Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Karim Kaabeche"'
Publikováno v:
The American Journal of Pathology. 169:1303-1311
Genetic mutations of Twist, a basic helix-loop-helix transcription factor, induce premature fusion of cranial sutures in Saethre-Chotzen syndrome (SCS). We report here a previously undescribed mechanism involved in the altered osteoblastogenesis in S
Autor:
Karim Kaabeche, P. J. Marie
Publikováno v:
PPAR Research, Vol 2006 (2006)
PPAR Research
PPAR Research
Bone loss occuring with unloading is associated with decreased osteoblastogenesis and increased bone marrow adipogenesis, resulting in bone loss and decreased bone formation. Here, we review the present knowledge on the role of PPARγin the control o
Publikováno v:
Journal of Biological Chemistry. 279:36259-36267
Fibroblast growth factors (FGFs) play an important regulatory role in skeletal development and bone formation. However, the FGF signaling mechanisms controlling osteoblast function are poorly understood. Here, we identified a role for the Src family
Publikováno v:
BONE
BONE, Elsevier, 2008, 42 (6), pp.1032-9. ⟨10.1016/j.bone.2008.02.009⟩
BONE, 2008, 42 (6), pp.1032-9. ⟨10.1016/j.bone.2008.02.009⟩
BONE, Elsevier, 2008, 42 (6), pp.1032-9. ⟨10.1016/j.bone.2008.02.009⟩
BONE, 2008, 42 (6), pp.1032-9. ⟨10.1016/j.bone.2008.02.009⟩
International audience; Fibroblast growth factor receptor (FGFR) signaling plays an important role in skeletogenesis. The molecular mechanisms triggered by activated FGFR in bone forming cells are however not fully understood. In this study, we ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baebb583dad90f441a8ae9dfed7522fc
https://www.hal.inserm.fr/inserm-00346884
https://www.hal.inserm.fr/inserm-00346884
Publikováno v:
Frontiers of oral biology. 12
Recent advances in molecular genetics have led to a better understanding of the role of specific genes such as fibroblast growth factor receptor (FGFR) and Twist in cranial bone formation. Specifically, the analysis of osteoblast abnormalities induce
Recent advances in molecular genetics have led to a better understanding of the role of specific genes such as fibroblast growth factor receptor (FGFR) and Twist in cranial bone formation. Specifically, the analysis of osteoblast abnormalities induce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be1804e240accc08c89557971d25377d
https://doi.org/10.1159/000115036
https://doi.org/10.1159/000115036
Publikováno v:
Human molecular genetics. 14(11)
Genetic mutations of Twist, a bHLH transcription factor, induce premature fusion of cranial sutures (craniosynostosis) in the Saethre-Chotzen syndrome (SCS). The mechanisms by which Twist haploinsufficiency may alter osteoblast differentiation are po
Autor:
Pierre J. Marie, Hind Guenou, Nadège Didelot, Karim Kaabeche, Daniel Bouvard, Antoine Listrat
Publikováno v:
Journal of cell science. 118(Pt 6)
Fibroblast growth factor receptor signaling is an important mechanism regulating osteoblast function. To gain an insight into the regulatory role of FGF receptor-2 (FGFR2) signaling in osteoblasts, we investigated integrin-mediated attachment and cel