RAB23 coordinates early osteogenesis by repressing FGF10-pERK1/2 and GLI1
Author:
Affiliation:
1. Craniofacial Development and Malformations research group, Orthodontics, Oral and Maxillofacial Diseases, University of Helsinki, Helsinki, Finland
2. Oral and Maxillofacial Diseases, Helsinki University Hospital, Helsinki, Finland
Abstract
Funder
Suomen Akatemia
Sigrid Juséliuksen Säätiö
Helsinki University Hospital Research Foundation
Publisher
eLife Sciences Publications, Ltd
Subject
General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience
Link
https://cdn.elifesciences.org/articles/55829/elife-55829-v2.pdf
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3. Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an alu element insertion from a new subfamily;Bochukova;Human Mutation,2009
4. Acrocephaly, with other congenital malformations;Carpenter;Proceedings of the Royal Society of Medicine,1909
5. Rab23 negatively regulates Gli1 transcriptional factor in a su(Fu)-dependent manner;Chi;Cellular Signalling,2012
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