Identification of ICR170-induced XPD mutations in UV-sensitive CHO cells.

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The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutations

P2860

Q24622650-677426E9-0405-427E-85FB-73E5068F7F36

P2860

Identification of ICR170-induced XPD mutations in UV-sensitive CHO cells.

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http://www.wikidata.org/entity/Q43825648

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2001 nî lūn-bûn

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2001年の論文

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2001年学术文章

@wuu

2001年学术文章

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2001年学术文章

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2001年学术文章

@zh-hans

2001年学术文章

@zh-my

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@zh-sg

2001年學術文章

@yue

2001年學術文章

@zh-hant

name

Identification of ICR170-induced XPD mutations in UV-sensitive CHO cells.

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Identification of ICR170-induced XPD mutations in UV-sensitive CHO cells.

@nl

type

Item

label

Identification of ICR170-induced XPD mutations in UV-sensitive CHO cells.

@en

Identification of ICR170-induced XPD mutations in UV-sensitive CHO cells.

@nl

prefLabel

Identification of ICR170-induced XPD mutations in UV-sensitive CHO cells.

@en

Identification of ICR170-induced XPD mutations in UV-sensitive CHO cells.

@nl

P1476

Identification of ICR170-induced XPD mutations in UV-sensitive CHO cells.

@en

P2093

Salazar EP

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

Tebbs RS

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

Thompson LH

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

P2860

Genomic organization and promoter characterization of two human UHS keratin genes

Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein

Molecular cloning and biological characterization of a human gene, ERCC2, that corrects the nucleotide excision repair defect in CHO UV5 cells

ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs

The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases

Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorder

Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II

Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19

Summary of complementation groups of UV-sensitive CHO cell mutants isolated by large-scale screening

Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH

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111-117

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

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scholarly article

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10.1002/EM.1060

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2-3

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P478

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

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2001-01-01T00:00:00Z

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

P698

11746743

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

Identification of ICR170-induced XPD mutations in UV-sensitive CHO cells.

about

P2860

P2860

Identification of ICR170-induced XPD mutations in UV-sensitive CHO cells.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698