BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 30304693)

  • 1. 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]  

  • 2. FADS1-FADS2 and ELOVL2 gene polymorphisms in susceptibility to autism spectrum disorders in Chinese children.
    Sun C; Zou M; Wang X; Xia W; Ma Y; Liang S; Hao Y; Wu L; Fu S
    BMC Psychiatry; 2018 Sep; 18(1):283. PubMed ID: 30180836
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1.
    Sicca F; Imbrici P; D'Adamo MC; Moro F; Bonatti F; Brovedani P; Grottesi A; Guerrini R; Masi G; Santorelli FM; Pessia M
    Neurobiol Dis; 2011 Jul; 43(1):239-47. PubMed ID: 21458570
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neurexin gene family variants as risk factors for autism spectrum disorder.
    Wang J; Gong J; Li L; Chen Y; Liu L; Gu H; Luo X; Hou F; Zhang J; Song R
    Autism Res; 2018 Jan; 11(1):37-43. PubMed ID: 29045040
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Potassium channel activity and glutamate uptake are impaired in astrocytes of seizure-susceptible DBA/2 mice.
    Inyushin M; Kucheryavykh LY; Kucheryavykh YV; Nichols CG; Buono RJ; Ferraro TN; Skatchkov SN; Eaton MJ
    Epilepsia; 2010 Sep; 51(9):1707-13. PubMed ID: 20831751
    [TBL] [Abstract][Full Text] [Related]  

  • 7. SHANK1 polymorphisms and SNP-SNP interactions among SHANK family: A possible cue for recognition to autism spectrum disorder in infant age.
    Qiu S; Li Y; Bai Y; Shi J; Cui H; Gu Y; Ren Y; Zhao Q; Zhang K; Lu M; Wang Y; Li Y; Zhong W; Zhu X; Liu Y; Cheng Y; Qiao Y; Liu Y
    Autism Res; 2019 Mar; 12(3):375-383. PubMed ID: 30629339
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A study of single nucleotide polymorphisms in CD157, AIM2 and JARID2 genes in Han Chinese children with autism spectrum disorder.
    Mo W; Liu J; Zhang Z; Yu H; Yang A; Qu F; Hu P; Liu Z; Hu F
    Nord J Psychiatry; 2018 Apr; 72(3):179-183. PubMed ID: 29216786
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association between SHANK3 polymorphisms and susceptibility to autism spectrum disorder.
    Qiu S; Li Y; Li Y; Zhong W; Shi M; Zhao Q; Zhang K; Wang Y; Lu M; Zhu X; Jiang H; Yu Y; Cheng Y; Liu Y
    Gene; 2018 Apr; 651():100-105. PubMed ID: 29408620
    [TBL] [Abstract][Full Text] [Related]  

  • 10. No association between the KCNH1, KCNJ10 and KCNN3 genes and schizophrenia in the Han Chinese population.
    Shen Q; Zhang J; Wang Y; Liu B; Li X; Zhao Q; Chen S; Ji J; Yang F; Wan C; Gao L; Xu Y; Feng G; He L; He G
    Neurosci Lett; 2011 Jan; 487(1):61-5. PubMed ID: 20933057
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism.
    Li J; Zhao L; You Y; Lu T; Jia M; Yu H; Ruan Y; Yue W; Liu J; Lu L; Zhang D; Wang L
    PLoS One; 2015; 10(7):e0133247. PubMed ID: 26204268
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Common Signal Patch Drives AP-1 Protein-dependent Golgi Export of Inwardly Rectifying Potassium Channels.
    Li X; Ortega B; Kim B; Welling PA
    J Biol Chem; 2016 Jul; 291(29):14963-72. PubMed ID: 27226616
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Electrophysiological features of sleep in children with Kir4.1 channel mutations and Autism-Epilepsy phenotype: a preliminary study.
    Cucchiara F; Frumento P; Banfi T; Sesso G; Di Galante M; D'Ascanio P; Valvo G; Sicca F; Faraguna U
    Sleep; 2020 Apr; 43(4):. PubMed ID: 31722434
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association Between DCC Polymorphisms and Susceptibility to Autism Spectrum Disorder.
    Li Y; Qiu S; Zhong W; Li Y; Liu Y; Cheng Y; Liu Y
    J Autism Dev Disord; 2020 Oct; 50(10):3800-3809. PubMed ID: 32144606
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population.
    Zhang L; Qin Y; Gong X; Peng R; Cai C; Zheng Y; Du Y; Wang H
    Transl Psychiatry; 2019 Jan; 9(1):31. PubMed ID: 30670685
    [TBL] [Abstract][Full Text] [Related]  

  • 18. GABA
    Yang S; Guo X; Dong X; Han Y; Gao L; Su Y; Dai W; Zhang X
    Sci Rep; 2017 Jun; 7(1):3290. PubMed ID: 28607477
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Expression, localization, and functional properties of inwardly rectifying K
    Manis AD; Hodges MR; Staruschenko A; Palygin O
    Am J Physiol Renal Physiol; 2020 Feb; 318(2):F332-F337. PubMed ID: 31841387
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The role of an inwardly rectifying K(+) channel (Kir4.1) in the inner ear and hearing loss.
    Chen J; Zhao HB
    Neuroscience; 2014 Apr; 265():137-46. PubMed ID: 24480364
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.