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yoda1 shed spheroids  (MedChemExpress)


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    Structured Review

    MedChemExpress yoda1 shed spheroids
    Schematic illustration showing the generation, mechanism, and application of self-mineralized <t>Yoda1+</t> BOs from Piezo1-activated SHED spheroids .
    Yoda1 Shed Spheroids, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 96/100, based on 134 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/yoda1 shed spheroids/product/MedChemExpress
    Average 96 stars, based on 134 article reviews
    yoda1 shed spheroids - by Bioz Stars, 2026-02
    96/100 stars

    Images

    1) Product Images from "Piezo1 mediated scaffold-free rapid generation of self-mineralized bone organoids via activating Wnt signaling"

    Article Title: Piezo1 mediated scaffold-free rapid generation of self-mineralized bone organoids via activating Wnt signaling

    Journal: Materials Today Bio

    doi: 10.1016/j.mtbio.2025.102620

    Schematic illustration showing the generation, mechanism, and application of self-mineralized Yoda1+ BOs from Piezo1-activated SHED spheroids .
    Figure Legend Snippet: Schematic illustration showing the generation, mechanism, and application of self-mineralized Yoda1+ BOs from Piezo1-activated SHED spheroids .

    Techniques Used:

    Piezo1 activation promotes SHED spheroids assembly through up-regulating adhesion molecules. (A) Illustration of the preparation process of Yoda1+ SEHDs spheroids. (B) Optical microscopy images showing the formation of SHED spheroids within 48 h. (C) The cell viability and morphology of cell spheroids observed by HE staining and live/dead staining. (D) & (E) Immunofluorescence staining to visualize the expression of Piezo1 and the morphology of F-actin cytoskeleton in SHED spheroids. (F) & (G) IHC staining and quantitative analysis to visualize the expression of E-cadherin and N-cadherin. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.
    Figure Legend Snippet: Piezo1 activation promotes SHED spheroids assembly through up-regulating adhesion molecules. (A) Illustration of the preparation process of Yoda1+ SEHDs spheroids. (B) Optical microscopy images showing the formation of SHED spheroids within 48 h. (C) The cell viability and morphology of cell spheroids observed by HE staining and live/dead staining. (D) & (E) Immunofluorescence staining to visualize the expression of Piezo1 and the morphology of F-actin cytoskeleton in SHED spheroids. (F) & (G) IHC staining and quantitative analysis to visualize the expression of E-cadherin and N-cadherin. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Techniques Used: Activation Assay, Microscopy, Staining, Immunofluorescence, Expressing, Immunohistochemistry

    Piezo1 activation enhances the osteogenic potential of SHED spheroids . (A) hBMSCs were cultured with conditioned media of Yoda1+ SHED spheroids. (B) The expressions of RUNX2 and BMP2 genes related to osteogenic differentiation. (C) & (D) IF staining and quantitative analysis to visualize the expression of RUNX2 and BMP2. (E) Wound healing assay and corresponding quantitative analysis on cell migration of hBMSCs. (F) ALP staining and Alizarin red staining. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.
    Figure Legend Snippet: Piezo1 activation enhances the osteogenic potential of SHED spheroids . (A) hBMSCs were cultured with conditioned media of Yoda1+ SHED spheroids. (B) The expressions of RUNX2 and BMP2 genes related to osteogenic differentiation. (C) & (D) IF staining and quantitative analysis to visualize the expression of RUNX2 and BMP2. (E) Wound healing assay and corresponding quantitative analysis on cell migration of hBMSCs. (F) ALP staining and Alizarin red staining. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Techniques Used: Activation Assay, Cell Culture, Staining, Expressing, Wound Healing Assay, Migration

    Piezo1 activation enhances the angiogenic potential of SHED spheroids . HUVECs were cultured with conditioned media of Yoda1+ SHED spheroids. (A) IHC staining and quantitative analysis to visualize the expression of CD31. (B) The expressions of ANG1 and CD31 genes related to osteogenic differentiation. (C) Wound healing assay and corresponding quantitative analysis on cell migration of HUVECs. (D) In vitro tube formation of HUVECs for neovascularization with corresponding quantitative analysis. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.
    Figure Legend Snippet: Piezo1 activation enhances the angiogenic potential of SHED spheroids . HUVECs were cultured with conditioned media of Yoda1+ SHED spheroids. (A) IHC staining and quantitative analysis to visualize the expression of CD31. (B) The expressions of ANG1 and CD31 genes related to osteogenic differentiation. (C) Wound healing assay and corresponding quantitative analysis on cell migration of HUVECs. (D) In vitro tube formation of HUVECs for neovascularization with corresponding quantitative analysis. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Techniques Used: Activation Assay, Cell Culture, Immunohistochemistry, Expressing, Wound Healing Assay, Migration, In Vitro

