154 related articles for article (PubMed ID: 8513330)
1. An alternative dystrophin transcript specific to peripheral nerve.
Byers TJ; Lidov HG; Kunkel LM
Nat Genet; 1993 May; 4(1):77-81. PubMed ID: 8513330
[TBL] [Abstract][Full Text] [Related]
2. New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin.
Cox GA; Phelps SF; Chapman VM; Chamberlain JS
Nat Genet; 1993 May; 4(1):87-93. PubMed ID: 8099842
[TBL] [Abstract][Full Text] [Related]
3. A second alternative transcript of the gap junction gene connexin32 is expressed in murine Schwann cells and modulated in injured sciatic nerve.
Söhl G; Gillen C; Bosse F; Gleichmann M; Müller HW; Willecke K
Eur J Cell Biol; 1996 Mar; 69(3):267-75. PubMed ID: 8900491
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Infidelity in the structure of ectopic transcripts: a novel exon in lymphocyte dystrophin transcripts.
Roberts RG; Bentley DR; Bobrow M
Hum Mutat; 1993; 2(4):293-9. PubMed ID: 8401537
[TBL] [Abstract][Full Text] [Related]
6. Evolution of the neuron-specific alternative splicing product of the c-src proto-oncogene.
Raulf F; Robertson SM; Schartl M
J Neurosci Res; 1989 Sep; 24(1):81-8. PubMed ID: 2478722
[TBL] [Abstract][Full Text] [Related]
7. Identification of Dp71e, a new dystrophin with a novel carboxy-terminal end.
Saint Martín A; Aragón J; Depardon-Benítez F; Sánchez-Trujillo A; Mendoza-Hernández G; Ceja V; Montañez C
FEBS J; 2012 Jan; 279(1):66-77. PubMed ID: 22008482
[TBL] [Abstract][Full Text] [Related]
8. Differentially expressed genes after peripheral nerve injury.
Gillen C; Gleichmann M; Spreyer P; Müller HW
J Neurosci Res; 1995 Oct; 42(2):159-71. PubMed ID: 8568916
[TBL] [Abstract][Full Text] [Related]
9. An exon skipping-associated nonsense mutation in the dystrophin gene uncovers a complex interplay between multiple antagonistic splicing elements.
Disset A; Bourgeois CF; Benmalek N; Claustres M; Stevenin J; Tuffery-Giraud S
Hum Mol Genet; 2006 Mar; 15(6):999-1013. PubMed ID: 16461336
[TBL] [Abstract][Full Text] [Related]
10. Towards a therapeutic inhibition of dystrophin exon 23 splicing in mdx mouse muscle induced by antisense oligoribonucleotides (splicomers): target sequence optimisation using oligonucleotide arrays.
Graham IR; Hill VJ; Manoharan M; Inamati GB; Dickson G
J Gene Med; 2004 Oct; 6(10):1149-58. PubMed ID: 15386737
[TBL] [Abstract][Full Text] [Related]
11. A novel cryptic exon in intron 2 of the human dystrophin gene evolved from an intron by acquiring consensus sequences for splicing at different stages of anthropoid evolution.
Dwi Pramono ZA; Takeshima Y; Surono A; Ishida T; Matsuo M
Biochem Biophys Res Commun; 2000 Jan; 267(1):321-8. PubMed ID: 10623618
[TBL] [Abstract][Full Text] [Related]
12. Genomic organization of the mouse dystrobrevin gene: comparative analysis with the dystrophin gene.
Ambrose HJ; Blake DJ; Nawrotzki RA; Davies KE
Genomics; 1997 Feb; 39(3):359-69. PubMed ID: 9119373
[TBL] [Abstract][Full Text] [Related]
13. A novel BDNF gene promoter directs expression to skeletal muscle.
Heinrich G
BMC Neurosci; 2003 Jun; 4():11. PubMed ID: 12812528
[TBL] [Abstract][Full Text] [Related]
14. Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus.
Feener CA; Koenig M; Kunkel LM
Nature; 1989 Apr; 338(6215):509-11. PubMed ID: 2648158
[TBL] [Abstract][Full Text] [Related]
15. Dp140: alternatively spliced isoforms in brain and kidney.
Lidov HG; Kunkel LM
Genomics; 1997 Oct; 45(1):132-9. PubMed ID: 9339369
[TBL] [Abstract][Full Text] [Related]
16. Purine-rich exon sequences are not necessarily splicing enhancer sequence in the dystrophin gene.
Ito T; Takeshima Y; Sakamoto H; Nakamura H; Matsuo M
Kobe J Med Sci; 2001 Oct; 47(5):193-202. PubMed ID: 11781497
[TBL] [Abstract][Full Text] [Related]
17. An autosomal transcript in skeletal muscle with homology to dystrophin.
Love DR; Hill DF; Dickson G; Spurr NK; Byth BC; Marsden RF; Walsh FS; Edwards YH; Davies KE
Nature; 1989 May; 339(6219):55-8. PubMed ID: 2541343
[TBL] [Abstract][Full Text] [Related]
18. The human thrombospondin 3 gene: analysis of transcription initiation and an alternatively spliced transcript.
Adolph KW; Bornstein P
Mol Cell Biol Res Commun; 1999 Jul; 2(1):47-52. PubMed ID: 10527891
[TBL] [Abstract][Full Text] [Related]
19. Dystrophin gene transcribed from different promoters in neuronal and glial cells.
Chelly J; Hamard G; Koulakoff A; Kaplan JC; Kahn A; Berwald-Netter Y
Nature; 1990 Mar; 344(6261):64-5. PubMed ID: 2406613
[TBL] [Abstract][Full Text] [Related]
20. In vitro splicing analysis showed that availability of a cryptic splice site is not a determinant for alternative splicing patterns caused by +1G-->A mutations in introns of the dystrophin gene.
Habara Y; Takeshima Y; Awano H; Okizuka Y; Zhang Z; Saiki K; Yagi M; Matsuo M
J Med Genet; 2009 Aug; 46(8):542-7. PubMed ID: 19001018
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
