scholarly article | Q13442814 |
P2093 | author name string | Rivier F | |
Fabbrizio E | |||
Mornet D | |||
Latouche J | |||
Hugon G | |||
P2860 | cites work | Tissue distribution of the dystrophin-related gene product and expression in the mdx and dy mouse | Q24563536 |
Dystroglycan is a binding protein of laminin and merosin in peripheral nerve | Q28238540 | ||
An autosomal transcript in skeletal muscle with homology to dystrophin | Q28251871 | ||
Detection of dystrophin in the postsynaptic density of rat brain and deficiency in a mouse model of Duchenne muscular dystrophy | Q30273955 | ||
Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells | Q31157622 | ||
G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brain. | Q34369312 | ||
Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse | Q35493060 | ||
Increased calcium influx in dystrophic muscle | Q36530501 | ||
An alternative dystrophin transcript specific to peripheral nerve | Q36785316 | ||
Apo-dystrophin-3: a 2.2kb transcript from the DMD locus encoding the dystrophin glycoprotein binding site | Q36785926 | ||
A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues | Q37055980 | ||
Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy. | Q41418979 | ||
Apo-dystrophin-1 and apo-dystrophin-2, products of the Duchenne muscular dystrophy locus: expression during mouse embryogenesis and in cultured cell lines | Q41451557 | ||
A novel product of the Duchenne muscular dystrophy gene which greatly differs from the known isoforms in its structure and tissue distribution | Q41712336 | ||
Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy gene | Q41748776 | ||
Abnormal localization of laminin subunits in muscular dystrophies | Q42503064 | ||
Characterization and localization of a 77 kDa protein related to the dystrophin gene family | Q42835422 | ||
Dp71, the nonmuscle product of the Duchenne muscular dystrophy gene is associated with the cell membrane | Q48233687 | ||
Laminin-binding protein 120 from brain is closely related to the dystrophin-associated glycoprotein, dystroglycan, and binds with high affinity to the major heparin binding domain of laminin | Q48249023 | ||
Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters | Q48429125 | ||
Duchenne muscular dystrophy gene product is not identical in muscle and brain. | Q52066801 | ||
Full-length and short forms of utrophin, the dystrophin-related protein. | Q55481178 | ||
Utrophin localization in normal and dystrophin-deficient heart | Q58105046 | ||
Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus | Q59070435 | ||
A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal andmdxmice Immunological evidence | Q67689028 | ||
Localization and quantitation of the chromosome 6-encoded dystrophin-related protein in normal and pathological human muscle | Q70579629 | ||
Monoclonal antibodies targeted against the C-terminal domain of dystrophin or utrophin | Q70680908 | ||
Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin | Q72285816 | ||
Differential expression of dystrophin, utrophin and dystrophin-associated proteins in peripheral nerve | Q72615801 | ||
Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice | Q72640306 | ||
Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients | Q72706803 | ||
Dystrophin and dystrophin-related protein expression in Torpedo marmorata electric organ | Q72903853 | ||
P407 | language of work or name | English | Q1860 |
P1104 | number of pages | 6 | |
P304 | page(s) | 309-314 | |
P577 | publication date | 1995-11-01 | |
P1433 | published in | Biochemical Journal | Q864221 |
P1476 | title | Re-evaluation of the distributions of dystrophin and utrophin in sciatic nerve | |
P478 | volume | 312 ( Pt 1) |
Q40070831 | Dp71, utrophin and beta-dystroglycan expression and distribution in PC12/L6 cell cocultures |
Q37335465 | Dystroglycan receptor is involved in integrin activation in intestinal epithelia |
Q46427690 | Dystrophin Dp116: A yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene |
Q73667417 | Dystrophin and its isoforms in a sympathetic ganglion of normal and dystrophic mdx mice: immunolocalization by electron microscopy and biochemical characterization |
Q33961107 | Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies |
Q35987510 | Effect of beta-dystroglycan processing on utrophin/Dp116 anchorage in normal and mdx mouse Schwann cell membrane. |
Q73176423 | Expression of a new M(r) 70-kDa dystrophin-related protein in the axon of peripheral nerves from Torpedo marmorata |
Q37915435 | Glia unglued: how signals from the extracellular matrix regulate the development of myelinating glia |
Q28344625 | Immunolocalisation of neuronal nitric oxide synthase at the neuromuscular junction of MDX mice: a confocal microscopy study |
Q77131893 | Molecular mechanisms and putative signalling events controlling utrophin expression in mammalian skeletal muscle fibres |
Q42379475 | Pathological pattern of Mdx mice diaphragm correlates with gradual expression of the short utrophin isoform Up71. |
Q30820172 | Presence of invertebrate dystrophin-like products in obliquely striated muscle of the leech, Pontobdella muricata (Annelida, Hirudinea). |
Q33887124 | Regulation and functional significance of utrophin expression at the mammalian neuromuscular synapse |
Q43044129 | The ABCA1 cholesterol transporter associates with one of two distinct dystrophin-based scaffolds in Schwann cells |
Q48378746 | The dystrophin / utrophin homologues in Drosophila and in sea urchin |
Q41160197 | Utrophin: a structural and functional comparison to dystrophin |
Q24672189 | ZZ domain of dystrophin and utrophin: topology and mapping of a beta-dystroglycan interaction site |
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