MOLECULAR-BIOLOGY OF DUCHENNE MUSCULAR-DYSTROPHY

被引：27

作者：

BROWN, RH

HOFFMAN, EP

机构：

[1] HARVARD UNIV,SCH MED,DEPT PEDIAT,BOSTON,MA 02115

[2] HARVARD UNIV,CHILDRENS HOSP,DIV GENET,BOSTON,MA 02115

来源：

TRENDS IN NEUROSCIENCES | 1988年 / 11卷 / 11期

关键词：

D O I：

10.1016/0166-2236(88)90006-9

中图分类号：

Q189 [神经科学];

学科分类号：

071006 ;

摘要：

引用

页码：480 / 484

页数：5

共 32 条

[1] DUCHENNE MUSCULAR-DYSTROPHY - DEFICIENCY OF DYSTROPHIN AT THE MUSCLE-CELL SURFACE [J].

BONILLA, E ;

SAMITT, CE ;

MIRANDA, AF ;

HAYS, AP ;

SALVIATI, G ;

DIMAURO, S ;

KUNKEL, LM ;

HOFFMAN, EP ;

ROWLAND, LP .

CELL, 1988, 54 (04) :447-452

[2] X-CHROMOSOME-LINKED MUSCULAR-DYSTROPHY (MDX) IN THE MOUSE [J].

BULFIELD, G ;

SILLER, WG ;

WIGHT, PAL ;

MOORE, KJ .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (04) :1189-1192

[3] EXPRESSION OF THE MURINE DUCHENNE MUSCULAR-DYSTROPHY GENE IN MUSCLE AND BRAIN [J].

CHAMBERLAIN, JS ;

PEARLMAN, JA ;

MUZNY, DM ;

GIBBS, RA ;

RANIER, JE ;

REEVES, AA ;

CASKEY, CT .

SCIENCE, 1988, 239 (4846) :1416-1418

[4] THE HOMOLOG OF THE DUCHENNE LOCUS IS DEFECTIVE IN X-LINKED MUSCULAR-DYSTROPHY OF DOGS [J].

COOPER, BJ ;

WINAND, NJ ;

STEDMAN, H ;

VALENTINE, BA ;

HOFFMAN, EP ;

KUNKEL, LM ;

SCOTT, MO ;

FISCHBECK, KH ;

KORNEGAY, JN ;

AVERY, RJ ;

WILLIAMS, JR ;

SCHMICKEL, RD ;

SYLVESTER, JE .

NATURE, 1988, 334 (6178) :154-156

[5] LINKAGE ANALYSIS OF 2 CLONED DNA-SEQUENCES FLANKING THE DUCHENNE MUSCULAR-DYSTROPHY LOCUS ON THE SHORT ARM OF THE HUMAN X-CHROMOSOME [J].

DAVIES, KE ;

PEARSON, PL ;

HARPER, PS ;

MURRAY, JM ;

OBRIEN, T ;

SARFARAZI, M ;

WILLIAMSON, R .

NUCLEIC ACIDS RESEARCH, 1983, 11 (08) :2303-2312

[6] DIRECT DETECTION OF MORE THAN 50-PERCENT OF THE DUCHENNE MUSCULAR-DYSTROPHY MUTATIONS BY FIELD INVERSION GELS [J].

DENDUNNEN, JT ;

BAKKER, E ;

BRETELER, EGK ;

PEARSON, PL ;

VANOMMEN, GJB .

NATURE, 1987, 329 (6140) :640-642

[7]

DUBOWITZ V, 1977, PATHOGENESIS HUMAN M, P688

[8]

Engel A., 1986, MYOLOGY, P1185

[9]

FRANCKE U, 1985, AM J HUM GENET, V37, P250

[10] MOLECULAR MECHANISMS OF MCARDLES DISEASE (MUSCLE GLYCOGEN-PHOSPHORYLASE DEFICIENCY) - RNA AND DNA ANALYSIS [J].

GAUTRON, S ;

DAEGELEN, D ;

MENNECIER, F ;

DUBOCQ, D ;

KAHN, A ;

DREYFUS, JC .

JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (01) :275-281

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