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 *

118 related articles for article (PubMed ID: 38934198)

  • 1. Whole Exome Sequencing Indicating GGCCTG Hexanucleotide Repeat in Patients with Spinocerebellar Ataxia Type 36.
    Chen R; Zhou C; Peng Y; Huang P; Yu Y; Zhu M; Zhou M; Hong D; Tan D
    Neurodegener Dis; 2024; 24(2):71-79. PubMed ID: 38934198
    [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. 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]  

  • 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. Repeat expansions in
    Lam T; Rocca C; Ibanez K; Dalmia A; Tallman S; Hadjivassiliou M; Hensiek A; Nemeth A; Facchini S; ; Wood N; Cortese A; Houlden H; Tucci A
    Brain Commun; 2023; 5(5):fcad244. PubMed ID: 37810464
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Hexanucleotide repeat expansion in SCA36 reduces the expression of genes involved in ribosome biosynthesis and protein translation.
    Morikawa T; Miura S; Uchiyama Y; Hiruki S; Sun Y; Fujioka R; Shibata H
    J Hum Genet; 2024 Sep; 69(9):411-416. PubMed ID: 38811808
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. '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]  

  • 13. 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]  

  • 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. 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]  

  • 16. Fast and reliable detection of repeat expansions in spinocerebellar ataxia using exomes.
    Méreaux JL; Davoine CS; Coutelier M; Guillot-Noël L; Castrioto A; Charles P; Coarelli G; Ewenczyk C; Klebe S; Heinzmann A; Méneret A; Fauret-Amsellem AL; de Sainte Agathe JM; Brice A; Durr A
    J Med Genet; 2023 Jul; 60(7):717-721. PubMed ID: 36599645
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [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]  

  • 19. 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]  

  • 20. Diagnosis of Spinocerebellar Ataxias Caused by Trinucleotide Repeat Expansions.
    Martindale JE
    Curr Protoc Hum Genet; 2017 Jan; 92():9.30.1-9.30.22. PubMed ID: 28075481
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.