Unwrapping the genes of myelin.

Protein zero gene expression is regulated by the glial transcription factor Sox10. Mol Cell Biol (2000) 2.11

Pelizaeus-Merzbacher disease: an X-linked neurologic disorder of myelin metabolism with a novel mutation in the gene encoding proteolipid protein. Am J Hum Genet (1989) 1.64

Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13). J Cell Biol (1992) 1.56

Tst-1, a member of the POU domain gene family, binds the promoter of the gene encoding the cell surface adhesion molecule P0. Mol Cell Biol (1991) 1.56

Drosophila chaoptin, a member of the leucine-rich repeat family, is a photoreceptor cell-specific adhesion molecule. EMBO J (1990) 1.43

Myelin basic protein gene contains separate enhancers for oligodendrocyte and Schwann cell expression. J Cell Biol (1992) 1.43

A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse. Proc Natl Acad Sci U S A (1992) 1.36

Mutation of the proteolipid protein gene PLP in a human X chromosome-linked myelin disorder. Proc Natl Acad Sci U S A (1989) 1.32

The oligodendrocyte-myelin glycoprotein belongs to a distinct family of proteins and contains the HNK-1 carbohydrate. J Cell Biol (1990) 1.19

Identification of an embryonic isoform of myelin basic protein that is expressed widely in the mouse embryo. Proc Natl Acad Sci U S A (1993) 1.19

Myelin/oligodendrocyte glycoprotein is a member of a subset of the immunoglobulin superfamily encoded within the major histocompatibility complex. Proc Natl Acad Sci U S A (1993) 1.13

Distinct functions for thyroid hormone receptors alpha and beta in brain development indicated by differential expression of receptor genes. EMBO J (1991) 1.13

Membrane structure in isolated and intact myelins. Biophys J (1989) 1.11

Axon-regulated expression of a Schwann cell transcript that is homologous to a 'growth arrest-specific' gene. EMBO J (1991) 1.10

Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipid. Proc Natl Acad Sci U S A (1991) 1.06

Immune tolerance in multiple sclerosis. Immunol Rev (2011) 1.03

Molecular anatomy and genetics of myelin proteins in the peripheral nervous system. J Anat (1995) 1.02

Animal models for inherited peripheral neuropathies. J Anat (1997) 1.00

Embryonic Schwann cell development: the biology of Schwann cell precursors and early Schwann cells. J Anat (1997) 0.90

Tetrameric assembly of full-sequence protein zero myelin glycoprotein by synchrotron x-ray scattering. Biophys J (1999) 0.86

Dominant-negative action of the jimpy mutation in mice complemented with an autosomal transgene for myelin proteolipid protein. Proc Natl Acad Sci U S A (1995) 0.83

Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene. Brain (2015) 0.81

Transgenic mouse model for neurocristopathy: Schwannomas and facial bone tumors. Proc Natl Acad Sci U S A (1993) 0.78

Differential expression of sodium channels in acutely isolated myelinating and non-myelinating Schwann cells of rabbits. J Physiol (1993) 0.77

Two novel missense mutations in the myelin protein zero gene causes Charcot-Marie-Tooth type 2 and Déjérine-Sottas syndrome. BMC Res Notes (2010) 0.75

Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family. Neurogenetics (2003) 0.75

Isolation and analysis of the gene encoding peripheral myelin protein zero. Neuron (1988) 2.07