R01 AG019698/AG/NIA NIH HHS/United States[Grants and Funding] - Search Results

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Subject: R01 AG019698/AG/NIA NIH HHS/United States[Grants - PubMed

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Evaluation of gene expression profiling in a mouse model of L-gulonolactone oxidase gene deficiency.

Yan J, Jiao Y, Li X, Jiao F, Beamer WG, Rosen CJ, Gu W. Yan J, et al. Genet Mol Biol. 2007;30(2):322-329. doi: 10.1590/s1415-47572007000300004. Genet Mol Biol. 2007. PMID: 18167513 Free PMC article.

A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis.

Donahue LR, Chang B, Mohan S, Miyakoshi N, Wergedal JE, Baylink DJ, Hawes NL, Rosen CJ, Ward-Bailey P, Zheng QY, Bronson RT, Johnson KR, Davisson MT. Donahue LR, et al. J Bone Miner Res. 2003 Sep;18(9):1612-21. doi: 10.1359/jbmr.2003.18.9.1612. J Bone Miner Res. 2003. PMID: 12968670 Free PMC article.

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