    RNA sequencing of Yoda1+ SHED spheroids. (A) Volcano plot of significantly upregulated and downregulated genes (Yoda1+ vs. Yoda1-). (B) The clustered heatmap of differentially expressed genes in Yoda1+ SHED spheroids compared with Yoda1- SHED spheroids related to mechanical stimulus. (C) KEGG enrichment analysis. (D) The clustered heatmap of differentially expressed genes in Yoda1+ SHED spheroids compared with Yoda1- SHED spheroids related to Wnt signaling pathway. (E) Western blot and quantitative analysis of the expression of markers including Piezo1, WNT7B and RUNX2. (F) The schematic illustration that under Yoda1 stimulation, the Piezo1 channel is activated, triggering the activation Wnt signaling pathway and increased expression of RUNX2. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.
    Figure Legend Snippet: RNA sequencing of Yoda1+ SHED spheroids. (A) Volcano plot of significantly upregulated and downregulated genes (Yoda1+ vs. Yoda1-). (B) The clustered heatmap of differentially expressed genes in Yoda1+ SHED spheroids compared with Yoda1- SHED spheroids related to mechanical stimulus. (C) KEGG enrichment analysis. (D) The clustered heatmap of differentially expressed genes in Yoda1+ SHED spheroids compared with Yoda1- SHED spheroids related to Wnt signaling pathway. (E) Western blot and quantitative analysis of the expression of markers including Piezo1, WNT7B and RUNX2. (F) The schematic illustration that under Yoda1 stimulation, the Piezo1 channel is activated, triggering the activation Wnt signaling pathway and increased expression of RUNX2. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Techniques Used: RNA Sequencing, Western Blot, Expressing, Activation Assay

    The formation and characterizations of Yoda1+ BOs. (A) Illustration of the formation process of bone organoids. The BOs were fixed, dehydrated and stained or lysed to extract mRNA for further qPCR assays. (B) IHC staining and quantitative analysis to visualize the expression of RUNX2 and OCN in BOs after osteogenic induction. (C) The expressions of four genes related to osteogenic differentiation of BOs. (D) Scanning electron microscopy (SEM) to observe the surface morphology and elemental distribution of BOs after 14-day osteogenic induction. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.
    Figure Legend Snippet: The formation and characterizations of Yoda1+ BOs. (A) Illustration of the formation process of bone organoids. The BOs were fixed, dehydrated and stained or lysed to extract mRNA for further qPCR assays. (B) IHC staining and quantitative analysis to visualize the expression of RUNX2 and OCN in BOs after osteogenic induction. (C) The expressions of four genes related to osteogenic differentiation of BOs. (D) Scanning electron microscopy (SEM) to observe the surface morphology and elemental distribution of BOs after 14-day osteogenic induction. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Techniques Used: Staining, Immunohistochemistry, Expressing, Electron Microscopy

    Yoda1+ BOs promotes calvarial bone regeneration. (A) A schematic illustration showing the design of the in vivo study. (B) Micro-CT images, (C) BV/TV values, and BMD values of various groups. The diameter of red circles = 3 mm. (D) Histological analysis by H&E, Masson's trichrome staining and IHC staining of OPN and OCN of calvarial bone sections. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.
    Figure Legend Snippet: Yoda1+ BOs promotes calvarial bone regeneration. (A) A schematic illustration showing the design of the in vivo study. (B) Micro-CT images, (C) BV/TV values, and BMD values of various groups. The diameter of red circles = 3 mm. (D) Histological analysis by H&E, Masson's trichrome staining and IHC staining of OPN and OCN of calvarial bone sections. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Techniques Used: In Vivo, Micro-CT, Staining, Immunohistochemistry



