Bhlha9 regulates apical ectodermal ridge formation during limb development-Reference-Cited by-同舟云学术

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Bhlha9 regulates apical ectodermal ridge formation during limb development

Published:2017-03-21 Issue:1 Volume:36 Page:64-72
ISSN:0914-8779
Container-title:Journal of Bone and Mineral Metabolism
language:en
Short-container-title:J Bone Miner Metab

Author:

Kataoka Kensuke,Matsushima Takahide,Ito Yoshiaki,Sato Tempei,Yokoyama Shigetoshi,Asahara Hiroshi

Funder

National Institutes of Health

Japan Society for the Promotion of Science

Core Research for Evolutional Science and Technology, Japan Science and Technology Agency

Bristol-Myers K.K. RA Clinical Investigation

Naito Foundation

Japan Agency for Medical Research and Development

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Orthopedics and Sports Medicine,General Medicine,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/article/10.1007/s00774-017-0820-0/fulltext.html

Reference30 articles.

1. Gurrieri F, Everman DB (2013) Clinical, genetic, and molecular aspects of split-hand/foot malformation: an update. Am J Med Genet A 11:2860–2872

2. Ianakiev P, Kilpatrick MW, Toudjarska I, Basel D, Beighton P, Tsipouras P (2000) Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27. Am J Hum Genet 1:59–66

3. van Bokhoven H, Hamel BC, Bamshad M, Sangiorgi E, Gurrieri F et al (2001) p63 gene mutations in EEC syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation. Am J Hum Genet 3:481–492

4. Yang A, Kaghad M, Wang Y, Gillett E, Fleming MD, Dotsch V, Andrews NC, Caput D, McKeon F (1998) p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities. Mol Cell 3:305–316

5. Yang A, Schweitzer R, Sun D, Kaghad M, Walker N, Bronson RT, Tabin C, Sharpe A, Caput D, Crum C, McKeon F (1999) p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development. Nature 6729:714–718

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3. BHLHA9 homozygous duplication in a consanguineous family: A challenge for genetic counseling;American Journal of Medical Genetics Part A;2022-12-24

4. Refining the Clinical Spectrum of the 17p13.3 Microduplication Syndrome: Case-Report of a Familial Small Microduplication;Biomedicines;2022-11-30

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