174 related articles for article (PubMed ID: 8215976)
21. 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]
22. Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues.
Taneja KL; McCurrach M; Schalling M; Housman D; Singer RH
J Cell Biol; 1995 Mar; 128(6):995-1002. PubMed ID: 7896884
[TBL] [Abstract][Full Text] [Related]
23. Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation.
Wang J; Pegoraro E; Menegazzo E; Gennarelli M; Hoop RC; Angelini C; Hoffman EP
Hum Mol Genet; 1995 Apr; 4(4):599-606. PubMed ID: 7543316
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?
Zatz M; Passos-Bueno MR; Cerqueira A; Marie SK; Vainzof M; Pavanello RC
Hum Mol Genet; 1995 Mar; 4(3):401-6. PubMed ID: 7795594
[TBL] [Abstract][Full Text] [Related]
26. [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]
27. Normal levels of DM RNA and myotonin protein kinase in skeletal muscle from adult myotonic dystrophy (DM) patients.
Bhagavati S; Ghatpande A; Leung B
Biochim Biophys Acta; 1996 Dec; 1317(3):155-7. PubMed ID: 8988229
[TBL] [Abstract][Full Text] [Related]
28. Triplet-primed PCR is more sensitive than southern blotting-long PCR for the diagnosis of myotonic dystrophy type1.
Addis M; Serrenti M; Meloni C; Cau M; Melis MA
Genet Test Mol Biomarkers; 2012 Dec; 16(12):1428-31. PubMed ID: 23030650
[TBL] [Abstract][Full Text] [Related]
29. Myotonic dystrophy--no evidence for preferential transmission of the mutated allele: a prenatal analysis.
Zunz E; Abeliovich D; Halpern GJ; Magal N; Shohat M
Am J Med Genet A; 2004 May; 127A(1):50-53. PubMed ID: 15103717
[TBL] [Abstract][Full Text] [Related]
30. Instability of the (CTG)n repeat in congenital myotonic dystrophy.
Wong LJ; Ashizawa T
Am J Hum Genet; 1997 Dec; 61(6):1445-8. PubMed ID: 9399912
[No Abstract] [Full Text] [Related]
31. Report on MDA workshop on myotonic dystrophy, 10 October 1994, Montreal, Quebec, Canada.
Johnson K; Siciliano MJ
J Med Genet; 1995 Aug; 32(8):662-5. PubMed ID: 7473665
[No Abstract] [Full Text] [Related]
32. New founder haplotypes at the myotonic dystrophy locus in southern Africa.
Goldman A; Ramsay M; Jenkins T
Am J Hum Genet; 1995 Jun; 56(6):1373-8. PubMed ID: 7762560
[TBL] [Abstract][Full Text] [Related]
33. Additive influence of maternal and offspring DM-kinase gene CTG repeat lengths in the genesis of congenital myotonic dystrophy.
Barceló JM; Pluscauskas M; MacKenzie AE; Tsilfidis C; Narang M; Korneluk RG
Am J Hum Genet; 1994 Jun; 54(6):1124-5. PubMed ID: 8198135
[No Abstract] [Full Text] [Related]
34. Somatic instability of the CTG repeat in mice transgenic for the myotonic dystrophy region is age dependent but not correlated to the relative intertissue transcription levels and proliferative capacities.
Lia AS; Seznec H; Hofmann-Radvanyi H; Radvanyi F; Duros C; Saquet C; Blanche M; Junien C; Gourdon G
Hum Mol Genet; 1998 Aug; 7(8):1285-91. PubMed ID: 9668171
[TBL] [Abstract][Full Text] [Related]
35. Molecular and clinical study of two myotonic dystrophy homozygotes.
Akbas F; Serdaroglu P; Deymeer F; Aysal F; Erginel-Unaltuna N
J Med Genet; 2001 Nov; 38(11):E40. PubMed ID: 11694554
[No Abstract] [Full Text] [Related]
36. [DNA diagnosis in myotonic dystrophy].
Tachi N
Hokkaido Igaku Zasshi; 1996 Jan; 71(1):3-8. PubMed ID: 8727368
[TBL] [Abstract][Full Text] [Related]
37. Paternal transmission of congenital myotonic dystrophy.
Bergoffen J; Kant J; Sladky J; McDonald-McGinn D; Zackai EH; Fischbeck KH
J Med Genet; 1994 Jul; 31(7):518-20. PubMed ID: 7966187
[TBL] [Abstract][Full Text] [Related]
38. Homozygous myotonic dystrophy with craniosynostosis.
Cerghet M; Tapos D; Serajee FJ; Mahbubul Huq AH
J Child Neurol; 2008 Aug; 23(8):930-3. PubMed ID: 18474935
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy.
Amiel J; Raclin V; Jouannic JM; Morichon N; Hoffman-Radvanyi H; Dommergues M; Feingold J; Munnich A; Bonnefont JP
J Med Genet; 2001 Dec; 38(12):850-2. PubMed ID: 11768387
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