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    Image Search Results


    GI 50 determination of active drugs from 2-D screen against a panel of three TNBC cell lines. Relative cell proliferation (as a percentage of controls) and cytotoxicity was determined in response to the indicated concentrations of drugs tested against SUM-159, HCC1806 and MDA-MB-231, as indicated. All cell lines were grown in 2-D. Immediately after drug treatment, confluency and CellTox Green dye fluorescence (cytotoxicity) was monitored for 72 h with the Incucyte. Relative cell proliferation was calculated by subtracting the initial confluency (based the first read) from the final confluency measurement for each well and normalized to controls. Therefore, a 0% value indicates no change in confluency compared to the start of the assay. Relative cell death after 72 h was calculated by dividing the area of green dye fluorescence by the total confluency area (based on brightfield imaging) and multiplying by 100. Separate plots are provided for cell proliferation and cytotoxicity for (A and B, respectively) adefovir, (C and D, respectively) eltrombopag, (E and F, respectively) mozavaptan, (G and H, respectively) mycophenolic acid, (I and J, respectively) pentamidine and (K and L, respectively) halofantrine. Data shown are representative of n≥3 independent experiments and the data points and error bars represent the mean ± standard deviation of triplicate technical replicates. GI, growth inhibition; TNBC, triple-negative breast cancer; 2-D, two-dimension.

    Journal: Oncology Letters

    Article Title: Identification of non-oncology drugs with activity against inflammatory and triple-negative breast cancer cell lines

    doi: 10.3892/ol.2025.15428

    Figure Lengend Snippet: GI 50 determination of active drugs from 2-D screen against a panel of three TNBC cell lines. Relative cell proliferation (as a percentage of controls) and cytotoxicity was determined in response to the indicated concentrations of drugs tested against SUM-159, HCC1806 and MDA-MB-231, as indicated. All cell lines were grown in 2-D. Immediately after drug treatment, confluency and CellTox Green dye fluorescence (cytotoxicity) was monitored for 72 h with the Incucyte. Relative cell proliferation was calculated by subtracting the initial confluency (based the first read) from the final confluency measurement for each well and normalized to controls. Therefore, a 0% value indicates no change in confluency compared to the start of the assay. Relative cell death after 72 h was calculated by dividing the area of green dye fluorescence by the total confluency area (based on brightfield imaging) and multiplying by 100. Separate plots are provided for cell proliferation and cytotoxicity for (A and B, respectively) adefovir, (C and D, respectively) eltrombopag, (E and F, respectively) mozavaptan, (G and H, respectively) mycophenolic acid, (I and J, respectively) pentamidine and (K and L, respectively) halofantrine. Data shown are representative of n≥3 independent experiments and the data points and error bars represent the mean ± standard deviation of triplicate technical replicates. GI, growth inhibition; TNBC, triple-negative breast cancer; 2-D, two-dimension.

    Article Snippet: The Incucyte Spheroid (Sartorius) software module was used to determine spheroid area by phase contrast and total green fluorescence of the well.

    Techniques: CellTox Assay, Fluorescence, Imaging, Standard Deviation, Inhibition

    Schematic illustration showing the generation, mechanism, and application of self-mineralized Yoda1+ BOs from Piezo1-activated SHED spheroids .

    Journal: Materials Today Bio

    Article Title: Piezo1 mediated scaffold-free rapid generation of self-mineralized bone organoids via activating Wnt signaling

    doi: 10.1016/j.mtbio.2025.102620

    Figure Lengend Snippet: Schematic illustration showing the generation, mechanism, and application of self-mineralized Yoda1+ BOs from Piezo1-activated SHED spheroids .

    Article Snippet: Yoda1-and Yoda1+ SHED spheroids were treated with Teplinovivint (MedChemExpress, USA), inhibitor of the Wnt/β-catenin pathway.

    Techniques:

    Piezo1 activation promotes SHED spheroids assembly through up-regulating adhesion molecules. (A) Illustration of the preparation process of Yoda1+ SEHDs spheroids. (B) Optical microscopy images showing the formation of SHED spheroids within 48 h. (C) The cell viability and morphology of cell spheroids observed by HE staining and live/dead staining. (D) & (E) Immunofluorescence staining to visualize the expression of Piezo1 and the morphology of F-actin cytoskeleton in SHED spheroids. (F) & (G) IHC staining and quantitative analysis to visualize the expression of E-cadherin and N-cadherin. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Piezo1 mediated scaffold-free rapid generation of self-mineralized bone organoids via activating Wnt signaling

