BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

314 related articles for article (PubMed ID: 23583740)

  • 1. 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]  

  • 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. 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. 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]  

  • 5. 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]  

  • 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
    Biochim Biophys Acta; 2016 Oct; 1859(10):1306-13. PubMed ID: 27424220
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).
    Reamon-Buettner SM; Cho SH; Borlak J
    BMC Med Genet; 2007 Jun; 8():38. PubMed ID: 17592645
    [TBL] [Abstract][Full Text] [Related]  

  • 8. MiR-196a binding-site SNP regulates RAP1A expression contributing to esophageal squamous cell carcinoma risk and metastasis.
    Wang K; Li J; Guo H; Xu X; Xiong G; Guan X; Liu B; Li J; Chen X; Yang K; Bai Y
    Carcinogenesis; 2012 Nov; 33(11):2147-54. PubMed ID: 22859270
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects.
    Salazar M; Consoli F; Villegas V; Caicedo V; Maddaloni V; Daniele P; Caianiello G; Pachón S; Nuñez F; Limongelli G; Pacileo G; Marino B; Bernal JE; De Luca A; Dallapiccola B
    Eur J Med Genet; 2011; 54(3):306-9. PubMed ID: 21276881
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Genetic screening of Gata4 and Nkx2.5 mutations in hereditary congenital heart defects: 5 familial cases].
    Pulignani S; Foffa I; Cresci M; Vittorini S; Ait-Ali L; Andreassi MG
    Recenti Prog Med; 2011 Mar; 102(3):120-5. PubMed ID: 21572484
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel Point Mutations in 3'-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects.
    Khatami M; Ghorbani S; Adriani MR; Bahaloo S; Naeini MA; Heidari MM; Hadadzadeh M
    Curr Med Sci; 2022 Feb; 42(1):129-143. PubMed ID: 34652630
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Search of Somatic Mutations of NKX2-5 and GATA4 Genes in Chinese Patients with Sporadic Congenital Heart Disease.
    Yin J; Qian J; Dai G; Wang C; Qin Y; Xu T; Li Z; Zhang H; Yang S
    Pediatr Cardiol; 2019 Jan; 40(1):17-22. PubMed ID: 30121862
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Screening of 99 Danish patients with congenital heart disease for GATA4 mutations.
    Zhang L; Tümer Z; Jacobsen JR; Andersen PS; Tommerup N; Larsen LA
    Genet Test; 2006; 10(4):277-80. PubMed ID: 17253934
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Regulation of the MIR155 host gene in physiological and pathological processes.
    Elton TS; Selemon H; Elton SM; Parinandi NL
    Gene; 2013 Dec; 532(1):1-12. PubMed ID: 23246696
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Characterization of 3'untranslated region (3'UTR) of the MICB gene.
    Pan F; Liu X; Huang J; Tian W
    Hum Immunol; 2013 Jun; 74(6):746-50. PubMed ID: 23380144
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.