A novel Phex mutation with defective glycosylation causes hypophosphatemia and rickets in mice.Xiong X., Qi X., Ge X., Gu P., Zhao J., Zhao Q., Gao X.View abstractCited forNUCLEOTIDE SEQUENCEStrainC57BL/6CategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCJ Biomed Sci 15:47-59 (2008)Cited in1Mapped to5
Genetic screening for X-linked hypophosphatemic mice and ontogenic characterization of the defect in the renal sodium-phosphate transporter.Muller Y.L., Collins J.F., Ghishan F.K.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 107489PubMedEurope PMCPediatr Res 44:633-638 (1998)Mapped to5
Intrinsic mineralization defect in Hyp mouse osteoblasts.Xiao Z.S., Crenshaw M., Guo R., Nesbitt T., Drezner M.K., Quarles L.D.View abstractCategoryFunctionSourceMGI: 107489PubMedEurope PMCAm J Physiol 275:E700-8 (1998)Mapped to5
Molecular cloning of a second human stanniocalcin homologue (STC2).Ishiabshi K., Miyamoto K., Taketani Y., Morita K., Takeda E., Sasaki S., Imai M.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCBiochem. Biophys. Res. Commun. 250:252-258 (1998)Cited in1Mapped to8
Characterization of genes encoding translation initiation factor eIF- 2gamma in mouse and human: sex chromosome localization, escape from X- inactivation and evolution.Ehrmann I.E., Ellis P.S., Mazeyrat S., Duthie S., Brockdorff N., Mattei M.-G., Gavin M.A., Affara N.A., Brown G.M.[...], Scott D.M.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCHum. Mol. Genet. 7:1725-1737 (1998)Cited in6Mapped to50
Partial deletion of both the spermine synthase gene and the Pex gene in the X-linked hypophosphatemic, gyro (Gy) mouse.Meyer R.A. Jr., Henley C.M., Meyer M.H., Morgan P.L., McDonald A.G., Mills C., Price D.K.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 107489PubMedEurope PMCGenomics 48:289-295 (1998)Mapped to8
Pex mRNA is localized in developing mouse osteoblasts and odontoblasts.Ruchon A.F., Marcinkiewicz M., Siegfried G., Tenenhouse H.S., DesGroseillers L., Crine P., Boileau G.View abstractCategoryExpressionSourceMGI: 107489PubMedEurope PMCJ Histochem Cytochem 46:459-468 (1998)Mapped to5
An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome.Blair H.J., Uwechue I.C., Barsh G.S., Rowe P.S., Boyd Y.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCGenomics 48:128-131 (1998)Mapped to17
Mouse mutants carrying deletions that remove the genes mutated in Coffin- Lowry syndrome and lactic acidosis.Blair H.J., Gormally E., Uwechue I.C., Boyd Y.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCHum Mol Genet 7:549-555 (1998)Mapped to15
Spermine deficiency in Gy mice caused by deletion of the spermine synthase gene.Lorenz B., Francis F., Gempel K., Boeddrich A., Josten M., Schmahl W., Schmidt J., Lehrach H., Meitinger T., Strom T.M.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 107489PubMedEurope PMCHum. Mol. Genet. 7:541-547 (1998)Cited in1Mapped to7
Osteocalcin production in primary osteoblast cultures derived from normal and Hyp mice.Carpenter T.O., Moltz K.C., Ellis B., Andreoli M., McCarthy T.L., Centrella M., Bryan D., Gundberg C.M.View abstractCategoryExpressionSourceMGI: 107489PubMedEurope PMCEndocrinology 139:35-43 (1998)Mapped to5
Positional cloning of the PEX gene: new insights into the pathophysiology of X-linked hypophosphatemic rickets.Econs M.J., Francis F.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCAm J Physiol 273:F489-98 (1997)Mapped to5
