(Q46828004)

25 December 2017

title

Polymorphisms of LIG4 and XRCC4 involved in the NHEJ pathway interact to modify risk of glioma (English)

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25 December 2017

Zhonghui Xu

6

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Hongliang Liu

object named as

Hongliang Liu

8

0 references

author name string

Yanhong Liu

1

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25 December 2017

Keke Zhou

2

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25 December 2017

Haishi Zhang

3

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25 December 2017

Yin Yao Shugart

4

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25 December 2017

Lina Chen

5

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25 December 2017

Yu Zhong

7

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25 December 2017

Li Jin

9

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25 December 2017

Qingyi Wei

10

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25 December 2017

Fengping Huang

11

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25 December 2017

Daru Lu

12

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25 December 2017

Liangfu Zhou

13

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25 December 2017

publication date

1 March 2008

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25 December 2017

published in

Human Mutation

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25 December 2017

volume

29

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25 December 2017

issue

3

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25 December 2017

page(s)

381-389

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25 December 2017

A patient with mutations in DNA Ligase IV: clinical features and overlap with Nijmegen breakage syndrome.

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A Role for XRCC4 in Age at Diagnosis and Breast Cancer Risk

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Targeted disruption of the gene encoding DNA ligase IV leads to lethality in embryonic mice

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Genome instability and DNA repair in brain, ageing and neurological disease

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Epidemiologic studies of pilots and aircrew

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7 January 2021

Gamma-radiation sensitivity and risk of glioma

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7 January 2021

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

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7 January 2021

Interactions of the DNA ligase IV-XRCC4 complex with DNA ends and the DNA-dependent protein kinase

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7 January 2021

Multifactor-dimensionality reduction shows a two-locus interaction associated with Type 2 diabetes mellitus.

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7 January 2021

Mammalian DNA double-strand break repair protein XRCC4 interacts with DNA ligase IV

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7 January 2021

Microarray data mining with visual programming.

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7 January 2021

Late embryonic lethality and impaired V(D)J recombination in mice lacking DNA ligase IV

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7 January 2021

The structure of haplotype blocks in the human genome

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7 January 2021

A critical role for DNA end-joining proteins in both lymphogenesis and neurogenesis

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7 January 2021

Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses

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7 January 2021

Analysis of DNA ligase IV mutations found in LIG4 syndrome patients: the impact of two linked polymorphisms

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7 January 2021

Polymorphisms in DNA double-strand break repair genes and breast cancer risk in the Nurses' Health Study

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7 January 2021

A genotype of the polymorphic DNA repair gene MGMT is associated with de novo glioblastoma

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7 January 2021

Crystal structure of the Xrcc4 DNA repair protein and implications for end joining

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7 January 2021

DNA double-strand breaks: signaling, repair and the cancer connection

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7 January 2021

Variants in DNA double-strand break repair genes and breast cancer susceptibility

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https://api.crossref.org/works/10.1002%2FHUMU.20645

7 January 2021

The XRCC4 gene product is a target for and interacts with the DNA-dependent protein kinase

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7 January 2021

Mechanism and regulation of human non-homologous DNA end-joining

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7 January 2021

Risks of brain tumour following treatment for cancer in childhood: modification by genetic factors, radiotherapy and chemotherapy

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7 January 2021

Tagging SNPs in non-homologous end-joining pathway genes and risk of glioma

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7 January 2021

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism

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7 January 2021

New strategies for identifying gene-gene interactions in hypertension

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7 January 2021

A flexible computational framework for detecting, characterizing, and interpreting statistical patterns of epistasis in genetic studies of human disease susceptibility

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7 January 2021

New primary neoplasms of the central nervous system in survivors of childhood cancer: a report from the Childhood Cancer Survivor Study.

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7 January 2021

DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20645

7 January 2021

Possible association of p53 codon 72 polymorphism with susceptibility to adult and pediatric high-grade astrocytomas.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20645

7 January 2021

Mechanisms of disease: DNA repair defects and neurological disease

1 reference

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7 January 2021

Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer

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7 January 2021

Genetic variants of NHEJ DNA ligase IV can affect the risk of developing multiple myeloma, a tumour characterised by aberrant class switch recombination

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20645

7 January 2021

Score tests for association between traits and haplotypes when linkage phase is ambiguous

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20645

7 January 2021

Crystal structure of an Xrcc4-DNA ligase IV complex

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https://api.crossref.org/works/10.1002%2FHUMU.20645

7 January 2021

Renin-angiotensin system gene polymorphisms and atrial fibrillation

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7 January 2021

Chromosomal stability and the DNA double-stranded break connection

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20645

7 January 2021

Polymorphisms of DNA repair genes and risk of glioma.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20645

7 January 2021

Bladder cancer predisposition: a multigenic approach to DNA-repair and cell-cycle-control genes.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20645

7 January 2021

Polymorphisms in GLTSCR1 and ERCC2 are associated with the development of oligodendrogliomas.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20645

7 January 2021

Identifiers

DOI

10.1002/HUMU.20645

1 reference

25 December 2017

1 reference

25 December 2017