scholarly article | Q13442814 |
P50 | author | Michael T Longaker | Q90219405 |
Harsh N Shah | Q90350061 | ||
Ankit Salhotra | Q59755654 | ||
P2093 | author name string | Benjamin Levi | |
P2860 | cites work | A Revised Perspective of Skeletal Stem Cell Biology | Q90403557 |
Disruption of Neutrophil Extracellular Traps (NETs) Links Mechanical Strain to Post-traumatic Inflammation | Q91218186 | ||
Murine Tissue-Resident PDGFRα+ Fibro-Adipogenic Progenitors Spontaneously Acquire Osteogenic Phenotype in an Altered Inflammatory Environment | Q91597163 | ||
Coordinating Tissue Regeneration Through Transforming Growth Factor-β Activated Kinase 1 Inactivation and Reactivation | Q91749884 | ||
Mesenchymal VEGFA induces aberrant differentiation in heterotopic ossification | Q91995141 | ||
Hox11 expressing regional skeletal stem cells are progenitors for osteoblasts, chondrocytes and adipocytes throughout life | Q92002734 | ||
Sensory Nerves Affect Bone Regeneration in Rabbit Mandibular Distraction Osteogenesis | Q92135250 | ||
Immobilization after injury alters extracellular matrix and stem cell fate | Q97553355 | ||
Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb patterning and skeletogenesis | Q21145242 | ||
Hedgehog-regulated processing of Gli3 produces an anterior/posterior repressor gradient in the developing vertebrate limb | Q22253250 | ||
The novel zinc finger-containing transcription factor osterix is required for osteoblast differentiation and bone formation | Q24292169 | ||
FIAT represses ATF4-mediated transcription to regulate bone mass in transgenic mice | Q24303541 | ||
TAZ, a transcriptional modulator of mesenchymal stem cell differentiation | Q24314991 | ||
Receptor specificity of the fibroblast growth factor family | Q24320178 | ||
TGF beta signals through a heteromeric protein kinase receptor complex | Q24337608 | ||
Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein | Q24536172 | ||
CCN1/Cyr61 is regulated by the canonical Wnt signal and plays an important role in Wnt3A-induced osteoblast differentiation of mesenchymal stem cells | Q24544140 | ||
A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait | Q24561917 | ||
RANK is essential for osteoclast and lymph node development | Q24598872 | ||
Sclerostin is an osteocyte-expressed negative regulator of bone formation, but not a classical BMP antagonist | Q24646652 | ||
TGF-β and BMP signaling in osteoblast, skeletal development, and bone formation, homeostasis and disease | Q26738766 | ||
Fate decision of mesenchymal stem cells: adipocytes or osteoblasts? | Q26766574 | ||
Recent biological trends in management of fracture non-union | Q26781878 | ||
The role of microRNAs in bone remodeling | Q26799815 | ||
Skeletal stem cells | Q26823973 | ||
Transcriptional regulatory cascades in Runx2-dependent bone development | Q26830666 | ||
Gremlin 1 identifies a skeletal stem cell with bone, cartilage, and reticular stromal potential. | Q27323315 | ||
LRP5 and LRP6 in development and disease | Q27692072 | ||
Multilineage potential of adult human mesenchymal stem cells | Q27860737 | ||
Vertebrate Smoothened functions at the primary cilium | Q27919682 | ||
Biological and molecular profile of fracture non-union tissue: current insights | Q28082618 | ||
Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development | Q28119185 | ||
Negative regulation of BMP/Smad signaling by Tob in osteoblasts | Q28143428 | ||
High bone density due to a mutation in LDL-receptor-related protein 5 | Q28217891 | ||
Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation | Q28240596 | ||
Sclerostin binds to LRP5/6 and antagonizes canonical Wnt signaling | Q28240767 | ||
Mechanical stimulation of bone in vivo reduces osteocyte expression of Sost/sclerostin | Q28261537 | ||
Developmental localization of the splicing alternatives of fibroblast growth factor receptor-2 (FGFR2) | Q28263694 | ||
Osteocytes, not Osteoblasts or Lining Cells, are the Main Source of the RANKL Required for Osteoclast Formation in Remodeling Bone | Q28267634 | ||
Sclerostin is a delayed secreted product of osteocytes that inhibits bone formation | Q28269067 | ||
Notch-1 signalling requires ligand-induced proteolytic release of intracellular domain | Q28273268 | ||
The roles of FGFs in the early development of vertebrate limbs | Q28273288 | ||
