KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome. - Wikidata - wikimedia - TriplyDB

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

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

http://www.wikidata.org/entity/Q34464896

about

Krüppeling erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants Activation of KLF1 Enhances the Differentiation and Maturation of Red Blood Cells from Human Pluripotent Stem Cells.An international effort to cure a global health problem: A report on the 19th Hemoglobin Switching Conference.Krüppel-like factors compete for promoters and enhancers to fine-tune transcription.2p15-p16.1 microdeletions encompassing and proximal to BCL11A are associated with elevated HbF in addition to neurologic impairment Krüppel-Like Transcription Factor KLF1 Is Required for Optimal γ- and β-Globin Expression in Human Fetal Erythroblasts.A novel 33-Gene targeted resequencing panel provides accurate, clinical-grade diagnosis and improves patient management for rare inherited anaemias A case of congenital dyserythropoietic anemia type IV.Diagnosis and management of congenital dyserythropoietic anemias.Direct targets of pSTAT5 signalling in erythropoiesis.Orchestration of late events in erythropoiesis by KLF1/EKLF.An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations.EKLF/KLF1-regulated cell cycle exit is essential for erythroblast enucleation.Recent progress in understanding and manipulating haemoglobin switching for the haemoglobinopathies.From Erythroblasts to Mature Red Blood Cells: Organelle Clearance in Mammals.Deficiency in interferon type 1 receptor improves definitive erythropoiesis in Klf1 null mice.Genetic variation of Krüppel-like factor 1 (KLF1) and fetal hemoglobin (HbF) levels in β0-thalassemia/HbE disease.KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IV: Insights Into the Variable Clinical Severity.Krüppel-like factors: Crippling and un-crippling metabolic pathways.

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P2860

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

http://www.wikidata.org/entity/Q34464896

description

2015 nî lūn-bûn

@nan

2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

name

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

@ast

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

@en

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

@nl

type

label

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

@ast

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

@en

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

@nl

prefLabel

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

@ast

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

@en

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

@nl

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BLOOD-2014-08-590968

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P1476

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

@en

P2093

Bronwyn Williams

http://www.w3.org/2001/XMLSchema#string

Graham W Magor

http://www.w3.org/2001/XMLSchema#string

Michael R Tallack

http://www.w3.org/2001/XMLSchema#string

Naomi McCallum

http://www.w3.org/2001/XMLSchema#string

P2860

Basic Krüppel-like factor functions within a network of interacting haematopoietic transcription factors

Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

SWELL1, a plasma membrane protein, is an essential component of volume-regulated anion channel

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts

A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia

Hsp90-Cdc37 chaperone complex regulates Ulk1- and Atg13-mediated mitophagy

Cloning and characterization of mCtBP2, a co-repressor that associates with basic Krüppel-like factor and other mammalian transcriptional regulators

SOX6 binds CtBP2 to repress transcription from the Fgf-3 promoter

A global role for EKLF in definitive and primitive erythropoiesis

Sox6 directly silences epsilon globin expression in definitive erythropoiesis.

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2405-2417

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scholarly article

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10.1182/BLOOD-2014-08-590968

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15

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125

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Andrew C Perkins

Kevin R Gillinder

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2015-02-27T00:00:00Z

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272945596

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25724378

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4521397

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