    doi: 10.1016/j.mtbio.2025.102620

    Figure Lengend Snippet: Piezo1 activation promotes SHED spheroids assembly through up-regulating adhesion molecules. (A) Illustration of the preparation process of Yoda1+ SEHDs spheroids. (B) Optical microscopy images showing the formation of SHED spheroids within 48 h. (C) The cell viability and morphology of cell spheroids observed by HE staining and live/dead staining. (D) & (E) Immunofluorescence staining to visualize the expression of Piezo1 and the morphology of F-actin cytoskeleton in SHED spheroids. (F) & (G) IHC staining and quantitative analysis to visualize the expression of E-cadherin and N-cadherin. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Article Snippet: Yoda1-and Yoda1+ SHED spheroids were treated with Teplinovivint (MedChemExpress, USA), inhibitor of the Wnt/β-catenin pathway.

    Techniques: Activation Assay, Microscopy, Staining, Immunofluorescence, Expressing, Immunohistochemistry

    Piezo1 activation enhances the osteogenic potential of SHED spheroids . (A) hBMSCs were cultured with conditioned media of Yoda1+ SHED spheroids. (B) The expressions of RUNX2 and BMP2 genes related to osteogenic differentiation. (C) & (D) IF staining and quantitative analysis to visualize the expression of RUNX2 and BMP2. (E) Wound healing assay and corresponding quantitative analysis on cell migration of hBMSCs. (F) ALP staining and Alizarin red staining. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Piezo1 mediated scaffold-free rapid generation of self-mineralized bone organoids via activating Wnt signaling

    doi: 10.1016/j.mtbio.2025.102620

    Figure Lengend Snippet: Piezo1 activation enhances the osteogenic potential of SHED spheroids . (A) hBMSCs were cultured with conditioned media of Yoda1+ SHED spheroids. (B) The expressions of RUNX2 and BMP2 genes related to osteogenic differentiation. (C) & (D) IF staining and quantitative analysis to visualize the expression of RUNX2 and BMP2. (E) Wound healing assay and corresponding quantitative analysis on cell migration of hBMSCs. (F) ALP staining and Alizarin red staining. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Article Snippet: Yoda1-and Yoda1+ SHED spheroids were treated with Teplinovivint (MedChemExpress, USA), inhibitor of the Wnt/β-catenin pathway.

    Techniques: Activation Assay, Cell Culture, Staining, Expressing, Wound Healing Assay, Migration

    Piezo1 activation enhances the angiogenic potential of SHED spheroids . HUVECs were cultured with conditioned media of Yoda1+ SHED spheroids. (A) IHC staining and quantitative analysis to visualize the expression of CD31. (B) The expressions of ANG1 and CD31 genes related to osteogenic differentiation. (C) Wound healing assay and corresponding quantitative analysis on cell migration of HUVECs. (D) In vitro tube formation of HUVECs for neovascularization with corresponding quantitative analysis. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Piezo1 mediated scaffold-free rapid generation of self-mineralized bone organoids via activating Wnt signaling

    doi: 10.1016/j.mtbio.2025.102620

    Figure Lengend Snippet: Piezo1 activation enhances the angiogenic potential of SHED spheroids . HUVECs were cultured with conditioned media of Yoda1+ SHED spheroids. (A) IHC staining and quantitative analysis to visualize the expression of CD31. (B) The expressions of ANG1 and CD31 genes related to osteogenic differentiation. (C) Wound healing assay and corresponding quantitative analysis on cell migration of HUVECs. (D) In vitro tube formation of HUVECs for neovascularization with corresponding quantitative analysis. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Article Snippet: Yoda1-and Yoda1+ SHED spheroids were treated with Teplinovivint (MedChemExpress, USA), inhibitor of the Wnt/β-catenin pathway.