Mutations affecting segment number and polarity in Drosophila | Q28273492 | ||
WNT signaling in bone homeostasis and disease: from human mutations to treatments | Q28285090 | ||
Regulation of type I collagen genes expression | Q28295942 | ||
Where Wnts went: the exploding field of Lrp5 and Lrp6 signaling in bone | Q28303536 | ||
Mice lacking JunB are osteopenic due to cell-autonomous osteoblast and osteoclast defects | Q28505493 | ||
Maturational disturbance of chondrocytes in Cbfa1-deficient mice | Q28506259 | ||
Hand2 controls osteoblast differentiation in the branchial arch by inhibiting DNA binding of Runx2 | Q28506661 | ||
Decreased BMD and limb deformities in mice carrying mutations in both Lrp5 and Lrp6 | Q28506732 | ||
A twist code determines the onset of osteoblast differentiation | Q28510533 | ||
Lrp6 hypomorphic mutation affects bone mass through bone resorption in mice and impairs interaction with Mesd | Q28512189 | ||
Sox9 is required for cartilage formation | Q28588649 | ||
Fgf-10 is required for both limb and lung development and exhibits striking functional similarity to Drosophila branchless | Q28589182 | ||
OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis | Q28589430 | ||
Gli1 protein participates in Hedgehog-mediated specification of osteoblast lineage during endochondral ossification | Q28591410 | ||
Intraflagellar transport, cilia, and mammalian Hedgehog signaling: analysis in mouse embryonic fibroblasts | Q28591555 | ||
The transcription factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6 | Q28593218 | ||
Bone development | Q28606488 | ||
Patched1 regulates hedgehog signaling at the primary cilium | Q29547515 | ||
Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts | Q29547605 | ||
Developmental roles and clinical significance of hedgehog signaling | Q29614988 | ||
Sonic hedgehog mediates the polarizing activity of the ZPA | Q29616565 | ||
Developmental regulation of the growth plate | Q29618969 | ||
Self-renewing osteoprogenitors in bone marrow sinusoids can organize a hematopoietic microenvironment | Q29620053 | ||
Trauma-induced heterotopic bone formation and the role of the immune system: A review | Q36395829 | ||
The postnatal role of Sox9 in cartilage | Q36412996 | ||
Dual function of Bmpr1a signaling in restricting preosteoblast proliferation and stimulating osteoblast activity in mouse | Q36497710 | ||
Inhibition of Hif1α prevents both trauma-induced and genetic heterotopic ossification | Q36498232 | ||
Hox11 genes regulate postnatal longitudinal bone growth and growth plate proliferation | Q36506634 | ||
Osteoblast lineage-specific effects of notch activation in the skeleton | Q36542861 | ||
Development of the endochondral skeleton | Q36629738 | ||
Notch Signaling and the Skeleton | Q36960089 | ||
Phenotype of five cases of prenatally diagnosed campomelic dysplasia harboring novel mutations of the SOX9 gene | Q84974960 | ||
Gli1-labeled adult mesenchymal stem/progenitor cells and hedgehog signaling contribute to endochondral heterotopic ossification | Q88379043 | ||
Osteoblast precursors and inflammatory cells arrive simultaneously to sites of a trabecular-bone injury | Q88981561 | ||
Mouse Cre Models for the Study of Bone Diseases | Q89208054 | ||
Regulation of heterotopic ossification by monocytes in a mouse model of aberrant wound healing | Q89555563 | ||
Skeletal Stem Cell-Schwann Cell Circuitry in Mandibular Repair | Q90060968 | ||
Tuning Macrophage Phenotype to Mitigate Skeletal Muscle Fibrosis | Q90244027 | ||
Analysis of Bone-Cartilage-Stromal Progenitor Populations in Trauma Induced and Genetic Models of Heterotopic Ossification | Q36968379 | ||
Loss of BMP signaling through BMPR1A in osteoblasts leads to greater collagen cross-link maturation and material-level mechanical properties in mouse femoral trabecular compartments | Q36984640 | ||
Genetic and molecular control of osterix in skeletal formation | Q37051825 | ||
The role of Dickkopf-1 in bone development, homeostasis, and disease | Q37066218 | ||
Clonal precursor of bone, cartilage, and hematopoietic niche stromal cells. | Q37068608 | ||
Wnt and hedgehog signaling pathways in bone development | Q37091510 | ||
Endothelial Notch activity promotes angiogenesis and osteogenesis in bone | Q37091548 | ||
