Literature DB >> 15645197

Phosphate's fate made easier.

Friedrich C Luft1.   

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Year:  2005        PMID： 15645197     DOI： 10.1007/s00109-004-0614-4

Source DB:  PubMed          Journal:  J Mol Med (Berl)        ISSN： 0946-2716            Impact factor:   4.599


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  4 in total

1.  Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders.

Authors:  Yaacov Frishberg; Orit Topaz; Reuven Bergman; Doron Behar; Drora Fisher; Derek Gordon; Gabriele Richard; Eli Sprecher
Journal:  J Mol Med (Berl)       Date:  2004-12-15       Impact factor: 4.599

Review 2.  The phosphatonin pathway: new insights in phosphate homeostasis.

Authors:  Susan C Schiavi; Rajiv Kumar
Journal:  Kidney Int       Date:  2004-01       Impact factor: 10.612

3.  Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis.

Authors:  Orit Topaz; Daniel L Shurman; Reuven Bergman; Margarita Indelman; Paulina Ratajczak; Mordechai Mizrachi; Ziad Khamaysi; Doron Behar; Dan Petronius; Vered Friedman; Israel Zelikovic; Sharon Raimer; Arieh Metzker; Gabriele Richard; Eli Sprecher
Journal:  Nat Genet       Date:  2004-05-09       Impact factor: 38.330

Review 4.  FGF23, PHEX, and MEPE regulation of phosphate homeostasis and skeletal mineralization.

Authors:  L Darryl Quarles
Journal:  Am J Physiol Endocrinol Metab       Date:  2003-07       Impact factor: 4.310
  4 in total

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