Stem and progenitor cell dysfunction in human trisomies
Trisomy 21, the commonest constitutional aneuploidy in humans, causes profound perturbation of stem and progenitor cell growth, which is both cell context dependent and developmental stage specific and mediated by complex genetic mechanisms beyond increased Hsa21 gene dosage. While proliferation of...
Main Authors: | Liu, B, Filippi, S, Roy, A, Roberts, I |
---|---|
Format: | Journal article |
Language: | English |
Published: |
EMBO Press
2014
|
Similar Items
-
Genome wide dysregulation of gene expression by Trisomy 21 in fetal liver haematopoietic stem and progenitor cells
by: Roy, A, et al.
Published: (2016) -
Perturbation of fetal liver hematopoietic stem and progenitor cell development by trisomy 21.
by: Roy, A, et al.
Published: (2012) -
Chromosome 7 and 19 trisomy in cultured human neural progenitor cells.
by: Dhruv Sareen, et al.
Published: (2009-10-01) -
The impact of trisomy 21 on early human hematopoiesis.
by: Roy, A, et al.
Published: (2013) -
Trisomy 21 expands the megakaryocyte-erythroid progenitor compartment in human fetal liver-implications for down syndrome AMKL.
by: Tunstall-Pedoe, O, et al.
Published: (2006)