Dimorphic effects of Notch signaling in bone homeostasis. | Q37165102 | ||
Reconciling the roles of FAK in osteoblast differentiation, osteoclast remodeling, and bone regeneration | Q37234953 | ||
Hox11 genes are required for regional patterning and integration of muscle, tendon and bone | Q37280961 | ||
Notch signaling maintains bone marrow mesenchymal progenitors by suppressing osteoblast differentiation | Q37339719 | ||
Fibroblast growth factor 2 control of vascular tone | Q37362801 | ||
Regulation of bone development and extracellular matrix protein genes by RUNX2. | Q37569808 | ||
Notch1 and Notch2 expression in osteoblast precursors regulates femoral microarchitecture | Q37675480 | ||
Integration of BMP, Wnt, and notch signaling pathways in osteoblast differentiation. | Q37906474 | ||
Combinatorial control of ATF4-dependent gene transcription in osteoblasts | Q37955971 | ||
Building strong bones: molecular regulation of the osteoblast lineage | Q37970567 | ||
Fracture healing under healthy and inflammatory conditions | Q37980336 | ||
Stem cells and bone: a historical perspective | Q38244680 | ||
Cbfa1 isoforms exert functional differences in osteoblast differentiation | Q38327457 | ||
Roles of bone morphogenetic protein type I receptors and Smad proteins in osteoblast and chondroblast differentiation. | Q38614636 | ||
BMP signalling in skeletal development, disease and repair. | Q38740288 | ||
Osteogenic Differentiation of Periosteal Cells During Fracture Healing | Q38805665 | ||
SOX9 and the many facets of its regulation in the chondrocyte lineage | Q38820782 | ||
Hox genes in the adult skeleton: Novel functions beyond embryonic development | Q39057750 | ||
Regionally Restricted Hox Function in Adult Bone Marrow Multipotent Mesenchymal Stem/Stromal Cells | Q39112663 | ||
The Role of Skeletal Stem Cells in the Reconstruction of Bone Defects | Q39407264 | ||
Development of the peripheral nervous system from the neural crest | Q39544468 | ||
Hedgehog-Gli activators direct osteo-chondrogenic function of bone morphogenetic protein toward osteogenesis in the perichondrium. | Q39615611 | ||
Wnt proteins promote bone regeneration | Q39709638 | ||
Runx2 determines bone maturity and turnover rate in postnatal bone development and is involved in bone loss in estrogen deficiency | Q40133754 | ||
Cooperative interactions between activating transcription factor 4 and Runx2/Cbfa1 stimulate osteoblast-specific osteocalcin gene expression | Q40401302 | ||
Two tissue-resident progenitor lineages drive distinct phenotypes of heterotopic ossification. | Q40459563 | ||
Connective tissue growth factor (CTGF) is regulated by Wnt and bone morphogenetic proteins signaling in osteoblast differentiation of mesenchymal stem cells | Q40501696 | ||
ATF4 is a substrate of RSK2 and an essential regulator of osteoblast biology; implication for Coffin-Lowry Syndrome | Q40562872 | ||
Campomelic dysplasia with XY sex reversal: diverse phenotypes resulting from mutations in a single gene | Q41029780 | ||
A role for FGF-8 in the initiation and maintenance of vertebrate limb bud outgrowth | Q41331703 | ||
Cell-matrix signals specify bone endothelial cells during developmental osteogenesis. | Q41591466 | ||
Reduced affinity to and inhibition by DKK1 form a common mechanism by which high bone mass-associated missense mutations in LRP5 affect canonical Wnt signaling | Q41878594 | ||
Coupling of angiogenesis and osteogenesis by a specific vessel subtype in bone | Q41881171 | ||
Sonic hedgehog-expressing cells in the developing limb measure time by an intrinsic cell cycle clock | Q42206249 | ||
Ihh/Gli2 signaling promotes osteoblast differentiation by regulating Runx2 expression and function | Q42530363 | ||
CXCL12 in early mesenchymal progenitors is required for haematopoietic stem-cell maintenance | Q43226905 | ||
Osteoblast precursors, but not mature osteoblasts, move into developing and fractured bones along with invading blood vessels. | Q30531794 | ||
Identification, characterization, and isolation of a common progenitor for osteoclasts, macrophages, and dendritic cells from murine bone marrow and periphery | Q30538833 | ||
FoxO-mediated defense against oxidative stress in osteoblasts is indispensable for skeletal homeostasis in mice | Q33645103 | ||
