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 *

212 related articles for article (PubMed ID: 34303089)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. CARASIL families from India with 3 novel null mutations in the
    Preethish-Kumar V; Nozaki H; Tiwari S; Vengalil S; Bhat M; Prasad C; Onodera O; Uemura M; Doniparthi S; Saini J; Nashi S; Polavarapu K; Nalini A
    Neurology; 2017 Dec; 89(23):2392-2394. PubMed ID: 29101275
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. Report of two pedigrees with heterozygous HTRA1 variants-related cerebral small vessel disease and literature review.
    Zhou H; Jiao B; Ouyang Z; Wu Q; Shen L; Fang L
    Mol Genet Genomic Med; 2022 Oct; 10(10):e2032. PubMed ID: 35946346
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Shifting the CARASIL paradigm: report of a non-Asian family and literature review.
    Menezes Cordeiro I; Nzwalo H; Sá F; Ferreira RB; Alonso I; Afonso L; Basílio C
    Stroke; 2015 Apr; 46(4):1110-2. PubMed ID: 25712943
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. HTRA1 expression profile and activity on TGF-β signaling in HTRA1 mutation carriers.
    Fasano A; Formichi P; Taglia I; Bianchi S; Di Donato I; Battisti C; Federico A; Dotti MT
    J Cell Physiol; 2020 Oct; 235(10):7120-7127. PubMed ID: 32017060
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Clinical manifestations and neuroradiological findings of CARASIL with a novel mutation].
    Shibata M
    Rinsho Shinkeigaku; 2012; 52(11):1363-4. PubMed ID: 23196619
    [TBL] [Abstract][Full Text] [Related]  

  • 18. CADASIL and CARASIL.
    Tikka S; Baumann M; Siitonen M; Pasanen P; Pöyhönen M; Myllykangas L; Viitanen M; Fukutake T; Cognat E; Joutel A; Kalimo H
    Brain Pathol; 2014 Sep; 24(5):525-44. PubMed ID: 25323668
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genotype-phenotype correlations of heterozygous HTRA1-related cerebral small vessel disease: case report and systematic review.
    Zhang H; Qin X; Shi Y; Gao X; Wang F; Wang H; Shang J; Zhao J; Zhang J; Shao F
    Neurogenetics; 2021 Jul; 22(3):187-194. PubMed ID: 33963955
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.