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Journal Abstract Search

152 related items for PubMed ID: 22902553

  • 1. Proteolipid protein dimerization at cysteine 108: Implications for protein structure.
    Daffu G, Sohi J, Kamholz J.
    Neurosci Res; 2012 Oct; 74(2):144-55. PubMed ID: 22902553
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  • 2. A common mechanism of PLP/DM20 misfolding causes cysteine-mediated endoplasmic reticulum retention in oligodendrocytes and Pelizaeus-Merzbacher disease.
    Dhaunchak AS, Nave KA.
    Proc Natl Acad Sci U S A; 2007 Nov 06; 104(45):17813-8. PubMed ID: 17962415
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  • 3. PLP/DM20 expression and turnover in a transgenic mouse model of Pelizaeus-Merzbacher disease.
    Karim SA, Barrie JA, McCulloch MC, Montague P, Edgar JM, Iden DL, Anderson TJ, Nave KA, Griffiths IR, McLaughlin M.
    Glia; 2010 Nov 01; 58(14):1727-38. PubMed ID: 20629189
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  • 6. Overexpression of DM20 messenger RNA in two brothers with Pelizaeus-Merzbacher disease.
    Carango P, Funanage VL, Quirós RE, Debruyn CS, Marks HG.
    Ann Neurol; 1995 Oct 01; 38(4):610-7. PubMed ID: 7574457
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  • 10. Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating Disease.
    Cailloux F, Gauthier-Barichard F, Mimault C, Isabelle V, Courtois V, Giraud G, Dastugue B, Boespflug-Tanguy O.
    Eur J Hum Genet; 2000 Nov 01; 8(11):837-45. PubMed ID: 11093273
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  • 11. A cellular mechanism governing the severity of Pelizaeus-Merzbacher disease.
    Gow A, Lazzarini RA.
    Nat Genet; 1996 Aug 01; 13(4):422-8. PubMed ID: 8696336
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  • 13. Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transport.
    Gow A, Friedrich VL, Lazzarini RA.
    J Neurosci Res; 1994 Apr 01; 37(5):574-83. PubMed ID: 7518006
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  • 14. Peripheral neuropathy caused by proteolipid protein gene mutations.
    Garbern JY, Cambi F, Lewis R, Shy M, Sima A, Kraft G, Vallat JM, Bosch EP, Hodes ME, Dlouhy S, Raskind W, Bird T, Macklin W, Kamholz J.
    Ann N Y Acad Sci; 1999 Sep 14; 883():351-65. PubMed ID: 10586260
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  • 15. PLP1 splicing abnormalities identified in Pelizaeus-Merzbacher disease and SPG2 fibroblasts are associated with different types of mutations.
    Bonnet-Dupeyron MN, Combes P, Santander P, Cailloux F, Boespflug-Tanguy O, Vaurs-Barrière C.
    Hum Mutat; 2008 Aug 14; 29(8):1028-36. PubMed ID: 18470932
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  • 16. Monoclonal antibody O10 defines a conformationally sensitive cell-surface epitope of proteolipid protein (PLP): evidence that PLP misfolding underlies dysmyelination in mutant mice.
    Jung M, Sommer I, Schachner M, Nave KA.
    J Neurosci; 1996 Dec 15; 16(24):7920-9. PubMed ID: 8987820
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  • 17. Proteolipid protein interactions in transfectants: implications for myelin assembly.
    Sinoway MP, Kitagawa K, Timsit S, Hashim GA, Colman DR.
    J Neurosci Res; 1994 Apr 01; 37(5):551-62. PubMed ID: 7518004
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  • 19. PLP1 gene duplication causes overexpression and alteration of the PLP/DM20 splicing balance in fibroblasts from Pelizaeus-Merzbacher disease patients.
    Regis S, Grossi S, Corsolini F, Biancheri R, Filocamo M.
    Biochim Biophys Acta; 2009 Jun 01; 1792(6):548-54. PubMed ID: 19376225
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  • 20. A PLP splicing abnormality is associated with an unusual presentation of PMD.
    Hobson GM, Huang Z, Sperle K, Stabley DL, Marks HG, Cambi F.
    Ann Neurol; 2002 Oct 01; 52(4):477-88. PubMed ID: 12325077
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