FGF23 Deficiency Leads to Mixed Hearing Loss and Middle Ear Malformation in Mice
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Title
FGF23 Deficiency Leads to Mixed Hearing Loss and Middle Ear Malformation in Mice
Authors
Keywords
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Journal
PLoS One
Volume 9, Issue 9, Pages e107681
Publisher
Public Library of Science (PLoS)
Online
2014-09-23
DOI
10.1371/journal.pone.0107681
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Related references
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- (2010) Masaya Takumida et al. ACTA OTO-LARYNGOLOGICA
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- (2010) Clemens Bergwitz et al. Annual Review of Medicine
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- (2009) S. G. Kujawa et al. JOURNAL OF NEUROSCIENCE
- Isolated C-terminal tail of FGF23 alleviates hypophosphatemia by inhibiting FGF23-FGFR-Klotho complex formation
- (2009) R. Goetz et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The Kidney and Ear: Emerging Parallel Functions
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- Klotho as a regulator of oxidative stress and senescence
- (2008) Makoto Kuro-o BIOLOGICAL CHEMISTRY
- Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)
- (2008) Osama Alsmadi et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- In vivo genetic evidence for klotho-dependent, fibroblast growth factor 23 (Fgf23) -mediated regulation of systemic phosphate homeostasis
- (2008) Teruyo Nakatani et al. FASEB JOURNAL
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