A new mib allele with a chromosomal deletion covering foxc1a exhibits anterior somite specification defect

mib(nn2002), found from an allele screen, showed early segmentation defect and severe cell death phenotypes, which are different from previously known mib mutants. Despite distinct morphological phenotypes, the typical mib molecular phenotypes: her4 down-regulation, neurogenic phenotype and cold sen...

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Detalles Bibliográficos
Autores principales: Hsu, Chia-Hao, Lin, Ji-Sheng, Po Lai, Keng, Li, Jing-Woei, Chan, Ting-Fung, You, May-Su, Tse, William Ka Fai, Jiang, Yun-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4454137/
https://www.ncbi.nlm.nih.gov/pubmed/26039894
http://dx.doi.org/10.1038/srep10673

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4454137/
https://www.ncbi.nlm.nih.gov/pubmed/26039894
http://dx.doi.org/10.1038/srep10673

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