Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene

[1]  K. Mikoshiba,et al.  Fate of Jimpy‐Type Oligodendrocytes in Jimpy Heterozygote , 1994, Journal of neurochemistry.

[2]  C. Readhead,et al.  Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage , 1994, Neuron.

[3]  C. Ackerley,et al.  Demyelination in a transgenic mouse: A model for multiple sclerosis , 1993, Journal of neuroscience research.

[4]  K. Kitagawa,et al.  A proteolipid protein gene family: Expression in sharks and rays and possible evolution from an ancestral gene encoding a pore-forming polypeptide , 1993, Neuron.

[5]  Yimin Yan,et al.  Molecular cloning of M6: Identification of a PLP/DM20 gene family , 1993, Neuron.

[6]  A. Warrington,et al.  The oligodendrocyte and its many cellular processes. , 1993, Trends in cell biology.

[7]  J. Schleutker,et al.  Linkage of a new mutation in the proteolipid protein (PLP) gene to Pelizaeus-Merzbacher disease (PMD) in a large Finnish kindred. , 1993, American journal of human genetics.

[8]  K. Mikoshiba,et al.  Novel Isoforms of Mouse Myelin Basic Protein Predominantly Expressed in Embryonic Stage , 1993, Journal of neurochemistry.

[9]  D. Pham‐Dinh,et al.  Pelizaeus-Merzbacher disease: a frameshift deletion/insertion event in the myelin proteolipid gene. , 1993, Human molecular genetics.

[10]  A. Warrington,et al.  Proliferation and differentiation of O4+ oligodendrocytes in postnatal rat cerebellum: Analysis in unfixed tissue slices using anti‐glycolipid antibodies , 1992, Journal of neuroscience research.

[11]  Sue Malcolm,et al.  Pelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosis. , 1992, American journal of human genetics.

[12]  C. Campagnoni,et al.  DM20 mRNA splice product of the myelin proteolipid protein gene is expressed in the murine heart , 1992, Journal of neuroscience research.

[13]  K. Nave,et al.  Uncoupling of hypomyelination and glial cell death by a mutation in the proteolipid protein gene , 1992, Nature.

[14]  K. Hayasaka,et al.  Isolation and sequence determination of cDNA encoding PMP-22 (PAS-II/SR13/Gas-3) of human peripheral myelin. , 1992, Biochemical and biophysical research communications.

[15]  R. Schiffmann,et al.  Molecular diagnostics for myelin proteolipid protein gene mutations in Pelizaeus-Merzbacher disease. , 1992, American journal of human genetics.

[16]  B. Trask,et al.  The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1A , 1992, Nature Genetics.

[17]  K. Mikoshiba,et al.  Selective Expression of DM‐20, an Alternatively Spliced Myelin Proteolipid Protein Gene Product, in Developing Nervous System and in Nonglial Cells , 1992, Journal of neurochemistry.

[18]  P. De Jonghe,et al.  The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication , 1992, Nature Genetics.

[19]  D. Housman,et al.  The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1A , 1992, Nature Genetics.

[20]  M. Hodes,et al.  New variant in exon 3 of the proteolipid protein (PLP) gene in a family with Pelizaeus-Merzbacher disease. , 1992, American journal of medical genetics.

[21]  T. Bird,et al.  Peripheral myelin protein–22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot–Marie–Tooth 1A , 1992, Nature Genetics.

[22]  E. Shooter,et al.  Trembler mouse carries a point mutation in a myelin gene , 1992, Nature.

[23]  S. Timsit,et al.  DM‐20 mRNA Is Expressed During the Embryonic Development of the Nervous System of the Mouse , 1992, Journal of neurochemistry.

[24]  C. Williams,et al.  Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease. , 1991, American journal of human genetics.

[25]  D. Pham‐Dinh,et al.  Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipid. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[26]  E. Shooter,et al.  A myelin protein is encoded by the homologue of a growth arrest-specific gene. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[27]  A. Campagnoni,et al.  Oligodendrocytes of the jimpy phenotype can be partially restored by environmental factors in vivo , 1991, Journal of neuroscience research.

[28]  K. Mikoshiba,et al.  Developmental Expression of Myelin Protein Genes in Dysmyelinating Mutant Mice: Analysis by Nuclear Run‐Off Transcription Assay, In Situ Hybridization, and Immunohistochemistry , 1991, Journal of neurochemistry.

[29]  D. Pham‐Dinh,et al.  Proteolipid DM-20 predominates over PLP in peripheral nervous system. , 1991, Neuroreport.

[30]  K. Mikoshiba,et al.  Myelin Basic Protein Gene and the Function of Antisense RNA in Its Repression in Myelin‐Deficient Mutant Mouse , 1991, Journal of neurochemistry.

[31]  T. Weimbs,et al.  A point mutation at the X-chromosomal proteolipid protein locus in Pelizaeus-Merzbacher disease leads to disruption of myelinogenesis. , 1990, Biological chemistry Hoppe-Seyler.

[32]  J. Monreal,et al.  Calcium Movements Mediated by Proteolipid Protein and Nucleotides in Liposomes Prepared with the Endogenous Lipids from Brain White Matter , 1990, Journal of neurochemistry.

