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 *

154 related articles for article (PubMed ID: 27106293)

  • 1. Genetic fitness and selection intensity in a population affected with high-incidence spinocerebellar ataxia type 1.
    Platonov FA; Tyryshkin K; Tikhonov DG; Neustroyeva TS; Sivtseva TM; Yakovleva NV; Nikolaev VP; Sidorova OG; Kononova SK; Goldfarb LG; Renwick NM
    Neurogenetics; 2016 Jul; 17(3):179-85. PubMed ID: 27106293
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
    Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J
    Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 families.
    Zhou YX; Qiao WH; Gu WH; Xie H; Tang BS; Zhou LS; Yang BX; Takiyama Y; Tsuji S; He HY; Deng CX; Goldfarb LG; Wang GX
    Arch Neurol; 2001 May; 58(5):789-94. PubMed ID: 11346374
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
    Brusco A; Gellera C; Cagnoli C; Saluto A; Castucci A; Michielotto C; Fetoni V; Mariotti C; Migone N; Di Donato S; Taroni F
    Arch Neurol; 2004 May; 61(5):727-33. PubMed ID: 15148151
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
    Pujana MA; Corral J; Gratacòs M; Combarros O; Berciano J; Genís D; Banchs I; Estivill X; Volpini V
    Hum Genet; 1999 Jun; 104(6):516-22. PubMed ID: 10453742
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Distribution of the CAG Triplet Repeat in ATXN1, ATXN3, and CACNA1A Loci in Peruvian Population.
    Gonzales-Sáenz C; Cruz-Rodriguez C; Espinoza-Huertas K; Véliz-Otani D; Marca V; Ortega O; Milla-Neyra K; Alvarez-Tejada J; Mazzetti P; Cornejo-Olivas M
    Cerebellum; 2020 Aug; 19(4):527-535. PubMed ID: 32285347
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Generation of induced pluripotent stem cell(iPSC)line CJUHi001-A derived peripheral blood mononuclear cells of spinocerebellar ataxia type 1(SCA1) the CAG repeat mutation in ATXN1 gene.
    Jin Y; Nan G
    Stem Cell Res; 2023 Feb; 66():102975. PubMed ID: 36459834
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Simulation of the distribution of spinocerebellar ataxia type 1 in Yakut populations: model parameters and results of simulation].
    Koneva LA; Konev AV; Kucher AN
    Genetika; 2010 Jul; 46(7):990-9. PubMed ID: 20795504
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CAT Interruption as a Protective Factor in Chinese Patients with Spinocerebellar Ataxia Type 1.
    Shao YR; Yu JY; Ma Y; Dong Y; Wu ZY
    Cerebellum; 2024 Jun; 23(3):1211-1214. PubMed ID: 37491649
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic characterization of Spinocerebellar ataxia 1 in a South Indian cohort.
    Kumaran D; Balagopal K; Tharmaraj RG; Aaron S; George K; Muliyil J; Sivadasan A; Danda S; Alexander M; Hasan G
    BMC Med Genet; 2014 Oct; 15():114. PubMed ID: 25344417
    [TBL] [Abstract][Full Text] [Related]  

  • 11. (CAG)
    Wang P; Chen Z; Peng Y; Cao L; Li X; Wang C; Yang H; Peng H; Shi Y; Zhou X; Li T; Feng L; Wu C; Qiu R; Xia K; Tang B; Jiang H
    Eur J Neurol; 2019 Aug; 26(8):1130-1136. PubMed ID: 30891880
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Therapeutic Strategies for Spinocerebellar Ataxia Type 1.
    Kerkhof LMC; van de Warrenburg BPC; van Roon-Mom WMC; Buijsen RAM
    Biomolecules; 2023 May; 13(5):. PubMed ID: 37238658
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detection Methods and Status of CAT Interruption of
    Jang JH; Yoon SJ; Kim SK; Cho JW; Kim JW
    Ann Lab Med; 2022 Mar; 42(2):274-277. PubMed ID: 34635619
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].
    Tang B; Wang D; Xia J
    Zhonghua Yi Xue Za Zhi; 1997 Nov; 77(11):819-22. PubMed ID: 9772474
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ataxin-1 regulates the cerebellar bioenergetics proteome through the GSK3β-mTOR pathway which is altered in Spinocerebellar ataxia type 1 (SCA1).
    Sánchez I; Balagué E; Matilla-Dueñas A
    Hum Mol Genet; 2016 Sep; 25(18):4021-4040. PubMed ID: 27466200
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Frequency and distribution of polyQ disease intermediate-length repeat alleles in healthy Italian population.
    Mongelli A; Magri S; Salvatore E; Rizzo E; De Rosa A; Fico T; Gatti M; Gellera C; Taroni F; Mariotti C; Nanetti L
    Neurol Sci; 2020 Jun; 41(6):1475-1482. PubMed ID: 31940111
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spinocerebellar ataxias types 1, 2 and 3: age adjusted clinical severity of disease at presentation correlates with size of CAG repeat lengths.
    Netravathi M; Pal PK; Purushottam M; Thennarasu K; Mukherjee M; Jain S
    J Neurol Sci; 2009 Feb; 277(1-2):83-6. PubMed ID: 19049837
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Selective Forces Related to Spinocerebellar Ataxia Type 2.
    Sena LS; Castilhos RM; Mattos EP; Furtado GV; Pedroso JL; Barsottini O; de Amorim MMP; Godeiro C; Pereira MLS; Jardim LB
    Cerebellum; 2019 Apr; 18(2):188-194. PubMed ID: 30219976
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.
    Jacobi H; du Montcel ST; Bauer P; Giunti P; Cook A; Labrum R; Parkinson MH; Durr A; Brice A; Charles P; Marelli C; Mariotti C; Nanetti L; Panzeri M; Rakowicz M; Sulek A; Sobanska A; Schmitz-Hübsch T; Schöls L; Hengel H; Baliko L; Melegh B; Filla A; Antenora A; Infante J; Berciano J; van de Warrenburg BP; Timmann D; Szymanski S; Boesch S; Kang JS; Pandolfo M; Schulz JB; Molho S; Diallo A; Klockgether T
    Lancet Neurol; 2015 Nov; 14(11):1101-8. PubMed ID: 26377379
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Insights into the mutational history and prevalence of SCA1 in the Indian population through anchored polymorphisms.
    Mittal U; Sharma S; Chopra R; Dheeraj K; Pal PK; Srivastava AK; Mukerji M
    Hum Genet; 2005 Oct; 118(1):107-14. PubMed ID: 16133185
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.