BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 17879446)

  • 1. Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).
    Ferreira S; Silva RS; Oliveira JP
    Hum Genet; 2007 Jun; 121(5):649. PubMed ID: 17879446
    [No Abstract]   [Full Text] [Related]  

  • 2. Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).
    Ferreira S; Fontoura P; Guerreiro R; Oliveira JP
    Hum Genet; 2007 Jun; 121(5):649-50. PubMed ID: 17879447
    [No Abstract]   [Full Text] [Related]  

  • 3. Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).
    Ferreira S; Costa C; Oliveira JP
    Hum Genet; 2007 Jun; 121(5):649. PubMed ID: 17879445
    [No Abstract]   [Full Text] [Related]  

  • 4. Archetypal Arg169Cys mutation in NOTCH3 does not drive the pathogenesis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy via a loss-of-function mechanism.
    Cognat E; Baron-Menguy C; Domenga-Denier V; Cleophax S; Fouillade C; Monet-Leprêtre M; Dewerchin M; Joutel A
    Stroke; 2014 Mar; 45(3):842-9. PubMed ID: 24425116
    [TBL] [Abstract][Full Text] [Related]  

  • 5. New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).
    Abramycheva N; Stepanova M; Kalashnikova L; Zakharova M; Maximova M; Tanashyan M; Lagoda O; Fedotova E; Klyushnikov S; Konovalov R; Sakharova A; Illarioshkin S
    J Neurol Sci; 2015 Feb; 349(1-2):196-201. PubMed ID: 25623805
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel Notch3 deletion mutation in a Chinese patient with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).
    Weiming F; Yuliang W; Youjie L; Xinsheng L; Shuyang X; Zhaoxia L
    J Clin Neurosci; 2013 Feb; 20(2):322-3. PubMed ID: 23151434
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new de novo Notch3 mutation causing CADASIL.
    Coto E; Menéndez M; Navarro R; García-Castro M; Alvarez V
    Eur J Neurol; 2006 Jun; 13(6):628-31. PubMed ID: 16796587
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Two novel mutations of the NOTCH3 gene in Korean patients with CADASIL.
    Kim Y; Kim JS; Kim G; No YJ; Yoo HW
    Mutat Res; 2006 Jan; 593(1-2):116-20. PubMed ID: 16256149
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [CADASIL and CARASIL].
    López JI; Vilanova JR
    Neurologia; 2009 Mar; 24(2):125-30. PubMed ID: 19322691
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Study of the familiar form of vascular dementia (CADASIL)].
    Takahashi K; Yoshizaki K
    Nihon Shinkei Seishin Yakurigaku Zasshi; 2007 Jun; 27(3):141-5. PubMed ID: 17633526
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo mutation in the NOTCH3 gene causing CADASIL.
    Stojanov D; Grozdanović D; Petrović S; Benedeto-Stojanov D; Stefanović I; Stojanović N; Ilić DN
    Bosn J Basic Med Sci; 2014 Feb; 14(1):48-50. PubMed ID: 24579972
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Identification of a novel NOTCH3 mutation in a family featuring cerebral autosomal dominant arteriopathy with subcortical infarct and leucoencephalopathy].
    Zhu Y; Wang J; Wu Y; Wang G; Hu B; Xu A
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):578-81. PubMed ID: 25297585
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): a patient from Sri Lanka.
    De Silva KR; Gamage R; Dunuwille J; Gunarathna D; Sirisena D; Weerasinghe A; Amarasinghe PH; Hosomi A; Mizuno T
    J Clin Neurosci; 2009 Nov; 16(11):1492-3. PubMed ID: 19683925
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysis.
    Milunsky A; Konialis C; Shim SH; Maher TA; Spengos K; Ito M; Pangalos C
    Prenat Diagn; 2005 Nov; 25(11):1057-8. PubMed ID: 16302168
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A case report about CADASlL: mutation in the NOTCH 3 receptor.
    Delibas S; Guven H; Comoglu SS
    Acta Neurol Taiwan; 2009 Dec; 18(4):262-6. PubMed ID: 20329594
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [CADASIL syndrome - cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
    Dziewulska D; Kwieciński H
    Neurol Neurochir Pol; 2008; 42(2):123-30. PubMed ID: 18512169
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Cappelli A; Ragno M; Cacchiò G; Scarcella M; Staffolani P; Pianese L
    Neurosci Lett; 2009 Sep; 462(2):176-8. PubMed ID: 19576955
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Notch3 Arg170Cys knock-in mice display pathologic and clinical features of the neurovascular disorder cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Wallays G; Nuyens D; Silasi-Mansat R; Souffreau J; Callaerts-Vegh Z; Van Nuffelen A; Moons L; D'Hooge R; Lupu F; Carmeliet P; Collen D; Dewerchin M
    Arterioscler Thromb Vasc Biol; 2011 Dec; 31(12):2881-8. PubMed ID: 21940951
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.