Bloom syndrome radials are predominantly non-homologous and are suppressed by phosphorylated BLM

about

First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease.RB localizes to DNA double-strand breaks and promotes DNA end resection and homologous recombination through the recruitment of BRG1.

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Q37251210-1000F66D-595A-4D99-A4FE-5AADF656A752 Q37507931-787AC479-5D26-47DA-88D0-EDAE08D8564D

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Bloom syndrome radials are predominantly non-homologous and are suppressed by phosphorylated BLM

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http://www.wikidata.org/entity/Q39882128

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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2014年學術文章

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Bloom syndrome radials are pre ...... ppressed by phosphorylated BLM

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Bloom syndrome radials are pre ...... pressed by phosphorylated BLM.

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type

Item

label

Bloom syndrome radials are pre ...... ppressed by phosphorylated BLM

@en

Bloom syndrome radials are pre ...... pressed by phosphorylated BLM.

@nl

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Bloom syndrome radials are pre ...... ppressed by phosphorylated BLM

@en

Bloom syndrome radials are pre ...... pressed by phosphorylated BLM.

@nl

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Bloom syndrome radials are pre ...... ppressed by phosphorylated BLM

@en

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Amy Hanlon Newell

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

James Hejna

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

Navid Ziaie

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

Nichole Owen

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

Robb E Moses

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

Scott Rennie

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

Susan B Olson

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The Bloom's syndrome gene product is homologous to RecQ helicases

Molecular pathogenesis and clinical management of Fanconi anemia

A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome

Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients

Identification of Holliday junction resolvases from humans and yeast.

Caretaker tumour suppressor genes that defend genome integrity

Cellular and molecular consequences of defective Fanconi anemia proteins in replication-coupled DNA repair: mechanistic insights

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

The molecular basis of common and rare fragile sites

Novel pro- and anti-recombination activities of the Bloom's syndrome helicase.

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255-263

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scholarly article

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10.1159/000375247

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144

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Asia D Mitchell

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2014-01-01T00:00:00Z

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25766002

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phosphorylation

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4406812

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Bloom syndrome radials are predominantly non-homologous and are suppressed by phosphorylated BLM

about

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P2860

Bloom syndrome radials are predominantly non-homologous and are suppressed by phosphorylated BLM

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932