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 *

186 related articles for article (PubMed ID: 19043263)

  • 1. Two Japanese CADASIL families exhibiting Notch3 mutation R75P not involving cysteine residue.
    Mizuno T; Muranishi M; Torugun T; Tango H; Nagakane Y; Kudeken T; Kawase Y; Kawabe K; Oshima F; Yaoi T; Itoh K; Fushiki S; Nakagawa M
    Intern Med; 2008; 47(23):2067-72. PubMed ID: 19043263
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A novel cysteine-sparing G73A mutation of NOTCH3 in a Chinese CADASIL family.
    Huang L; Li W; Li Y; Song C; Wang P; Wang H; Sun X
    Neurogenetics; 2020 Jan; 21(1):39-49. PubMed ID: 31720972
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Pro-Hemorrhagic Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Associated with NOTCH3 p.R75P Mutation with Low Vascular NOTCH3 Aggregation Property.
    Ishiyama H; Kim H; Saito S; Takeda S; Takegami M; Yamamoto Y; Abe S; Nakazawa S; Tanaka T; Washida K; Morita Y; Oh ST; Jung HJ; Choi JC; Nakaoku Y; Nakahara J; Koga M; Toyoda K; Amemiya K; Ikeda Y; Hatakeyama K; Mizuta I; Mizuno T; Kim KK; Ihara M
    Ann Neurol; 2024 Jun; 95(6):1040-1054. PubMed ID: 38520151
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The R110C mutation in Notch3 causes variable clinical features in two Turkish families with CADASIL syndrome.
    Uyguner ZO; Siva A; Kayserili H; Saip S; Altintaş A; Apak MY; Albayram S; Işik N; Akman-Demir G; Taşyürekli M; Oz B; Wollnik B
    J Neurol Sci; 2006 Jul; 246(1-2):123-30. PubMed ID: 16730748
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family.
    Pavlovic AM; Dobricic V; Semnic R; Lackovic V; Novakovic I; Bajcetic M; Sternic N
    Acta Neurol Belg; 2013 Sep; 113(3):299-302. PubMed ID: 23319290
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A novel cysteine-sparing NOTCH3 mutation in a Chinese family with CADASIL.
    Ge W; Kuang H; Wei B; Bo L; Xu Z; Xu X; Geng D; Sun M
    PLoS One; 2014; 9(8):e104533. PubMed ID: 25098330
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Therapeutic NOTCH3 cysteine correction in CADASIL using exon skipping: in vitro proof of concept.
    Rutten JW; Dauwerse HG; Peters DJ; Goldfarb A; Venselaar H; Haffner C; van Ommen GJ; Aartsma-Rus AM; Lesnik Oberstein SA
    Brain; 2016 Apr; 139(Pt 4):1123-35. PubMed ID: 26912635
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients.
    Pantoni L; Pescini F; Nannucci S; Sarti C; Bianchi S; Dotti MT; Federico A; Inzitari D
    Neurology; 2010 Jan; 74(1):57-63. PubMed ID: 20038773
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. First report of a pathogenic mutation on exon 24 of the NOTCH3 gene in a CADASIL family.
    Valenti R; Bianchi S; Pescini F; D'Eramo C; Inzitari D; Dotti MT; Pantoni L
    J Neurol; 2011 Sep; 258(9):1632-6. PubMed ID: 21409506
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CADASIL with a novel mutation in exon 7 of NOTCH3 (C388Y).
    Ishida C; Sakajiri K; Yoshita M; Joutel A; Cave-Riant F; Yamada M
    Intern Med; 2006; 45(16):981-5. PubMed ID: 16974063
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.