BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 11013451)

  • 1. Molecular anatomy of CTG expansion in myotonin protein kinase gene among myotonic dystrophy patients from eastern India.
    Basu P; Gangopadhaya PK; Mukherjee SC; Das SK; Sinha KK; Bhattacharyya NP
    Hum Mutat; 2000 Oct; 16(4):372. PubMed ID: 11013451
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Expansion of CTG repeat in myotonin protein kinase gene on Alu(ins)-HinfI-I background in a myotonic dystrophy patient from India. Mutations in brief no. 210. Online.
    Basu P; Gangopadhaya PK; Murkherjee SC; Sinha KK; Bhattacharyya NP
    Hum Mutat; 1999; 13(1):84. PubMed ID: 10189221
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Haplotype analysis of the DM1 locus in the Serbian population.
    Krndija D; Savić D; Mladenović J; Rakocević-Stojanović V; Apostolski S; Todorović S; Romac S
    Acta Neurol Scand; 2005 Apr; 111(4):274-7. PubMed ID: 15740580
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CTG repeat lengths of the DMPK gene in myotonic dystrophy patients compared to healthy controls in Thailand.
    Theerasasawat S; Papsing C; Pulkes T
    J Clin Neurosci; 2010 Dec; 17(12):1520-2. PubMed ID: 20801043
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Allelic polymorphism and analysis of haplotypes of the muscle protein kinase genes and haplotype analysis in residents of northwestern Russia and patients with myotonic dystrophy].
    Malysheva OV; Ivashchenko TE; Vasil'eva TN; Saĭkova LA; Baranov VS
    Genetika; 1998 Feb; 34(2):295-9. PubMed ID: 9589858
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in Taiwan: implications for low prevalence and founder mutations of Taiwanese myotonic dystrophy type 1.
    Pan H; Lin HM; Ku WY; Li TC; Li SY; Lin CC; Hsiao KM
    Eur J Hum Genet; 2001 Aug; 9(8):638-41. PubMed ID: 11528511
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CTG repeat number in the nonaffected allele of myotonic dystrophy patients is not critical for disease expression.
    Cipollaro M; Galderisi U; Iacomino G; Galano G; Di Bernardo G; Lus G; Cotrufo R; Orsini A; Santoro L; Pastore L; Sarrantonio C; Salvatore F; Cascino A
    Hum Biol; 1997 Dec; 69(6):887-90. PubMed ID: 9353981
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy.
    Frisch R; Singleton KR; Moses PA; Gonzalez IL; Carango P; Marks HG; Funanage VL
    Mol Genet Metab; 2001; 74(1-2):281-91. PubMed ID: 11592825
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [DNA diagnosis in myotonic dystrophy].
    Tachi N
    Hokkaido Igaku Zasshi; 1996 Jan; 71(1):3-8. PubMed ID: 8727368
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Instability of the expanded (CTG)n repeats in the myotonin protein kinase gene in cultured lymphoblastoid cell lines from patients with myotonic dystrophy.
    Ashizawa T; Monckton DG; Vaishnav S; Patel BJ; Voskova A; Caskey CT
    Genomics; 1996 Aug; 36(1):47-53. PubMed ID: 8812415
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Correlation between degrees of the CTG repeat expansion and clinical features of myotonic dystrophy].
    Eguchi I; Koike R; Onodera O; Tanaka K; Kondo H; Tsuji S
    Rinsho Shinkeigaku; 1994 Feb; 34(2):118-23. PubMed ID: 8194263
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [CTG-repeat analysis of myotonin protein kinase gene in Bashkortostan patients with myotonic dystrophy].
    Khidiiatova IM; Fatkhlislamova RI; magzhanov RV; Popova SN; Slominskiĭ PA; Limborskaia SA; Khusnutdinova EK
    Zh Nevrol Psikhiatr Im S S Korsakova; 2002; 102(3):54-8. PubMed ID: 11957350
    [TBL] [Abstract][Full Text] [Related]  

  • 13. (CTG)n expansion at DMPK locus seen only in muscle tissue: a novel case.
    Hasan Q; Mohan V; Ahuja YR
    Indian J Exp Biol; 2004 Sep; 42(9):937-40. PubMed ID: 15462191
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Somatic mosaicism of p(CTG)n expansion in a case of myotonic dystrophy with parotid tumor].
    Ogata K; Takahashi A; Oguchi N; Ishitoya J; Fuse S; Shimpo T
    Rinsho Shinkeigaku; 1998 Aug; 38(8):736-8. PubMed ID: 9916519
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CTG expansion & haplotype analysis in DM1 gene in healthy Iranian population.
    Shojasaffar B; Moradin N; Kahrizi K; Cobo AM; Najmabadi H
    Can J Neurol Sci; 2008 May; 35(2):216-9. PubMed ID: 18574937
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characteristics of myotonic dystrophy in Istria: molecular genetics approach--mutation analysis.
    Medica I; Logar N; Batagelj M; Peterlin B
    Coll Antropol; 1998 Dec; 22(2):477-84. PubMed ID: 9887603
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [CTG-repeat in myotonin protein kinase].
    Sorimachi H; Sasagawa N; Maruyama K; Arahata K; Ishiura S; Suzuki K
    Rinsho Shinkeigaku; 1994 Dec; 34(12):1230-2. PubMed ID: 7774120
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular analysis of GAA repeats and four linked bi-allelic markers in and around the frataxin gene in patients and normal populations from India.
    Chattopadhyay B; Gupta S; Gangopadhyay PK; Das SK; Roy T; Mukherjee SC; Sinha KK; Singhal BS; Bhattacharyya NP
    Ann Hum Genet; 2004 May; 68(Pt 3):189-95. PubMed ID: 15180699
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Haplotype analysis and LD detection at DM1 locus.
    Kumar A; Agarwal S; Pradhan S
    Gene; 2015 Aug; 567(1):45-50. PubMed ID: 25934189
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1.
    Savić D; Rakocvic-Stojanovic V; Keckarevic D; Culjkovic B; Stojkovic O; Mladenovic J; Todorovic S; Apostolski S; Romac S
    Hum Mutat; 2002 Feb; 19(2):131-9. PubMed ID: 11793472
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.