713 related articles for article (PubMed ID: 27424220)
1. A 3'UTR polymorphism marks differential KLRG1 mRNA levels through disruption of a miR-584-5p binding site and associates with pemphigus foliaceus susceptibility.
Cipolla GA; Park JK; de Oliveira LA; Lobo-Alves SC; de Almeida RC; Farias TD; Lemos Dde S; Malheiros D; Lavker RM; Petzl-Erler ML
Biochim Biophys Acta; 2016 Oct; 1859(10):1306-13. PubMed ID: 27424220
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. In silico analysis of microRNAS targeting the HLA-G 3' untranslated region alleles and haplotypes.
Castelli EC; Moreau P; Oya e Chiromatzo A; Mendes-Junior CT; Veiga-Castelli LC; Yaghi L; Giuliatti S; Carosella ED; Donadi EA
Hum Immunol; 2009 Dec; 70(12):1020-5. PubMed ID: 19664672
[TBL] [Abstract][Full Text] [Related]
4. Polymorphisms in lipid metabolism related miRNA binding sites and risk of metabolic syndrome.
Ye Q; Zhao X; Xu K; Li Q; Cheng J; Gao Y; Du J; Shi H; Zhou L
Gene; 2013 Oct; 528(2):132-8. PubMed ID: 23911300
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Tumor-promoting function of single nucleotide polymorphism rs1836724 (C3388T) alters multiple potential legitimate microRNA binding sites at the 3'-untranslated region of ErbB4 in breast cancer.
Bagheri F; Mesrian Tanha H; Mojtabavi Naeini M; Ghaedi K; Azadeh M
Mol Med Rep; 2016 May; 13(5):4494-8. PubMed ID: 27035115
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. A variant in a microRNA binding site in NEIL2 3'UTR confers susceptibility to age-related cataracts.
Kang L; Zou X; Zhang G; Xiang J; Wang Y; Yang M; Chen X; Wu J; Guan H
FASEB J; 2019 Sep; 33(9):10469-10476. PubMed ID: 31253066
[TBL] [Abstract][Full Text] [Related]
9. Functional Characterization of a Single Nucleotide Polymorphism in the 3' Untranslated Region of Sheep DLX3 Gene.
Rong E; Zhang Z; Qiao S; Yang H; Yan X; Li H; Wang N
PLoS One; 2015; 10(9):e0137135. PubMed ID: 26332462
[TBL] [Abstract][Full Text] [Related]
10. Germline hereditary, somatic mutations and microRNAs targeting-SNPs in congenital heart defects.
Sabina S; Pulignani S; Rizzo M; Cresci M; Vecoli C; Foffa I; Ait-Ali L; Pitto L; Andreassi MG
J Mol Cell Cardiol; 2013 Jul; 60():84-9. PubMed ID: 23583740
[TBL] [Abstract][Full Text] [Related]
11. A functional polymorphism of PON1 interferes with microRNA binding to increase the risk of ischemic stroke and carotid atherosclerosis.
Liu ME; Liao YC; Lin RT; Wang YS; Hsi E; Lin HF; Chen KC; Juo SH
Atherosclerosis; 2013 May; 228(1):161-7. PubMed ID: 23497787
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. The impact of 3'UTR variants on differential expression of candidate cancer susceptibility genes.
Skeeles LE; Fleming JL; Mahler KL; Toland AE
PLoS One; 2013; 8(3):e58609. PubMed ID: 23472213
[TBL] [Abstract][Full Text] [Related]
14. A miR-151 binding site polymorphism in the 3'-untranslated region of the cyclin E1 gene associated with nasopharyngeal carcinoma.
Liu Y; Cai H; Liu J; Fan H; Wang Z; Wang Q; Shao M; Sun X; Diao J; Liu Y; Shi Y; Fan Q
Biochem Biophys Res Commun; 2013 Mar; 432(4):660-5. PubMed ID: 23416081
[TBL] [Abstract][Full Text] [Related]
15. Association of Cytotoxic T-Lymphocyte Antigen 4 (CTLA4) and Thyroglobulin (TG) Genetic Variants with Autoimmune Hypothyroidism.
Patel H; Mansuri MS; Singh M; Begum R; Shastri M; Misra A
PLoS One; 2016; 11(3):e0149441. PubMed ID: 26963610
[TBL] [Abstract][Full Text] [Related]
16. 3'UTR SNPs and Haplotypes in the GATA4 Gene Contribute to the Genetic Risk of Congenital Heart Disease.
Pulignani S; Vecoli C; Sabina S; Foffa I; Ait-Ali L; Andreassi MG
Rev Esp Cardiol (Engl Ed); 2016 Aug; 69(8):760-5. PubMed ID: 27118528
[TBL] [Abstract][Full Text] [Related]
17. Altered gene expression in late-onset Alzheimer's disease due to SNPs within 3'UTR microRNA response elements.
Roy J; Mallick B
Genomics; 2017 Jul; 109(3-4):177-185. PubMed ID: 28286146
[TBL] [Abstract][Full Text] [Related]
18. Fixed differences in the 3'UTR of buffalo PRNP gene provide binding sites for miRNAs post-transcriptional regulation.
Zhao H; Wang S; Guo L; Du Y; Liu L; Ma T; Otecko NO; Li C; Zhang Y
Oncotarget; 2017 Jul; 8(28):46006-46019. PubMed ID: 28545018
[TBL] [Abstract][Full Text] [Related]
19. Genetic 3'UTR variation is associated with human pigmentation characteristics and sensitivity to sunlight.
Hernando B; Peña-Chilet M; Ibarrola-Villava M; Martin-Gonzalez M; Gomez-Fernandez C; Ribas G; Martinez-Cadenas C
Exp Dermatol; 2017 Oct; 26(10):896-903. PubMed ID: 28266728
[TBL] [Abstract][Full Text] [Related]
20. Genetic variants in microRNAs and their binding sites within gene 3'UTRs associate with susceptibility to age-related macular degeneration.
Ghanbari M; Erkeland SJ; Xu L; Colijn JM; Franco OH; Dehghan A; Klaver CCW; Meester-Smoor MA
Hum Mutat; 2017 Jul; 38(7):827-838. PubMed ID: 28397307
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]