[33]  I. Duncan,et al.  A point mutation in the proteolipid protein gene of the 'shaking pup' interrupts oligodendrocyte development. , 1990, Development.

[34]  L. Hudson,et al.  Conservative amino acid substitution in the myelin proteolipid protein of jimpymsd mice , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[35]  M. Hodes,et al.  Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[36]  W. Stoffel,et al.  Myelin‐deficient rat: a point mutation in exon III (A‐‐‐‐C, Thr75‐‐‐‐Pro) of the myelin proteolipid protein causes dysmyelination and oligodendrocyte death. , 1989, The EMBO journal.

[37]  J. Berndt,et al.  Mutation of the proteolipid protein gene PLP in a human X chromosome-linked myelin disorder. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[38]  M. Ambler,et al.  Pelizaeus-Merzbacher disease: an X-linked neurologic disorder of myelin metabolism with a novel mutation in the gene encoding proteolipid protein. , 1989, American journal of human genetics.

[39]  I. Griffiths,et al.  Expression of myelin protein genes in Schwann cells , 1989, Journal of neurocytology.

[40]  Lennart Philipson,et al.  Genes specifically expressed at growth arrest of mammalian cells , 1988, Cell.

[41]  M. Ghandour,et al.  Expression of galactocerebroside in developing normal and jimpy oligodendrocytesin situ , 1988, Journal of neurocytology.

[42]  †Klaus‐Armin Nave,et al.  A Single Nucleotide Difference in the Gene for Myelin Proteolipid Protein Defines the Jimpy Mutation in Mouse , 1987, Journal of neurochemistry.

[43]  K. Kampf,et al.  An AG→GG transition at a splice site in the myelin proteolipid protein gene in jimpy mice results in the removal of an exon , 1987, FEBS letters.

[44]  B D Trapp,et al.  Spatial segregation of mRNA encoding myelin-specific proteins. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[45]  R. Skoff,et al.  A defect in the cell cycle of neuroglia in the myelin deficient jimpy mouse. , 1987, Brain research.

[46]  G. Roussel,et al.  Arrest of proteolipid transport through the Golgi apparatus in Jimpy brain , 1987, Journal of neurocytology.

[47]  R. Skoff,et al.  Oligodendroglial cell death in jimpy mice: an explanation for the myelin deficit , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[48]  K. Mullis,et al.  Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. , 1985, Science.

[49]  J. Sutcliffe,et al.  Nucleotide sequences of two mRNAs for rat brain myelin proteolipid protein , 1985, Cell.

[50]  H. Clark,et al.  Electron Microscopic Immunocytochemical Localization of Myelin Proteolipid Protein and Myelin Basic Protein to Oligodendrocytes in Rat Brain During Myelination , 1985, Journal of neurochemistry.

[51]  A. van Dorsselaer,et al.  Brain proteolipids. Isolation, purification and effect on ionic permeability of membranes. , 1983, European journal of biochemistry.

[52]  M. Schachner,et al.  Monoclonal antibodies (O1 to O4) to oligodendrocyte cell surfaces: an immunocytological study in the central nervous system. , 1981, Developmental biology.

[53]  D. Silberberg,et al.  Galactocerebroside is a specific cell-surface antigenic marker for oligodendrocytes in culture , 1978, Nature.

[54]  R. Skoff,et al.  Myelin deficit in the Jimpy mouse may be due to cellular abnormalities in astroglia , 1976, Nature.

[55]  W. Demyer,et al.  Pelizaeus-Merzbacher Disease , 2017 .

[56]  J. Tateishi,et al.  A missense mutation in the proteolipid protein gene responsible for Pelizaeus-Merzbacher disease in a Japanese family. , 1993, Human molecular genetics.

[57]  M. Hodes,et al.  A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher disease. , 1991, American journal of medical genetics.

[58]  M. Levine,et al.  Gene expression in the jimpy mutant: evidence for fewer oligodendrocytes expressing myelin protein genes and impaired translocation of myelin basic protein mRNA. , 1990, Developmental neuroscience.

[59]  R. Skoff,et al.  Death of individual oligodendrocytes in jimpy brain precedes expression of proteolipid protein. , 1990, Developmental neuroscience.

[60]  K. Mikoshiba,et al.  Developmental profile and differential localization of mRNAs of myelin proteins (MBP and PLP) in oligodendrocytes in the brain and in culture. , 1989, Brain research. Developmental brain research.

[61]  R. Skoff,et al.  Glial conditioned medium enables jimpy oligodendrocytes to express properties of normal oligodendrocytes: Production of myelin antigens and membranes , 1988, Glia.

[62]  K. Mikoshiba,et al.  The fifth exon of the myelin proteolipid protein-coding gene is not utilized in the brain of jimpy mutant mice. , 1987, Gene.

[63]  V. Friedrich,et al.  Myelin‐specific proteolipid protein is expressed in myelinating schwann cells but is not incorporated into myelin sheaths , 1987, Journal of neuroscience research.

[64]  T. Terashima,et al.  The glioarchitectonics of the chicken brain. IV. Electron microscopic study. , 1986, Okajimas folia anatomica Japonica.

[65]  E. Hogan,et al.  Animal Models of Genetic Disorders of Myelin , 1984 .

[66]  P. Braun,et al.  Proteins of Myelin , 1977 .