Similar articles for PMID: 28502511

Year	Number of Results
2002	1
2007	5
2008	1
2009	5
2011	10
2012	8
2013	5
2014	10
2015	12
2016	14
2017	17
2018	10
2019	6
2020	15
2021	16
2022	2
2023	5
2024	0

1

Functional analysis of new 3' untranslated regions genetic variants in genes associated with genetic hypercholesterolemias.

Pérez-Campo FM, De Castro-Orós I, Noriega A, Cofán M, Lamiquiz-Moneo I, Cenarro A, Ros E, Civeira F, Pocoví M, Rodríguez-Rey JC. Pérez-Campo FM, et al. J Clin Lipidol. 2017 Mar-Apr;11(2):532-542. doi: 10.1016/j.jacl.2017.02.004. Epub 2017 Feb 28. J Clin Lipidol. 2017. PMID: 28502511

2

Bioinformatics Analysis Revealed Novel 3'UTR Variants Associated with Intellectual Disability.

Yang J, Liu A, He I, Bai Y. Yang J, et al. Genes (Basel). 2020 Aug 26;11(9):998. doi: 10.3390/genes11090998. Genes (Basel). 2020. PMID: 32858868 Free PMC article.

3

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. Ye Q, et al. Gene. 2013 Oct 10;528(2):132-8. doi: 10.1016/j.gene.2013.07.036. Epub 2013 Jul 31. Gene. 2013. PMID: 23911300

4

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. Safdar M, et al. Mamm Genome. 2021 Oct;32(5):389-400. doi: 10.1007/s00335-021-09880-6. Epub 2021 Jun 4. Mamm Genome. 2021. PMID: 34089082 Free PMC article.

5

An 11-nt sequence polymorphism at the 3'UTR of human SFTPA1 and SFTPA2 gene variants differentially affect gene expression levels and miRNA regulation in cell culture.

Silveyra P, DiAngelo SL, Floros J. Silveyra P, et al. Am J Physiol Lung Cell Mol Physiol. 2014 Jul 1;307(1):L106-19. doi: 10.1152/ajplung.00313.2013. Epub 2014 May 2. Am J Physiol Lung Cell Mol Physiol. 2014. PMID: 24793167 Free PMC article.

6

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. Cipolla GA, et al. Biochim Biophys Acta. 2016 Oct;1859(10):1306-13. doi: 10.1016/j.bbagrm.2016.07.006. Epub 2016 Jul 14. Biochim Biophys Acta. 2016. PMID: 27424220 Free PMC article.

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; kConFab; 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. Brewster BL, et al. Hum Mutat. 2012 Dec;33(12):1665-75. doi: 10.1002/humu.22159. Epub 2012 Aug 2. Hum Mutat. 2012. PMID: 22753153

8

Analysis of DNA variants in miRNAs and miRNA 3'UTR binding sites in female infertility patients.

Tyc KM, Wong A, Scott RT Jr, Tao X, Schindler K, Xing J. Tyc KM, et al. Lab Invest. 2021 Apr;101(4):503-512. doi: 10.1038/s41374-020-00498-x. Epub 2020 Oct 17. Lab Invest. 2021. PMID: 33070169 Free PMC article.

9

Brain derived neurotrophic factor (BDNF) expression is regulated by microRNAs miR-26a and miR-26b allele-specific binding.

Caputo V, Sinibaldi L, Fiorentino A, Parisi C, Catalanotto C, Pasini A, Cogoni C, Pizzuti A. Caputo V, et al. PLoS One. 2011;6(12):e28656. doi: 10.1371/journal.pone.0028656. Epub 2011 Dec 14. PLoS One. 2011. PMID: 22194877 Free PMC article.

10

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. Ghanbari M, et al. Hum Mutat. 2017 Jul;38(7):827-838. doi: 10.1002/humu.23226. Epub 2017 May 4. Hum Mutat. 2017. PMID: 28397307

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

130 results

Results by year