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Unraveling the Mechano-Molecular Mechanisms of TRAP Activity Using CRISPR/Cas9 Mediated Fluorescent Reporter Mice

https://doi.org/10.2139/ssrn.4668846
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/hon.2900010404openalex-extracted
Tartrate‐resistant acid phosphatase as a differentiation marker for the human mononuclear phagocyte system
inferredcites →https://doi.org/10.1002/jbmr.1989openalex-extracted
Siglec-15 Regulates Osteoclast Differentiation by Modulating RANKL-Induced Phosphatidylinositol 3-Kinase/Akt and Erk Pathways in Association With Signaling Adaptor DAP12
inferredcites →https://doi.org/10.1002/jbmr.2528openalex-extracted
Aging Leads to a Dysregulation in Mechanically Driven Bone Formation and Resorption
inferredcites →https://doi.org/10.1002/jcp.30312openalex-extracted
Mechanical stretch induces osteogenesis through the alternative activation of macrophages
inferredcites →https://doi.org/10.1006/excr.2002.5612openalex-extracted
Osteoclasts from Mice Deficient in Tartrate-Resistant Acid Phosphatase Have Altered Ruffled Borders and Disturbed Intracellular Vesicular Transport
inferredcites →https://doi.org/10.1007/s00223-007-9032-2openalex-extracted
Altered Collagen in Tartrate-Resistant Acid Phosphatase (TRAP)-Deficient Mice: A Role for TRAP in Bone Collagen Metabolism
inferredcites →https://doi.org/10.1007/s10237-011-0327-xopenalex-extracted
Bone morphology allows estimation of loading history in a murine model of bone adaptation
inferredcites →https://doi.org/10.1007/s10237-019-01266-7openalex-extracted
A novel algorithm to predict bone changes in the mouse tibia properties under physiological conditions
inferredcites →https://doi.org/10.1007/s10875-016-0252-yopenalex-extracted
Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey
inferredcites →https://doi.org/10.1016/0092-8674(93)90429-topenalex-extracted
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
inferredcites →https://doi.org/10.1016/j.bone.2011.08.035openalex-extracted
Mouse tail vertebrae adapt to cyclic mechanical loading by increasing bone formation rate and decreasing bone resorption rate as shown by time-lapsed in vivo imaging of dynamic bone morphometry
inferredcites →https://doi.org/10.1016/j.bone.2013.09.024openalex-extracted
FGF2 stimulates osteogenic differentiation through ERK induced TAZ expression
inferredcites →https://doi.org/10.1016/j.bone.2013.10.019openalex-extracted
Effects of age on bone mRNA levels of sclerostin and other genes relevant to bone metabolism in humans
inferredcites →https://doi.org/10.1016/j.bone.2015.02.027openalex-extracted
Monitoring in vivo (re)modeling: A computational approach using 4D microCT data to quantify bone surface movements
inferredcites →https://doi.org/10.1016/j.jbiomech.2014.11.020openalex-extracted
Bone adaptation to cyclic loading in murine caudal vertebrae is maintained with age and directly correlated to the local micromechanical environment
inferredcites →https://doi.org/10.1016/j.mod.2012.04.003openalex-extracted
Role of tartrate-resistant acid phosphatase (TRAP) in long bone development
inferredcites →https://doi.org/10.1016/j.parco.2011.08.001openalex-extracted
A scalable memory efficient multigrid solver for micro-finite element analyses based on CT images
inferredcites →https://doi.org/10.1016/s0021-9258(17)36541-9openalex-extracted
Dephosphorylation of osteopontin and bone sialoprotein by osteoclastic tartrate-resistant acid phosphatase. Modulation of osteoclast adhesion in vitro.
inferredcites →https://doi.org/10.1016/s0169-6009(08)80025-6openalex-extracted
Induction of bone formation in rat tail vertebrae by mechanical loading
inferredcites →https://doi.org/10.1016/s8756-3282(01)00488-4openalex-extracted
Modulation of appositional and longitudinal bone growth in the rat ulna by applied static and dynamic force
inferredcites →https://doi.org/10.1016/s8756-3282(01)00619-6openalex-extracted
Targeted and nontargeted remodeling
inferredcites →https://doi.org/10.1016/s8756-3282(01)00642-1openalex-extracted
Targeted and nontargeted bone remodeling: relationship to basic multicellular unit origination and progression
inferredcites →https://doi.org/10.1016/s8756-3282(02)00736-6openalex-extracted
Estimation of distal radius failure load with micro-finite element analysis models based on three-dimensional peripheral quantitative computed tomography images
inferredcites →https://doi.org/10.1017/cbo9780511802843openalex-extracted
Bootstrap Methods and their Application
inferredcites →https://doi.org/10.1038/nature01658openalex-extracted
Osteoclast differentiation and activation
inferredcites →https://doi.org/10.1038/nature10137openalex-extracted
Role of YAP/TAZ in mechanotransduction
inferredcites →https://doi.org/10.1038/s41598-020-57461-5openalex-extracted
The association between mineralised tissue formation and the mechanical local in vivo environment: Time-lapsed quantification of a mouse defect healing model
inferredcites →https://doi.org/10.1038/s41598-020-75835-7openalex-extracted
A versatile toolbox for semi-automatic cell-by-cell object-based colocalization analysis
inferredcites →https://doi.org/10.1038/s41598-021-02368-yopenalex-extracted
Individualized cyclic mechanical loading improves callus properties during the remodelling phase of fracture healing in mice as assessed from time-lapsed in vivo imaging
inferredcites →https://doi.org/10.1038/srep07595openalex-extracted
Comprehensive profiling analysis of actively resorbing osteoclasts identifies critical signaling pathways regulated by bone substrate
inferredcites →https://doi.org/10.1042/bj3430063openalex-extracted
Tartrate-resistant purple acid phosphatase is synthesized as a latent proenzyme and activated by cysteine proteinases
inferredcites →https://doi.org/10.1046/j.1365-2567.2001.01145.xopenalex-extracted
Mice lacking tartrate‐resistant acid phosphatase (Acp 5) have disordered macrophage inflammatory responses and reduced clearance of the pathogen, Staphylococcus aureus
inferredcites →https://doi.org/10.1073/pnas.87.12.4473openalex-extracted
Osteopontin--a possible anchor of osteoclasts to bone.
