Osteopotentia regulates osteoblast maturation, bone formation, and skeletal integrity in mice

scientific journal article

Osteopotentia regulates osteoblast maturation, bone formation, and skeletal integrity in mice is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1083/JCB.201003006
P932PMC publication ID2867309
P698PubMed publication ID20440000
P5875ResearchGate publication ID44570895

P2093author name stringAndreas Mohr
Frank Roemer
Yebin Jiang
Michael L. Sohaskey
Richard M. Harland
Jenny J. Zhao
P2860cites workProlyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfectaQ24295351
FIAT represses ATF4-mediated transcription to regulate bone mass in transgenic miceQ24303541
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Capturing genes encoding membrane and secreted proteins important for mouse developmentQ24563626
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Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiencyQ28264927
Role of matrix metalloproteinase 13 in both endochondral and intramembranous ossification during skeletal regenerationQ28504637
JAWS coordinates chondrogenesis and synovial joint positioningQ28512176
CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfectaQ28592442
Indian hedgehog signals independently of PTHrP to promote chondrocyte hypertrophyQ28592610
Osteoclast differentiation and activationQ29547556
Role of insulin-like growth factors in embryonic and postnatal growthQ29620034
Osteoblast expression of an engineered Gs-coupled receptor dramatically increases bone massQ30481229
Osteogenesis imperfecta type III: mutations in the type I collagen structural genes, COL1A1 and COL1A2, are not necessarily responsibleQ33595459
Procollagen folding and assembly: the role of endoplasmic reticulum enzymes and molecular chaperonesQ33794216
Osteocyte function, osteocyte death and bone fracture resistance.Q33845290
Increased bone formation by prevention of osteoblast apoptosis with parathyroid hormoneQ33857424
Type V osteogenesis imperfecta: a new form of brittle bone diseaseQ33917008
Quantitative trait loci, genes, and polymorphisms that regulate bone mineral density in mouseQ33980500
Collagens, modifying enzymes and their mutations in humans, flies and wormsQ34544297
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Transcriptional control of skeletogenesisQ34820209
Bone matrix proteins: their function, regulation, and relationship to osteoporosisQ35121395
Insulin-like growth factor I and bone mineral density: experience from animal models and human observational studiesQ35840269
Concepts of osteoblast growth and differentiation: basis for modulation of bone cell development and tissue formationQ36043951
Proteins of rough microsomal membranes related to ribosome binding. I. Identification of ribophorins I and II, membrane proteins characteristics of rough microsomesQ36199162
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Bringing KASH under the SUN: the many faces of nucleo-cytoskeletal connectionsQ37323130
ATF4 is a substrate of RSK2 and an essential regulator of osteoblast biology; implication for Coffin-Lowry SyndromeQ40562872
A model for intramembranous ossification during fracture healingQ40626986
Growth on type I collagen promotes expression of the osteoblastic phenotype in human osteosarcoma MG-63 cellsQ41099942
Does adult fracture repair recapitulate embryonic skeletal formation?Q41691669
A network of nuclear envelope membrane proteins linking centromeres to microtubulesQ42044145
Altered fracture repair in the absence of MMP9Q42641175
The influence of type I collagen on the development and maintenance of the osteoblast phenotype in primary and passaged rat calvarial osteoblasts: modification of expression of genes supporting cell growth, adhesion, and extracellular matrix mineralQ46294804
IGF-I receptor is required for the anabolic actions of parathyroid hormone on boneQ46771350
Application of micro-CT assessment of 3-D bone microstructure in preclinical and clinical studiesQ46776300
Functional analysis of secreted and transmembrane proteins critical to mouse development.Q46905044
Osteogenesis imperfecta type VI: a form of brittle bone disease with a mineralization defect.Q50502089
SUN1 is required for telomere attachment to nuclear envelope and gametogenesis in mice.Q51984300
Osteocyte density in woven bone.Q52085750
Osteogenesis imperfecta type VII: an autosomal recessive form of brittle bone diseaseQ59286854
Homozygous osteogenesis imperfecta unlinked to collagen I genesQ60641444
Factors that promote progressive development of the osteoblast phenotype in cultured fetal rat calvaria cellsQ68768271
Phenotypical features of an unique Irish family with severe autosomal recessive osteogenesis imperfectaQ69495455
Fibrogenesis imperfecta ossium (Baker's disease): a case studied at autopsyQ73289456
Fibrogenesis imperfecta ossium; a generalised disease of bone characterised by defective formation of the collagen fibres of the bone matrixQ73933621
P4510describes a project that usesImageJQ1659584
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectosteoblastQ917177
P304page(s)511–525
P577publication date2010-05-03
P1433published inJournal of Cell BiologyQ1524550
P1476titleOsteopotentia regulates osteoblast maturation, bone formation, and skeletal integrity in mice
P478volume189

Reverse relations

cites work (P2860)
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