Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 81

1.

The Interplay between miRNA-Related Variants and Age-Related Macular Degeneration: EVIDENCE of Association of MIR146A and MIR27A.

Strafella C, Errichiello V, Caputo V, Aloe G, Ricci F, Cusumano A, Novelli G, Giardina E, Cascella R.

Int J Mol Sci. 2019 Mar 29;20(7). pii: E1578. doi: 10.3390/ijms20071578.

2.

A DAAM1 3'-UTR SNP mutation regulates breast cancer metastasis through affecting miR-208a-5p-DAAM1-RhoA axis.

Mei J, Yan T, Huang Y, Xia T, Chang F, Shen S, Hao L, Chen Y, Wang Z, Jiang X, Xu B, Zhu Y.

Cancer Cell Int. 2019 Mar 11;19:55. doi: 10.1186/s12935-019-0747-8. eCollection 2019.

3.

Relationship of common variants in Interleukin 33 gene with susceptibility and prognosis of osteosarcoma in Han Chinese population.

Kang C, Zhao J, Wang Y, Yang C, Chen J, Zhi L.

J Cancer. 2019 Jan 29;10(5):1138-1144. doi: 10.7150/jca.29086. eCollection 2019.

4.

Computational Methods for the Pharmacogenetic Interpretation of Next Generation Sequencing Data.

Zhou Y, Fujikura K, Mkrtchian S, Lauschke VM.

Front Pharmacol. 2018 Dec 4;9:1437. doi: 10.3389/fphar.2018.01437. eCollection 2018. Review.

5.

regQTLs: Single nucleotide polymorphisms that modulate microRNA regulation of gene expression in tumors.

Wilk G, Braun R.

PLoS Genet. 2018 Dec 17;14(12):e1007837. doi: 10.1371/journal.pgen.1007837. eCollection 2018 Dec.

6.

miRNA Mediated Noise Making of 3'UTR Mutations in Cancer.

Wu W, Wu L, Zhu M, Wang Z, Wu M, Li P, Nie Y, Lin X, Hu J, Eskilsson E, Wang Q, Shao J, Lyu S.

Genes (Basel). 2018 Nov 12;9(11). pii: E545. doi: 10.3390/genes9110545.

7.

Framework for microRNA variant annotation and prioritization using human population and disease datasets.

Oak N, Ghosh R, Huang KL, Wheeler DA, Ding L, Plon SE.

Hum Mutat. 2019 Jan;40(1):73-89. doi: 10.1002/humu.23668. Epub 2018 Nov 8.

PMID:
30302893
8.

Uncovering association networks through an eQTL analysis involving human miRNAs and lincRNAs.

Branco PR, de Araújo GS, Barrera J, Suarez-Kurtz G, de Souza SJ.

Sci Rep. 2018 Oct 9;8(1):15050. doi: 10.1038/s41598-018-33420-z.

9.

MicroRNA-17 as a promising diagnostic biomarker of gastric cancer: An investigation combining TCGA, GEO, meta-analysis, and bioinformatics.

Hu G, Lv Q, Yan J, Chen L, Du J, Zhao K, Xu W.

FEBS Open Bio. 2018 Aug 30;8(9):1508-1523. doi: 10.1002/2211-5463.12496. eCollection 2018 Sep.

10.

Polymorphism studies on microRNA targetome of thalassemia.

Galehdari H, Azarshin SZ, Bijanzadeh M, Shafiei M.

Bioinformation. 2018 May 31;14(5):252-258. doi: 10.6026/97320630014252. eCollection 2018.

11.

PASSPORT-seq: A Novel High-Throughput Bioassay to Functionally Test Polymorphisms in Micro-RNA Target Sites.

Ipe J, Collins KS, Hao Y, Gao H, Bhatia P, Gaedigk A, Liu Y, Skaar TC.

Front Genet. 2018 Jun 15;9:219. doi: 10.3389/fgene.2018.00219. eCollection 2018.

12.

MicroRNA-Related Genetic Variants Associated with Survival of Head and Neck Squamous Cell Carcinoma.

Wilkins OM, Titus AJ, Salas LA, Gui J, Eliot M, Butler RA, Sturgis EM, Li G, Kelsey KT, Christensen BC.

Cancer Epidemiol Biomarkers Prev. 2019 Jan;28(1):127-136. doi: 10.1158/1055-9965.EPI-18-0002. Epub 2018 Jun 7.

PMID:
29880533
13.

Integrative Analysis Identifies Genetic Variants Associated With Autoimmune Diseases Affecting Putative MicroRNA Binding Sites.

de Almeida RC, Chagas VS, Castro MAA, Petzl-Erler ML.

Front Genet. 2018 Apr 26;9:139. doi: 10.3389/fgene.2018.00139. eCollection 2018.

