scholarly article | Q13442814 |
P2093 | author name string | Shu Takeda | |
Omri Bauer | |||
Yoram Groner | |||
Ayako Kimura | |||
Amnon Sharir | |||
Shay Hantisteanu | |||
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Cbfβ deletion in mice recapitulates cleidocranial dysplasia and reveals multiple functions of Cbfβ required for skeletal development. | Q33767459 | ||
The genetic transformation of bone biology | Q33796568 | ||
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Osteo-chondroprogenitor cells are derived from Sox9 expressing precursors | Q34055618 | ||
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Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture | Q34268288 | ||
HES1 (Hairy and Enhancer of Split 1) Is a Determinant of Bone Mass | Q34509386 | ||
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Loss of Runx2 in committed osteoblasts impairs postnatal skeletogenesis. | Q34790965 | ||
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A Cbfa1-dependent genetic pathway controls bone formation beyond embryonic development | Q35194624 | ||
Structure and regulated expression of mammalian RUNX genes | Q35779684 | ||
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Overexpression of Cbfa1 in osteoblasts inhibits osteoblast maturation and causes osteopenia with multiple fractures | Q36293998 | ||
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Functionally improved bone in calbindin-D28k knockout mice | Q36631885 | ||
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Adiponectin regulates bone mass via opposite central and peripheral mechanisms through FoxO1. | Q36920314 | ||
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Role of Runx genes in chondrocyte differentiation | Q38289933 | ||
The Runx3 transcription factor regulates development and survival of TrkC dorsal root ganglia neurons | Q39644959 | ||
Runx3/AML2/Cbfa3 regulates early and late chondrocyte differentiation. | Q40135256 | ||
Genomic regions identified for BMD in a large sample including epistatic interactions and gender-specific effects | Q40285853 | ||
Runx3 regulates mouse TGF-beta-mediated dendritic cell function and its absence results in airway inflammation | Q40734155 | ||
Basic biomechanical measurements of bone: a tutorial | Q40797364 | ||
Isolation of osteoprogenitors from murine bone marrow by selection of CD11b negative cells | Q41924062 | ||
The protein tyrosine phosphatase Rptpzeta is expressed in differentiated osteoblasts and affects bone formation in mice | Q42818523 | ||
Mouse alpha1(I)-collagen promoter is the best known promoter to drive efficient Cre recombinase expression in osteoblast | Q43434401 | ||
Association of a common polymorphism in the methylenetetrahydrofolate reductase (MTHFR) gene with bone phenotypes depends on plasma folate status | Q44812034 | ||
Region-specific expression in early chick and mouse embryos of Ghox-lab and Hox 1.6, vertebrate homeobox-containing genes related to Drosophila labial | Q45859555 | ||
Multiple osteoporosis susceptibility genes on chromosome 1p36 in Chinese. | Q46012022 | ||
Phylogenesis and regulated expression of the RUNT domain transcription factors RUNX1 and RUNX3. | Q47396753 | ||
Association of the -381T/C promoter variation of the brain natriuretic peptide gene with low bone-mineral density and rapid postmenopausal bone loss | Q48381397 | ||
Confirmation and fine mapping of chromosomal regions influencing peak bone mass in mice | Q48657499 | ||
An analysis of skeletal development in osteoblast-specific and chondrocyte-specific runt-related transcription factor-2 (Runx2) knockout mice | Q50235797 | ||
Distinct roles for Hedgehog and canonical Wnt signaling in specification, differentiation and maintenance of osteoblast progenitors. | Q50722204 | ||
Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S. | Q50941844 | ||
Regulation of skeletal development by the Runx family of transcription factors. | Q50974881 | ||
Runx3-deficient mouse strains circa 2008: resemblance and dissimilarity. | Q51808089 | ||
Quantitative trait loci for bone density in mice: the genes determining total skeletal density and femur density show little overlap in F2 mice. | Q52115495 | ||
Spatial and temporal expression pattern of Runx3 (Aml2) and Runx1 (Aml1) indicates non-redundant functions during mouse embryogenesis. | Q52126883 | ||
Col2a1-directed expression of Cre recombinase in differentiating chondrocytes in transgenic mice. | Q52169988 | ||
Developmental expression of mouse stromelysin-3 mRNA. | Q52209103 | ||
Core binding factor β of osteoblasts maintains cortical bone mass via stabilization of Runx2 in mice. | Q53252888 | ||
Cbf beta regulates Runx2 function isoform-dependently in postnatal bone development. | Q53615857 | ||
The distinct role of the Runx proteins in chondrocyte differentiation and intervertebral disc degeneration: findings in murine models and in human disease. | Q54517855 | ||
Achondroplasia | Q57751572 | ||
First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q | Q57783993 | ||
Mice deficient in Abl are osteoporotic and have defects in osteoblast maturation | Q58085524 | ||
Criteria to evaluate bone mineralization in cattle: I. Effect of dietary phosphorus on chemical, physical, and mechanical properties | Q70214014 | ||
Association of a polymorphism in the TNFR2 gene with low bone mineral density | Q73995317 | ||
Regulation of matrix metalloproteinases (MMP-2, -3, -9, and -13) by interleukin-1 and interleukin-6 in mouse calvaria: association of MMP induction with bone resorption | Q74278303 | ||
Variance component linkage analysis indicates a QTL for femoral neck bone mineral density on chromosome 1p36 | Q77105209 | ||
Expression of Runx1, -2 and -3 during tooth, palate and craniofacial bone development | Q79096024 | ||
High-throughput tool for discovery of bone regulating factors | Q79398611 | ||
Interleukin 10-deficient mice develop osteopenia, decreased bone formation, and mechanical fragility of long bones | Q80552322 | ||
Univariate and bivariate variance component linkage analysis of a whole-genome scan for loci contributing to bone mineral density | Q81644880 | ||
Meta-analysis of genome-wide linkage studies for bone mineral density | Q82811612 | ||
Cbfb regulates bone development by stabilizing Runx family proteins | Q85644607 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | congenital disorder | Q727096 |
osteoblast | Q917177 | ||
P304 | page(s) | 1097-1109 | |
P577 | publication date | 2015-01-20 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | Loss of osteoblast Runx3 produces severe congenital osteopenia | |
P478 | volume | 35 |
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Q64264178 | Identification of Genes Differentially Expressed in Simvastatin-Induced Alveolar Bone Formation |
Q41636712 | Identification of a p53 target, CD137L, that mediates growth suppression and immune response of osteosarcoma cells. |
Q52765383 | Identification of differentially expressed miRNAs associated with chronic kidney disease-mineral bone disorder. |
Q61818043 | Identification of key transcription factors - gene regulatory network related with osteogenic differentiation of human mesenchymal stem cells based on transcription factor prognosis system |
Q36530809 | In Vitro Expansion of Bone Marrow Derived Mesenchymal Stem Cells Alters DNA Double Strand Break Repair of Etoposide Induced DNA Damage |
Q92377245 | Molecular Mechanism of Runx2-Dependent Bone Development |
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Q92291499 | Osteoporosis genome-wide association study variant c.3781 C>A is regulated by a novel anti-osteogenic factor miR-345-5p |
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Q64902344 | RUNX family: Oncogenes or tumor suppressors (Review). |
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Q36309953 | The RUNX Genes as Conditional Oncogenes: Insights from Retroviral Targeting and Mouse Models |
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