BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 35822697)

  • 1. Genetic spectrum of NOTCH3 and clinical phenotype of CADASIL patients in different populations.
    Ni W; Zhang Y; Zhang L; Xie JJ; Li HF; Wu ZY
    CNS Neurosci Ther; 2022 Nov; 28(11):1779-1789. PubMed ID: 35822697
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype and Phenotype Differences in CADASIL from an Asian Perspective.
    Kim Y; Bae JS; Lee JY; Song HK; Lee JH; Lee M; Kim C; Lee SH
    Int J Mol Sci; 2022 Sep; 23(19):. PubMed ID: 36232798
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles.
    Liao YC; Hsiao CT; Fuh JL; Chern CM; Lee WJ; Guo YC; Wang SJ; Lee IH; Liu YT; Wang YF; Chang FC; Chang MH; Soong BW; Lee YC
    PLoS One; 2015; 10(8):e0136501. PubMed ID: 26308724
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Mönkäre S; Kuuluvainen L; Schleutker J; Myllykangas L; Pöyhönen M
    Acta Neurol Scand; 2022 Nov; 146(5):643-651. PubMed ID: 36086804
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in Chinese.
    Lee YC; Yang AH; Liu HC; Wong WJ; Lu YC; Chang MH; Soong BW
    J Neurol Sci; 2006 Jul; 246(1-2):111-5. PubMed ID: 16580020
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characteristics of CADASIL in Korea: a novel cysteine-sparing Notch3 mutation.
    Kim Y; Choi EJ; Choi CG; Kim G; Choi JH; Yoo HW; Kim JS
    Neurology; 2006 May; 66(10):1511-6. PubMed ID: 16717210
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) associated with a novel C82R mutation in the NOTCH3 gene.
    Zea-Sevilla MA; Bermejo-Velasco P; Serrano-Heranz R; Calero M
    J Alzheimers Dis; 2015; 43(2):363-7. PubMed ID: 25096610
    [TBL] [Abstract][Full Text] [Related]  

  • 10. NOTCH3 mutations and clinical features in 33 mainland Chinese families with CADASIL.
    Wang Z; Yuan Y; Zhang W; Lv H; Hong D; Chen B; Liu Y; Luan X; Xie S; Wu S
    J Neurol Neurosurg Psychiatry; 2011 May; 82(5):534-9. PubMed ID: 20935329
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cysteine-sparing CADASIL mutations in NOTCH3 show proaggregatory properties in vitro.
    Wollenweber FA; Hanecker P; Bayer-Karpinska A; Malik R; Bäzner H; Moreton F; Muir KW; Müller S; Giese A; Opherk C; Dichgans M; Haffner C; Duering M
    Stroke; 2015 Mar; 46(3):786-92. PubMed ID: 25604251
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and imaging features of patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and cysteine-sparing NOTCH3 mutations.
    Kim H; Lim YM; Lee EJ; Oh YJ; Kim KK
    PLoS One; 2020; 15(6):e0234797. PubMed ID: 32555735
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    Lee YC; Chung CP; Chang MH; Wang SJ; Liao YC
    Neurology; 2020 Jan; 94(1):e87-e96. PubMed ID: 31792094
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Phenotypic and mutational spectrum in patients from mainland China.
    Yin X; Wu D; Wan J; Yan S; Lou M; Zhao G; Zhang B
    Int J Neurosci; 2015; 125(8):585-92. PubMed ID: 25105908
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Systematic Review of Cysteine-Sparing NOTCH3 Missense Mutations in Patients with Clinical Suspicion of CADASIL.
    Muiño E; Gallego-Fabrega C; Cullell N; Carrera C; Torres N; Krupinski J; Roquer J; Montaner J; Fernández-Cadenas I
    Int J Mol Sci; 2017 Sep; 18(9):. PubMed ID: 28902129
    [TBL] [Abstract][Full Text] [Related]  

  • 17. NOTCH3 mutations in a cohort of Portuguese patients within CADASIL spectrum phenotype.
    Almeida MR; Elias I; Fernandes C; Machado R; Galego O; Santo G
    Neurogenetics; 2022 Jan; 23(1):1-9. PubMed ID: 34851492
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Family Members With a Pathogenic
    Hack RJ; Gravesteijn G; Cerfontaine MN; Hegeman IM; Mulder AA; Lesnik Oberstein SAJ; Rutten JW
    Stroke; 2022 Jun; 53(6):1964-1974. PubMed ID: 35300531
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical Features of 4 Novel NOTCH3 Mutations of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy in China.
    Qin W; Ren Z; Xia M; Yang M; Shi Y; Huang Y; Guo X; Zhang J
    Med Sci Monit Basic Res; 2019 Sep; 25():199-209. PubMed ID: 31554780
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain.
    Monet-Leprêtre M; Bardot B; Lemaire B; Domenga V; Godin O; Dichgans M; Tournier-Lasserve E; Cohen-Tannoudji M; Chabriat H; Joutel A
    Brain; 2009 Jun; 132(Pt 6):1601-12. PubMed ID: 19293235
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.