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 *

180 related articles for article (PubMed ID: 28229454)

  • 1. Analysis of a fully penetrant spinocerebellar ataxia type 8 Brazilian family.
    Cintra VP; Lourenço CM; Rocha MMV; Tomaselli PJ; Marques W
    Acta Neurol Scand; 2017 Nov; 136(5):541-545. PubMed ID: 28229454
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.
    Ikeda Y; Dalton JC; Moseley ML; Gardner KL; Bird TD; Ashizawa T; Seltzer WK; Pandolfo M; Milunsky A; Potter NT; Shoji M; Vincent JB; Day JW; Ranum LP
    Am J Hum Genet; 2004 Jul; 75(1):3-16. PubMed ID: 15152344
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Bidirectional expression of the SCA8 expansion mutation: one mutation, two genes.
    Ikeda Y; Daughters RS; Ranum LP
    Cerebellum; 2008; 7(2):150-8. PubMed ID: 18418692
    [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. SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance.
    Moseley ML; Schut LJ; Bird TD; Koob MD; Day JW; Ranum LP
    Hum Mol Genet; 2000 Sep; 9(14):2125-30. PubMed ID: 10958651
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy.
    Cellini E; Nacmias B; Forleo P; Piacentini S; Guarnieri BM; Serio A; Calabrò A; Renzi D; Sorbi S
    Arch Neurol; 2001 Nov; 58(11):1856-9. PubMed ID: 11708995
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.
    Silveira I; Miranda C; Guimarães L; Moreira MC; Alonso I; Mendonça P; Ferro A; Pinto-Basto J; Coelho J; Ferreirinha F; Poirier J; Parreira E; Vale J; Januário C; Barbot C; Tuna A; Barros J; Koide R; Tsuji S; Holmes SE; Margolis RL; Jardim L; Pandolfo M; Coutinho P; Sequeiros J
    Arch Neurol; 2002 Apr; 59(4):623-9. PubMed ID: 11939898
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Yugoslavia.
    Topisirovic I; Dragasevic N; Savic D; Ristic A; Keckarevic M; Keckarevic D; Culjkovic B; Petrovic I; Romac S; Kostic VS
    Clin Genet; 2002 Oct; 62(4):321-4. PubMed ID: 12372061
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular genetics of spinocerebellar ataxia type 8 (SCA8).
    Mosemiller AK; Dalton JC; Day JW; Ranum LP
    Cytogenet Genome Res; 2003; 100(1-4):175-83. PubMed ID: 14526178
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High germinal instability of the (CTG)n at the SCA8 locus of both expanded and normal alleles.
    Silveira I; Alonso I; Guimarães L; Mendonça P; Santos C; Maciel P; Fidalgo De Matos JM; Costa M; Barbot C; Tuna A; Barros J; Jardim L; Coutinho P; Sequeiros J
    Am J Hum Genet; 2000 Mar; 66(3):830-40. PubMed ID: 10712199
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications.
    Wu YR; Chen IC; Soong BW; Kao SH; Lee GC; Huang SY; Fung HC; Lee-Chen GJ; Chen CM
    Hum Genet; 2009 May; 125(4):437-44. PubMed ID: 19229559
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10.
    Raskin S; Ashizawa T; Teive HA; Arruda WO; Fang P; Gao R; White MC; Werneck LC; Roa B
    Arch Neurol; 2007 Apr; 64(4):591-4. PubMed ID: 17420323
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spinocerebellar ataxia type 8: clinical features in a large family.
    Day JW; Schut LJ; Moseley ML; Durand AC; Ranum LP
    Neurology; 2000 Sep; 55(5):649-57. PubMed ID: 10980728
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
    Oda M; Maruyama H; Komure O; Morino H; Terasawa H; Izumi Y; Imamura T; Yasuda M; Ichikawa K; Ogawa M; Matsumoto M; Kawakami H
    Arch Neurol; 2004 Feb; 61(2):209-12. PubMed ID: 14967767
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locus.
    Vincent JB; Neves-Pereira ML; Paterson AD; Yamamoto E; Parikh SV; Macciardi F; Gurling HM; Potkin SG; Pato CN; Macedo A; Kovacs M; Davies M; Lieberman JA; Meltzer HY; Petronis A; Kennedy JL
    Am J Hum Genet; 2000 Mar; 66(3):819-29. PubMed ID: 10712198
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.
    Moseley ML; Zu T; Ikeda Y; Gao W; Mosemiller AK; Daughters RS; Chen G; Weatherspoon MR; Clark HB; Ebner TJ; Day JW; Ranum LP
    Nat Genet; 2006 Jul; 38(7):758-69. PubMed ID: 16804541
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Haplotype diversity and somatic instability in normal and expanded SCA8 alleles.
    Martins S; Seixas AI; Magalhães P; Coutinho P; Sequeiros J; Silveira I
    Am J Med Genet B Neuropsychiatr Genet; 2005 Nov; 139B(1):109-14. PubMed ID: 16184604
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Studies on the CTA/CTG trinucleotide repeats of ATXN8OS gene in Chinese Hans].
    Wang J; Zhang S; Xu Q; Li X; Song X; Jiang H; Shen L; Yan X; Pan Q; Xia K; Tang B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):511-4. PubMed ID: 18841561
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion.
    Obayashi M; Stevanin G; Synofzik M; Monin ML; Duyckaerts C; Sato N; Streichenberger N; Vighetto A; Desestret V; Tesson C; Wichmann HE; Illig T; Huttenlocher J; Kita Y; Izumi Y; Mizusawa H; Schöls L; Klopstock T; Brice A; Ishikawa K; Dürr A
    J Neurol Neurosurg Psychiatry; 2015 Sep; 86(9):986-95. PubMed ID: 25476002
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinicopathologic investigation of a family with expanded SCA8 CTA/CTG repeats.
    Ito H; Kawakami H; Wate R; Matsumoto S; Imai T; Hirano A; Kusaka H
    Neurology; 2006 Oct; 67(8):1479-81. PubMed ID: 17060579
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.