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 *

176 related articles for article (PubMed ID: 38110787)

  • 1. Generation of iPSC lines (KAIMRCi003A, KAIMRCi003B) from a Saudi patient with Dravet syndrome carrying homozygous mutation in the CPLX1 gene and heterozygous mutation in SCN9A.
    Alowaysi M; Al-Shehri M; Badkok A; Attas H; Aboalola D; Baadhaim M; Alzahrani H; Daghestani M; Zia A; Al-Ghamdi K; Al-Ghamdi A; Zakri S; Aouabdi S; Tegner J; Alsayegh K
    Hum Cell; 2024 Mar; 37(2):502-510. PubMed ID: 38110787
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Generation of Human iPSC Lines from Three Individuals with Dravet Syndrome and Characterization of Neural Differentiation Markers in iPSC-Derived Ventral Forebrain Organoid Model.
    Zayat V; Kuczynska Z; Liput M; Metin E; Rzonca-Niewczas S; Smyk M; Mazurczak T; Goszczanska-Ciuchta A; Leszczynski P; Hoffman-Zacharska D; Buzanska L
    Cells; 2023 Jan; 12(2):. PubMed ID: 36672274
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome.
    Mulley JC; Hodgson B; McMahon JM; Iona X; Bellows S; Mullen SA; Farrell K; Mackay M; Sadleir L; Bleasel A; Gill D; Webster R; Wirrell EC; Harbord M; Sisodiya S; Andermann E; Kivity S; Berkovic SF; Scheffer IE; Dibbens LM
    Epilepsia; 2013 Sep; 54(9):e122-6. PubMed ID: 23895530
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Generation of three human induced pluripotent stem cell (iPSC) lines from three patients with Dravet syndrome carrying distinct SCN1A gene mutations.
    Schuster J; Fatima A; Sobol M; Norradin FH; Laan L; Dahl N
    Stem Cell Res; 2019 Aug; 39():101523. PubMed ID: 31400703
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Generation of a human iPSC line (UUIGPi015-A) from a patient with Dravet syndrome and a 2.9 Mb deletion spanning SCN1A on chromosome 2.
    Schuster J; de Guidi C; Tripathi R; Klar J; Dahl N
    Stem Cell Res; 2022 Apr; 60():102712. PubMed ID: 35203050
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and molecular analysis of epilepsy-related genes in patients with Dravet syndrome.
    Jiang T; Shen Y; Chen H; Yuan Z; Mao S; Gao F
    Medicine (Baltimore); 2018 Dec; 97(50):e13565. PubMed ID: 30558019
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in the sodium channel genes SCN1A, SCN3A, and SCN9A in children with epilepsy with febrile seizures plus(EFS+).
    Ma H; Guo Y; Chen Z; Wang L; Tang Z; Zhang J; Miao Q; Zhai Q
    Seizure; 2021 May; 88():146-152. PubMed ID: 33895391
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.
    Singh NA; Pappas C; Dahle EJ; Claes LR; Pruess TH; De Jonghe P; Thompson J; Dixon M; Gurnett C; Peiffer A; White HS; Filloux F; Leppert MF
    PLoS Genet; 2009 Sep; 5(9):e1000649. PubMed ID: 19763161
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome.
    Ogiwara I; Nakayama T; Yamagata T; Ohtani H; Mazaki E; Tsuchiya S; Inoue Y; Yamakawa K
    Epilepsia; 2012 Dec; 53(12):e200-3. PubMed ID: 23148524
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic exploration of Dravet syndrome: two case report.
    Triono A; Herini ES; Gunadi
    J Med Case Rep; 2024 Apr; 18(1):215. PubMed ID: 38649973
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients.
    Sun Y; Paşca SP; Portmann T; Goold C; Worringer KA; Guan W; Chan KC; Gai H; Vogt D; Chen YJ; Mao R; Chan K; Rubenstein JL; Madison DV; Hallmayer J; Froehlich-Santino WM; Bernstein JA; Dolmetsch RE
    Elife; 2016 Jul; 5():. PubMed ID: 27458797
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?
    Lim BC; Hwang H; Kim H; Chae JH; Choi J; Kim KJ; Hwang YS; Yum MS; Ko TS
    Epilepsy Res; 2015 Jan; 109():34-9. PubMed ID: 25524840
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Variable epilepsy phenotypes associated with heterozygous mutation in the SCN9A gene: report of two cases.
    Yang C; Hua Y; Zhang W; Xu J; Xu L; Gao F; Jiang P
    Neurol Sci; 2018 Jun; 39(6):1113-1115. PubMed ID: 29500686
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The incidence of SCN1A-related Dravet syndrome in Denmark is 1:22,000: a population-based study from 2004 to 2009.
    Bayat A; Hjalgrim H; Møller RS
    Epilepsia; 2015 Apr; 56(4):e36-9. PubMed ID: 25778844
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Establishment of isogenic iPSCs from an individual with SCN1A mutation mosaicism as a model for investigating neurocognitive impairment in Dravet syndrome.
    Maeda H; Chiyonobu T; Yoshida M; Yamashita S; Zuiki M; Kidowaki S; Isoda K; Yamakawa K; Morimoto M; Nakahata T; Saito MK; Hosoi H
    J Hum Genet; 2016 Jun; 61(6):565-9. PubMed ID: 26841829
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dravet syndrome and Dravet syndrome-like phenotype: a systematic review of the SCN1A and PCDH19 variants.
    Rampazzo ACM; Dos Santos RRP; Maluf FA; Simm RF; Marson FAL; Ortega MM; de Aguiar PHP
    Neurogenetics; 2021 May; 22(2):105-115. PubMed ID: 33937968
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Generation of D1-1 TALEN isogenic control cell line from Dravet syndrome patient iPSCs using TALEN-mediated editing of the SCN1A gene.
    Tanaka Y; Sone T; Higurashi N; Sakuma T; Suzuki S; Ishikawa M; Yamamoto T; Mitsui J; Tsuji H; Okano H; Hirose S
    Stem Cell Res; 2018 Apr; 28():100-104. PubMed ID: 29453127
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Generation of SCN1A Knock out induced pluripotent stem cell (iPSC) line.
    Shan W; Yang X; Ren Q; Wang Q
    Stem Cell Res; 2021 Aug; 55():102452. PubMed ID: 34247112
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Establishment of a human induced stem cell line (FUi002-A) from Dravet syndrome patient carrying heterozygous R1525X mutation in SCN1A gene.
    Tanaka Y; Higurashi N; Shirasu N; Yasunaga S; Moreira KM; Okano H; Hirose S
    Stem Cell Res; 2018 Aug; 31():11-15. PubMed ID: 29981888
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Generation of corrected-hiPSC (USTCi001-A-1) from epilepsy patient iPSCs using TALEN-mediated editing of the SCN1A gene.
    Zhao H; He L; Li S; Huang H; Tang F; Han X; Lin Z; Tian C; Huang R; Zhou P; Huang J; Deng S; Li Z
    Stem Cell Res; 2020 Jul; 46():101864. PubMed ID: 32544858
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.