167 related articles for article (PubMed ID: 2479544)
1. Myelin-deficient rat: a point mutation in exon III (A----C, Thr75----Pro) of the myelin proteolipid protein causes dysmyelination and oligodendrocyte death.
Boison D; Stoffel W
EMBO J; 1989 Nov; 8(11):3295-302. PubMed ID: 2479544
[TBL] [Abstract][Full Text] [Related]
2. Single base substitution in codon 74 of the MD rat myelin proteolipid protein gene.
Simons R; Riordan JR
Ann N Y Acad Sci; 1990; 605():146-54. PubMed ID: 1702593
[TBL] [Abstract][Full Text] [Related]
3. Gene expression and oligodendrocyte development in the myelin deficient rat.
Nadon NL; Duncan ID
J Neurosci Res; 1995 May; 41(1):96-104. PubMed ID: 7674382
[TBL] [Abstract][Full Text] [Related]
4. Oligodendrocyte survival and function in the long-lived strain of the myelin deficient rat.
Duncan ID; Nadon NL; Hoffman RL; Lunn KF; Csiza C; Wells MR
J Neurocytol; 1995 Oct; 24(10):745-62. PubMed ID: 8586995
[TBL] [Abstract][Full Text] [Related]
5. The myelin-deficient rat has a single base substitution in the third exon of the myelin proteolipid protein gene.
Simons R; Riordan JR
J Neurochem; 1990 Mar; 54(3):1079-81. PubMed ID: 1689377
[TBL] [Abstract][Full Text] [Related]
6. Transcriptional regulation studies of myelin-associated genes in myelin-deficient mutant rats.
Kumar S; Macklin WB; Gordon MN; Espinosa de los Monteros A; Cole R; Scully SA; de Vellis J
Dev Neurosci; 1990; 12(4-5):316-25. PubMed ID: 1705212
[TBL] [Abstract][Full Text] [Related]
7. Evolution of the myelin integral membrane proteins of the central nervous system.
Schliess F; Stoffel W
Biol Chem Hoppe Seyler; 1991 Sep; 372(9):865-74. PubMed ID: 1722981
[TBL] [Abstract][Full Text] [Related]
8. A point mutation in the proteolipid protein gene of the 'shaking pup' interrupts oligodendrocyte development.
Nadon NL; Duncan ID; Hudson LD
Development; 1990 Oct; 110(2):529-37. PubMed ID: 1723945
[TBL] [Abstract][Full Text] [Related]
9. Mutations in the myelin proteolipid protein gene alter oligodendrocyte gene expression in jimpy and jimpymsd mice.
Macklin WB; Gardinier MV; Obeso ZO; King KD; Wight PA
J Neurochem; 1991 Jan; 56(1):163-71. PubMed ID: 1702830
[TBL] [Abstract][Full Text] [Related]
10. Mutations in the rat myelin basic protein gene are associated with specific alterations in other myelin gene expression.
Carré JL; Goetz BD; O'Connor LT; Bremer Q; Duncan ID
Neurosci Lett; 2002 Sep; 330(1):17-20. PubMed ID: 12213624
[TBL] [Abstract][Full Text] [Related]
11. Myelin protein expression in the myelin-deficient rat brain and cultured oligodendrocytes.
Zeller NK; Dubois-Dalcq M; Lazzarini RA
J Mol Neurosci; 1989; 1(3):139-49. PubMed ID: 2484440
[TBL] [Abstract][Full Text] [Related]
12. Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene.
Kagawa T; Ikenaka K; Inoue Y; Kuriyama S; Tsujii T; Nakao J; Nakajima K; Aruga J; Okano H; Mikoshiba K
Neuron; 1994 Aug; 13(2):427-42. PubMed ID: 7520255
[TBL] [Abstract][Full Text] [Related]
13. Intracellular distribution of myelin protein gene products is altered in oligodendrocytes of the taiep rat.
O'Connor LT; Goetz BD; Couve E; Song J; Duncan ID
Mol Cell Neurosci; 2000 Oct; 16(4):396-407. PubMed ID: 11085877
[TBL] [Abstract][Full Text] [Related]
14. Normal temporal and spatial distribution of oligodendrocyte progenitors in the myelin-deficient (md) rat.
Pringle NP; Nadon NL; Rhode DM; Richardson WD; Duncan ID
J Neurosci Res; 1997 Feb; 47(3):264-70. PubMed ID: 9039648
[TBL] [Abstract][Full Text] [Related]
15. Paralytic tremor (pt): a new allele of the proteolipid protein gene in rabbits.
Tosic M; Dolivo M; Domańska-Janik K; Matthieu JM
J Neurochem; 1994 Dec; 63(6):2210-6. PubMed ID: 7525875
[TBL] [Abstract][Full Text] [Related]
16. Oligodendrocytes expressing exclusively the DM20 isoform of the proteolipid protein gene: myelination and development.
Spörkel O; Uschkureit T; Büssow H; Stoffel W
Glia; 2002 Jan; 37(1):19-30. PubMed ID: 11746780
[TBL] [Abstract][Full Text] [Related]
17. A combination of PLP and DM20 transgenes promotes partial myelination in the jimpy mouse.
Nadon NL; Arnheiter H; Hudson LD
J Neurochem; 1994 Sep; 63(3):822-33. PubMed ID: 7519661
[TBL] [Abstract][Full Text] [Related]
18. A missense mutation in the proteolipid protein gene responsible for Pelizaeus-Merzbacher disease in a Japanese family.
Iwaki A; Muramoto T; Iwaki I; Furumi H; Dario-deLeon ML; Tateishi J; Fukumaki Y
Hum Mol Genet; 1993 Jan; 2(1):19-22. PubMed ID: 7683951
[TBL] [Abstract][Full Text] [Related]
19. A single nucleotide difference in the gene for myelin proteolipid protein defines the jimpy mutation in mouse.
Nave KA; Bloom FE; Milner RJ
J Neurochem; 1987 Dec; 49(6):1873-7. PubMed ID: 2445921
[TBL] [Abstract][Full Text] [Related]
20. Conservative amino acid substitution in the myelin proteolipid protein of jimpymsd mice.
Gencic S; Hudson LD
J Neurosci; 1990 Jan; 10(1):117-24. PubMed ID: 1688931
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]