BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

239 related articles for article (PubMed ID: 23963851)

  • 1. A novel mutation of the high-temperature requirement A serine peptidase 1 (HTRA1) gene in a Chinese family with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL).
    Chen Y; He Z; Meng S; Li L; Yang H; Zhang X
    J Int Med Res; 2013 Oct; 41(5):1445-55. PubMed ID: 23963851
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL.
    Nozaki H; Kato T; Nihonmatsu M; Saito Y; Mizuta I; Noda T; Koike R; Miyazaki K; Kaito M; Ito S; Makino M; Koyama A; Shiga A; Uemura M; Sekine Y; Murakami A; Moritani S; Hara K; Yokoseki A; Kuwano R; Endo N; Momotsu T; Yoshida M; Nishizawa M; Mizuno T; Onodera O
    Neurology; 2016 May; 86(21):1964-74. PubMed ID: 27164673
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Establishment and identification of a novel HTRA1 mutation mice model.
    Li C; Jin W; Wang X; Li T; Wang M; Cao B
    Rev Cardiovasc Med; 2019 Sep; 20(3):179-186. PubMed ID: 31601092
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population.
    Cai B; Zeng J; Lin Y; Lin Y; Lin W; Lin W; Li Z; Wang N
    Neurol Sci; 2015 Aug; 36(8):1387-91. PubMed ID: 25772074
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Heterozygous HTRA1 mutations with mimicking symptoms of CARASIL in two families.
    Kono Y; Nishioka K; Li Y; Komatuzaki Y; Ito Y; Yoshino H; Tanaka R; Iguchi Y; Hattori N
    Clin Neurol Neurosurg; 2018 Sep; 172():174-176. PubMed ID: 30031255
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mutation in the HTRA1 gene identified in Chinese CARASIL pedigree.
    Wang XL; Li CF; Guo HW; Cao BZ
    CNS Neurosci Ther; 2012 Oct; 18(10):867-9. PubMed ID: 22900900
    [No Abstract]   [Full Text] [Related]  

  • 7. A CARASIL Patient from Americas with Novel Mutation and Atypical Features: Case Presentation and Literature Review.
    Ibrahimi M; Nozaki H; Lee A; Onodera O; Reichwein R; Wicklund M; El-Ghanem M
    Cerebrovasc Dis; 2017; 44(3-4):135-140. PubMed ID: 28628911
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Chinese CARASIL Patient Caused by Novel Compound Heterozygous Mutations in HTRA1.
    Xie F; Zhang LS
    J Stroke Cerebrovasc Dis; 2018 Oct; 27(10):2840-2842. PubMed ID: 30068478
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetically Confirmed CARASIL: Case Report with Novel HTRA1 Mutation and Literature Review.
    Yu Z; Cao S; Wu A; Yue H; Zhang C; Wang J; Xia M; Wu J
    World Neurosurg; 2020 Nov; 143():121-128. PubMed ID: 32445900
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A Case of Leukoencephalopathy and Small Vessels Disease Caused by a Novel HTRA1 Homozygous Mutation.
    Gündüz T; Demirkol Y; Doğan Ö; Demir S; Akçakaya NH
    J Stroke Cerebrovasc Dis; 2019 Nov; 28(11):104354. PubMed ID: 31494012
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CARASIL)].
    Uemura M; Nozaki H; Onodera O
    Brain Nerve; 2017 Jan; 69(1):25-33. PubMed ID: 28126975
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cerebral small vessel disease-related protease HtrA1 processes latent TGF-β binding protein 1 and facilitates TGF-β signaling.
    Beaufort N; Scharrer E; Kremmer E; Lux V; Ehrmann M; Huber R; Houlden H; Werring D; Haffner C; Dichgans M
    Proc Natl Acad Sci U S A; 2014 Nov; 111(46):16496-501. PubMed ID: 25369932
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation in the HTRA1 gene in a patient with degenerated spine as a component of CARASIL syndrome.
    Bayrakli F; Balaban H; Gurelik M; Hizmetli S; Topaktas S
    Turk Neurosurg; 2014; 24(1):67-9. PubMed ID: 24535794
    [TBL] [Abstract][Full Text] [Related]  

  • 14. One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family.
    Bekircan-Kurt CE; Çetinkaya A; Gocmen R; Koşukcu C; Soylemezoglu F; Arsava EM; Tuncer A; Erdem-Ozdamar S; Akarsu NA; Topcuoglu MA
    J Stroke Cerebrovasc Dis; 2021 Sep; 30(9):105997. PubMed ID: 34303089
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): A challenging diagnosis and a rare multiple sclerosis mimic.
    Shirah B; Algahtani H; Algahtani R; Alfares A; Hassan A
    J Stroke Cerebrovasc Dis; 2023 Aug; 32(8):107225. PubMed ID: 37348440
    [TBL] [Abstract][Full Text] [Related]  

  • 16. HTRA1-related autosomal dominant cerebral small vessel disease.
    Liu JY; Zhu YC; Zhou LX; Wei YP; Mao CH; Cui LY; Peng B; Yao M
    Chin Med J (Engl); 2020 Oct; 134(2):178-184. PubMed ID: 33109952
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.
    Hara K; Shiga A; Fukutake T; Nozaki H; Miyashita A; Yokoseki A; Kawata H; Koyama A; Arima K; Takahashi T; Ikeda M; Shiota H; Tamura M; Shimoe Y; Hirayama M; Arisato T; Yanagawa S; Tanaka A; Nakano I; Ikeda S; Yoshida Y; Yamamoto T; Ikeuchi T; Kuwano R; Nishizawa M; Tsuji S; Onodera O
    N Engl J Med; 2009 Apr; 360(17):1729-39. PubMed ID: 19387015
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel HTRA1 exon 2 mutation causes loss of protease activity in a Pakistani CARASIL patient.
    Khaleeli Z; Jaunmuktane Z; Beaufort N; Houlden H; Haffner C; Brandner S; Dichgans M; Werring D
    J Neurol; 2015 May; 262(5):1369-72. PubMed ID: 25957642
    [No Abstract]   [Full Text] [Related]  

  • 19. A novel heterozygous HTRA1 mutation in an Asian family with CADASIL-like disease.
    Cao H; Liu J; Tian W; Ji X; Wang Q; Luan S; Dong X; Dong H
    J Clin Lab Anal; 2022 Feb; 36(2):e24174. PubMed ID: 34951056
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel c.971A>G mutation in the HTRA1 gene in a Chinese family with CARASIL.
    Hou MM; Mao XW; Liu XB; Liu YQ; Bi XY; Hou XJ
    J Biol Regul Homeost Agents; 2020; 34(4):1407-1410. PubMed ID: 32895092
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.