Cargando…
MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1
BACKGROUND: Through in vivo loss-of-function studies, vertebrate members of the Male abnormal 21 (mab-21) gene family have been implicated in gastrulation, neural tube formation and eye morphogenesis. Despite mounting evidence of their considerable importance in development, the biochemical properti...
Autores principales: | Baldessari, Danila, Badaloni, Aurora, Longhi, Renato, Zappavigna, Vincenzo, Consalez, G Giacomo |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2004
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC545073/ https://www.ncbi.nlm.nih.gov/pubmed/15613244 http://dx.doi.org/10.1186/1471-2121-5-48 |
Ejemplares similares
-
A conditional transgenic reporter of presynaptic terminals reveals novel features of the mouse corticospinal tract
por: D’Acunzo, Pasquale, et al.
Publicado: (2014) -
miR-21 synergizes with BMP9 in osteogenic differentiation by activating the BMP9/Smad signaling pathway in murine multilineage cells
por: SONG, QILING, et al.
Publicado: (2015) -
Mab21l2 Is Essential for Embryonic Heart and Liver Development
por: Saito, Yohei, et al.
Publicado: (2012) -
Identification of missense MAB21L1 variants in microphthalmia and aniridia
por: Seese, Sarah E., et al.
Publicado: (2021) -
Mutations in MAB21L2 Result in Ocular Coloboma, Microcornea and Cataracts
por: Deml, Brett, et al.
Publicado: (2015)