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 *

130 related articles for article (PubMed ID: 35510647)

  • 1. CAG Somatic Instability in a Huntington Disease Expansion Carrier Presenting with a Progressive Supranuclear Palsy-like Phenotype.
    Dewan R; Jaunmuktane Z; Garcia-Segura ME; Strand C; Wild E; Villar J; Dalgard CL; Tabrizi SJ; Traynor BJ; Proukakis C
    Mov Disord; 2022 Jul; 37(7):1555-1557. PubMed ID: 35510647
    [No Abstract]   [Full Text] [Related]  

  • 2. Loss of TDP-43 promotes somatic CAG repeat expansion in Huntington's disease knock-in mice.
    Bai D; Zhu L; Jia Q; Duan X; Chen L; Wang X; Hou J; Jiang G; Yang S; Li S; Li XJ; Yin P
    Prog Neurobiol; 2023 Aug; 227():102484. PubMed ID: 37315918
    [TBL] [Abstract][Full Text] [Related]  

  • 3. MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice.
    Tomé S; Manley K; Simard JP; Clark GW; Slean MM; Swami M; Shelbourne PF; Tillier ER; Monckton DG; Messer A; Pearson CE
    PLoS Genet; 2013; 9(2):e1003280. PubMed ID: 23468640
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Patterns of CAG repeat instability in the central nervous system and periphery in Huntington's disease and in spinocerebellar ataxia type 1.
    Mouro Pinto R; Arning L; Giordano JV; Razghandi P; Andrew MA; Gillis T; Correia K; Mysore JS; Grote Urtubey DM; Parwez CR; von Hein SM; Clark HB; Nguyen HP; Förster E; Beller A; Jayadaev S; Keene CD; Bird TD; Lucente D; Vonsattel JP; Orr H; Saft C; Petrasch-Parwez E; Wheeler VC
    Hum Mol Genet; 2020 Aug; 29(15):2551-2567. PubMed ID: 32761094
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Stoichiometry of base excision repair proteins correlates with increased somatic CAG instability in striatum over cerebellum in Huntington's disease transgenic mice.
    Goula AV; Berquist BR; Wilson DM; Wheeler VC; Trottier Y; Merienne K
    PLoS Genet; 2009 Dec; 5(12):e1000749. PubMed ID: 19997493
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Msh2 acts in medium-spiny striatal neurons as an enhancer of CAG instability and mutant huntingtin phenotypes in Huntington's disease knock-in mice.
    Kovalenko M; Dragileva E; St Claire J; Gillis T; Guide JR; New J; Dong H; Kucherlapati R; Kucherlapati MH; Ehrlich ME; Lee JM; Wheeler VC
    PLoS One; 2012; 7(9):e44273. PubMed ID: 22970194
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington's disease knock-in mice is blocked by Mlh1 knock-out.
    Loupe JM; Pinto RM; Kim KH; Gillis T; Mysore JS; Andrew MA; Kovalenko M; Murtha R; Seong I; Gusella JF; Kwak S; Howland D; Lee R; Lee JM; Wheeler VC; MacDonald ME
    Hum Mol Genet; 2020 Nov; 29(18):3044-3053. PubMed ID: 32876667
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches.
    Pinto RM; Dragileva E; Kirby A; Lloret A; Lopez E; St Claire J; Panigrahi GB; Hou C; Holloway K; Gillis T; Guide JR; Cohen PE; Li GM; Pearson CE; Daly MJ; Wheeler VC
    PLoS Genet; 2013 Oct; 9(10):e1003930. PubMed ID: 24204323
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Progressive Polyglutamine Repeat Expansion in Peripheral Blood Cells and Sperm of Transgenic Huntington's Disease Monkeys.
    Clever F; Cho IK; Yang J; Chan AWS
    J Huntingtons Dis; 2019; 8(4):443-448. PubMed ID: 31561381
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Age-dependent and tissue-specific CAG repeat instability occurs in mouse knock-in for a mutant Huntington's disease gene.
    Ishiguro H; Yamada K; Sawada H; Nishii K; Ichino N; Sawada M; Kurosawa Y; Matsushita N; Kobayashi K; Goto J; Hashida H; Masuda N; Kanazawa I; Nagatsu T
    J Neurosci Res; 2001 Aug; 65(4):289-97. PubMed ID: 11494364
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Modifiers of Somatic Repeat Instability in Mouse Models of Friedreich Ataxia and the Fragile X-Related Disorders: Implications for the Mechanism of Somatic Expansion in Huntington's Disease.
    Zhao X; Kumari D; Miller CJ; Kim GY; Hayward B; Vitalo AG; Pinto RM; Usdin K
    J Huntingtons Dis; 2021; 10(1):149-163. PubMed ID: 33579860
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transcription elongation and tissue-specific somatic CAG instability.
    Goula AV; Stys A; Chan JP; Trottier Y; Festenstein R; Merienne K
    PLoS Genet; 2012; 8(11):e1003051. PubMed ID: 23209427
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetics of Huntington disease.
    Nance MA
    Handb Clin Neurol; 2017; 144():3-14. PubMed ID: 28947123
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Reply to: "Reply to Late onset Huntington's disease with 29 CAG repeat expansion" JNS-D-16-00732.
    Garcia-Ruiz PJ; Garcia-Caldentey J; Herranz A; Del Val J; Feliz C; Martínez-Castrillo JC
    J Neurol Sci; 2016 Oct; 369():390. PubMed ID: 27431298
    [No Abstract]   [Full Text] [Related]  

  • 15. Reply: Late onset Huntington's disease with 29 CAG repeat expansion.
    Oosterloo M; Van Belzen MJ; Bijlsma EK; Roos RA
    J Neurol Sci; 2016 Sep; 368():343. PubMed ID: 27538661
    [No Abstract]   [Full Text] [Related]  

  • 16. Late onset Huntington's disease with 29 CAG repeat expansion.
    Garcia-Ruiz PJ; Garcia-Caldentey J; Feliz C; del Val J; Herranz A; Martínez-Castrillo JC
    J Neurol Sci; 2016 Apr; 363():114-5. PubMed ID: 27000233
    [No Abstract]   [Full Text] [Related]  

  • 17. DNA Mismatch Repair and its Role in Huntington's Disease.
    Iyer RR; Pluciennik A
    J Huntingtons Dis; 2021; 10(1):75-94. PubMed ID: 33579865
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comparison of Huntington's disease CAG Repeat Length Stability in Human Motor Cortex and Cingulate Gyrus.
    Geraerts FC; Snell RG; Faull RL; Williams L; Jacobsen JC; Reid SJ
    J Huntingtons Dis; 2016 Oct; 5(3):297-301. PubMed ID: 27716680
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Investigations of Huntington's Disease and Huntington's Disease-Like Syndromes in Indian Choreatic Patients.
    Kaur J; Parveen S; Shamim U; Sharma P; Suroliya V; Sonkar AK; Ahmad I; Garg J; Anand KS; Laskar S; Chowdhury D; Kushwaha S; Goyal V; Srivastava AK; Singh G; Faruq M
    J Huntingtons Dis; 2020; 9(3):283-289. PubMed ID: 32675418
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neil1 is a genetic modifier of somatic and germline CAG trinucleotide repeat instability in R6/1 mice.
    Møllersen L; Rowe AD; Illuzzi JL; Hildrestrand GA; Gerhold KJ; Tveterås L; Bjølgerud A; Wilson DM; Bjørås M; Klungland A
    Hum Mol Genet; 2012 Nov; 21(22):4939-47. PubMed ID: 22914735
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.