222 related articles for article (PubMed ID: 31253066)
21. rs78378222 polymorphism in the 3'-untranslated region of TP53 contributes to development of age-associated cataracts by modifying microRNA-125b-induced apoptosis of lens epithelial cells.
Zhao Y; Li X; Zhu S
Mol Med Rep; 2016 Sep; 14(3):2305-10. PubMed ID: 27431420
[TBL] [Abstract][Full Text] [Related]
22. DNA glycosylase NEIL2 functions in multiple cellular processes.
Sarker AH; Cooper PK; Hazra TK
Prog Biophys Mol Biol; 2021 Sep; 164():72-80. PubMed ID: 33753087
[TBL] [Abstract][Full Text] [Related]
23. Long non‑coding RNA NONHSAT143692.2 is involved in oxidative DNA damage repair in the lens by regulating the miR‑4728‑5p/OGG1 axis.
Zhou T; Zhang J; Qin B; Xu H; Zhang S; Guan H
Int J Mol Med; 2020 Nov; 46(5):1838-1848. PubMed ID: 33000245
[TBL] [Abstract][Full Text] [Related]
24. A functional SNP in miR-625-5p binding site of AKT2 3'UTR is associated with noise-induced hearing loss susceptibility in the Chinese population.
Miao L; Wang B; Zhang J; Yin L; Pu Y
Environ Sci Pollut Res Int; 2021 Aug; 28(30):40782-40792. PubMed ID: 33768461
[TBL] [Abstract][Full Text] [Related]
25. Cervical carcinoma risk associate with genetic polymorphisms of NEIL2 gene in Chinese population and its significance as predictive biomarker.
Ye F; Liu J; Wang H; Chen X; Cheng Q; Chen H
Sci Rep; 2020 Mar; 10(1):5136. PubMed ID: 32198476
[TBL] [Abstract][Full Text] [Related]
26. MiR-196a binding-site SNP regulates RAP1A expression contributing to esophageal squamous cell carcinoma risk and metastasis.
Wang K; Li J; Guo H; Xu X; Xiong G; Guan X; Liu B; Li J; Chen X; Yang K; Bai Y
Carcinogenesis; 2012 Nov; 33(11):2147-54. PubMed ID: 22859270
[TBL] [Abstract][Full Text] [Related]
27. Recognition of the oxidized lesions spiroiminodihydantoin and guanidinohydantoin in DNA by the mammalian base excision repair glycosylases NEIL1 and NEIL2.
Hailer MK; Slade PG; Martin BD; Rosenquist TA; Sugden KD
DNA Repair (Amst); 2005 Jan; 4(1):41-50. PubMed ID: 15533836
[TBL] [Abstract][Full Text] [Related]
28. The Relevance of SNPs at 3'UTR Region of CASP7 and miR-371b-5p Associated Diseases: A Computational Analysis.
Safdar M; Zaheer S; Khailany RA; Parvez S; Naveed M; Bhuiyan P; Ozaslan M; Moatasam R; Al-Attar MS; Khan MA; Junejo Y
Cell Biochem Biophys; 2020 Dec; 78(4):541-557. PubMed ID: 32951155
[TBL] [Abstract][Full Text] [Related]
29. G-A variant in miR-200c binding site of EFNA1 alters susceptibility to gastric cancer.
Li Y; Nie Y; Cao J; Tu S; Lin Y; Du Y; Li Y
Mol Carcinog; 2014 Mar; 53(3):219-29. PubMed ID: 23065816
[TBL] [Abstract][Full Text] [Related]
30. Nei Endonuclease VIII-like 2 Gene rs8191670 Polymorphism affects the Sensitivity of Non-small Cell Lung Cancer to Cisplatin by binding with MiR-548a.
He W; Pang L; Gong S; Wang X; Hou L
J Cancer; 2020; 11(16):4801-4809. PubMed ID: 32626527
[No Abstract] [Full Text] [Related]
31. SNPs at 3'UTR of APOL1 and miR-6741-3p target sites associated with kidney diseases more susceptible to SARS-COV-2 infection: in silco and in vitro studies.
