Pages that link to "Q36785316"
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The following pages link to An alternative dystrophin transcript specific to peripheral nerve (Q36785316):
Displaying 50 items.
- Dystrophin Dp71 is required for neurite outgrowth in PC12 cells (Q24293534) (← links)
- Dystrophin Dp71: the smallest but multifunctional product of the Duchenne muscular dystrophy gene (Q24298098) (← links)
- Syntrophin binds to an alternatively spliced exon of dystrophin (Q24312273) (← links)
- Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24 (Q24314323) (← links)
- Dystrophins and dystrobrevins (Q24805434) (← links)
- Characterization of DRP2, a novel human dystrophin homologue (Q28114838) (← links)
- Immunolocalisation of neuronal nitric oxide synthase at the neuromuscular junction of MDX mice: a confocal microscopy study (Q28344625) (← links)
- Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization (Q28508732) (← links)
- Identification of Dp71e, a new dystrophin with a novel carboxy-terminal end (Q28565042) (← links)
- Dystrophin Dp71f associates with the beta1-integrin adhesion complex to modulate PC12 cell adhesion (Q28578480) (← links)
- Differential expression and subcellular distribution of dystrophin Dp71 isoforms during differentiation process (Q28579272) (← links)
- Phosphorylation of dystrophin Dp71d by Ca2+/calmodulin-dependent protein kinase II modulates the Dp71d nuclear localization in PC12 cells (Q28583921) (← links)
- Identification of Dp71 isoforms in the platelet membrane cytoskeleton. Potential role in thrombin-mediated platelet adhesion (Q28589594) (← links)
- C6ORF32 is upregulated during muscle cell differentiation and induces the formation of cellular filopodia (Q29347282) (← links)
- Molecular analysis of a spontaneous dystrophin 'knockout' dog. (Q30735735) (← links)
- The dystrotelin, dystrophin and dystrobrevin superfamily: new paralogues and old isoforms. (Q33269611) (← links)
- Splicing mutations in DMD/BMD detected by RT-PCR/PTT: detection of a 19AA insertion in the cysteine rich domain of dystrophin compatible with BMD (Q33678004) (← links)
- Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides. (Q33868227) (← links)
- Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies (Q33961107) (← links)
- Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter (Q34183444) (← links)
- Dystrophin and mutations: one gene, several proteins, multiple phenotypes (Q34278933) (← links)
- Somitic origin of limb muscle satellite and side population cells (Q34304849) (← links)
- The human dystrophin gene requires 16 hours to be transcribed and is cotranscriptionally spliced (Q34308679) (← links)
- Searching for the 1 in 2,400,000: a review of dystrophin gene point mutations (Q34324968) (← links)
- G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brain. (Q34369312) (← links)
- Phosphorylation within the cysteine-rich region of dystrophin enhances its association with β-dystroglycan and identifies a potential novel therapeutic target for skeletal muscle wasting (Q34575694) (← links)
- Abnormal turning behavior in Drosophila larvae. Identification and molecular analysis of scribbler (sbb) (Q34609833) (← links)
- Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models. (Q34699458) (← links)
- Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation (Q34797193) (← links)
- The role of utrophin in the potential therapy of Duchenne muscular dystrophy (Q34807150) (← links)
- ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy (Q35432074) (← links)
- The identification of point mutations in Duchenne muscular dystrophy patients by using reverse-transcription PCR and the protein truncation test (Q35644562) (← links)
- Molecular microdomains in a sensory terminal, the vestibular calyx ending (Q35748331) (← links)
- Experience and strategy for the molecular testing of Duchenne muscular dystrophy (Q35789975) (← links)
- Effect of beta-dystroglycan processing on utrophin/Dp116 anchorage in normal and mdx mouse Schwann cell membrane. (Q35987510) (← links)
- Nonmechanical Roles of Dystrophin and Associated Proteins in Exercise, Neuromuscular Junctions, and Brains (Q36105739) (← links)
- Regulation of myogenic progenitor proliferation in human fetal skeletal muscle by BMP4 and its antagonist Gremlin (Q36118952) (← links)
- Gastrointestinal Dysfunction in Patients with Duchenne Muscular Dystrophy (Q36162530) (← links)
- Laminins and their receptors in Schwann cells and hereditary neuropathies (Q36164129) (← links)
- Absence of extraocular muscle pathology in Duchenne's muscular dystrophy: role for calcium homeostasis in extraocular muscle sparing (Q36365256) (← links)
- Melanocytes--a novel tool to study mitochondrial dysfunction in Duchenne muscular dystrophy (Q36695834) (← links)
- Dystrophin and utrophin isoforms are expressed in glia, but not neurons, of the avian parasympathetic ciliary ganglion (Q36832586) (← links)
- Effect of dystrophin antisense oligonucleotides on cultured human neurons (Q36874732) (← links)
- Mutation types and aging differently affect revertant fiber expansion in dystrophic mdx and mdx52 mice (Q37042659) (← links)
- Characterization of a Dmd (EGFP) reporter mouse as a tool to investigate dystrophin expression (Q37064342) (← links)
- Assessment of the structural and functional impact of in-frame mutations of the DMD gene, using the tools included in the eDystrophin online database (Q37109015) (← links)
- Association between loss of dp140 and cognitive impairment in duchenne and becker dystrophies (Q37328965) (← links)
- Dystroglycan receptor is involved in integrin activation in intestinal epithelia (Q37335465) (← links)
- Gene therapy in large animal models of muscular dystrophy (Q37396408) (← links)
- Mouse regenerating myofibers detected as false-positive donor myofibers with anti-human spectrin (Q37508255) (← links)