BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

344 related articles for article (PubMed ID: 21683323)

  • 1. Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.
    Kobayashi H; Abe K; Matsuura T; Ikeda Y; Hitomi T; Akechi Y; Habu T; Liu W; Okuda H; Koizumi A
    Am J Hum Genet; 2011 Jul; 89(1):121-30. PubMed ID: 21683323
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Clinical features of SCA36: a novel spinocerebellar ataxia with motor neuron involvement (Asidan).
    Ikeda Y; Ohta Y; Kobayashi H; Okamoto M; Takamatsu K; Ota T; Manabe Y; Okamoto K; Koizumi A; Abe K
    Neurology; 2012 Jul; 79(4):333-41. PubMed ID: 22744658
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China.
    Zeng S; Zeng J; He M; Zeng X; Zhou Y; Liu Z; Xia K; Pan Q; Jiang H; Shen L; Yan X; Tang B; Wang J
    Clin Genet; 2016 Aug; 90(2):141-8. PubMed ID: 26661328
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Spinocerebellar ataxia type 36 (nicknamed Asidan)].
    Abe K; Ikeda Y
    Brain Nerve; 2012 Aug; 64(8):937-41. PubMed ID: 22868885
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Suppression of the yeast elongation factor Spt4 ortholog reduces expanded SCA36 GGCCUG repeat aggregation and cytotoxicity.
    Furuta N; Tsukagoshi S; Hirayanagi K; Ikeda Y
    Brain Res; 2019 May; 1711():29-40. PubMed ID: 30610877
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Porphyrins ameliorate spinocerebellar ataxia type 36 GGCCTG repeat expansion-mediated cytotoxicity.
    Hirayanagi K; Ozaki H; Tsukagoshi S; Furuta N; Ikeda Y
    Neurosci Res; 2021 Oct; 171():92-102. PubMed ID: 33705846
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Long-read sequencing identified intronic (GGCCTG)n expansion in NOP56 in one SCA36 family and literature review.
    Wang Q; Zhang C; Liu S; Liu T; Ni R; Liu X; Zhong P; Wu Q; Xu T; Ke H; Tian W; Cao L
    Clin Neurol Neurosurg; 2022 Dec; 223():107503. PubMed ID: 36368168
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterization.
    García-Murias M; Quintáns B; Arias M; Seixas AI; Cacheiro P; Tarrío R; Pardo J; Millán MJ; Arias-Rivas S; Blanco-Arias P; Dapena D; Moreira R; Rodríguez-Trelles F; Sequeiros J; Carracedo A; Silveira I; Sobrido MJ
    Brain; 2012 May; 135(Pt 5):1423-35. PubMed ID: 22492559
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Recent advances in clinical and genetic research of spinocerebellar ataxia type 36].
    Zeng S; Tang B; Wang J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):886-9. PubMed ID: 26663071
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spinocerebellar ataxia type 36 in the Han Chinese.
    Lee YC; Tsai PC; Guo YC; Hsiao CT; Liu GT; Liao YC; Soong BW
    Neurol Genet; 2016 Jun; 2(3):e68. PubMed ID: 27123487
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characteristic RNA foci of the abnormal hexanucleotide GGCCUG repeat expansion in spinocerebellar ataxia type 36 (Asidan).
    Liu W; Ikeda Y; Hishikawa N; Yamashita T; Deguchi K; Abe K
    Eur J Neurol; 2014 Nov; 21(11):1377-86. PubMed ID: 24985895
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan.
    Abe K; Ikeda Y; Kurata T; Ohta Y; Manabe Y; Okamoto M; Takamatsu K; Ohta T; Takao Y; Shiro Y; Shoji M; Kamiya T; Kobayashi H; Koizumi A
    Eur J Neurol; 2012 Aug; 19(8):1070-8. PubMed ID: 22353375
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
    Wang JL; Yang X; Xia K; Hu ZM; Weng L; Jin X; Jiang H; Zhang P; Shen L; Guo JF; Li N; Li YR; Lei LF; Zhou J; Du J; Zhou YF; Pan Q; Wang J; Wang J; Li RQ; Tang BS
    Brain; 2010 Dec; 133(Pt 12):3510-8. PubMed ID: 21106500
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.
    Stevanin G; Bouslam N; Thobois S; Azzedine H; Ravaux L; Boland A; Schalling M; Broussolle E; Dürr A; Brice A
    Ann Neurol; 2004 Jan; 55(1):97-104. PubMed ID: 14705117
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia.
    Seixas AI; Loureiro JR; Costa C; Ordóñez-Ugalde A; Marcelino H; Oliveira CL; Loureiro JL; Dhingra A; Brandão E; Cruz VT; Timóteo A; Quintáns B; Rouleau GA; Rizzu P; Carracedo Á; Bessa J; Heutink P; Sequeiros J; Sobrido MJ; Coutinho P; Silveira I
    Am J Hum Genet; 2017 Jul; 101(1):87-103. PubMed ID: 28686858
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spinocerebellar ataxia 36 (SCA36): «Costa da Morte ataxia».
    Arias M; García-Murias M; Sobrido MJ
    Neurologia; 2017; 32(6):386-393. PubMed ID: 25593102
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes.
    Aydin G; Dekomien G; Hoffjan S; Gerding WM; Epplen JT; Arning L
    BMC Neurol; 2018 Jan; 18(1):3. PubMed ID: 29316893
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Chinese SCA36 pedigree analysis of
    Zou J; Wang F; Gong Z; Wang R; Chen S; Zhang H; Sun R; Gao C; Li W; Shang J; Zhang J
    Front Genet; 2023; 14():1110307. PubMed ID: 37051597
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 18.