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| Characterization of mouse Clpp protease cDNA, gene, and protein. Andresen B.S., Corydon T.J., Wilsbech M., Bross P., Schroeder L.D., Hindkjaer T.F., Bolund L., Gregersen N.
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| Functional annotation of a full-length mouse cDNA collection. Kawai J., Shinagawa A., Shibata K., Yoshino M., Itoh M., Ishii Y., Arakawa T., Hara A., Fukunishi Y., Konno H. et al.
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| Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Okazaki Y., Furuno M., Kasukawa T., Adachi J., Bono H., Kondo S., Nikaido I., Osato N., Saito R., Suzuki H. et al.
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| A large-scale, gene-driven mutagenesis approach for the functional analysis of the mouse genome. Hansen J., Floss T., Van Sloun P., Fuchtbauer E.M., Vauti F., Arnold H.H., Schnutgen F., Wurst W., von Melchner H., Ruiz P.
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| Mice bearing Acads mutation display altered postingestive but not 5-s orosensory response to dietary fat. Smith Richards B.K., Belton B.N., York B., Volaufova J.
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| Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria. Mootha V.K., Bunkenborg J., Olsen J.V., Hjerrild M., Wisniewski J.R., Stahl E., Bolouri M.S., Ray H.N., Sihag S., Kamal M. et al.
Cell 115:629-640(2003) MGI 87868 · UniProtKB (15) · Mapped (987) |
| Influence of dietary fatty acid chain-length on metabolic tolerance in mouse models of inherited defects in mitochondrial fatty acid beta-oxidation. Schuler A.M., Gower B.A., Matern D., Rinaldo P., Wood P.A.
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| Synergistic heterozygosity in mice with inherited enzyme deficiencies of mitochondrial fatty acid beta-oxidation. Schuler A.M., Gower B.A., Matern D., Rinaldo P., Vockley J., Wood P.A.
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| The transcriptional landscape of the mammalian genome. Carninci P., Kasukawa T., Katayama S., Gough J., Frith M.C., Maeda N., Oyama R., Ravasi T., Lenhard B., Wells C. et al.
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| Molecular cloning, functional expression, and chromosomal localization of mouse hepatocyte nuclear factor 1. Kuo C.J., Conley P.B., Hsieh C.L., Francke U., Crabtree G.R.
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| Organic aciduria and butyryl CoA dehydrogenase deficiency in BALB/cByJ mice. Schiffer S.P., Prochazka M., Jezyk P.F., Roderick T.H., Yudkoff M., Patterson D.F.
Biochem. Genet. 27:47-58(1989) MGI 87868 · Mapped (11) |
| Structural and functional studies of the early T lymphocyte activation 1 (Eta-1) gene. Definition of a novel T cell-dependent response associated with genetic resistance to bacterial infection. Patarca R., Freeman G.J., Singh R.P., Wei F.-Y., Durfee T., Blattner F., Regnier D.C., Kozak C.A., Mock B.A., Morse H.C. III et al.
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| The structural gene for F liver protein (Flp) maps to chromosome 5 of the mouse. Winchester G., Mitchison N.A., Taylor B.A.
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| Genetics and ontogeny of butyryl CoA dehydrogenase in the mouse and linkage of Bcd-1 with Dao-1. Seeley T.L., Holmes R.S.
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| The gamma phosphorylase kinase gene, Phkg, maps to mouse chromosome 5 near Gus. Maichele A.J., Chamberlain J.S.
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| Pathologic characterization of short-chain acyl-CoA dehydrogenase deficiency in BALB/cByJ mice. Armstrong D.L., Masiowski M.L., Wood P.A.
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| Null allele at Bcd-1 locus in BALB/cByJ mice is due to a deletion in the short-chain acyl-CoA dehydrogenase gene and results in missplicing of mRNA. Hinsdale M.E., Kelly C.L., Wood P.A.
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| Breeding experiments to combine the X-linked sparse-fur (spf) mutation with the autosomal recessive BALB/cByJ strain: testing the biochemical phenotype of double-mutant mice as a model for ammonia: fatty acyl CoA synergism. Qureshi I.A., Leblanc D., Cyr D., Giguere R., Mitchell G.
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| Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome. Pontoglio M., Barra J., Hadchouel M., Doyen A., Kress C., Bach J.P., Babinet C., Yaniv M.
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| Cloning and characterization of the mouse short-chain acyl-CoA dehydrogenase gene. Kelly C.L., Wood P.A.
Mamm. Genome 7:262-264(1996) MGI 87868 · UniProtKB (1) · Mapped (2) |
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