Domain-specific Mutations of a Transforming Growth Factor (TGF)-β1 Latency-associated Peptide Cause Camurati-Engelmann Disease Because of the Formation of a Constitutively Active Form of TGF-β1-Reference-Cited by-同舟云学术

Domain-specific Mutations of a Transforming Growth Factor (TGF)-β1 Latency-associated Peptide Cause Camurati-Engelmann Disease Because of the Formation of a Constitutively Active Form of TGF-β1

Published:2001-04 Issue:15 Volume:276 Page:11469-11472
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Saito Takashi,Kinoshita Akira,Yoshiura Koh-ichiro,Makita Yoshio,Wakui Keiko,Honke Koichi,Niikawa Norio,Taniguchi Naoyuki

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference25 articles.

1. Glucocorticoid activity, inactivity and the osteoblast

2. Decreased bone mass and bone elasticity in mice lacking the transforming growth factor-β1 gene

3. Transforming Growth Factor-β Stimulates Bone Matrix Apposition and Bone Cell Replication in Cultured Fetal Rat Calvariae*

4. Osteoblastic Responses to TGF-β during Bone Remodeling

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