Safdar M; Khan MS; Karim AY; Omar SA; Smail SW; Saeed M; Zaheer S; Ali M; Ahmad B; Tasleem M; Junejo Y
Mamm Genome; 2021 Oct; 32(5):389-400. PubMed ID: 34089082
[TBL] [Abstract][Full Text] [Related]
32. Correlation Between Single Nucleotide Polymorphisms of an miRNA Binding Site in the 3'UTR of
Yu A; Zhang J; Mei Y; Zhong H; Chen S; Song Q
Genet Test Mol Biomarkers; 2020 Jul; 24(7):381-389. PubMed ID: 32552146
[No Abstract] [Full Text] [Related]
33. Structural investigation of a viral ortholog of human NEIL2/3 DNA glycosylases.
Prakash A; Eckenroth BE; Averill AM; Imamura K; Wallace SS; Doublié S
DNA Repair (Amst); 2013 Dec; 12(12):1062-71. PubMed ID: 24120312
[TBL] [Abstract][Full Text] [Related]
34. Different organization of base excision repair of uracil in DNA in nuclei and mitochondria and selective upregulation of mitochondrial uracil-DNA glycosylase after oxidative stress.
Akbari M; Otterlei M; Peña-Diaz J; Krokan HE
Neuroscience; 2007 Apr; 145(4):1201-12. PubMed ID: 17101234
[TBL] [Abstract][Full Text] [Related]
35. A GDF15 3' UTR variant, rs1054564, results in allele-specific translational repression of GDF15 by hsa-miR-1233-3p.
Teng MS; Hsu LA; Juan SH; Lin WC; Lee MC; Su CW; Wu S; Ko YL
PLoS One; 2017; 12(8):e0183187. PubMed ID: 28806401
[TBL] [Abstract][Full Text] [Related]
36. Single nucleotide polymorphisms of DNA base-excision repair genes (APE1, OGG1 and XRCC1) associated with breast cancer risk in a Chinese population.
Luo H; Li Z; Qing Y; Zhang SH; Peng Y; Li Q; Wang D
Asian Pac J Cancer Prev; 2014; 15(3):1133-40. PubMed ID: 24606430
[TBL] [Abstract][Full Text] [Related]
37. Identification of fifteen novel germline variants in the BRCA1 3'UTR reveals a variant in a breast cancer case that introduces a functional miR-103 target site.
Brewster BL; Rossiello F; French JD; Edwards SL; Wong M; Wronski A; Whiley P; Waddell N; Chen X; Bove B; ; Hopper JL; John EM; Andrulis I; Daly M; Volorio S; Bernard L; Peissel B; Manoukian S; Barile M; Pizzamiglio S; Verderio P; Spurdle AB; Radice P; Godwin AK; Southey MC; Brown MA; Peterlongo P
Hum Mutat; 2012 Dec; 33(12):1665-75. PubMed ID: 22753153
[TBL] [Abstract][Full Text] [Related]
38. Significance of amino acid substitution variants of DNA repair genes in radiosusceptibility of cervical cancer patients; a pilot study.
Farkasova T; Gurska S; Witkovsky V; Gabelova A
Neoplasma; 2008; 55(4):330-7. PubMed ID: 18505345
[TBL] [Abstract][Full Text] [Related]
39. Multiple microRNA regulation of lipoprotein lipase gene abolished by 3'UTR polymorphisms in a triglyceride-lowering haplotype harboring p.Ser474Ter.
Caussy C; Charrière S; Meirhaeghe A; Dallongeville J; Lefai E; Rome S; Cuerq C; Euthine V; Delay M; Marmontel O; Di Filippo M; Lagarde M; Moulin P; Marçais C
Atherosclerosis; 2016 Mar; 246():280-6. PubMed ID: 26820803
[TBL] [Abstract][Full Text] [Related]
40. Functional variants of the NEIL1 and NEIL2 genes and risk and progression of squamous cell carcinoma of the oral cavity and oropharynx.
Zhai X; Zhao H; Liu Z; Wang LE; El-Naggar AK; Sturgis EM; Wei Q
Clin Cancer Res; 2008 Jul; 14(13):4345-52. PubMed ID: 18594018
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
