XRCC5 VNTR, XRCC6 -61C>G, and XRCC7 6721G>T Gene Polymorphisms Associated with Male Infertility Risk: Evidences from Case-Control and In Silico Studies

Association Between Functional Polymorphisms of DNA Double-Strand Breaks in Repair GenesXRCC5,XRCC6andXRCC7with the Risk of Systemic Lupus Erythematosus in South East Iran

(2015) Danial Jahantigh et al.   DNA AND CELL BIOLOGY

Association Between the XRCC6 Polymorphisms and Cancer Risks

(2015) Jing Jia et al.   MEDICINE

The UCSC Genome Browser database: 2016 update

(2015) Matthew L. Speir et al.   NUCLEIC ACIDS RESEARCH

Ku70 and non-homologous end joining protect testicular cells from DNA damage

(2013) E. A. Ahmed et al.   JOURNAL OF CELL SCIENCE

Polymorphisms in double-strand breaks repair genes are associated with impaired fertility in Chinese population

(2013) Guixiang Ji et al.   REPRODUCTION

Association of XRCC5 VNTR polymorphism with the development of chronic myeloid leukemia

(2013) Manjula Gorre et al.   TUMOR BIOLOGY

The novel allele (3R) of the VNTR polymorphism in the XRCC5 promoter region dramatically decreases the gene expression

(2012) Mehrdad Rajaei et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertility

(2012) Guixiang Ji et al.   BMC Medicine

Functional analysis of promoter variants in KU70 and their role in cancer susceptibility

(2012) Manon Ouimet et al.   GENES CHROMOSOMES & CANCER

Interaction between Polymorphisms of DNA Repair Genes Significantly Modulated Bladder Cancer Risk

(2012) Yi Zhi et al.   International Journal of Medical Sciences

A functional polymorphism C-1310G in the promoter region ofKu70/XRCC6is associated with risk of renal cell carcinoma

(2012) Wei Wang et al.   MOLECULAR CARCINOGENESIS

SNPnexus: a web server for functional annotation of novel and publicly known genetic variants (2012 update)

(2012) A. Z. Dayem Ullah et al.   NUCLEIC ACIDS RESEARCH

SpliceAid 2: A database of human splicing factors expression data and RNA target motifs

(2011) Francesco Piva et al.   HUMAN MUTATION

The Mechanism of Double-Strand DNA Break Repair by the Nonhomologous DNA End-Joining Pathway

(2010) Michael R. Lieber   Annual Review of Biochemistry

Genetic probing of homologous recombination and non-homologous end joining during meiotic prophase in irradiated mouse spermatocytes

(2010) Emad A. Ahmed et al.   MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS

ERCC1 and ERCC2 polymorphisms and risk of idiopathic azoospermia in a Chinese population

(2010) Guixiang Ji et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Polymorphisms of nucleotide-excision repair genes may contribute to sperm DNA fragmentation and male infertility

(2010) Aihua Gu et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Joint Effects of XRCC1 Polymorphisms and Polycyclic Aromatic Hydrocarbons Exposure on Sperm DNA Damage and Male Infertility

(2010) Guixiang Ji et al.   TOXICOLOGICAL SCIENCES

RNA and Disease

(2009) Thomas A. Cooper et al.   CELL

XPCgene polymorphisms and risk of idiopathic azoospermia or oligozoospermia in a Chinese population

(2009) Jie Liang et al.   INTERNATIONAL JOURNAL OF ANDROLOGY

Human Splicing Finder: an online bioinformatics tool to predict splicing signals

(2009) François-Olivier Desmet et al.   NUCLEIC ACIDS RESEARCH

Alternative splicing and disease

(2008) Jamal Tazi et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Correlation between DNA damage and sperm parameters: a prospective study of 1,633 patients

(2008) Paul Cohen-Bacrie et al.   FERTILITY AND STERILITY

A novel variable number of tandem repeats (VNTR) polymorphism containing Sp1 binding elements in the promoter of XRCC5 is a risk factor for human bladder cancer

(2007) Shouyu Wang et al.   MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS