Re-evaluation of the distributions of dystrophin and utrophin in sciatic nerve

scientific article published on November 1995

Re-evaluation of the distributions of dystrophin and utrophin in sciatic nerve is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1042/BJ3120309
P932PMC publication ID1136260
P698PubMed publication ID7492329
P5875ResearchGate publication ID15707430

P2093author name stringRivier F
Fabbrizio E
Mornet D
Latouche J
Hugon G
P2860cites workTissue distribution of the dystrophin-related gene product and expression in the mdx and dy mouseQ24563536
Dystroglycan is a binding protein of laminin and merosin in peripheral nerveQ28238540
An autosomal transcript in skeletal muscle with homology to dystrophinQ28251871
Detection of dystrophin in the postsynaptic density of rat brain and deficiency in a mouse model of Duchenne muscular dystrophyQ30273955
Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cellsQ31157622
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 mouseQ35493060
Increased calcium influx in dystrophic muscleQ36530501
An alternative dystrophin transcript specific to peripheral nerveQ36785316
Apo-dystrophin-3: a 2.2kb transcript from the DMD locus encoding the dystrophin glycoprotein binding siteQ36785926
A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissuesQ37055980
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 linesQ41451557
A novel product of the Duchenne muscular dystrophy gene which greatly differs from the known isoforms in its structure and tissue distributionQ41712336
Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy geneQ41748776
Abnormal localization of laminin subunits in muscular dystrophiesQ42503064
Characterization and localization of a 77 kDa protein related to the dystrophin gene familyQ42835422
Dp71, the nonmuscle product of the Duchenne muscular dystrophy gene is associated with the cell membraneQ48233687
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 lamininQ48249023
Expression of four alternative dystrophin transcripts in brain regions regulated by different promotersQ48429125
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 heartQ58105046
Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminusQ59070435
A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal andmdxmice Immunological evidenceQ67689028
Localization and quantitation of the chromosome 6-encoded dystrophin-related protein in normal and pathological human muscleQ70579629
Monoclonal antibodies targeted against the C-terminal domain of dystrophin or utrophinQ70680908
Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophinQ72285816
Differential expression of dystrophin, utrophin and dystrophin-associated proteins in peripheral nerveQ72615801
Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx miceQ72640306
Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patientsQ72706803
Dystrophin and dystrophin-related protein expression in Torpedo marmorata electric organQ72903853
P407language of work or nameEnglishQ1860
P1104number of pages6
P304page(s)309-314
P577publication date1995-11-01
P1433published inBiochemical JournalQ864221
P1476titleRe-evaluation of the distributions of dystrophin and utrophin in sciatic nerve
P478volume312 ( Pt 1)

Reverse relations

cites work (P2860)
Q40070831Dp71, utrophin and beta-dystroglycan expression and distribution in PC12/L6 cell cocultures
Q37335465Dystroglycan receptor is involved in integrin activation in intestinal epithelia
Q46427690Dystrophin Dp116: A yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene
Q73667417Dystrophin and its isoforms in a sympathetic ganglion of normal and dystrophic mdx mice: immunolocalization by electron microscopy and biochemical characterization
Q33961107Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies
Q35987510Effect of beta-dystroglycan processing on utrophin/Dp116 anchorage in normal and mdx mouse Schwann cell membrane.
Q73176423Expression of a new M(r) 70-kDa dystrophin-related protein in the axon of peripheral nerves from Torpedo marmorata
Q37915435Glia unglued: how signals from the extracellular matrix regulate the development of myelinating glia
Q28344625Immunolocalisation of neuronal nitric oxide synthase at the neuromuscular junction of MDX mice: a confocal microscopy study
Q77131893Molecular mechanisms and putative signalling events controlling utrophin expression in mammalian skeletal muscle fibres
Q42379475Pathological pattern of Mdx mice diaphragm correlates with gradual expression of the short utrophin isoform Up71.
Q30820172Presence of invertebrate dystrophin-like products in obliquely striated muscle of the leech, Pontobdella muricata (Annelida, Hirudinea).
Q33887124Regulation and functional significance of utrophin expression at the mammalian neuromuscular synapse
Q43044129The ABCA1 cholesterol transporter associates with one of two distinct dystrophin-based scaffolds in Schwann cells
Q48378746The dystrophin / utrophin homologues in Drosophila and in sea urchin
Q41160197Utrophin: a structural and functional comparison to dystrophin
Q24672189ZZ domain of dystrophin and utrophin: topology and mapping of a beta-dystroglycan interaction site

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