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 *

142 related articles for article (PubMed ID: 11719278)

  • 1. SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia.
    Holmes SE; Hearn EO; Ross CA; Margolis RL
    Brain Res Bull; 2001 Oct-Nov 1; 56(3-4):397-403. PubMed ID: 11719278
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Why is SCA12 different from other SCAs?
    Holmes SE; O'Hearn E; Margolis RL
    Cytogenet Genome Res; 2003; 100(1-4):189-97. PubMed ID: 14526180
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evidence of a common founder for SCA12 in the Indian population.
    Bahl S; Virdi K; Mittal U; Sachdeva MP; Kalla AK; Holmes SE; O'Hearn E; Margolis RL; Jain S; Srivastava AK; Mukerji M
    Ann Hum Genet; 2005 Sep; 69(Pt 5):528-34. PubMed ID: 16138911
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical behaviour of spinocerebellar ataxia type 12 and intermediate length abnormal CAG repeats in PPP2R2B.
    Srivastava AK; Takkar A; Garg A; Faruq M
    Brain; 2017 Jan; 140(1):27-36. PubMed ID: 27864267
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spinocerebellar ataxia type 12.
    O'Hearn E; Holmes SE; Margolis RL
    Handb Clin Neurol; 2012; 103():535-47. PubMed ID: 21827912
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12.
    O'Hearn EE; Hwang HS; Holmes SE; Rudnicki DD; Chung DW; Seixas AI; Cohen RL; Ross CA; Trojanowski JQ; Pletnikova O; Troncoso JC; Margolis RL
    Mov Disord; 2015 Nov; 30(13):1813-1824. PubMed ID: 26340331
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of 46 CAG repeats within PPP2R2B as probably the shortest pathogenic allele for SCA12.
    Dong Y; Wu JJ; Wu ZY
    Parkinsonism Relat Disord; 2015 Apr; 21(4):398-401. PubMed ID: 25634432
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Molecular and clinical correlation in five Indian families with spinocerebellar ataxia 12.
    Srivastava AK; Choudhry S; Gopinath MS; Roy S; Tripathi M; Brahmachari SK; Jain S
    Ann Neurol; 2001 Dec; 50(6):796-800. PubMed ID: 11761478
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Polymorphism of trinucleotide repeats in non-translated regions of SCA8 and SCA12 genes: allele distribution in a Polish control group.
    Sułek A; Hoffman-Zacharska D; Bednarska-Makaruk M; Szirkowiec W; Zaremba J
    J Appl Genet; 2004; 45(1):101-5. PubMed ID: 14960773
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.
    Holmes SE; O'Hearn EE; McInnis MG; Gorelick-Feldman DA; Kleiderlein JJ; Callahan C; Kwak NG; Ingersoll-Ashworth RG; Sherr M; Sumner AJ; Sharp AH; Ananth U; Seltzer WK; Boss MA; Vieria-Saecker AM; Epplen JT; Riess O; Ross CA; Margolis RL
    Nat Genet; 1999 Dec; 23(4):391-2. PubMed ID: 10581021
    [No Abstract]   [Full Text] [Related]  

  • 14. SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family.
    Fujigasaki H; Verma IC; Camuzat A; Margolis RL; Zander C; Lebre AS; Jamot L; Saxena R; Anand I; Holmes SE; Ross CA; Dürr A; Brice A
    Ann Neurol; 2001 Jan; 49(1):117-21. PubMed ID: 11198281
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.
    Sato K; Yabe I; Fukuda Y; Soma H; Nakahara Y; Tsuji S; Sasaki H
    Arch Neurol; 2010 Oct; 67(10):1257-62. PubMed ID: 20937954
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spinocerebellar ataxia type 12: clues to pathogenesis.
    Cohen RL; Margolis RL
    Curr Opin Neurol; 2016 Dec; 29(6):735-742. PubMed ID: 27748686
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Generation of a human induced pluripotent stem cell line JHUi003-A with homozygous mutation for spinocerebellar ataxia type 12 using genome editing.
    Feng H; Li Q; Margolis RL; Li PP
    Stem Cell Res; 2021 May; 53():102346. PubMed ID: 34087983
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spinocerebellar ataxia type 2 (SCA2): clinical features and genetic analysis.
    Mutesa L; Pierquin G; Segers K; Vanbellinghen JF; Gahimbare L; Bours V
    J Trop Pediatr; 2008 Oct; 54(5):350-2. PubMed ID: 18499737
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Unusual cerebral white matter change in a Chinese family with Spinocerebellar ataxia type 12.
    Hu T; Zhao B; Wei QQ; Shang H
    J Neurol Sci; 2015 Feb; 349(1-2):243-5. PubMed ID: 25586539
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.