134 related articles for article (PubMed ID: 2158637)
1. Enormous dystrophin in a patient with Becker muscular dystrophy.
Angelini C; Beggs AH; Hoffman EP; Fanin M; Kunkel LM
Neurology; 1990 May; 40(5):808-12. PubMed ID: 2158637
[TBL] [Abstract][Full Text] [Related]
2. A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophy.
Gold R; Kress W; Bettecken T; Reichmann H; Müller CR
J Neurol; 1994 Mar; 241(5):331-4. PubMed ID: 8006687
[TBL] [Abstract][Full Text] [Related]
3. Duplication of dystrophin gene and dissimilar clinical phenotype in the same family.
Toscano A; Vitiello L; Comi GP; Galvagni F; Miorin M; Prelle A; Fortunato F; Bardoni A; Mora M; Fiumara A
Neuromuscul Disord; 1995 Nov; 5(6):475-81. PubMed ID: 8580729
[TBL] [Abstract][Full Text] [Related]
4. Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.
Malhotra SB; Hart KA; Klamut HJ; Thomas NS; Bodrug SE; Burghes AH; Bobrow M; Harper PS; Thompson MW; Ray PN
Science; 1988 Nov; 242(4879):755-9. PubMed ID: 3055295
[TBL] [Abstract][Full Text] [Related]
5. Absence of dystrophin in two patients with Becker type Xp21 muscular dystrophy.
Mongini T; Palmucci L; Doriguzzi C; Chiadoò-Piat L; Restagno G
Neurosci Lett; 1992 Nov; 147(1):37-40. PubMed ID: 1480320
[TBL] [Abstract][Full Text] [Related]
6. Very mild muscular dystrophy associated with the deletion of 46% of dystrophin.
England SB; Nicholson LV; Johnson MA; Forrest SM; Love DR; Zubrzycka-Gaarn EE; Bulman DE; Harris JB; Davies KE
Nature; 1990 Jan; 343(6254):180-2. PubMed ID: 2404210
[TBL] [Abstract][Full Text] [Related]
7. Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy.
Nicholson LV; Johnson MA; Gardner-Medwin D; Bhattacharya S; Harris JB
Acta Neuropathol; 1990; 80(3):239-50. PubMed ID: 2205076
[TBL] [Abstract][Full Text] [Related]
8. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.
Den Dunnen JT; Grootscholten PM; Bakker E; Blonden LA; Ginjaar HB; Wapenaar MC; van Paassen HM; van Broeckhoven C; Pearson PL; van Ommen GJ
Am J Hum Genet; 1989 Dec; 45(6):835-47. PubMed ID: 2573997
[TBL] [Abstract][Full Text] [Related]
9. A case of Becker muscular dystrophy resulting from the skipping of four contiguous exons (71-74) of the dystrophin gene during mRNA maturation.
Patria SY; Alimsardjono H; Nishio H; Takeshima Y; Nakamura H; Matsuo M
Proc Assoc Am Physicians; 1996 Jul; 108(4):308-14. PubMed ID: 8863344
[TBL] [Abstract][Full Text] [Related]
10. Defective dystrophin in Duchenne and Becker dystrophy myotubes in cell culture.
Sklar RM; Beggs AH; Lev AA; Specht L; Shapiro F; Brown RH
Neurology; 1990 Dec; 40(12):1854-8. PubMed ID: 1701042
[TBL] [Abstract][Full Text] [Related]
11. Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy.
Miranda AF; Francke U; Bonilla E; Martucci G; Schmidt B; Salviati G; Rubin M
Am J Med Genet; 1989 Feb; 32(2):268-73. PubMed ID: 2648829
[TBL] [Abstract][Full Text] [Related]
12. Transcription of the dystrophin gene in Duchenne muscular dystrophy muscle.
Muntoni F; Strong PN
FEBS Lett; 1989 Jul; 252(1-2):95-8. PubMed ID: 2668030
[TBL] [Abstract][Full Text] [Related]
13. Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy.
Bonilla E; Schmidt B; Samitt CE; Miranda AF; Hays AP; de Oliveira AB; Chang HW; Servidei S; Ricci E; Younger DS
Am J Pathol; 1988 Dec; 133(3):440-5. PubMed ID: 3059802
[TBL] [Abstract][Full Text] [Related]
14. Prevalent cardiac involvement in dystrophin Becker type mutation.
Siciliano G; Fanin M; Angelini C; Pollina LE; Miorin M; Saad FA; Freda MP; Muratorio A
Neuromuscul Disord; 1994 Jul; 4(4):381-6. PubMed ID: 7981595
[TBL] [Abstract][Full Text] [Related]
15. Quantitative Southern blot analysis in the dystrophin gene of Japanese patients with Duchenne or Becker muscular dystrophy: a high frequency of duplications.
Hiraishi Y; Kato S; Ishihara T; Takano T
J Med Genet; 1992 Dec; 29(12):897-901. PubMed ID: 1362223
[TBL] [Abstract][Full Text] [Related]
16. Multiplicity of abnormal dystrophin in Becker muscular dystrophy. A Becker muscular dystrophy gene frequently produced two smaller sizes of dystrophin.
Hori S; Ohtani S; Shimizu T; Ibi T; Sahashi K; Nonaka I; Miyamoto K; Tanabe H
J Neurol Sci; 1994 Feb; 121(2):183-9. PubMed ID: 8158213
[TBL] [Abstract][Full Text] [Related]
17. An unusual variant of Becker muscular dystrophy.
de Visser M; Bakker E; Defesche JC; Bolhuis PA; van Ommen GJ
Ann Neurol; 1990 May; 27(5):578-81. PubMed ID: 2193611
[TBL] [Abstract][Full Text] [Related]
18. Improved diagnosis of Becker muscular dystrophy by dystrophin testing.
Hoffman EP; Kunkel LM; Angelini C; Clarke A; Johnson M; Harris JB
Neurology; 1989 Aug; 39(8):1011-7. PubMed ID: 2668783
[TBL] [Abstract][Full Text] [Related]
19. Molecular genetics of Duchenne and Becker muscular dystrophy: emphasis on improved diagnosis.
Kunkel LM; Beggs AH; Hoffman EP
Clin Chem; 1989 Jul; 35(7 Suppl):B21-4. PubMed ID: 2663232
[TBL] [Abstract][Full Text] [Related]
20. Absence of dystrophin in Becker muscular dystrophy.
Patel K; Leevers S; Abbs S; Hart KA; Heckmatt JZ; Bobrow M; Dubowitz V
Lancet; 1989 Jan; 1(8628):47. PubMed ID: 2563029
[No Abstract] [Full Text] [Related]
[Next] [New Search]