These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

294 related articles for article (PubMed ID: 27473590)

  • 1. The genetic variants in 3' untranslated region of voltage-gated sodium channel alpha 1 subunit gene affect the mRNA-microRNA interactions and associate with epilepsy.
    Li T; Kuang Y; Li B
    BMC Genet; 2016 Jul; 17(1):111. PubMed ID: 27473590
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A specific haplotype in potential miRNAs binding sites of secreted frizzled-related protein 1 (SFRP1) is associated with BMD variation in osteoporosis.
    Amjadi-Moheb F; Hosseini SR; Kosari-Monfared M; Ghadami E; Nooreddini H; Akhavan-Niaki H
    Gene; 2018 Nov; 677():132-141. PubMed ID: 30055306
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Single-Base Gene Variants in
    Buainain RP; Sodré AR; Dos Santos JS; Takazaki KAG; Queiroz LS; de Oliveira CTP; de Aguiar PHP; Marson FAL; Ortega MM
    Int J Mol Sci; 2024 May; 25(11):. PubMed ID: 38892194
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Significance of 3'UTR and Pathogenic Haplotype in Glucose-6-Phosphate Deficiency.
    Chaowanathikhom M; Nuchnoi P; Palasuwan D
    Lab Med; 2017 Feb; 48(1):73-88. PubMed ID: 28138089
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Influence of common SCN1A promoter variants on the severity of SCN1A-related phenotypes.
    de Lange IM; Weuring W; van 't Slot R; Gunning B; Sonsma ACM; McCormack M; de Kovel C; van Gemert LJJM; Mulder F; van Kempen MJA; Knoers NVAM; Brilstra EH; Koeleman BPC
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00727. PubMed ID: 31144463
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Bioinformatics Analysis Revealed Novel 3'UTR Variants Associated with Intellectual Disability.
    Yang J; Liu A; He I; Bai Y
    Genes (Basel); 2020 Aug; 11(9):. PubMed ID: 32858868
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A novel variant in the 3' UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH's binding.
    Zeng T; Dong ZF; Liu SJ; Wan RP; Tang LJ; Liu T; Zhao QH; Shi YW; Yi YH; Liao WP; Long YS
    Hum Genet; 2014 Jun; 133(6):801-11. PubMed ID: 24464349
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. The association of SCN1A p.Thr1067Ala polymorphism with epilepsy risk and the response to antiepileptic drugs in Slovenian children and adolescents with epilepsy.
    Bertok S; Dolžan V; Goričar K; Podkrajšek KT; Battelino T; Rener-Primec Z
    Seizure; 2017 Oct; 51():9-13. PubMed ID: 28753467
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Association of single nucleotide polymorphisms in the 3'UTR of ERAP1 gene with essential hypertension in the Northeastern Han Chinese.
    Yang S; Liu X; Gao Y; Ding M; Li B; Sun H; He Y; Yang P
    Gene; 2015 Apr; 560(2):211-6. PubMed ID: 25665737
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Determination of SCN1A genetic variants in Mexican patients with refractory epilepsy and Dravet syndrome.
    Jiménez-Arredondo RE; Brambila-Tapia AJL; Mercado-Silva FM; Magaña-Torres MT; Figuera LE
    Genet Mol Res; 2017 May; 16(2):. PubMed ID: 28525652
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel SCN1A variants in Dravet syndrome and evaluating a wide approach of patient selection.
    Surovy M; Soltysova A; Kolnikova M; Sykora P; Ilencikova D; Ficek A; Radvanszky J; Kadasi L
    Gen Physiol Biophys; 2016 Jul; 35(3):333-42. PubMed ID: 27045673
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [Sequence analyses of HIRA gene 3'UTR region and related microRNA].
    Wang X; Zhang J; Cao Y; Diao L; Wang H; Ma X; Ma D; Huang G
    Zhonghua Yi Xue Za Zhi; 2014 Apr; 94(16):1223-6. PubMed ID: 24924885
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.