메뉴 건너뛰기




Volumn 60, Issue 6, 1997, Pages 1555-1558

Up-regulation of the brain and Purkinje-cell forms of dystrophin transcripts, in Becker muscular dystrophy [8]

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; BECKER MUSCULAR DYSTROPHY; CASE REPORT; DUCHENNE MUSCULAR DYSTROPHY; GENE EXPRESSION; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; LETTER; MALE; MUSCLE BIOPSY; PRIORITY JOURNAL; PROMOTER REGION; PURKINJE CELL; RECEPTOR UPREGULATION;

EID: 0030908641     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0002-9297(07)64253-0     Document Type: Letter
Times cited : (21)

References (11)
  • 1
    • 0023215347 scopus 로고
    • X-linked dilated cardiomyopathy
    • BA Berko M Swift X-linked dilated cardiomyopathy N Engl J Med 316 1987 1186 1191
    • (1987) N Engl J Med , vol.316 , pp. 1186-1191
    • Berko, BA1    Swift, M2
  • 3
    • 0029824347 scopus 로고    scopus 로고
    • Identification of a transcriptional enhancer within muscle intron 1 of the human dystrophin gene
    • HJ Klamut LO Bosnoyan-Collins RG Worton PN Ray HL Davis Identification of a transcriptional enhancer within muscle intron 1 of the human dystrophin gene Hum Mol Genet 5 1996 1599 1606
    • (1996) Hum Mol Genet , vol.5 , pp. 1599-1606
    • Klamut, HJ1    Bosnoyan-Collins, LO2    Worton, RG3    Ray, PN4    Davis, HL5
  • 4
    • 0030028518 scopus 로고    scopus 로고
    • A point mutation in the 5′ splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy
    • J Milasin F Muntoni GM Severini L Bartoloni M Vatta M Krajinovic A Mateddu A point mutation in the 5′ splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy Hum Mol Genet 5 1996 73 79
    • (1996) Hum Mol Genet , vol.5 , pp. 73-79
    • Milasin, J1    Muntoni, F2    Severini, GM3    Bartoloni, L4    Vatta, M5    Krajinovic, M6    Mateddu, A7
  • 5
    • 0027265702 scopus 로고
    • Deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy
    • F Muntoni M Cau A Ganau R Congiu G Arvedi A Mateddu MG Marrosu Deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy N Engl J Med 329 1993 921 925
    • (1993) N Engl J Med , vol.329 , pp. 921-925
    • Muntoni, F1    Cau, M2    Ganau, A3    Congiu, R4    Arvedi, G5    Mateddu, A6    Marrosu, MG7
  • 6
    • 0028812128 scopus 로고
    • Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy
    • F Muntoni MA Melis A Ganau V Dubowitz Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy Am J Hum Genet 56 1995 151 157
    • (1995) Am J Hum Genet , vol.56 , pp. 151-157
    • Muntoni, F1    Melis, MA2    Ganau, A3    Dubowitz, V4
  • 8
    • 0026321742 scopus 로고
    • A screening for dystrophin gene deletions in Japanese patients with Duchenne/Becker muscular dystrophy by the multiplex polymerase chain reaction
    • H Sakuraba K Ishii M Shimmoto H Yamada Y Suzuki A screening for dystrophin gene deletions in Japanese patients with Duchenne/Becker muscular dystrophy by the multiplex polymerase chain reaction Brain Dev 13 1991 339 342
    • (1991) Brain Dev , vol.13 , pp. 339-342
    • Sakuraba, H1    Ishii, K2    Shimmoto, M3    Yamada, H4    Suzuki, Y5
  • 9
    • 0027193330 scopus 로고
    • X-linked dilated cardiomyopathy: molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus
    • JA Towbin JF Hejtmancik P Brink B Gelb XM Zhu JS Chamberlain ERB McCabe X-linked dilated cardiomyopathy: molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus Circulation 87 1993 1854 1865
    • (1993) Circulation , vol.87 , pp. 1854-1865
    • Towbin, JA1    Hejtmancik, JF2    Brink, P3    Gelb, B4    Zhu, XM5    Chamberlain, JS6    McCabe, ERB7
  • 10
    • 85114523455 scopus 로고
    • A novel cardio-specific dystrophin mutation as a cause of X-linked dilated cardiomyopathy (XLCM)
    • JA Towbin R Ortiz-Lopez D Bulman PN Ray W-M Franz H Katus M Swift A novel cardio-specific dystrophin mutation as a cause of X-linked dilated cardiomyopathy (XLCM) Pediatr Res Suppl 37 1994 36A
    • (1994) Pediatr Res Suppl , vol.37 , pp. 36A
    • Towbin, JA1    Ortiz-Lopez, R2    Bulman, D3    Ray, PN4    Franz, W-M5    Katus, H6    Swift, M7
  • 11
    • 0027482335 scopus 로고
    • Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy
    • K Yoshida S Ikeda A Nakamura M Kagoshima S Takeda S Shoji N Yanagisawa Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy Muscle Nerve 16 1993 1161 1166
    • (1993) Muscle Nerve , vol.16 , pp. 1161-1166
    • Yoshida, K1    Ikeda, S2    Nakamura, A3    Kagoshima, M4    Takeda, S5    Shoji, S6    Yanagisawa, N7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.