These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

69 related articles for article (PubMed ID: 9100242)

  • 1. Hypomyelinated pt mutant rabbit as a new model of Pelizeaus-Merzbacher disease.
    Sypecka J; Domańska-Janik K
    Neurol Neurochir Pol; 1996; 30 Suppl 2():43-7. PubMed ID: 9100242
    [No Abstract]   [Full Text] [Related]  

  • 2. Jimpy(msd) mouse mutation and connatal Pelizaeus-Merzbacher disease.
    Yamamoto T; Nanba E; Zhang H; Sasaki M; Komaki H; Takeshita K
    Am J Med Genet; 1998 Feb; 75(4):439-40. PubMed ID: 9482656
    [No Abstract]   [Full Text] [Related]  

  • 3. Myelin proteolipid protein mutation in the rabbit: a new model of Pelizaeus-Merzbacher disease.
    Tosic M; Dolivo M; Domanska-Janik K; Matthieu JM
    Schweiz Arch Neurol Psychiatr (1985); 1994; 145(3):24-6. PubMed ID: 7533932
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Connatal Pelizaeus-Merzbacher disease: a missense mutation in exon 4 of the proteolipid protein (PLP) gene.
    Nagao M; Kadowaki J
    J Hum Genet; 1998; 43(3):206-8. PubMed ID: 9747038
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rabbit paralytic tremor phenotype--a plp1 gene mutation as a model of human Pelizaeus-Merzbacher disease.
    Sypecka J; Domańska-Janik K
    Acta Neurobiol Exp (Wars); 2005; 65(2):221-9. PubMed ID: 15960310
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pelizaeus-Merzbacher disease in a family of Portuguese origin caused by a point mutation in exon 5 of the proteolipid protein gene.
    Pratt VM; Boyadjiev S; Dlouhy SR; Silver K; Der Kaloustian VM; Hodes ME
    Am J Med Genet; 1995 Feb; 55(4):402-4. PubMed ID: 7539212
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A G to T mutation at a splice site in a case of Pelizaeus-Merzbacher disease.
    Strautnieks S; Malcolm S
    Hum Mol Genet; 1993 Dec; 2(12):2191-2. PubMed ID: 7509235
    [No Abstract]   [Full Text] [Related]  

  • 8. Pelizaeus-Merzbacher disease caused by a de novo mutation that originated in exon 2 of the maternal great-grandfather of the propositus.
    Pratt VM; Boyadjiev S; Green K; Hodes ME; Dlouhy SR
    Am J Med Genet; 1995 Jul; 58(1):70-3. PubMed ID: 7573159
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 38(1):136-9. PubMed ID: 1707231
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Lipophilin (PLP) gene in X-linked myelin disorders.
    Fahim S; Riordan JR
    J Neurosci Res; 1986; 16(1):303-10. PubMed ID: 3746948
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Girl with signs of Pelizaeus-Merzbacher disease heterozygous for a mutation in exon 2 of the proteolipid protein gene.
    Hodes ME; DeMyer WE; Pratt VM; Edwards MK; Dlouhy SR
    Am J Med Genet; 1995 Feb; 55(4):397-401. PubMed ID: 7539211
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel nonsense proteolipid protein gene mutation as a cause of X-linked spastic paraplegia in twin males.
    Osaka H; Kawanishi C; Inoue K; Uesugi H; Hiroshi K; Nishiyama K; Yamada Y; Suzuki K; Kimura S; Kosaka K
    Biochem Biophys Res Commun; 1995 Oct; 215(3):835-41. PubMed ID: 7488049
    [TBL] [Abstract][Full Text] [Related]  

  • 13. X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus.
    Saugier-Veber P; Munnich A; Bonneau D; Rozet JM; Le Merrer M; Gil R; Boespflug-Tanguy O
    Nat Genet; 1994 Mar; 6(3):257-62. PubMed ID: 8012387
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Adrenoleukodystrophy and adrenomyeloneuropathy in 2 brothers].
    Leipner N; Köster O; Rosskamp R; Nadstawek J
    Rofo; 1984 Mar; 140(3):341-2. PubMed ID: 6423494
    [No Abstract]   [Full Text] [Related]  

  • 15. Uncoupling of hypomyelination and glial cell death by a mutation in the proteolipid protein gene.
    Schneider A; Montague P; Griffiths I; Fanarraga M; Kennedy P; Brophy P; Nave KA
    Nature; 1992 Aug; 358(6389):758-61. PubMed ID: 1380672
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A de novo mutation (C755T; Ser252Phe) in exon 6 of the proteolipid protein gene responsible for Pelizaeus-Merzbacher disease.
    Hodes ME; Aydanian A; Dlouhy SR; Whelan DT; Heshka T; Ronen G
    Clin Genet; 1998 Sep; 54(3):248-9. PubMed ID: 9788732
    [No Abstract]   [Full Text] [Related]  

  • 17. Pelizaeus-Merzbacher disease.
    Anderson TJ; Griffiths IR
    Lab Anim Sci; 1999 Feb; 49(1):54-7. PubMed ID: 10090095
    [No Abstract]   [Full Text] [Related]  

  • 18. Family with Pelizaeus-Merzbacher disease/X-linked spastic paraplegia and a nonsense mutation in exon 6 of the proteolipid protein gene.
    Bond C; Si X; Crisp M; Wong P; Paulson GW; Boesel CP; Dlouhy SR; Hodes ME
    Am J Med Genet; 1997 Aug; 71(3):357-60. PubMed ID: 9268109
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [On a case of spongio-cavitary leukopathia].
    Macchi G; Taramelli M; Borri PF
    Acta Neurol (Napoli); 1969; 24(4):565-71. PubMed ID: 5402752
    [No Abstract]   [Full Text] [Related]  

  • 20. [Sex-related neurologic diseases. Pelizaeus-Merzbacher-type leukodystrophy. Adrenoleukodystrophy. Fabry's disease].
    Pascual-Castroviejo I
    An Esp Pediatr; 1984 Oct; 21 Suppl 20():44-7. PubMed ID: 6440461
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.