18
results
for uniprot:Q9WU79
in citationmapping
| Mitochondrial proline dehydrogenase deficiency in hyperprolinemic PRO/Re mice: genetic and enzymatic analyses. Blake R.L., Hall J.G., Russell E.S. |
| Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2. Lund J., Roe B., Chen F., Budarf M., Galili N., Riblet R., Miller R.D., Emanuel B.S., Reeves R.H. |
| Role of epithelial architecture and intracellular metabolism in proline uptake and transtubular reclamation in PRO/re mouse kidney. Scriver C.R., McInnes R.R., Mohyuddin F. Proc. Natl. Acad. Sci. U.S.A. 72:1431-1435(1975) MGI 97770 · Mapped (3) |
| Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2. Lund J., Chen F., Hua A., Roe B., Budarf M., Emanuel B.S., Reeves R.H. |
| Dissection of behavior and psychiatric disorders using the mouse as a model. Tarantino L.M., Bucan M. |
| Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region. Puech A., Saint-Jore B., Merscher S., Russell R.G., Cherif D., Sirotkin H., Xu H., Factor S., Kucherlapati R., Skoultchi A.I. Proc. Natl. Acad. Sci. U.S.A. 97:10090-10095(2000) MGI 97770 · Mapped (52) |
| 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. Nature 420:563-573(2002) MGI 97770 · UniProtKB (17,858) · Mapped (12,469) |
| Proteomic analysis of the mouse liver mitochondrial inner membrane. Da Cruz S., Xenarios I., Langridge J., Vilbois F., Parone P.A., Martinou J.-C. J. Biol. Chem. 278:41566-41571(2003) MGI 97770 · UniProtKB (1) · Mapped (334) |
| Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention. Zambrowicz B.P., Abuin A., Ramirez-Solis R., Richter L.J., Piggott J., BeltrandelRio H., Buxton E.C., Edwards J., Finch R.A., Friddle C.J. et al. Proc. Natl. Acad. Sci. U.S.A. 100:14109-14114(2003) MGI 97770 · Mapped (17,104) |
| A comprehensive analysis of 22q11 gene expression in the developing and adult brain. Maynard T.M., Haskell G.T., Peters A.Z., Sikich L., Lieberman J.A., LaMantia A.S. Proc. Natl. Acad. Sci. U.S.A. 100:14433-14438(2003) MGI 97770 · Mapped (73) |
| Hepatocyte nuclear factors 1alpha and 4alpha control expression of proline oxidase in adult liver. Kamiya A., Inoue Y., Kodama T., Gonzalez F.J. FEBS Lett. 578:63-68(2004) MGI 97770 · UniProtKB (1) · Mapped (8) |
| 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. Science 309:1559-1563(2005) MGI 97770 · UniProtKB (27,417) · Mapped (5,721) |
| Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice. Paterlini M., Zakharenko S.S., Lai W.S., Qin J., Zhang H., Mukai J., Westphal K.G., Olivier B., Sulzer D., Pavlidis P. et al. |
| Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome. Meechan D.W., Maynard T.M., Wu Y., Gopalakrishna D., Lieberman J.A., LaMantia A.S. Mol. Cell. Neurosci. 33:412-428(2006) MGI 97770 · Mapped (34) |
| A mitochondrial protein compendium elucidates complex I disease biology. Pagliarini D.J., Calvo S.E., Chang B., Sheth S.A., Vafai S.B., Ong S.E., Walford G.A., Sugiana C., Boneh A., Chen W.K. et al. Cell 134:112-123(2008) MGI 97770 · UniProtKB (2) · Mapped (1,816) |
| Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes. Maynard T.M., Meechan D.W., Dudevoir M.L., Gopalakrishna D., Peters A.Z., Heindel C.C., Sugimoto T.J., Wu Y., Lieberman J.A., Lamantia A.S. Mol. Cell. Neurosci. 39:439-451(2008) MGI 97770 · Mapped (22) |
| Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome. Meechan D.W., Tucker E.S., Maynard T.M., LaMantia A.S. Proc. Natl. Acad. Sci. U.S.A. 106:16434-16445(2009) MGI 97770 · Mapped (50) |
| Hyperprolinemia and prolinuria in a new inbred strain of mice, PRO-Re. Blake R.L., Russell E.S. |
