Pages that link to "Q41182264"

The following pages link to Myelin mutants: model systems for the study of normal and abnormal myelination (Q41182264):

Displaying 33 items.

• Teneurin-4 is a novel regulator of oligodendrocyte differentiation and myelination of small-diameter axons in the CNS (Q28505398) (← links)
• Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene (Q28509913) (← links)
• CNS myelin and sertoli cell tight junction strands are absent in Osp/claudin-11 null mice (Q28512612) (← links)
• Insertion of a retrotransposon in Mbp disrupts mRNA splicing and myelination in a new mutant rat (Q28580564) (← links)
• Characterization of the optic nerve and retinal ganglion cell layer in the dysmyelinated adult Long Evans Shaker rat: evidence for axonal sprouting (Q28582134) (← links)
• A mutation in the gene encoding mitochondrial Mg² channel MRS2 results in demyelination in the rat. (Q29347166) (← links)
• Transcriptional profile of the human peripheral nervous system by serial analysis of gene expression (Q30956325) (← links)
• Identification of a new exon in the myelin proteolipid protein gene encoding novel protein isoforms that are restricted to the somata of oligodendrocytes and neurons (Q31402007) (← links)
• A mutation in the canine gene encoding folliculin-interacting protein 2 (FNIP2) associated with a unique disruption in spinal cord myelination (Q33631202) (← links)
• Trembler as a mouse model of CMT1A? (Q33787366) (← links)
• Myelin and disorders that affect the formation and maintenance of this sheath (Q33971574) (← links)
• New perspectives on the function of myelin galactolipids. (Q34066203) (← links)
• A molecular view on paranodal junctions of myelinated fibers. (Q34470090) (← links)
• Motor training compensates for cerebellar dysfunctions caused by oligodendrocyte ablation (Q35122690) (← links)
• The Myelin Mutants as Models to Study Myelin Repair in the Leukodystrophies (Q35648148) (← links)
• DTI abnormalities in anterior corpus callosum of rats with spike-wave epilepsy (Q37266785) (← links)
• Highly malignant behavior of a murine oligodendrocyte precursor cell line following transplantation into the demyelinated and nondemyelinated central nervous system. (Q39379307) (← links)
• The monoclonal antibody 23E9 defines a novel developmentally-regulated Schwann cell surface antigen (Q40789313) (← links)
• The transcription factor Yin Yang 1 is essential for oligodendrocyte progenitor differentiation. (Q42591243) (← links)
• Oligodendroglial pathology in the development of myelin breakdown in the dmy mutant rat (Q44141971) (← links)
• A physical map of the genomic region on mouse chromosome 3 containing the hindshaker (hsh) mutation (Q47284024) (← links)
• Current concepts of PLP and its role in the nervous system (Q47808566) (← links)
• Axonal Swellings and Degeneration in Mice Lacking the Major Proteolipid of Myelin (Q48004959) (← links)
• Neural disease: Drosophila degenerates for a good cause (Q48352728) (← links)
• Myelin proteolipid protein (Plp) intron 1 DNA is required to temporally regulate Plp gene expression in the brain (Q48477173) (← links)
• Myelin galactolipids are essential for proper node of Ranvier formation in the CNS. (Q48519848) (← links)
• Fatty acid synthase expression during peripheral nervous system myelination. (Q48607391) (← links)
• Modification of Schwann cell phenotype withPlp transgenes: Evidence that the PLP and DM20 isoproteins are targeted to different cellular domains (Q48615163) (← links)
• Narrowing critical regions and determining penetrance for selected 18q- phenotypes. (Q54040009) (← links)
• Insertion of proteolipid protein into mitochondria but not DM20 regulates metabolism of cells (Q61855835) (← links)
• A transgenic mouse model for inducible and reversible dysmyelination (Q73066534) (← links)
• Acetyl-CoA carboxylase and SREBP expression during peripheral nervous system myelination (Q73198853) (← links)
• Loss of Wwox Causes Defective Development of Cerebral Cortex with Hypomyelination in a Rat Model of Lethal Dwarfism with Epilepsy (Q92150549) (← links)