Growth hormone normalizes renal 1,25-dihydroxyvitamin D3-24-hydroxylase gene expression but not Na+-phosphate cotransporter (Npt2) mRNA in phosphate-deprived Hyp mice.Roy S., Martel J., Tenenhouse H.S.View abstractCategoriesFunction, Expression, Phenotypes & VariantsSourceMGI: 107489PubMedEurope PMCJ Bone Miner Res 12:1672-1680 (1997)Mapped to17
Parathyroid hormone gene expression in Hyp mice fed a low-phosphate diet.Marks K.H., Kilav R., Berman E., Naveh-Many T., Silver J.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 107489PubMedEurope PMCNephrol Dial Transplant 12:1581-1585 (1997)Mapped to5
Skeletal casein kinase activity defect in the HYP mouse.Rifas L., Cheng S., Halstead L.R., Gupta A., Hruska K.A., Avioli L.V.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCCalcif Tissue Int 61:256-259 (1997)Mapped to5
Mammalian membrane metallopeptidases: NEP, ECE, KELL, and PEX.Turner A.J., Tanzawa K.View abstractCategoriesFunction, SequencesSourceMGI: 107489PubMedEurope PMCFASEB J 11:355-364 (1997)Mapped to11
Lack of effect of vitamin D and its metabolites on intestinal phosphate transport in familial hypophosphatemia of mice.O'Doherty P.J., DeLuca H.F., Eicher E.M.View abstractCategoryFunctionSourceMGI: 107489PubMedEurope PMCEndocrinology 101:1325-1330 (1977)Mapped to5
Pex/PEX tissue distribution and evidence for a deletion in the 3' region of the Pex gene in X-linked hypophosphatemic mice.Beck L., Soumounou Y., Martel J., Krishnamurthy G., Gauthier C., Goodyer C.G., Tenenhouse H.S.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCJ. Clin. Invest. 99:1200-1209 (1997)Cited in2Mapped to4
Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia.Strom T.M., Francis F., Lorenz B., Boeddrich A., Econs M.J., Lehrach H., Meitinger T.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCHum. Mol. Genet. 6:165-171 (1997)Cited in2Mapped to6
Osteocalcin abnormalities in Hyp mice reflect altered genetic expression and are not due to altered clearance, affinity for mineral, or ambient phosphorus levels.Carpenter T.O., Gundberg C.M.View abstractCategoriesFunction, Expression, Phenotypes & VariantsSourceMGI: 107489PubMedEurope PMCEndocrinology 137:5213-5219 (1996)Mapped to5
Renal expression of Na+-phosphate cotransporter mRNA and protein: effect of the Gy mutation and low phosphate diet.Beck L., Tenenhouse H.S., Meyer R.A., Meyer M.H., Biber J., Murer H.View abstractCategoryExpressionSourceMGI: 107489PubMedEurope PMCPflugers Arch 431:936-941 (1996)Mapped to5
Direct demonstration of a humorally-mediated inhibition of renal phosphate transport in the Hyp mouse.Lajeunesse D., Meyer R.A. Jr., Hamel L.CategoryFunctionSourceMGI: 107489PubMedEurope PMCKidney Int 50:1531-1538 (1996)Mapped to5
Fine genetic mapping of the Hyp mutation on mouse chromosome X.Du L., Desbarats M., Cornibert S., Malo D., Ecarot B.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCGenomics 32:177-183 (1996)Mapped to18
cDNA cloning of the murine Pex gene implicated in X-linked hypophosphatemia and evidence for expression in bone.Du L., Desbarats M., Viel J., Glorieux F.H., Cawthorn C., Ecarot B.View abstractCategorySequencesSourceMGI: 107489PubMedEurope PMCGenomics 36:22-28 (1996)Cited in1Mapped to4
Comparison of 22-oxacalcitriol and 1,25(OH)2D3 on bone metabolism in young X-linked hypophosphatemic male mice.Halstead L.R., Weinstein R.S., Cheng S.L., Rifas L., Avioli L.V.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 107489PubMedEurope PMCAm J Physiol 270:E141-7 (1996)Mapped to5