MAB21L1 modulates gene expression and DNA metabolic processes in the lens placode

Mutations in human MAB21L1 cause aberrations in lens ectoderm morphogenesis and lead to congenital cerebellar, ocular, craniofacial and genital (COFG) syndrome. Murine Mab21l1-null mutations cause severe cell-autonomous defects in lens formation, leading to microphthalmia; therefore, Mab21l1-null mi...

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Detalles Bibliográficos
Autores principales: Yamada, Ryuichi, Oguri, Akira, Fujiki, Katsunori, Shirahige, Katsuhiko, Hirate, Yoshikazu, Kanai-Azuma, Masami, Takezoe, Hirotaka, Akimoto, Yoshihiro, Takahashi, Naoki, Kanai, Yoshiakira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8713989/
https://www.ncbi.nlm.nih.gov/pubmed/34779479
http://dx.doi.org/10.1242/dmm.049251

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8713989/
https://www.ncbi.nlm.nih.gov/pubmed/34779479
http://dx.doi.org/10.1242/dmm.049251

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