MPP1/p55 gene deletion in a hemophilia A patient with ectrodactyly and severe developmental defects-Reference-Cited by-同舟云学术

MPP1/p55 gene deletion in a hemophilia A patient with ectrodactyly and severe developmental defects

Published:2018-12-02 Issue:1 Volume:94 Page:E29-E32
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am J Hematol

Author:

Fritz Daniel I.¹²,Hanada Toshihiko¹,Lu Yunzhe¹,Martin Johnston J.³,Chishti Athar H.¹²^ORCID

Affiliation:

1. Department of Developmental, Molecular, and Chemical Biology; Tufts University School of Medicine; Boston Massachusetts

2. Sackler School of Graduate Biomedical Sciences, Program in Cellular, Molecular, and Developmental Biology; Tufts University School of Medicine; Boston Massachusetts

3. Hematology/Oncology; The Children's Hospital at Memorial University Medical Center, Mercer University School of Medicine; Savannah Georgia

Funder

American Heart Association

National Institutes of Health

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.25323/fullpdf

Reference14 articles.

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2. Evolution of the MAGUK protein gene family in premetazoan lineages;Mendoza;BMC Evol Biol,2010

3. Molecular identification of a major palmitoylated erythrocyte membrane protein containing the src homology 3 motif;Ruff;Proc Natl Acad Sci U S A.,1991

4. Palmitoylation of MPP1 (membrane-palmitoylated protein 1)/p55 is crucial for lateral membrane organization in erythroid cells;Lach;J Biol Chem,2012

5. MPP1 links the usher protein network and the crumbs protein complex in the retina;Gosens;Hum Mol Genet.,2007

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