Meclozine Promotes Longitudinal Skeletal Growth in Transgenic Mice with Achondroplasia Carrying a Gain-of-Function Mutation in the FGFR3 Gene-Reference-Cited by-同舟云学术

Meclozine Promotes Longitudinal Skeletal Growth in Transgenic Mice with Achondroplasia Carrying a Gain-of-Function Mutation in the FGFR3 Gene

Published:2014-12-02 Issue:2 Volume:156 Page:548-554
ISSN:0013-7227
Container-title:Endocrinology
language:en
Short-container-title:

Author:

Matsushita Masaki¹²,Hasegawa Satoru¹,Kitoh Hiroshi²,Mori Kensaku³,Ohkawara Bisei¹,Yasoda Akihiro⁴,Masuda Akio¹,Ishiguro Naoki²,Ohno Kinji¹

Affiliation:

1. Division of Neurogenetics, Center for Neurological Diseases and Cancer (M.M., S.H., B.O., A.M., K.O.), Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan

2. Department of Orthopaedic Surgery (M.M., H.K., N.I.), Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan

3. Department of Media Science (K.M.), Graduate School of Information Science, Nagoya University, Nagoya 466-8550, Japan

4. Department of Diabetes, Endocrinology and Nutrition (A.Y.), Kyoto University Graduate School of Medicine, Kyoto 606-8501, Japan

Publisher

The Endocrine Society

Subject

Endocrinology

Link

http://academic.oup.com/endo/article-pdf/156/2/548/8989945/endo0548.pdf

Reference24 articles.

1. Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia;Rousseau;Nature,1994

2. Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia;Shiang;Cell,1994

3. A common FGFR3 gene mutation in hypochondroplasia;Prinos;Hum Mol Genet,1995

4. A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene;Tavormina;Am J Hum Genet,1999

5. Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3;Tavormina;Nat Genet,1995

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