BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 30342765)

  • 21. Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2.
    Wang C; Xu Y; Feng X; Ma J; Xie S; Zhang Y; Tang BS; Chan P
    Neurobiol Aging; 2015 Jan; 36(1):545.e1-7. PubMed ID: 25189117
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Periodic alternating nystagmus and rebound nystagmus in spinocerebellar ataxia type 6.
    Hashimoto T; Sasaki O; Yoshida K; Takei Y; Ikeda S
    Mov Disord; 2003 Oct; 18(10):1201-4. PubMed ID: 14534930
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Toxicity of pathogenic ataxin-2 in Drosophila shows dependence on a pure CAG repeat sequence.
    McGurk L; Rifai OM; Shcherbakova O; Perlegos AE; Byrns CN; Carranza FR; Zhou HW; Kim HJ; Zhu Y; Bonini NM
    Hum Mol Genet; 2021 Sep; 30(19):1797-1810. PubMed ID: 34077532
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Motor neurone disease/amyotrophic lateral sclerosis associated with intermediate-length CAG repeat expansions in Ataxin-2 does not have 1C2-positive polyglutamine inclusions.
    Highley JR; Lorente Pons A; Cooper-Knock J; Wharton SB; Ince PG; Shaw PJ; Wood J; Kirby J
    Neuropathol Appl Neurobiol; 2016 Jun; 42(4):377-89. PubMed ID: 26095883
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India.
    Basu P; Chattopadhyay B; Gangopadhaya PK; Mukherjee SC; Sinha KK; Das SK; Roychoudhury S; Majumder PP; Bhattacharyya NP
    Hum Genet; 2000 Jun; 106(6):597-604. PubMed ID: 10942107
    [TBL] [Abstract][Full Text] [Related]  

  • 26. FTLD-ALS of TDP-43 type and SCA2 in a family with a full ataxin-2 polyglutamine expansion.
    Bäumer D; East SZ; Tseu B; Zeman A; Hilton D; Talbot K; Ansorge O
    Acta Neuropathol; 2014 Oct; 128(4):597-604. PubMed ID: 24718895
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Sequencing analysis of the SCA6 CAG expansion excludes an influence of repeat interruptions on disease onset.
    Wiethoff S; O'Connor E; Haridy NA; Nethisinghe S; Wood N; Giunti P; Bettencourt C; Houlden H
    J Neurol Neurosurg Psychiatry; 2018 Nov; 89(11):1226-1227. PubMed ID: 29367260
    [No Abstract]   [Full Text] [Related]  

  • 28. Increased expression of alpha 1A Ca2+ channel currents arising from expanded trinucleotide repeats in spinocerebellar ataxia type 6.
    Piedras-Renteria ES; Watase K; Harata N; Zhuchenko O; Zoghbi HY; Lee CC; Tsien RW
    J Neurosci; 2001 Dec; 21(23):9185-93. PubMed ID: 11717352
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A case of amyotrophic lateral sclerosis with intermediate ATXN-1 CAG repeat expansion in a large family with spinocerebellar ataxia type 1.
    Spataro R; La Bella V
    J Neurol; 2014 Jul; 261(7):1442-3. PubMed ID: 24916831
    [No Abstract]   [Full Text] [Related]  

  • 30. Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders.
    Lattante S; Millecamps S; Stevanin G; Rivaud-Péchoux S; Moigneu C; Camuzat A; Da Barroca S; Mundwiller E; Couarch P; Salachas F; Hannequin D; Meininger V; Pasquier F; Seilhean D; Couratier P; Danel-Brunaud V; Bonnet AM; Tranchant C; LeGuern E; Brice A; Le Ber I; Kabashi E;
    Neurology; 2014 Sep; 83(11):990-5. PubMed ID: 25098532
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p.
    Jodice C; Mantuano E; Veneziano L; Trettel F; Sabbadini G; Calandriello L; Francia A; Spadaro M; Pierelli F; Salvi F; Ophoff RA; Frants RR; Frontali M
    Hum Mol Genet; 1997 Oct; 6(11):1973-8. PubMed ID: 9302278
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Intermediate-length CAG repeat in ATXN2 is associated with increased risk for amyotrophic lateral sclerosis in Brazilian patients.
    Tavares de Andrade HM; Cintra VP; de Albuquerque M; Piccinin CC; Bonadia LC; Duarte Couteiro RE; Sabino de Oliveira D; Claudino R; Magno Gonçalves MV; Dourado MET; de Souza LC; Teixeira AL; de Godoy Rousseff Prado L; Tumas V; Bulle Oliveira AS; Nucci A; Lopes-Cendes I; Marques W; França MC
    Neurobiol Aging; 2018 Sep; 69():292.e15-292.e18. PubMed ID: 29934271
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Association of ATXN2 intermediate-length CAG repeats with amyotrophic lateral sclerosis correlates with the distributions of normal CAG repeat alleles among individual ethnic populations.
    Naruse H; Matsukawa T; Ishiura H; Mitsui J; Takahashi Y; Takano H; Goto J; Toda T; Tsuji S
    Neurogenetics; 2019 May; 20(2):65-71. PubMed ID: 30847648
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Spinocerebellar ataxia type 6: channelopathy or glutamine repeat disorder?
    Frontali M
    Brain Res Bull; 2001 Oct-Nov 1; 56(3-4):227-31. PubMed ID: 11719255
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene.
    Tonelli A; D'Angelo MG; Salati R; Villa L; Germinasi C; Frattini T; Meola G; Turconi AC; Bresolin N; Bassi MT
    J Neurol Sci; 2006 Feb; 241(1-2):13-7. PubMed ID: 16325861
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The SCA12 mutation as a rare cause of spinocerebellar ataxia.
    Cholfin JA; Sobrido MJ; Perlman S; Pulst SM; Geschwind DH
    Arch Neurol; 2001 Nov; 58(11):1833-5. PubMed ID: 11708992
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [SCA6: From gene identification to recent progress on pathogenesis].
    Watase K; Ishikawa K; Mizusawa H
    Rinsho Shinkeigaku; 2010 Nov; 50(11):858-60. PubMed ID: 21921472
    [TBL] [Abstract][Full Text] [Related]  

  • 39. CAG repeat length in androgen receptor gene is not associated with amyotrophic lateral sclerosis.
    Bruson A; Sambataro F; Querin G; D'Ascenzo C; Palmieri A; Agostini J; Gaiani A; Angelini C; Galbiati M; Poletti A; Pennuto M; Pegoraro E; Clementi M; Soraru G
    Eur J Neurol; 2012 Oct; 19(10):1373-5. PubMed ID: 22233359
    [TBL] [Abstract][Full Text] [Related]  

  • 40. DnaJ-1 and karyopherin α3 suppress degeneration in a new Drosophila model of Spinocerebellar Ataxia Type 6.
    Tsou WL; Hosking RR; Burr AA; Sutton JR; Ouyang M; Du X; Gomez CM; Todi SV
    Hum Mol Genet; 2015 Aug; 24(15):4385-96. PubMed ID: 25954029
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.