Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation.
about
Constitutive nuclear expression of dentin matrix protein 1 fails to rescue the Dmp1-null phenotype.FGF23 in skeletal modeling and remodeling.Mineralizing enthesopathy is a common feature of renal phosphate-wasting disorders attributed to FGF23 and is exacerbated by standard therapy in hyp miceSkeletal Muscle, but not Cardiovascular Function, Is Altered in a Mouse Model of Autosomal Recessive Hypophosphatemic Rickets.Sclerostin antibody (Scl-Ab) improves osteomalacia phenotype in dentin matrix protein 1(Dmp1) knockout mice with little impact on serum levels of phosphorus and FGF23.Plasma FGF23 levels increase rapidly after acute kidney injury.Dmp1 Null Mice Develop a Unique Osteoarthritis-like Phenotype.The rachitic tooth.The skeleton as an endocrine organ.Osteocyte regulation of phosphate homeostasis and bone mineralization underlies the pathophysiology of the heritable disorders of rickets and osteomalacia.Phosphate homeostasis and genetic mutations of familial hypophosphatemic rickets.The dentin matrix acidic phosphoprotein 1 (DMP1) in the light of mammalian evolution.A novel auditory ossicles membrane and the development of conductive hearing loss in Dmp1-null mice.Genetic Causes of Rickets.Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23-related hypophosphatemia, dental anomalies, and ectopic calcification.
P2860
Q33985338-EE25EBF3-E82E-455A-894F-EC021F5B6F7AQ35707031-CBFD00EE-DF2D-4C78-A4BC-D54033FB2EA6Q36439625-47C4AC7C-6C46-4FB7-B396-F307375E9702Q36899883-F85C61DC-EEDD-45D2-AA31-802FFF545BE6Q36923887-59AFA0FF-9B46-450D-B8D5-070726AEE9CEQ37154351-6F18E3ED-1465-40D0-92B2-23B97AF7C25EQ37348702-D25415D7-68B6-4D5B-A57C-61F76AE88FC2Q37493998-B4E87218-1E83-4157-B4D5-DEAE22A4D61AQ38050402-6BA2CED5-554A-4977-9A58-29A6A1E437DDQ38081019-C99E6CB5-5DAF-4541-96E8-87F79F8D41A3Q38430631-0044DF3A-9FB5-4CB7-9B36-C2BE5A185432Q39476762-9B46898C-0C4E-4AE7-8448-D104F0474885Q50170613-ADDC4EB9-D1DA-4543-AE0F-A94ADD983C46Q52687353-37AF38D7-CFD0-4C67-BFAD-0AF0CA878A22Q54456673-740488BB-8E74-4323-A1CA-BFA0E09A3A69
P2860
Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation.
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Long-term clinical outcome and ...... used by a novel DMP1 mutation.
@ast
Long-term clinical outcome and ...... used by a novel DMP1 mutation.
@en
type
label
Long-term clinical outcome and ...... used by a novel DMP1 mutation.
@ast
Long-term clinical outcome and ...... used by a novel DMP1 mutation.
@en
prefLabel
Long-term clinical outcome and ...... used by a novel DMP1 mutation.
@ast
Long-term clinical outcome and ...... used by a novel DMP1 mutation.
@en
P2093
P2860
P356
P1476
Long-term clinical outcome and ...... used by a novel DMP1 mutation.
@en
P2093
Harald Jüppner
Heikki Kröger
Ilkka Kaitila
Murat Bastepe
Renata C Pereira
Tero Laine
William G Cole
P2860
P304
P356
10.1002/JBMR.105
P577
2010-10-01T00:00:00Z