Osteoblast-Specific Expression of the Fibrous Dysplasia (FD)-Causing MutationGsαR201CProduces a High Bone Mass Phenotype but Does Not Reproduce FD in the Mouse

Author:

Remoli Cristina1,Michienzi Stefano1,Sacchetti Benedetto1,Consiglio Alberto Di1,Cersosimo Stefania1,Spica Emanuela1,Robey Pamela G2,Holmbeck Kenn2,Cumano Ana3,Boyde Alan4,Davis Graham4,Saggio Isabella5,Riminucci Mara1,Bianco Paolo1

Affiliation:

1. Department of Molecular Medicine; Sapienza University of Rome; Rome Italy

2. Craniofacial and Skeletal Diseases Branch; National Institute of Dental and Craniofacial Research; National Institutes of Health; Department of Health and Human Services; Bethesda Maryland USA

3. Lymphopoiesis Unit; INSERM; Pasteur Institute; Paris France

4. Dental Physical Sciences; Queen Mary University of London; London UK

5. Department of Biology and Biotechnology “C. Darwin”; Sapienza University of Rome, and IBPM CNR; Rome Italy

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference70 articles.

1. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome;Weinstein;N Engl J Med.,1991

2. An activating Gs alpha mutation is present in fibrous dysplasia of bone in the McCune-Albright syndrome;Shenker;J Clin Endocrinol Metab.,1994

3. Constitutively active Gs alpha is associated with an increased phosphodiesterase activity in human growth hormone-secreting adenomas;Lania;J Clin Endocrinol Metab.,1998

4. Fibrous dysplasia of bone in the McCune-Albright syndrome: abnormalities in bone formation;Riminucci;Am J Pathol.,1997

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3