Dystrophin expression in heterozygous mdxl+ mice indicates imprinting of X chromosome inactivation by parent-of-origin-, tissue-, strain- and position-dependent factors

Dystrophin: The protein product of the duchenne muscular dystrophy locus

1987 • 4,477 citations

Gene Action in the X-chromosome of the Mouse (Mus musculus L.)

1961 • 3,881 citations

X chromosome-linked muscular dystrophy (mdx) in the mouse.

1984 • 1,678 citations

A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome

1991 • 1,469 citations

The Molecular Basis of Muscular Dystrophy in the mdx Mouse: a Point Mutation

1989 • 1,171 citations

The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus

1992 • 983 citations

Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse

1975 • 783 citations

The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

1988 • 658 citations

Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome

1991 • 617 citations

Characterization of a murine gene expressed from the inactive X chromosome

1991 • 529 citations

Disruption of insulin–like growth factor 2 imprinting in Beckwith–Wiedemann syndrome

1993 • 427 citations

Expression of Xist during mouse development suggests a role in the initiation of X chromosome inactivation

1993 • 369 citations

Decreased osmotic stability of dystrophin-less muscle cells from the mdx mouse

1991 • 331 citations

Preferential expression of the maternally derived X chromosome in the mouse yolk sac

1977 • 328 citations

The subcellular distribution of dystrophin in mouse skeletal, cardiac, and smooth muscle.

1991 • 228 citations

Dystrophin-deficient mdx muscle fibers are preferentially vulnerable to necrosis induced by experimental lengthening contractions

1990 • 221 citations

Tissue specificity of X-chromosome inactivation patterns

1994 • 193 citations

Dystrophinopathy in isolated cases of myopathy in females

1992 • 157 citations

CONTROLLING ELEMENTS IN THE MOUSE X CHROMOSOME

1967 • 141 citations

Mosaic Expression of Dystrophin in Symptomatic Carriers of Duchenne's Muscular Dystrophy

1989 • 141 citations

Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1

1993 • 136 citations

Controlling elements in the mouse: IV. Evidence of non-randomX-inactivation

1981 • 113 citations

Preferential paternal X inactivation in extraembryonic tissues of early mouse embryos

1982 • 109 citations

SOME MILESTONES IN THE HISTORY OF X-CHROMOSOME INACTIVATION

1992 • 107 citations

X-chromosome inactivation mosaicism in the three germ layers and the germ line of the mouse embryo

1983 • 102 citations

Imprinting: a gamete's point of view

1994 • 95 citations

Cardiomyopathy may be the only clinical manifestation in female carriers of Duchenne muscular dystrophy

1993 • 88 citations

Serum CK, calcium, magnesium, and oxidative phosphorylation in mdx mouse muscular dystrophy

1988 • 85 citations

Controlling elements in the mouse: V. Linkage tests with X-linked genes

1981 • 54 citations

Dystrophin distribution in heterozygote mdx mice

1989 • 54 citations

Age-Related Conversion of Dystrophin-Negative to -Positive Fiber Segments of Skeletal but not Cardiac Muscle Fibers in Heterozygote mdx Mice

1990 • 51 citations

A manifesting carrier of Duchenne muscular dystrophy with severe myocardial symptoms

1990 • 41 citations

Semi-automated assays for enzymopathies of carbohydrate metabolism in liver and erythrocytes, using a reaction rate analyser

1974 • 27 citations

Investigation of a female manifesting Becker muscular dystrophy.

1992 • 17 citations

Deleted Work

1955 • 0 citations