[1]
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NUCLEOTIDE SEQUENCE [MRNA].
DOI=10.1006/bbrc.2000.3696; PubMed=11032749 [NCBI, ExPASy, EBI, Israel, Japan]
Yamashita T.,
Yoshioka M.,
Itoh N.;
"Identification of a novel fibroblast growth factor, FGF-23, preferentially expressed in the ventrolateral thalamic nucleus of the brain.";
Biochem. Biophys. Res. Commun. 277:494-498(2000).
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[2]
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NUCLEOTIDE SEQUENCE [MRNA], VARIANTS ADHR GLN-176; GLN-179 AND TRP-179, AND VARIANT MET-239.
DOI=10.1038/81664; PubMed=11062477 [NCBI, ExPASy, EBI, Israel, Japan]
White K.E.,
Evans W.E.,
O'Riordan J.L.H.,
Speer M.C.,
Econs M.J.,
Lorenz-Depiereux B.,
Grabowski M.,
Meitinger T.,
Strom T.M.;
"Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23.";
Nat. Genet. 26:345-348(2000).
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[3]
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NUCLEOTIDE SEQUENCE [MRNA].
DOI=10.1073/pnas.101545198; PubMed=11344269 [NCBI, ExPASy, EBI, Israel, Japan]
Shimada T.,
Mizutani S.,
Muto T.,
Yoneya T.,
Hino R.,
Takeda S.,
Takeuchi Y.,
Fujita T.,
Fukumoto S.,
Yamashita T.;
"Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia.";
Proc. Natl. Acad. Sci. U.S.A. 98:6500-6505(2001).
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[4]
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NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
DOI=10.1101/gr.1293003; PubMed=12975309 [NCBI, ExPASy, EBI, Israel, Japan]
Clark H.F.,
Gurney A.L.,
Abaya E.,
Baker K.,
Baldwin D.T.,
Brush J.,
Chen J.,
Chow B.,
Chui C.,
Crowley C.,
Currell B.,
Deuel B.,
Dowd P.,
Eaton D.,
Foster J.S.,
Grimaldi C.,
Gu Q.,
Hass P.E.,
Heldens S., ![]()
Huang A.,
Kim H.S.,
Klimowski L.,
Jin Y.,
Johnson S.,
Lee J.,
Lewis L.,
Liao D.,
Mark M.R.,
Robbie E.,
Sanchez C.,
Schoenfeld J.,
Seshagiri S.,
Simmons L.,
Singh J.,
Smith V.,
Stinson J.,
Vagts A.,
Vandlen R.L.,
Watanabe C.,
Wieand D.,
Woods K.,
Xie M.-H.,
Yansura D.G.,
Yi S.,
Yu G.,
Yuan J.,
Zhang M.,
Zhang Z.,
Goddard A.D.,
Wood W.I.,
Godowski P.J.,
Gray A.M.;
"The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment.";
Genome Res. 13:2265-2270(2003).
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[5]
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NUCLEOTIDE SEQUENCE [GENOMIC DNA], AND VARIANTS SER-195 AND MET-239.
NIEHS SNPs program;
Submitted (MAR-2004) to the EMBL/GenBank/DDBJ databases.
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[6]
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NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
DOI=10.1101/gr.2596504; PubMed=15489334 [NCBI, ExPASy, EBI, Israel, Japan]
The MGC Project Team;
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).";
Genome Res. 14:2121-2127(2004).
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[7]
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PROTEIN SEQUENCE OF 25-39.
DOI=10.1110/ps.04682504; PubMed=15340161 [NCBI, ExPASy, EBI, Israel, Japan]
Zhang Z.,
Henzel W.J.;
"Signal peptide prediction based on analysis of experimentally verified cleavage sites.";
Protein Sci. 13:2819-2824(2004).
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[8]
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PROCESSING.
DOI=10.1210/jc.86.2.497; PubMed=11157998 [NCBI, ExPASy, EBI, Israel, Japan]
White K.E.,
Jonsson K.B.,
Carn G.,
Hampson G.,
Spector T.D.,
Mannstadt M.,
Lorenz-Depiereux B.,
Miyauchi A.,
Yang I.M.,
Ljunggren O.,
Meitinger T.,
Strom T.M.,
Jueppner H.,
Econs M.J.;
"The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting.";
J. Clin. Endocrinol. Metab. 86:497-500(2001).
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[9]
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PROCESSING.
DOI=10.1210/en.143.8.3179; PubMed=12130585 [NCBI, ExPASy, EBI, Israel, Japan]
Shimada T.,
Muto T.,
Urakawa I.,
Yoneya T.,
Yamazaki Y.,
Okawa K.,
Takeuchi Y.,
Fujita T.,
Fukumoto S.,
Yamashita T.;
"Mutant FGF-23 responsible for autosomal dominant hypophosphatemic rickets is resistant to proteolytic cleavage and causes hypophosphatemia in vivo.";
Endocrinology 143:3179-3182(2002).
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[10]
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PROCESSING BY PROPROTEIN CONVERTASES.
DOI=10.1016/j.bone.2004.04.002; PubMed=15268897 [NCBI, ExPASy, EBI, Israel, Japan]
Benet-Pages A.,
Lorenz-Depiereux B.,
Zischka H.,
White K.E.,
Econs M.J.,
Strom T.M.;
"FGF23 is processed by proprotein convertases but not by PHEX.";
Bone 35:455-462(2004).
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[11]
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X-RAY CRYSTALLOGRAPHY (1.5 ANGSTROMS) OF 25-179.
DOI=10.1128/MCB.02249-06; PubMed=17339340 [NCBI, ExPASy, EBI, Israel, Japan]
Goetz R.,
Beenken A.,
Ibrahimi O.A.,
Kalinina J.,
Olsen S.K.,
Eliseenkova A.V.,
Xu C.,
Neubert T.A.,
Zhang F.,
Linhardt R.J.,
Yu X.,
White K.E.,
Inagaki T.,
Kliewer S.A.,
Yamamoto M.,
Kurosu H.,
Ogawa Y.,
Kuro-o M.,
Lanske B., ![]()
Razzaque M.S.,
Mohammadi M.;
"Molecular insights into the klotho-dependent, endocrine mode of action of fibroblast growth factor 19 subfamily members.";
Mol. Cell. Biol. 27:3417-3428(2007).
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[12]
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VARIANT HFTC GLY-71.
DOI=10.1093/hmg/ddi034; PubMed=15590700 [NCBI, ExPASy, EBI, Israel, Japan]
Benet-Pages A.,
Orlik P.,
Strom T.M.,
Lorenz-Depiereux B.;
"An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia.";
Hum. Mol. Genet. 14:385-390(2005).
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