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Items: 1 to 20 of 56

1.

Whole exome sequencing for the identification of CYP3A7 variants associated with tacrolimus concentrations in kidney transplant patients.

Sohn M, Kim MG, Han N, Kim IW, Gim J, Min SI, Song EY, Kim YS, Jung HS, Shin YK, Ha J, Oh JM.

Sci Rep. 2018 Dec 24;8(1):18064. doi: 10.1038/s41598-018-36085-w.

2.

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.

3.

A Functional riboSNitch in the 3' Untranslated Region of FKBP5 Alters MicroRNA-320a Binding Efficiency and Mediates Vulnerability to Chronic Post-Traumatic Pain.

Linnstaedt SD, Riker KD, Rueckeis CA, Kutchko KM, Lackey L, McCarthy KR, Tsai YH, Parker JS, Kurz MC, Hendry PL, Lewandowski C, Datner E, Pearson C, O'Neil B, Domeier R, Kaushik S, Laederach A, McLean SA.

J Neurosci. 2018 Sep 26;38(39):8407-8420. doi: 10.1523/JNEUROSCI.3458-17.2018. Epub 2018 Aug 27.

4.

BRCA1 and BRCA2 gene variants and nonsyndromic cleft lip/palate.

Rodriguez N, Maili L, Chiquet BT, Blanton SH, Hecht JT, Letra A.

Birth Defects Res. 2018 Jul 17;110(12):1043-1048. doi: 10.1002/bdr2.1346. Epub 2018 Jun 19.

PMID:
29921024
5.

The SNPcurator: literature mining of enriched SNP-disease associations.

Tawfik NS, Spruit MR.

Database (Oxford). 2018 Jan 1;2018. doi: 10.1093/database/bay020.

6.

miRNAtools: Advanced Training Using the miRNA Web of Knowledge.

Stępień EŁ, Costa MC, Enguita FJ.

Noncoding RNA. 2018 Feb 16;4(1). pii: E5. doi: 10.3390/ncrna4010005.

7.

A meta-analysis of public microarray data identifies biological regulatory networks in Parkinson's disease.

Su L, Wang C, Zheng C, Wei H, Song X.

BMC Med Genomics. 2018 Apr 13;11(1):40. doi: 10.1186/s12920-018-0357-7.

8.

Novel candidate genes important for asthma and hypertension comorbidity revealed from associative gene networks.

Saik OV, Demenkov PS, Ivanisenko TV, Bragina EY, Freidin MB, Goncharova IA, Dosenko VE, Zolotareva OI, Hofestaedt R, Lavrik IN, Rogaev EI, Ivanisenko VA.

BMC Med Genomics. 2018 Feb 13;11(Suppl 1):15. doi: 10.1186/s12920-018-0331-4.

9.

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.

10.

Unraveling the determinants of microRNA mediated regulation using a massively parallel reporter assay.

Vainberg Slutskin I, Weingarten-Gabbay S, Nir R, Weinberger A, Segal E.

Nat Commun. 2018 Feb 6;9(1):529. doi: 10.1038/s41467-018-02980-z.

11.

MSDD: a manually curated database of experimentally supported associations among miRNAs, SNPs and human diseases.

Yue M, Zhou D, Zhi H, Wang P, Zhang Y, Gao Y, Guo M, Li X, Wang Y, Zhang Y, Ning S, Li X.

Nucleic Acids Res. 2018 Jan 4;46(D1):D181-D185. doi: 10.1093/nar/gkx1035.

12.

Variation in the α2A-adrenergic receptor gene and risk of gestational diabetes.

Kawai VK, Levinson RT, Adefurin A, Kurnik D, Collier SP, Conway D, Stein CM.

Pharmacogenomics. 2017 Oct;18(15):1381-1386. doi: 10.2217/pgs-2017-0079. Epub 2017 Oct 4.

13.

Structure and functional impact of seed region variant in MIR-499 gene family in bronchial asthma.

Toraih EA, Hussein MH, Al Ageeli E, Riad E, AbdAllah NB, Helal GM, Fawzy MS.

Respir Res. 2017 Sep 8;18(1):169. doi: 10.1186/s12931-017-0648-0.

14.

SNPs, linkage disequilibrium, and chronic mountain sickness in Tibetan Chinese.

Buroker NE, Ning XH, Zhou ZN, Li K, Cen WJ, Wu XF, Zhu WZ, Scott CR, Chen SH.

Hypoxia (Auckl). 2017 Jul 14;5:67-74. doi: 10.2147/HP.S117967. eCollection 2017.

15.

Exploring genetic associations with ceRNA regulation in the human genome.

Li MJ, Zhang J, Liang Q, Xuan C, Wu J, Jiang P, Li W, Zhu Y, Wang P, Fernandez D, Shen Y, Chen Y, Kocher JA, Yu Y, Sham PC, Wang J, Liu JS, Liu XS.

Nucleic Acids Res. 2017 Jun 2;45(10):5653-5665. doi: 10.1093/nar/gkx331.

16.

Genetic and epigenetic regulation of arrhythmogenic cardiomyopathy.

Mazurek S, Kim GH.

Biochim Biophys Acta Mol Basis Dis. 2017 Aug;1863(8):2064-2069. doi: 10.1016/j.bbadis.2017.04.020. Epub 2017 Apr 25. Review.

17.

MicroRNA-related genetic variants in iron regulatory genes, dietary iron intake, microRNAs and lung cancer risk.

Zhang L, Ye Y, Tu H, Hildebrandt MA, Zhao L, Heymach JV, Roth JA, Wu X.

Ann Oncol. 2017 May 1;28(5):1124-1129. doi: 10.1093/annonc/mdx046.

18.

SNPs in microRNA target sites and their potential role in human disease.

Moszyńska A, Gebert M, Collawn JF, Bartoszewski R.

Open Biol. 2017 Apr;7(4). pii: 170019. doi: 10.1098/rsob.170019. Review.

19.

Whole genome sequencing of an African American family highlights toll like receptor 6 variants in Kawasaki disease susceptibility.

Kim J, Shimizu C, Kingsmore SF, Veeraraghavan N, Levy E, Ribeiro Dos Santos AM, Yang H, Flatley J, Hoang LT, Hibberd ML, Tremoulet AH, Harismendy O, Ohno-Machado L, Burns JC.

PLoS One. 2017 Feb 2;12(2):e0170977. doi: 10.1371/journal.pone.0170977. eCollection 2017.

20.

Genetic variant rs3750625 in the 3'UTR of ADRA2A affects stress-dependent acute pain severity after trauma and alters a microRNA-34a regulatory site.

Linnstaedt SD, Walker MG, Riker KD, Nyland JE, Hu J, Rossi C, Swor RA, Jones JS, Diatchenko L, Bortsov AV, Peak DA, McLean SA.

Pain. 2017 Feb;158(2):230-239. doi: 10.1097/j.pain.0000000000000742.

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