BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 34119749)

  • 1. A Chinese CADASIL Family with a Novel Mutation on Exon 10 of Notch3 Gene.
    Liu Y; Huang S; Yu L; Li T; Diao S; Chen Z; Zhou G; Sheng X; Xu Y; Fang Q
    J Stroke Cerebrovasc Dis; 2021 Aug; 30(8):105674. PubMed ID: 34119749
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Novel Mutation Outside of the EGFr Encoding Exons of NOTCH3 Gene in a Chinese with CADASIL.
    Wang W; Ren Z; Shi Y; Zhang J
    J Stroke Cerebrovasc Dis; 2020 Dec; 29(12):105410. PubMed ID: 33254371
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.
    Algahtani H; Shirah B; Alharbi SY; Al-Qahtani MH; Abdulkareem AA; Naseer MI
    J Stroke Cerebrovasc Dis; 2020 Jul; 29(7):104832. PubMed ID: 32414585
    [TBL] [Abstract][Full Text] [Related]  

  • 4. First Report of Arg587Cys Mutation of Notch3 Gene in Two Chinese Families with CADASIL.
    You J; Liao S; Zhang F; Ma Z; Li G
    J Stroke Cerebrovasc Dis; 2017 Jan; 26(1):e1-e4. PubMed ID: 28341077
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Japanese Case of CADASIL with a Rare Mutation in Exon 24 of the NOTCH3 Gene.
    Ebihara Y; Mochizuki H; Ishii N; Mizuta I; Shiomi K; Mizuno T; Nakazato M
    Intern Med; 2018 Oct; 57(20):3011-3014. PubMed ID: 29780132
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The genetic spectrum and the evaluation of CADASIL screening scale in Chinese patients with NOTCH3 mutations.
    Liu X; Zuo Y; Sun W; Zhang W; Lv H; Huang Y; Xiao J; Yuan Y; Wang Z
    J Neurol Sci; 2015 Jul; 354(1-2):63-9. PubMed ID: 25982499
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The first Indian-origin family with genetically proven cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Yadav S; Bentley P; Srivastava P; Prasad K; Sharma P
    J Stroke Cerebrovasc Dis; 2013 Jan; 22(1):28-31. PubMed ID: 21737310
    [TBL] [Abstract][Full Text] [Related]  

  • 8. NOTCH3 Gene Mutation in a Chilean Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Family.
    Gallardo A; Latapiat V; Rivera A; Fonseca B; Roldan A; Sandoval P; Sánchez C; Matamala JM
    J Stroke Cerebrovasc Dis; 2020 Feb; 29(2):104530. PubMed ID: 31813735
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CADASIL with a novel NOTCH3 mutation (Cys478Tyr).
    Ozaki K; Irioka T; Ishikawa K; Mizusawa H
    J Stroke Cerebrovasc Dis; 2015 Mar; 24(3):e61-2. PubMed ID: 25595846
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese.
    Lee YC; Liu CS; Chang MH; Lin KP; Fuh JL; Lu YC; Liu YF; Soong BW
    J Neurol; 2009 Feb; 256(2):249-55. PubMed ID: 19242647
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel report of Cys1298Gly mutation in exon 24 of NOTCH3 gene in a Chinese family with CADASIL.
    Hu J; Qian J; Che Z; Tang B; Li Y; Gong Q; Lu X
    J Stroke Cerebrovasc Dis; 2023 Aug; 32(8):107208. PubMed ID: 37295172
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Tang SC; Lee MJ; Jeng JS; Yip PK
    J Neurol Sci; 2005 Feb; 228(2):125-8. PubMed ID: 15694192
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spectrum of NOTCH3 mutations in Korean patients with clinically suspicious cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Kim YE; Yoon CW; Seo SW; Ki CS; Kim YB; Kim JW; Bang OY; Lee KH; Kim GM; Chung CS; Na DL
    Neurobiol Aging; 2014 Mar; 35(3):726.e1-6. PubMed ID: 24139282
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel Mutation of the NOTCH3 Gene in a Chinese Pedigree with CADASIL.
    Hou X; He C; Jin Q; Niu Q; Ren G; Cheng H
    CNS Neurol Disord Drug Targets; 2017; 16(1):30-35. PubMed ID: 27781952
    [TBL] [Abstract][Full Text] [Related]  

  • 15. R54C Mutation of NOTCH3 Gene in the First Rungus Family with CADASIL.
    Lim KS; Tan AH; Lim CS; Chua KH; Lee PC; Ramli N; Rajahram GS; Hussin FT; Wong KT; Bhattacharjee MB; Ng CC
    PLoS One; 2015; 10(8):e0135470. PubMed ID: 26270344
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two novel mutations in NOTCH3 gene causes cerebral autosomal dominant arteriopathy with subcritical infarct and leucoencephalopathy in two Chinese families.
    Zhu Y; Wang J; Wu Y; Wang G; Hu B
    Int J Clin Exp Pathol; 2015; 8(2):1321-7. PubMed ID: 25973016
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel heterozygous NOTCH3 pathogenic variant found in two Chinese patients with CADASIL.
    Li S; Chen Y; Shan H; Ma F; Shi M; Xue J
    J Clin Neurosci; 2017 Dec; 46():85-89. PubMed ID: 28867359
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel mutation of the NOTCH3 gene in a Polish family with CADASIL.
    Buczek J; Błażejewska-Hyżorek B; Cudna A; Lusawa M; Lewandowska E; Kurkowska-Jastrzębska I; Członkowska A
    Neurol Neurochir Pol; 2016; 50(4):262-4. PubMed ID: 27375140
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Chinese CADASIL family with p.R578C mutation at exon 11 of the NOTCH3 gene.
    Wu X; Zhang A; Li Y; Lei X; Guo S; Tian T; Gong H; He D
    Clin Neurol Neurosurg; 2021 Sep; 208():106833. PubMed ID: 34352628
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Screening for NOTCH3 gene mutations among 151 consecutive Korean patients with acute ischemic stroke.
    Choi JC; Lee KH; Song SK; Lee JS; Kang SY; Kang JH
    J Stroke Cerebrovasc Dis; 2013 Jul; 22(5):608-14. PubMed ID: 22133740
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.