The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis. - Test2 - elhamkhani - TriplyDB

The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.

The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.

http://www.wikidata.org/entity/Q33944167

about

The DNA helicase recql4 is required for normal osteoblast expansion and osteosarcoma formation RNA editing by ADAR1 prevents MDA5 sensing of endogenous dsRNA as nonself Interaction of RECQ4 and MCM10 is important for efficient DNA replication origin firing in human cells.RECQL5 Suppresses Oncogenic JAK2-Induced Replication Stress and Genomic Instability.Adenosine-to-inosine RNA editing by ADAR1 is essential for normal murine erythropoiesis.Protein recoding by ADAR1-mediated RNA editing is not essential for normal development and homeostasis.Cell cycle-dependent phosphorylation regulates RECQL4 pathway choice and ubiquitination in DNA double-strand break repair.Protein sequestration at the nuclear periphery as a potential regulatory mechanism in premature aging.

P2860

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P2860

The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.

http://www.wikidata.org/entity/Q33944167

description

2014 nî lūn-bûn

@nan

2014 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.

@ast

The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.

@en

type

label

The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.

@ast

The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.

@en

prefLabel

The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.

@ast

The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.

@en

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P1433

Journal of Clinical Investigation

P1476

The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.

@en

P2093

David J Izon

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

Elisabetta DeLuca

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

Julie M Quach

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

Meaghan Wall

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

Monique F Smeets

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

P2860

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

Dual DNA unwinding activities of the Rothmund-Thomson syndrome protein, RECQ4

Distantly related sequences in the alpha- and beta-subunits of ATP synthase, myosin, kinases and other ATP-requiring enzymes and a common nucleotide binding fold

Molecular pathogenesis and clinical management of Fanconi anemia

RECQL5/Recql5 helicase regulates homologous recombination and suppresses tumor formation via disruption of Rad51 presynaptic filaments

Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus

Phosphorylation of Sld2 and Sld3 by cyclin-dependent kinases promotes DNA replication in budding yeast.

Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases

FANCM connects the genome instability disorders Bloom's Syndrome and Fanconi Anemia

Stage-specific apoptosis, developmental delay, and embryonic lethality in mice homozygous for a targeted disruption in the murine Bloom's syndrome gene

P304

3551-3565

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scholarly article

P356

10.1172/JCI75334

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P407

P433

8

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P478

124

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P50

Jörg Heierhorst

Alistair M Chalk

Louise E Purton

P577

2014-06-24T00:00:00Z

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P698

24960165

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P921

P932

4109528

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