1007 related articles for article (PubMed ID: 1310900)
1. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.
Brook JD; McCurrach ME; Harley HG; Buckler AJ; Church D; Aburatani H; Hunter K; Stanton VP; Thirion JP; Hudson T
Cell; 1992 Feb; 68(4):799-808. PubMed ID: 1310900
[TBL] [Abstract][Full Text] [Related]
2. Molecular analysis of the CTG trinucleotide repeat in South African myotonic dystrophy families--implications for diagnosis and counselling.
Goldman A; Ramsay M; Jenkins T
S Afr Med J; 1995 Nov; 85(11):1161-4. PubMed ID: 8597005
[TBL] [Abstract][Full Text] [Related]
3. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.
Brook JD; McCurrach ME; Harley HG; Buckler AJ; Church D; Aburatani H; Hunter K; Stanton VP; Thirion JP; Hudson T
Cell; 1992 Apr; 69(2):385. PubMed ID: 1568252
[No Abstract] [Full Text] [Related]
4. [DNA diagnosis in myotonic dystrophy].
Tachi N
Hokkaido Igaku Zasshi; 1996 Jan; 71(1):3-8. PubMed ID: 8727368
[TBL] [Abstract][Full Text] [Related]
5. A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat.
Boucher CA; King SK; Carey N; Krahe R; Winchester CL; Rahman S; Creavin T; Meghji P; Bailey ME; Chartier FL
Hum Mol Genet; 1995 Oct; 4(10):1919-25. PubMed ID: 8595416
[TBL] [Abstract][Full Text] [Related]
6. Minimal somatic instability of CTG repeat in congenital myotonic dystrophy.
Tachi N; Ohya K; Chiba S; Sato T; Kikuchi K
Pediatr Neurol; 1995 Jan; 12(1):81-3. PubMed ID: 7748368
[TBL] [Abstract][Full Text] [Related]
7. [Advances in molecular genetics of myotonic dystrophy].
Yamagata H; Yamanaka N; Miki T; Ogihara T
Nihon Rinsho; 1993 Sep; 51(9):2474-80. PubMed ID: 8411731
[TBL] [Abstract][Full Text] [Related]
8. [Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion].
Spranger M; Janssen B; Rating D; Spranger S
Nervenarzt; 1999 Feb; 70(2):131-5. PubMed ID: 10098148
[TBL] [Abstract][Full Text] [Related]
9. Myotonic dystrophy with no trinucleotide repeat expansion.
Thornton CA; Griggs RC; Moxley RT
Ann Neurol; 1994 Mar; 35(3):269-72. PubMed ID: 8122879
[TBL] [Abstract][Full Text] [Related]
10. Detection of the CTG repeat expansion in congenital myotonic dystrophy.
Ohya K; Tachi N; Sato T; Kon S; Kikuchi K; Chiba S
Jpn J Hum Genet; 1997 Mar; 42(1):169-80. PubMed ID: 9183996
[TBL] [Abstract][Full Text] [Related]
11. [Non-radioactive PCR southern method for analysis of CTG repeat in myotonic dystrophy].
Kozuka N; Tachi N; Ohya K; Uchida E; Kikuchi S; Sengoku Y
No To Hattatsu; 2003 Sep; 35(5):380-7. PubMed ID: 13677946
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Molecular and clinical characteristics of myotonic dystrophy type 1 in koreans.
Kim SY; Kim JY; Kim GP; Sung JJ; Lim KS; Lee KW; Chae JH; Hong YH; Seong MW; Park SS
Korean J Lab Med; 2008 Dec; 28(6):483-92. PubMed ID: 19127114
[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-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]
16. A molecular protocol for diagnosing myotonic dystrophy.
Guida M; Marger RS; Papp AC; Snyder PJ; Sedra MS; Kissel JT; Mendell JR; Prior TW
Clin Chem; 1995 Jan; 41(1):69-72. PubMed ID: 7813083
[TBL] [Abstract][Full Text] [Related]
17. [Molecular genetics of myotonic dystrophy--population genetics of the CTG repeat expansion of the MTPK gene].
Yamagata H; Miki T; Ogihara T
Nihon Rinsho; 1997 Dec; 55(12):3205-9. PubMed ID: 9436437
[TBL] [Abstract][Full Text] [Related]
18. Relative stability of a minimal CTG repeat expansion in a large kindred with myotonic dystrophy.
Simmons Z; Thornton CA; Seltzer WK; Richards CS
Neurology; 1998 May; 50(5):1501-4. PubMed ID: 9596022
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of congenital myotonic dystrophy and counseling of the pregnant mother: case report and literature review.
Geifman-Holtzman O; Fay K
Am J Med Genet; 1998 Jul; 78(3):250-3. PubMed ID: 9677060
[TBL] [Abstract][Full Text] [Related]
20. Reduction of serum IgG level and peripheral T-cell counts are correlated with CTG repeat lengths in myotonic dystrophy patients.
Nakamura A; Kojo T; Arahata K; Takeda S
Neuromuscul Disord; 1996 May; 6(3):203-10. PubMed ID: 8784809
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]