scholarly article | Q13442814 |
P50 | author | Catherine Chaussain | Q57020391 |
P2093 | author name string | Michèle Garabédian | |
Michel Goldberg | |||
Peter S Rowe | |||
Dominique Septier | |||
Frédéric Jehan | |||
Tchilalo Boukpessi | |||
Céline Gaucher | |||
P2860 | cites work | MEPE, a new gene expressed in bone marrow and tumors causing osteomalacia | Q24290092 |
A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium | Q24308202 | ||
Six genes expressed in bones and teeth encode the current members of the SIBLING family of proteins | Q28204658 | ||
Characterization of PHEX endopeptidase catalytic activity: identification of parathyroid-hormone-related peptide107-139 as a substrate and osteocalcin, PPi and phosphate as inhibitors | Q28363247 | ||
Role of matrix extracellular phosphoglycoprotein in the pathogenesis of X-linked hypophosphatemia | Q28511009 | ||
Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP). | Q30426917 | ||
Scanning electron microscope study of separated calcospherites from the matrices of different mineralizing systems | Q30768202 | ||
Post-translational modifications of sibling proteins and their roles in osteogenesis and dentinogenesis | Q34325799 | ||
Surface plasmon resonance (SPR) confirms that MEPE binds to PHEX via the MEPE-ASARM motif: a model for impaired mineralization in X-linked rickets (HYP) | Q35992810 | ||
MEPE has the properties of an osteoblastic phosphatonin and minhibin. | Q40590136 | ||
Inhibition of MEPE cleavage by Phex. | Q44130801 | ||
Dental abnormalities in patients with familial hypophosphatemic vitamin D-resistant rickets: prevention by early treatment with 1-hydroxyvitamin D. | Q44364335 | ||
Dentin structure in familial hypophosphatemic rickets: benefits of vitamin D and phosphate treatment. | Q46279337 | ||
CELLS AND EXTRACELLULAR MATRICES OF DENTIN AND PULP: A BIOLOGICAL BASIS FOR REPAIR AND TISSUE ENGINEERING. | Q51715110 | ||
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis. | Q54943458 | ||
Dentin Alteration of Deciduous Teeth in Human Hypophosphatemic Rickets | Q57736177 | ||
The dentino-enamel junction revisited | Q57736179 | ||
P433 | issue | 1-4 | |
P304 | page(s) | 219-223 | |
P577 | publication date | 2008-08-14 | |
P1433 | published in | Cells Tissues Organs | Q2167221 |
P1476 | title | Dentin noncollagenous matrix proteins in familial hypophosphatemic rickets | |
P478 | volume | 189 |
Q33617326 | Abnormal presence of the matrix extracellular phosphoglycoprotein-derived acidic serine- and aspartate-rich motif peptide in human hypophosphatemic dentin. |
Q35850452 | Age dependent regulation of bone-mass and renal function by the MEPE ASARM-motif |
Q47842811 | Defective Mineralization in X-Linked Hypophosphatemia Dental Pulp Cell Cultures. |
Q47822629 | Expression of Phosphate Transporters during Dental Mineralization. |
Q27002346 | Extracellular matrix mineralization in periodontal tissues: Noncollagenous matrix proteins, enzymes, and relationship to hypophosphatasia and X-linked hypophosphatemia |
Q34602567 | MEPE-derived ASARM peptide inhibits odontogenic differentiation of dental pulp stem cells and impairs mineralization in tooth models of X-linked hypophosphatemia |
Q57736114 | Magnetic Resonance Imaging Features as Surrogate Markers of X-Linked Hypophosphatemic Rickets Activity |
Q31161423 | PHEX mimetic (SPR4-peptide) corrects and improves HYP and wild type mice energy-metabolism |
Q39998029 | Periapical and endodontic status of permanent teeth in patients with hypophosphatemic rickets. |
Q27026805 | Regulation of bone-renal mineral and energy metabolism: the PHEX, FGF23, DMP1, MEPE ASARM pathway |
Q34221238 | The changing face of hypophosphatemic disorders in the FGF-23 era |
Q36074718 | The chicken or the egg: PHEX, FGF23 and SIBLINGs unscrambled |
Q37493998 | The rachitic tooth |
Q37648693 | Therapeutic management of hypophosphatemic rickets from infancy to adulthood. |
Q35575445 | Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations |
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