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Journal Abstract Search


138 related items for PubMed ID: 1719967

  • 1. Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin.
    Hayasaka K, Nanao K, Tahara M, Sato W, Takada G, Miura M, Uyemura K.
    Biochem Biophys Res Commun; 1991 Oct 31; 180(2):515-8. PubMed ID: 1719967
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  • 2. Isolation and sequence determination of cDNA encoding PMP-22 (PAS-II/SR13/Gas-3) of human peripheral myelin.
    Hayasaka K, Himoro M, Nanao K, Sato W, Miura M, Uyemura K, Takahashi E, Takada G.
    Biochem Biophys Res Commun; 1992 Jul 31; 186(2):827-31. PubMed ID: 1497668
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  • 3. Isolation and sequence determination of cDNA encoding P2 protein of human peripheral myelin.
    Hayasaka K, Nanao K, Tahara M, Sato W, Takada G, Miura M, Uyemura K.
    Biochem Biophys Res Commun; 1991 Nov 27; 181(1):204-7. PubMed ID: 1720307
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  • 4. Isolation and sequence of a cDNA encoding the major structural protein of peripheral myelin.
    Lemke G, Axel R.
    Cell; 1985 Mar 27; 40(3):501-8. PubMed ID: 2578885
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  • 5. Evolution of the myelin integral membrane proteins of the central nervous system.
    Schliess F, Stoffel W.
    Biol Chem Hoppe Seyler; 1991 Sep 27; 372(9):865-74. PubMed ID: 1722981
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  • 6. Molecular cloning and tissue expression of a cDNA encoding IP1--a P0-like glycoprotein of trout CNS myelin.
    Stratmann A, Jeserich G.
    J Neurochem; 1995 Jun 27; 64(6):2427-36. PubMed ID: 7539051
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  • 7. Molecular cloning of cDNA for the import precursor of human coupling factor 6 of H(+)-ATP synthase in mitochondria.
    Higuti T, Tsurumi C, Kawamura Y, Tsujita H, Osaka F, Yoshihara Y, Tani I, Tanaka K, Ichihara A.
    Biochem Biophys Res Commun; 1991 Jul 31; 178(2):793-9. PubMed ID: 1830479
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  • 10. DNA sequence, genomic organization, and chromosomal localization of the mouse peripheral myelin protein zero gene: identification of polymorphic alleles.
    You KH, Hsieh CL, Hayes C, Stahl N, Francke U, Popko B.
    Genomics; 1991 Apr 31; 9(4):751-7. PubMed ID: 1709914
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  • 11. Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.
    Giese KP, Martini R, Lemke G, Soriano P, Schachner M.
    Cell; 1992 Nov 13; 71(4):565-76. PubMed ID: 1384988
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  • 14. New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1.
    Himoro M, Yoshikawa H, Matsui T, Mitsui Y, Takahashi M, Kaido M, Nishimura T, Sawaishi Y, Takada G, Hayasaka K.
    Biochem Mol Biol Int; 1993 Sep 13; 31(1):169-73. PubMed ID: 7505151
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  • 15. Cloning and sequencing of a full length cDNA encoding ovine lipoprotein lipase.
    Edwards WD, Daniels SE, Page RA, Volpe CP, Kille P, Sweeney GE, Cryer A.
    Biochim Biophys Acta; 1993 Feb 20; 1172(1-2):167-70. PubMed ID: 8439555
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