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4. Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders. Willard HF, Riordan JR. Science; 1985 Nov 22; 230(4728):940-2. PubMed ID: 3840606 [Abstract] [Full Text] [Related]
5. The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice. Dautigny A, Mattei MG, Morello D, Alliel PM, Pham-Dinh D, Amar L, Arnaud D, Simon D, Mattei JF, Guenet JL. Nature; 1985 Nov 22; 321(6073):867-9. PubMed ID: 2425262 [Abstract] [Full Text] [Related]
9. Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease. Raskind WH, Williams CA, Hudson LD, Bird TD. Am J Hum Genet; 1991 Dec 22; 49(6):1355-60. PubMed ID: 1720927 [Abstract] [Full Text] [Related]
15. Proteolipid proteins: structure and genetic expression in normal and myelin-deficient mutant mice. Nave KA, Milner RJ. Crit Rev Neurobiol; 1989 Dec 22; 5(1):65-91. PubMed ID: 2670252 [Abstract] [Full Text] [Related]
16. PLP overexpression perturbs myelin protein composition and myelination in a mouse model of Pelizaeus-Merzbacher disease. Karim SA, Barrie JA, McCulloch MC, Montague P, Edgar JM, Kirkham D, Anderson TJ, Nave KA, Griffiths IR, McLaughlin M. Glia; 2007 Mar 22; 55(4):341-51. PubMed ID: 17133418 [Abstract] [Full Text] [Related]
17. 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 [Abstract] [Full Text] [Related]
19. A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher disease. Pratt VM, Trofatter JA, Schinzel A, Dlouhy SR, Conneally PM, Hodes ME. Am J Med Genet; 1991 Jan 01; 38(1):136-9. PubMed ID: 1707231 [Abstract] [Full Text] [Related]