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Hicham Drissi

Researcher at University of Massachusetts Medical School

Publications -  11
Citations -  1442

Hicham Drissi is an academic researcher from University of Massachusetts Medical School. The author has contributed to research in topics: Transcription factor & RUNX2. The author has an hindex of 10, co-authored 11 publications receiving 1375 citations.

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Journal ArticleDOI

Expression of the osteoblast differentiation factor RUNX2 (Cbfa1/AML3/Pebp2αA) is inhibited by tumor necrosis factor-α

TL;DR: The results indicate that TNF regulates RUNX2 expression at multiple levels including destabilization of mRNA and suppression of transcription, which may decrease osteoblast differentiation and inhibit bone formation in TNF excess states.
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Transcriptional autoregulation of the bone related CBFA1/RUNX2 gene.

TL;DR: Functional contributions of 5′ regulatory sequences conserved in rat, mouse and human CBFA1 genes to transcription are defined and indicate that the CB FA1 gene is autoregulated in part by negative feedback on its own promoter to stringently controlCBFA1 gene expression and function during bone formation.
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Phenotype discovery by gene expression profiling: mapping of biological processes linked to BMP-2-mediated osteoblast differentiation.

TL;DR: A global analysis identified a multistage molecular and cellular cascade that supports BMP‐2‐mediated osteoblast differentiation and resulted in the discovery of a class of genes, initially described in relation to differentiation of astrocytes and oligodendrocyte that are functionally coupled to signals for cellular extensions.
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1,25-(OH)2-Vitamin D3 Suppresses the Bone-Related Runx2/Cbfa1 Gene Promoter

TL;DR: It is established that Runx2 expression is regulated by VD3, which provides regulatory coupling between tissue-specific and steroid hormone-dependent control of genes during bone formation.
Journal Article

The Cell Cycle Regulator p27kip1 Contributes to Growth and Differentiation of Osteoblasts

TL;DR: expression of p27 and p21 indicates that p21, which predominates in the growth period, is related to proliferation control, suggesting that p27 plays a key role in regulating osteoblast differentiation by controlling proliferation-related events in bone cells.