BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

490 related articles for article (PubMed ID: 24378235)

  • 1. Genetic association of KCNJ10 rs1130183 with seizure susceptibility and computational analysis of deleterious non-synonymous SNPs of KCNJ10 gene.
    Phani NM; Acharya S; Xavy S; Bhaskaranand N; Bhat MK; Jain A; Rai PS; Satyamoorthy K
    Gene; 2014 Feb; 536(2):247-53. PubMed ID: 24378235
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility.
    Buono RJ; Lohoff FW; Sander T; Sperling MR; O'Connor MJ; Dlugos DJ; Ryan SG; Golden GT; Zhao H; Scattergood TM; Berrettini WH; Ferraro TN
    Epilepsy Res; 2004 Feb; 58(2-3):175-83. PubMed ID: 15120748
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy.
    Lenzen KP; Heils A; Lorenz S; Hempelmann A; Höfels S; Lohoff FW; Schmitz B; Sander T
    Epilepsy Res; 2005 Feb; 63(2-3):113-8. PubMed ID: 15725393
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Contribution of KCNJ10 gene polymorphisms in childhood epilepsy.
    Dai AI; Akcali A; Koska S; Oztuzcu S; Cengiz B; Demiryürek AT
    J Child Neurol; 2015 Mar; 30(3):296-300. PubMed ID: 25008907
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy.
    Heuser K; Nagelhus EA; Taubøll E; Indahl U; Berg PR; Lien S; Nakken S; Gjerstad L; Ottersen OP
    Epilepsy Res; 2010 Jan; 88(1):55-64. PubMed ID: 19864112
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Functional characterisation of missense variations in the Kir4.1 potassium channel (KCNJ10) associated with seizure susceptibility.
    Shang L; Lucchese CJ; Haider S; Tucker SJ
    Brain Res Mol Brain Res; 2005 Sep; 139(1):178-83. PubMed ID: 15936844
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene.
    Ferraro TN; Golden GT; Smith GG; Martin JF; Lohoff FW; Gieringer TA; Zamboni D; Schwebel CL; Press DM; Kratzer SO; Zhao H; Berrettini WH; Buono RJ
    Mamm Genome; 2004 Apr; 15(4):239-51. PubMed ID: 15112102
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Common variants of KCNJ10 are associated with susceptibility and anti-epileptic drug resistance in Chinese genetic generalized epilepsies.
    Guo Y; Yan KP; Qu Q; Qu J; Chen ZG; Song T; Luo XY; Sun ZY; Bi CL; Liu JF
    PLoS One; 2015; 10(4):e0124896. PubMed ID: 25874548
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exploration of deleterious single nucleotide polymorphisms in late-onset Alzheimer disease susceptibility genes.
    Masoodi TA; Al Shammari SA; Al-Muammar MN; Alhamdan AA; Talluri VR
    Gene; 2013 Jan; 512(2):429-37. PubMed ID: 22960267
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of KCNJ10 variants and the susceptibility to clinical epilepsy.
    Jiang C; Li L; Wu M; Hao M; Feng J
    Clin Neurol Neurosurg; 2021 Jan; 200():106340. PubMed ID: 33187755
    [TBL] [Abstract][Full Text] [Related]  

  • 11. In silico analysis of consequences of non-synonymous SNPs of Slc11a2 gene in Indian bovines.
    Patel SM; Koringa PG; Reddy BB; Nathani NM; Joshi CG
    Genom Data; 2015 Sep; 5():72-9. PubMed ID: 26484229
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exploration of deleterious single nucleotide polymorphisms in the components of human P bodies: an in silico approach.
    Venkatesh T; Suresh PS
    Gene; 2013 Oct; 528(2):360-3. PubMed ID: 23892092
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification and structural comparison of deleterious mutations in nsSNPs of ABL1 gene in chronic myeloid leukemia: a bio-informatics study.
    George Priya Doss C; Sudandiradoss C; Rajasekaran R; Purohit R; Ramanathan K; Sethumadhavan R
    J Biomed Inform; 2008 Aug; 41(4):607-12. PubMed ID: 18243808
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in human DNA repair genes.
    Nakken S; Alseth I; Rognes T
    Neuroscience; 2007 Apr; 145(4):1273-9. PubMed ID: 17055652
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Predicting the functional and structural consequences of nsSNPs in human methionine synthase gene using computational tools.
    Desai M; Chauhan JB
    Syst Biol Reprod Med; 2019 Aug; 65(4):288-300. PubMed ID: 30676783
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A bioinformatics approach for the phenotype prediction of nonsynonymous single nucleotide polymorphisms in human cytochromes P450.
    Wang LL; Li Y; Zhou SF
    Drug Metab Dispos; 2009 May; 37(5):977-91. PubMed ID: 19204079
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification and in silico analysis of functional SNPs of the BRCA1 gene.
    Rajasekaran R; Sudandiradoss C; Doss CG; Sethumadhavan R
    Genomics; 2007 Oct; 90(4):447-52. PubMed ID: 17719744
    [TBL] [Abstract][Full Text] [Related]  

  • 18. In silico searching for disease-associated functional DNA variants.
    Sethumadhavan R; Doss CG; Rajasekaran R
    Methods Mol Biol; 2011; 760():239-50. PubMed ID: 21780001
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association study between inwardly rectifying potassium channels 2.1 and 4.1 and autism spectrum disorders.
    Sun C; Zou M; Li L; Li D; Ma Y; Xia W; Wu L; Ren H
    Life Sci; 2018 Nov; 213():183-189. PubMed ID: 30304693
    [TBL] [Abstract][Full Text] [Related]  

  • 20. In silico analysis of non-synonymous single nucleotide polymorphisms in human DAZL gene associated with male infertility.
    Nailwal M; Chauhan JB
    Syst Biol Reprod Med; 2017 Aug; 63(4):248-258. PubMed ID: 28388287
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.