14.

Clustering Pattern and Functional Effect of SNPs in Human miRNA Seed Regions.

He S, Ou H, Zhao C, Zhang J.

Int J Genomics. 2018 Mar 6;2018:2456076. doi: 10.1155/2018/2456076. eCollection 2018.

15.

A Comprehensive in Silico Analysis of Regulatory SNPs of Human CLEC7A Gene and Its Validation as Genotypic and Phenotypic Disease Marker in Recurrent Vulvovaginal Infections.

Kalia N, Kaur M, Sharma S, Singh J.

Front Cell Infect Microbiol. 2018 Mar 20;8:65. doi: 10.3389/fcimb.2018.00065. eCollection 2018.

16.

Deficiency of immunoregulatory indoleamine 2,3-dioxygenase 1in juvenile diabetes.

Orabona C, Mondanelli G, Pallotta MT, Carvalho A, Albini E, Fallarino F, Vacca C, Volpi C, Belladonna ML, Berioli MG, Ceccarini G, Esposito SM, Scattoni R, Verrotti A, Ferretti A, De Giorgi G, Toni S, Cappa M, Matteoli MC, Bianchi R, Matino D, Iacono A, Puccetti M, Cunha C, Bicciato S, Antognelli C, Talesa VN, Chatenoud L, Fuchs D, Pilotte L, Van den Eynde B, Lemos MC, Romani L, Puccetti P, Grohmann U.

JCI Insight. 2018 Mar 22;3(6). pii: 96244. doi: 10.1172/jci.insight.96244.

17.

In silico analysis of single nucleotide polymorphisms (SNPs) in human FOXC2 gene.

Nimir M, Abdelrahim M, Abdelrahim M, Abdalla M, Ahmed WE, Abdullah M, Hamid MMA.

Version 2. F1000Res. 2017 Mar 9 [revised 2017 Jan 1];6:243. doi: 10.12688/f1000research.10937.2. eCollection 2017.

18.

A common variant alters SCN5A-miR-24 interaction and associates with heart failure mortality.

Zhang X, Yoon JY, Morley M, McLendon JM, Mapuskar KA, Gutmann R, Mehdi H, Bloom HL, Dudley SC, Ellinor PT, Shalaby AA, Weiss R, Tang WHW, Moravec CS, Singh M, Taylor AL, Yancy CW, Feldman AM, McNamara DM, Irani K, Spitz DR, Breheny P, Margulies KB, London B, Boudreau RL.

J Clin Invest. 2018 Mar 1;128(3):1154-1163. doi: 10.1172/JCI95710. Epub 2018 Feb 19.

19.

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.

Medina-Gomez C, Kemp JP, Trajanoska K, Luan J, Chesi A, Ahluwalia TS, Mook-Kanamori DO, Ham A, Hartwig FP, Evans DS, Joro R, Nedeljkovic I, Zheng HF, Zhu K, Atalay M, Liu CT, Nethander M, Broer L, Porleifsson G, Mullin BH, Handelman SK, Nalls MA, Jessen LE, Heppe DHM, Richards JB, Wang C, Chawes B, Schraut KE, Amin N, Wareham N, Karasik D, Van der Velde N, Ikram MA, Zemel BS, Zhou Y, Carlsson CJ, Liu Y, McGuigan FE, Boer CG, Bønnelykke K, Ralston SH, Robbins JA, Walsh JP, Zillikens MC, Langenberg C, Li-Gao R, Williams FMK, Harris TB, Akesson K, Jackson RD, Sigurdsson G, den Heijer M, van der Eerden BCJ, van de Peppel J, Spector TD, Pennell C, Horta BL, Felix JF, Zhao JH, Wilson SG, de Mutsert R, Bisgaard H, Styrkársdóttir U, Jaddoe VW, Orwoll E, Lakka TA, Scott R, Grant SFA, Lorentzon M, van Duijn CM, Wilson JF, Stefansson K, Psaty BM, Kiel DP, Ohlsson C, Ntzani E, van Wijnen AJ, Forgetta V, Ghanbari M, Logan JG, Williams GR, Bassett JHD, Croucher PI, Evangelou E, Uitterlinden AG, Ackert-Bicknell CL, Tobias JH, Evans DM, Rivadeneira F.

Am J Hum Genet. 2018 Jan 4;102(1):88-102. doi: 10.1016/j.ajhg.2017.12.005.

20.

Genetic variation at the microRNA binding site of CAV1 gene is associated with lung cancer susceptibility.

Fang X, Li X, Yin Z, Xia L, Quan X, Zhao Y, Zhou B.

Oncotarget. 2017 Oct 9;8(54):92943-92954. doi: 10.18632/oncotarget.21687. eCollection 2017 Nov 3.

Supplemental Content

Support Center