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Journal Abstract Search

101 related items for PubMed ID: 10072599

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  • 2. Assignment of the true and processed genes for human glycine decarboxylase to 9p23-24 and 4q12.
    Isobe M, Koyata H, Sakakibara T, Momoi-Isobe K, Hiraga K.
    Biochem Biophys Res Commun; 1994 Sep 30; 203(3):1483-7. PubMed ID: 7945295
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  • 4. Genetic polymorphism of murine C3 controlled by a single co-dominant locus on chromosome 17.
    Natsuume-Sakai S, Hayakawa JI, Takahashi M.
    J Immunol; 1978 Aug 30; 121(2):491-8. PubMed ID: 681746
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  • 5. A restriction fragment length polymorphism at murine Glud locus co-segregates with Rib-1, Es-10, and Tcra on chromosome 14.
    Shaughnessy J, Mock B, Duncan R, Potter M, Banner C.
    Nucleic Acids Res; 1989 Apr 11; 17(7):2881. PubMed ID: 2566156
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  • 11. The gas5 gene is disrupted by a frameshift mutation within its longest open reading frame in several inbred mouse strains and maps to murine chromosome 1.
    Muller AJ, Chatterjee S, Teresky A, Levine AJ.
    Mamm Genome; 1998 Sep 11; 9(9):773-4. PubMed ID: 9716666
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  • 13. Assignment of the human oxidized low-density lipoprotein receptor gene (OLR1) to chromosome 12p13.1-->p12.3, and identification of a polymorphic CA-repeat marker in the OLR1 gene.
    Li X, Bouzyk MM, Wang X.
    Cytogenet Cell Genet; 1998 Sep 11; 82(1-2):34-6. PubMed ID: 9763655
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  • 14. Structure and chromosomal assignment of the sterol 12alpha-hydroxylase gene (CYP8B1) in human and mouse: eukaryotic cytochrome P-450 gene devoid of introns.
    Gåfvels M, Olin M, Chowdhary BP, Raudsepp T, Andersson U, Persson B, Jansson M, Björkhem I, Eggertsen G.
    Genomics; 1999 Mar 01; 56(2):184-96. PubMed ID: 10051404
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  • 20. Novel mutations in the P-protein (glycine decarboxylase) gene in patients with glycine encephalopathy (non-ketotic hyperglycinemia).
    Toone JR, Applegarth DA, Kure S, Coulter-Mackie MB, Sazegar P, Kojima K, Ichinohe A.
    Mol Genet Metab; 2002 Jul 01; 76(3):243-9. PubMed ID: 12126939
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