Recent insights into bone development, homeostasis, and repair in type 1 neurofibromatosis (NF1).
about
Computational modeling of bone fracture non-unions: four clinically relevant case studiesFrom neurodevelopment to neurodegeneration: the interaction of neurofibromin and valosin-containing protein/p97 in regulation of dendritic spine formationConstruction of a novel oligonucleotide array-based transcription factor interaction assay platform and its uses for profiling STAT1 cofactors in mouse fibroblast cellsNF1 is a critical regulator of muscle development and metabolismPreliminary experience with the combined use of recombinant bone morphogenetic protein and bisphosphonates in the treatment of congenital pseudarthrosis of the tibia.Interplay of Nkx3.2, Sox9 and Pax3 regulates chondrogenic differentiation of muscle progenitor cells.Development of severe skeletal defects in induced SHP-2-deficient adult mice: a model of skeletal malformation in humans with SHP-2 mutationsDisturbed osteoblastic differentiation of fibrous hamartoma cell from congenital pseudarthrosis of the tibia associated with neurofibromatosis type I.Mice lacking Nf1 in osteochondroprogenitor cells display skeletal dysplasia similar to patients with neurofibromatosis type I.Perioperative management of neurofibromatosis type 1.Intrinsic ability of adult stem cell in skeletal muscle: an effective and replenishable resource to the establishment of pluripotent stem cellsDevelopment of an in vitro cell system from zebrafish suitable to study bone cell differentiation and extracellular matrix mineralization.The regulation of osteoclast function and bone resorption by small GTPasesAnimal models of scoliosis.Bringing computational models of bone regeneration to the clinic.Improved union and bone strength in a mouse model of NF1 pseudarthrosis treated with recombinant human bone morphogenetic protein-2 and zoledronic acid.Prevalence of neurofibromatosis type 1 in congenital pseudarthrosis of the tibia.Does pamidronate enhance the osteogenesis in mesenchymal stem cells derived from fibrous hamartoma in congenital pseudarthrosis of the tibia?Masquelet's procedure and bone morphogenetic protein in congenital pseudarthrosis of the tibia in children: a case series and meta-analysisCapturing the wide variety of impaired fracture healing phenotypes in Neurofibromatosis Type 1 with eight key factors: a computational study.Bone mineral metabolism in patients with neurofibromatosis type 1 (von Recklingausen disease).Gene expression profiles in guided bone regeneration using combinations of different biomaterials: a pilot animal study.In silico clinical trials for pediatric orphan diseases.Is double inactivation of the Nf1 gene responsible for the development of congenital pseudarthrosis of the tibia associated with NF1?Neurofibromatosis type 1
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P2860
Recent insights into bone development, homeostasis, and repair in type 1 neurofibromatosis (NF1).
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh
2007年學術文章
@zh-hant
name
Recent insights into bone deve ...... ype 1 neurofibromatosis (NF1).
@en
Recent insights into bone deve ...... ype 1 neurofibromatosis (NF1).
@nl
type
label
Recent insights into bone deve ...... ype 1 neurofibromatosis (NF1).
@en
Recent insights into bone deve ...... ype 1 neurofibromatosis (NF1).
@nl
prefLabel
Recent insights into bone deve ...... ype 1 neurofibromatosis (NF1).
@en
Recent insights into bone deve ...... ype 1 neurofibromatosis (NF1).
@nl
P1433
P1476
Recent insights into bone deve ...... ype 1 neurofibromatosis (NF1).
@en
P2093
Aaron Schindeler
David G Little
P304
P356
10.1016/J.BONE.2007.11.006
P577
2007-11-28T00:00:00Z