Active sites of human MEPE-ASARM regulating bone matrix mineralization-Reference-Cited by-同舟云学术

Active sites of human MEPE-ASARM regulating bone matrix mineralization

Published:2020-11 Issue: Volume:517 Page:110931
ISSN:0303-7207
Container-title:Molecular and Cellular Endocrinology
language:en
Short-container-title:Molecular and Cellular Endocrinology

Author:

Minamizaki Tomoko,Sakurai Kaoru,Hayashi Ikue,Toshishige Masaaki,Yoshioka Hirotaka,Kozai Katsuyuki,Yoshiko Yuji

Funder

Raffinee International Foundation

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

Reference33 articles.

1. Phosphorylation-dependent inhibition of mineralization by osteopontin ASARM peptides is regulated by PHEX cleavage;Addison;J. Bone Miner. Res.,2010

2. MEPE-ASARM peptides control extracellular matrix mineralization by binding to hydroxyapatite: an inhibition regulated by PHEX cleavage of ASARM;Addison;J. Bone Miner. Res.,2008

3. Mepe, the gene encoding a tumor-secreted protein in oncogenic hypophosphatemic osteomalacia, is expressed in bone;Argiro;Genomics,2001

4. Sclerostin is a locally acting regulator of late-osteoblast/preosteocyte differentiation and regulates mineralization through a MEPE-ASARM-dependent mechanism;Atkins;J. Bone Miner. Res.,2011

5. Small integrin-binding ligand N-linked glycoproteins (SIBLINGs): multifunctional proteins in cancer;Bellahcene;Nat. Rev. Canc.,2008

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