inferredcites →https://doi.org/10.1080/10255840802078014openalex-extracted
A novelin vivomouse model for mechanically stimulated bone adaptation – a combined experimental and computational validation study
inferredcites →https://doi.org/10.1093/bioinformatics/bts635openalex-extracted
STAR: ultrafast universal RNA-seq aligner
inferredcites →https://doi.org/10.1093/bioinformatics/btu638openalex-extracted
HTSeq—a Python framework to work with high-throughput sequencing data
inferredcites →https://doi.org/10.1093/nar/gkw398openalex-extracted
CHOPCHOP v2: a web tool for the next generation of CRISPR genome engineering
inferredcites →https://doi.org/10.1128/mcb.23.3.1004-1013.2003openalex-extracted
Transcriptional Coactivation of Bone-Specific Transcription Factor Cbfa1 by TAZ
inferredcites →https://doi.org/10.1172/jci8905openalex-extracted
Mice lacking β3 integrins are osteosclerotic because of dysfunctional osteoclasts
inferredcites →https://doi.org/10.1186/1471-2105-10-161openalex-extracted
GAGE: generally applicable gene set enrichment for pathway analysis
inferredcites →https://doi.org/10.1186/ar3379openalex-extracted
Negative regulation of osteoclastogenesis and bone resorption by cytokines and transcriptional repressors
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-extracted
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1242/dev.070987openalex-extracted
Hippo pathway regulation by cell morphology and stress fibers
inferredcites →https://doi.org/10.1242/dev.122.10.3151openalex-extracted
Mice lacking tartrate-resistant acid phosphatase (Acp 5) have disrupted endochondral ossification and mild osteopetrosis
inferredcites →https://doi.org/10.1242/dev.128.23.4899openalex-extracted
Overlapping functions of lysosomal acid phosphatase (LAP) and tartrate-resistant acid phosphatase (Acp5) revealed by doubly deficient mice
inferredcites →https://doi.org/10.1242/jcs.109.4.787openalex-extracted
Partial colocalization of glucocorticoid and mineralocorticoid receptors in discrete compartments in nuclei of rat hippocampus neurons
inferredcites →https://doi.org/10.1309/dgea9be2ve5vcfyhopenalex-extracted
Tartrate-Resistant Acid Phosphatase as an Immunohistochemical Marker for Inflammatory Macrophages
inferredcites →https://doi.org/10.1359/jbmr.040603openalex-extracted
Intracellular Machinery for Matrix Degradation in Bone-Resorbing Osteoclasts
inferredcites →https://doi.org/10.1359/jbmr.2000.15.1.103openalex-extracted
Transgenic Mice Overexpressing Tartrate-Resistant Acid Phosphatase Exhibit an Increased Rate of Bone Turnover
inferredcites →https://doi.org/10.1359/jbmr.2003.18.10.1905openalex-extracted
Tartrate-Resistant Acid Phosphatase Knockout Mice
inferredcites →https://doi.org/10.1371/journal.pone.0062172openalex-extracted
Local Mechanical Stimuli Regulate Bone Formation and Resorption in Mice at the Tissue Level
inferredcites →https://doi.org/10.1530/jme-15-0067openalex-extracted
Bone remodeling in the context of cellular and systemic regulation: the role of osteocytes and the nervous system
inferredcites →https://doi.org/10.3389/fbioe.2020.566346openalex-extracted
Mechano-Regulation of Trabecular Bone Adaptation Is Controlled by the Local in vivo Environment and Logarithmically Dependent on Loading Frequency
inferredcites →https://doi.org/10.3389/fbioe.2023.1140673openalex-extracted
Mechanostat parameters estimated from time-lapsed in vivo micro-computed tomography data of mechanically driven bone adaptation are logarithmically dependent on loading frequency
inferredcites →https://doi.org/10.3389/fcell.2022.856204openalex-extracted
Tissue-Level Regeneration and Remodeling Dynamics are Driven by Mechanical Stimuli in the Microenvironment in a Post-Bridging Loaded Femur Defect Healing Model in Mice
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