KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome-Reference-Cited by-同舟云学术

KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome

Published:2015-04-09 Issue:15 Volume:125 Page:2405-2417
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Magor Graham W.¹,Tallack Michael R.¹²,Gillinder Kevin R.¹,Bell Charles C.¹,McCallum Naomi³,Williams Bronwyn⁴,Perkins Andrew C.¹⁵

Affiliation:

1. Mater Research Institute, Faculty of Medicine and Biomedical Sciences, The University of Queensland, Woolloongabba, QLD, Australia;

2. School of Medicine, Faculty of Medicine and Biomedical Sciences, The University of Queensland, St Lucia, QLD, Australia;

3. Queensland Pathology, Brisbane, QLD, Australia;

4. Department of Hematology, Royal Brisbane and Women’s Hospital, Brisbane, QLD, Australia; and

5. Department of Cancer Services, Princess Alexandra Hospital, Brisbane, QLD, Australia

Abstract

Key Points Complete loss of KLF1 function is compatible with life but results in severe nonspherocytic hemolytic anemia and kernicterus. Human KLF1 regulates most aspects of red cell biology.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/125/15/2405/1384589/2405.pdf

Reference77 articles.

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4. Congenital dyserythropoietic anemias: molecular insights and diagnostic approach.;Iolascon;Blood,2013

5. Congenital dyserythropoietic anaemias: clinical features, haematological morphology and new biochemical data.;Wickramasinghe;Blood Rev,1998

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