BMP-2 modulates beta-catenin signaling through stimulation of Lrp5 expression and inhibition of beta-TrCP expression in osteoblasts | Q33723850 | ||
Generation and expression of a Hoxa11eGFP targeted allele in mice | Q33794230 | ||
Fibroblast growth factor signaling and basement membrane assembly are connected during epithelial morphogenesis of the embryoid body | Q33946703 | ||
Osteo-chondroprogenitor cells are derived from Sox9 expressing precursors | Q34055618 | ||
Multiple functions of Osterix are required for bone growth and homeostasis in postnatal mice | Q34059112 | ||
Indian hedgehog signaling regulates transcription and expression of collagen type X via Runx2/Smads interactions | Q34138974 | ||
A review of osteocyte function and the emerging importance of sclerostin | Q34264395 | ||
Minireview: transcriptional control of osteoblast differentiation | Q34287375 | ||
Fgf-8 expression in the post-gastrulation mouse suggests roles in the development of the face, limbs and central nervous system. | Q34319673 | ||
New aspects of Wnt signaling pathways in higher vertebrates | Q34353150 | ||
Fibroblast growth factor receptor-1 (FGFR-1) is essential for normal neural tube and limb development. | Q34427515 | ||
Disruption of the fibroblast growth factor-2 gene results in decreased bone mass and bone formation | Q34432447 | ||
Clonal analysis of mouse development reveals a polyclonal origin for yolk sac blood islands | Q34570196 | ||
The development of fibroblast colonies in monolayer cultures of guinea-pig bone marrow and spleen cells | Q34704081 | ||
TGFbeta-SMAD signal transduction: molecular specificity and functional flexibility | Q34713446 | ||
Transcription factors in bone: developmental and pathological aspects | Q34735288 | ||
Effects of aging on osteogenic response and heterotopic ossification following burn injury in mice | Q34920114 | ||
Functions of AP1 (Fos/Jun) in bone development | Q34963037 | ||
Identification and specification of the mouse skeletal stem cell | Q34979978 | ||
Fra-2/AP-1 controls bone formation by regulating osteoblast differentiation and collagen production | Q35005578 | ||
Regulation of fracture repair by growth factors | Q35317301 | ||
Role of gender in burn-induced heterotopic ossification and mesenchymal cell osteogenic differentiation | Q35662790 | ||
Proinflammatory Mediators Enhance the Osteogenesis of Human Mesenchymal Stem Cells after Lineage Commitment | Q35691834 | ||
Osteoclasts: New Insights | Q35755039 | ||
Glucose Uptake and Runx2 Synergize to Orchestrate Osteoblast Differentiation and Bone Formation | Q35762267 | ||
Identification and characterization of an injury-induced skeletal progenitor | Q35961149 | ||
Targeted disruption of fibroblast growth factor (FGF) receptor 2 suggests a role for FGF signaling in pregastrulation mammalian development | Q36064260 | ||
Signaling networks that control the lineage commitment and differentiation of bone cells | Q36082866 | ||
FGF signaling in the developing endochondral skeleton | Q36111408 | ||
Fibroblast growth factor receptor 1 signaling in the osteo-chondrogenic cell lineage regulates sequential steps of osteoblast maturation | Q36140903 | ||
Local application of recombinant human fibroblast growth factor-2 on bone repair: a dose-escalation prospective trial on patients with osteotomy | Q44226824 | ||
Actions of fibroblast growth factor-8 in bone cells in vitro | Q44296458 | ||
Mesenchymal stem cells from different organs are characterized by distinct topographic Hox codes | Q44468474 | ||
Fgf8 signalling from the AER is essential for normal limb development. | Q45967231 | ||
Pro-inflammatory M1 macrophages promote Osteogenesis by mesenchymal stem cells via the COX-2-prostaglandin E2 pathway. | Q46183672 | ||
Wnt 3a promotes proliferation and suppresses osteogenic differentiation of adult human mesenchymal stem cells | Q46284854 | ||
Roles for FGF8 in the induction, initiation, and maintenance of chick limb development | Q46448253 | ||
Fracture healing via periosteal callus formation requires macrophages for both initiation and progression of early endochondral ossification. | Q46665783 | ||
Hedgehog promotes primary osteoblast differentiation and increases PTHrP mRNA expression and iPTHrP secretion. | Q47827195 | ||
