BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

252 related articles for article (PubMed ID: 25900954)

  • 1. Spinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic population.
    Faruq M; Srivastava AK; Singh S; Gupta R; Dada T; Garg A; Behari M; Mukerji M
    Indian J Med Res; 2015 Feb; 141(2):187-98. PubMed ID: 25900954
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Complete Association of an intronic SNP rs6798742 with Origin of Spinocerebellar Ataxia Type 7-CAG Expansion Loci in the Indian and Mexican Population.
    Faruq M; Magaña JJ; Suroliya V; Narang A; Murillo-Melo NM; Hernández-Hernández O; Srivastava AK; Mukerji M
    Ann Hum Genet; 2017 Sep; 81(5):197-204. PubMed ID: 28597910
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian family.
    Martin J; Van Regemorter N; Del-Favero J; Löfgren A; Van Broeckhoven C
    J Neurol Sci; 1999 Sep; 168(1):37-46. PubMed ID: 10500272
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Molecular and clinical study of spinocerebellar ataxia type 7 in Chinese kindreds.
    Gu W; Wang Y; Liu X; Zhou B; Zhou Y; Wang G
    Arch Neurol; 2000 Oct; 57(10):1513-8. PubMed ID: 11030806
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spinocerebellar ataxia type-7: Report of a family in Northwest Nigeria.
    Alkali NH; Bwala SA; Alimi SA; Oyakhire SI
    Ann Afr Med; 2016; 15(2):87-90. PubMed ID: 27044733
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Spinocerebellar ataxia Type 7: clinical and genetic study of a new Moroccan family (case report).
    Bouzid FZ; Mansouri M; Abdelaziz C; Louhab N; Bernard S; Strubi-Vuillaume I; Dafir K; Aboussair N
    Pan Afr Med J; 2021; 38():162. PubMed ID: 33995769
    [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. Spinocerebellar ataxia 7 (SCA7).
    Lebre AS; Brice A
    Cytogenet Genome Res; 2003; 100(1-4):154-63. PubMed ID: 14526176
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
    Pujana MA; Corral J; Gratacòs M; Combarros O; Berciano J; Genís D; Banchs I; Estivill X; Volpini V
    Hum Genet; 1999 Jun; 104(6):516-22. PubMed ID: 10453742
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Slowing of voluntary and involuntary saccades: an early sign in spinocerebellar ataxia type 7.
    Oh AK; Jacobson KM; Jen JC; Baloh RW
    Ann Neurol; 2001 Jun; 49(6):801-4. PubMed ID: 11409434
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation.
    Johansson J; Forsgren L; Sandgren O; Brice A; Holmgren G; Holmberg M
    Hum Mol Genet; 1998 Feb; 7(2):171-6. PubMed ID: 9425223
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Post-zygotic de novo trinucleotide repeat expansion at spinocerebellar ataxia type 7 locus: evidence from an Indian family.
    Mittal U; Roy S; Jain S; Srivastava AK; Mukerji M
    J Hum Genet; 2005; 50(3):155-157. PubMed ID: 15750685
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Voice Alterations in Patients With Spinocerebellar Ataxia Type 7 (SCA7): Clinical-Genetic Correlations.
    Gómez-Coello A; Valadez-Jiménez VM; Cisneros B; Carrillo-Mora P; Parra-Cárdenas M; Hernández-Hernández O; Magaña JJ
    J Voice; 2017 Jan; 31(1):123.e1-123.e5. PubMed ID: 26992556
    [TBL] [Abstract][Full Text] [Related]  

  • 17. AAV-Mediated CAG-Targeting Selectively Reduces Polyglutamine-Expanded Protein and Attenuates Disease Phenotypes in a Spinocerebellar Ataxia Mouse Model.
    Niewiadomska-Cimicka A; Fievet L; Surdyka M; Jesion E; Keime C; Singer E; Eisenmann A; Kalinowska-Poska Z; Nguyen HHP; Fiszer A; Figiel M; Trottier Y
    Int J Mol Sci; 2024 Apr; 25(8):. PubMed ID: 38673939
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Studies on the CAG repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese Han].
    Wang J; Xu Q; Lei L; Shen L; Jiang H; Li X; Zhou Y; Yi J; Zhou J; Yan X; Pan Q; Xia K; Tang B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):620-5. PubMed ID: 19953482
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Somatic instability of expanded CAG repeats of ATXN7 in Japanese patients with spinocerebellar ataxia type 7.
    Katagiri S; Hayashi T; Takeuchi T; Yamada H; Gekka T; Kawabe K; Kurita A; Tsuneoka H
    Doc Ophthalmol; 2015 Jun; 130(3):189-95. PubMed ID: 25643591
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Trinucleotide expansions in the SCA7 gene in a large family with spinocerebellar ataxia and craniocervical dystonia.
    Lin Y; Zheng JY; Jin YH; Xie YC; Jin ZB
    Neurosci Lett; 2008 Mar; 434(2):230-3. PubMed ID: 18325672
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.