Cargando…
Interaction of sexual dimorphism and gene dosage imbalance in skeletal deficits associated with Down syndrome
All individuals with Down syndrome (DS), which results from trisomy of human chromosome 21 (Ts21), present with skeletal abnormalities typified by craniofacial features, short stature and low bone mineral density (BMD). Differences in skeletal deficits between males and females with DS suggest a sex...
Autores principales: | Thomas, Jared R., LaCombe, Jonathan, Long, Rachel, Lana-Elola, Eva, Watson-Scales, Sheona, Wallace, Joseph M., Fisher, Elizabeth M.C., Tybulewicz, Victor L.J., Roper, Randall J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262595/ https://www.ncbi.nlm.nih.gov/pubmed/32305495 http://dx.doi.org/10.1016/j.bone.2020.115367 |
Ejemplares similares
-
Genetic dissection of triplicated chromosome 21 orthologs yields varying skeletal traits in Down syndrome model mice
por: Sloan, Kourtney, et al.
Publicado: (2023) -
Down syndrome: searching for the genetic culprits
por: Lana-Elola, Eva, et al.
Publicado: (2011) -
Genetic dissection of Down syndrome-associated congenital heart defects using a new mouse mapping panel
por: Lana-Elola, Eva, et al.
Publicado: (2016) -
Correction: Genetic dissection of Down syndrome-associated congenital heart defects using a new mouse mapping panel
por: Lana-Elola, Eva, et al.
Publicado: (2020) -
Craniofacial dysmorphology in Down syndrome is caused by increased dosage of Dyrk1a and at least three other genes
por: Redhead, Yushi, et al.
Publicado: (2023)