(Q56994843)

17

Nathaniel Rothman

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Stephen Chanock

16

Stephen Chanock

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Theodore Holford

Theodore R. Holford

7

0 references

Meredith Yeager

9

Meredith Yeager

0 references

Daehee Kang

11

Daehee Kang

0 references

Shelia Hoar Zahm

5

Shelia H. Zahm

0 references

Tongzhang Zheng

2

Tongzhang Zheng

0 references

Kaiyong Zou

14

Kaiyong Zou

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Sophia S Wang

6

Sophia S. Wang

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author name string

Min Shen

1

0 references

Qing Lan

3

0 references

Yawei Zhang

4

0 references

Brian Leaderer

8

0 references

Robert Welch

10

0 references

Bing Zhang

13

0 references

Yong Zhu

https://scigraph.springernature.com/pub.10.1007/s00439-006-0177-2

15

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publication date

26 April 2006

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published in

Human Genetics

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volume

119

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issue

6

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page(s)

659-668

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exact match

0 references

cites work

Current advances in unraveling the function of the Werner syndrome protein

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-006-0177-2

Mechanisms of human DNA repair: an update

21 January 2018

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Dysregulation of DNA repair pathways in a transforming growth factor alpha/c-myc transgenic mouse model of accelerated hepatocarcinogenesis.

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Polymorphisms at the Werner locus: II. 1074Leu/Phe, 1367Cys/Arg, longevity, and atherosclerosis

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Epidemiology of the Revised European-American Lymphoma Classification subtypes

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Suppression of UV-induced apoptosis by the human DNA repair protein XPG

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Microarray analysis in the HSV-1 latently infected mouse trigeminal ganglion

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Mechanisms of formation of chromosomal aberrations: insights from studies with DNA repair-deficient cells

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Assessing the probability that a positive report is false: an approach for molecular epidemiology studies

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Reduced expression levels of nucleotide excision repair genes in lung cancer: a case-control analysis

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Chromosomal doubling: the significance of polyploidization in the development of human tumors: possibly relevant findings on a lymphoma

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Recurring chromosomal abnormalities in non-Hodgkin's lymphoma: biologic and clinical significance

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SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes

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Severe growth retardation and short life span of double-mutant mice lacking Xpa and exon 15 of Xpg.

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Single nucleotide polymorphisms in theXPGgene: Determination of role in DNA repair and breast cancer risk

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Functional link between Myc and the Werner gene in tumorigenesis.

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Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome

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Cellular dynamics and modulation of WRN protein is DNA damage specific

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Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population

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The involvement of key DNA repair pathways in the formation of chromosome rearrangements in embryonic stem cells

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Predicting deleterious amino acid substitutions

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Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation

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Alcohol use and risk of non-Hodgkin's lymphoma among Connecticut women (United States).

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Characterization of the nuclear localization signal in the DNA helicase involved in Werner's syndrome.

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Analysis of gene expression profiles associated with cisplatin resistance in human ovarian cancer cell lines and tissues using cDNA microarray.

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Expression of nucleotide excision repair genes and the risk for squamous cell carcinoma of the head and neck

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XRCC3 deficiency results in a defect in recombination and increased endoreduplication in human cells

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Genetic variation and willingness to participate in epidemiologic research: data from three studies

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Variant XRCC3 implicated in cancer is functional in homology-directed repair of double-strand breaks

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The enzymatic activities of the Werner syndrome protein are disabled by the amino acid polymorphism R834C.

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Collection of genomic DNA from adults in epidemiological studies by buccal cytobrush and mouthwash

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12 December 2020

Relationship between XPG codon 1104 polymorphism and risk of primary lung cancer.

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12 December 2020