    Techniques: Activation Assay, Cell Culture, Immunohistochemistry, Expressing, Wound Healing Assay, Migration, In Vitro

    RNA sequencing of Yoda1+ SHED spheroids. (A) Volcano plot of significantly upregulated and downregulated genes (Yoda1+ vs. Yoda1-). (B) The clustered heatmap of differentially expressed genes in Yoda1+ SHED spheroids compared with Yoda1- SHED spheroids related to mechanical stimulus. (C) KEGG enrichment analysis. (D) The clustered heatmap of differentially expressed genes in Yoda1+ SHED spheroids compared with Yoda1- SHED spheroids related to Wnt signaling pathway. (E) Western blot and quantitative analysis of the expression of markers including Piezo1, WNT7B and RUNX2. (F) The schematic illustration that under Yoda1 stimulation, the Piezo1 channel is activated, triggering the activation Wnt signaling pathway and increased expression of RUNX2. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Piezo1 mediated scaffold-free rapid generation of self-mineralized bone organoids via activating Wnt signaling

    doi: 10.1016/j.mtbio.2025.102620

    Figure Lengend Snippet: RNA sequencing of Yoda1+ SHED spheroids. (A) Volcano plot of significantly upregulated and downregulated genes (Yoda1+ vs. Yoda1-). (B) The clustered heatmap of differentially expressed genes in Yoda1+ SHED spheroids compared with Yoda1- SHED spheroids related to mechanical stimulus. (C) KEGG enrichment analysis. (D) The clustered heatmap of differentially expressed genes in Yoda1+ SHED spheroids compared with Yoda1- SHED spheroids related to Wnt signaling pathway. (E) Western blot and quantitative analysis of the expression of markers including Piezo1, WNT7B and RUNX2. (F) The schematic illustration that under Yoda1 stimulation, the Piezo1 channel is activated, triggering the activation Wnt signaling pathway and increased expression of RUNX2. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Article Snippet: Yoda1-and Yoda1+ SHED spheroids were treated with Teplinovivint (MedChemExpress, USA), inhibitor of the Wnt/β-catenin pathway.

    Techniques: RNA Sequencing, Western Blot, Expressing, Activation Assay

    The formation and characterizations of Yoda1+ BOs. (A) Illustration of the formation process of bone organoids. The BOs were fixed, dehydrated and stained or lysed to extract mRNA for further qPCR assays. (B) IHC staining and quantitative analysis to visualize the expression of RUNX2 and OCN in BOs after osteogenic induction. (C) The expressions of four genes related to osteogenic differentiation of BOs. (D) Scanning electron microscopy (SEM) to observe the surface morphology and elemental distribution of BOs after 14-day osteogenic induction. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Piezo1 mediated scaffold-free rapid generation of self-mineralized bone organoids via activating Wnt signaling

    doi: 10.1016/j.mtbio.2025.102620

    Figure Lengend Snippet: The formation and characterizations of Yoda1+ BOs. (A) Illustration of the formation process of bone organoids. The BOs were fixed, dehydrated and stained or lysed to extract mRNA for further qPCR assays. (B) IHC staining and quantitative analysis to visualize the expression of RUNX2 and OCN in BOs after osteogenic induction. (C) The expressions of four genes related to osteogenic differentiation of BOs. (D) Scanning electron microscopy (SEM) to observe the surface morphology and elemental distribution of BOs after 14-day osteogenic induction. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Article Snippet: Yoda1-and Yoda1+ SHED spheroids were treated with Teplinovivint (MedChemExpress, USA), inhibitor of the Wnt/β-catenin pathway.

    Techniques: Staining, Immunohistochemistry, Expressing, Electron Microscopy

    Yoda1+ BOs promotes calvarial bone regeneration. (A) A schematic illustration showing the design of the in vivo study. (B) Micro-CT images, (C) BV/TV values, and BMD values of various groups. The diameter of red circles = 3 mm. (D) Histological analysis by H&E, Masson's trichrome staining and IHC staining of OPN and OCN of calvarial bone sections. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Piezo1 mediated scaffold-free rapid generation of self-mineralized bone organoids via activating Wnt signaling

    doi: 10.1016/j.mtbio.2025.102620

    Figure Lengend Snippet: Yoda1+ BOs promotes calvarial bone regeneration. (A) A schematic illustration showing the design of the in vivo study. (B) Micro-CT images, (C) BV/TV values, and BMD values of various groups. The diameter of red circles = 3 mm. (D) Histological analysis by H&E, Masson's trichrome staining and IHC staining of OPN and OCN of calvarial bone sections. (n ≥ 3) ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

    Article Snippet: Yoda1-and Yoda1+ SHED spheroids were treated with Teplinovivint (MedChemExpress, USA), inhibitor of the Wnt/β-catenin pathway.

    Techniques: In Vivo, Micro-CT, Staining, Immunohistochemistry