Suppressor of Fused restraint of Hedgehog activity level is critical for osteogenic proliferation and differentiation during calvarial bone development | Q47971385 | ||
Macrophage-derived oncostatin M contributes to human and mouse neurogenic heterotopic ossifications | Q47991308 | ||
Abnormalities in cartilage and bone development in the Apert syndrome FGFR2(+/S252W) mouse | Q48837214 | ||
Pharmacological rescue of diabetic skeletal stem cell niches. | Q48873501 | ||
The early history of the Sox genes | Q48933333 | ||
An analysis of skeletal development in osteoblast-specific and chondrocyte-specific runt-related transcription factor-2 (Runx2) knockout mice | Q50235797 | ||
Scleraxis-Lineage Cells Contribute to Ectopic Bone Formation in Muscle and Tendon. | Q50321433 | ||
Strategic Targeting of Multiple BMP Receptors Prevents Trauma-Induced Heterotopic Ossification. | Q50885568 | ||
Bone Morphogenetic Proteins. | Q51724862 | ||
Integration of growth and specification in chick wing digit-patterning. | Q51961530 | ||
Bone regeneration is regulated by wnt signaling. | Q51978189 | ||
BMP2 activity, although dispensable for bone formation, is required for the initiation of fracture healing. | Q52002102 | ||
Beta-catenin signaling pathway is crucial for bone morphogenetic protein 2 to induce new bone formation. | Q52002734 | ||
Conditional inactivation of Fgfr1 in mouse defines its role in limb bud establishment, outgrowth and digit patterning. | Q52041047 | ||
Endothelial progenitor cells from peripheral blood support bone regeneration by provoking an angiogenic response. | Q53363266 | ||
Expression of nerve growth factor and vascular endothelial growth factor in the inferior alveolar nerve after distraction osteogenesis. | Q53597529 | ||
Skeletal stem cells in space and time. | Q53636612 | ||
Structural and Functional Diversity in the FGf Receptor Multigene Family | Q55919452 | ||
Increased bone formation and osteosclerosis in mice overexpressing the transcription factor Fra-1 | Q57675161 | ||
Mechanoresponsive stem cells acquire neural crest fate in jaw regeneration | Q57793634 | ||
Resting zone of the growth plate houses a unique class of skeletal stem cells | Q58570660 | ||
Classifying cells with Scasat, a single-cell ATAC-seq analysis tool | Q58600578 | ||
Characterizing the Circulating Cell Populations in Traumatic Heterotopic Ossification | Q58701151 | ||
Discovery of a periosteal stem cell mediating intramembranous bone formation | Q59066621 | ||
Identification of the Human Skeletal Stem Cell | Q59754893 | ||
Wnt Pathway in Bone Repair and Regeneration - What Do We Know So Far | Q60919373 | ||
Hip Fracture Nonunions: Diagnosis, Treatment, and Special Considerations in Elderly Patients | Q60947531 | ||
Heterotopic Ossification: A Comprehensive Review | Q64096225 | ||
Reactivation of a developmental signaling center is required for therapeutic control of the murine periosteal niche | Q64272396 | ||
Expression of the fibroblast growth factor receptor FGFR-1/flg during gastrulation and segmentation in the mouse embryo | Q67491933 | ||
Increased bone turnover in late postmenopausal women is a major determinant of osteoporosis | Q71644718 | ||
Inflammatory cells in normal human fracture healing | Q72846237 | ||
Transcriptional mechanisms in osteoblast differentiation and bone formation | Q73763993 | ||
Locally applied nerve growth factor enhances bone consolidation in a rabbit model of mandibular distraction osteogenesis | Q79139219 | ||
Wnt/beta-catenin signaling interacts differentially with Ihh signaling in controlling endochondral bone and synovial joint formation | Q80175014 | ||
Targeted ablation of osteocytes induces osteoporosis with defective mechanotransduction | Q80432871 | ||
Endogenous BMPR-IB signaling is required for early osteoblast differentiation of human bone cells | Q82771853 | ||
Regulation of osteoblast differentiation by Runx2 | Q84966232 | ||
P577 | publication date | 2020-09-08 | |
P1433 | published in | Nature Reviews Molecular Cell Biology | Q1573120 |
P1476 | title | Mechanisms of bone development and repair |
Q104802177 | Gaucher disease: Basic and translational science needs for more complete therapy and management | cites work | P2860 |
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