puy in a Japanese family: Ultrastructural aspect of the red cell skeleton-Reference-Cited by-同舟云学术

Hereditary elliptocytosis associated with spectrin Le Puy in a Japanese family: Ultrastructural aspect of the red cell skeleton

Published:2009-04-24 Issue:2 Volume:52 Page:92-98
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:

Author:

Maréchal Joelle,Wada Hideho,Koffa Trigona,Kanzaki Akio,Wilmotte Rick,Ikoma Kimiko,Yawata Ayumi,Inoue Takafumi,Takanashi Kaoru,Miura Akira,Alloisio Nicole,Delaunay Jean,Yawata Yoshihito

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1994.tb01292.x/fullpdf

Reference36 articles.

1. Erythrocyte spectrin is comprised of many homologous triple helical segments;Speicher;Nature,1984

2. Phasing the conformational unit of spectrin;Winograd;Proc Natl Acad Sci USA,1991

3. Spectrin genes in health and disease;Gallagher;Semin Hematol,1993

4. Location of the human red cell spectrin tetramer binding site and detection of a related “closed” hairpin loop dimer using proteolytic footprinting;Speicher;J Biol Chem,1993

5. Point mutation in the β-spectrin gene associated with αI/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association;Tse;J Clin Invest,1990

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Stop codon in exon 30 (E2069X) of β-spectrin gene associated with hereditary elliptocytosis in spectrin Nagoya;Human Mutation;1996

2. Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis;Human Mutation;1996

3. Genetic disorders of the red cell membrane;Critical Reviews in Oncology/Hematology;1995-06

4. A deletional frameshift mutation in spectrin β-gene associated with hereditary elliptocytosis in spectrin Napoli;British Journal of Haematology;1994-10