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Image Search Results
Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
Article Title: A MicroRNA-124 Polymorphism is Associated with Fracture Healing via Modulating BMP6 Expression.
doi: 10.1159/000475570
Figure Lengend Snippet: Fig. 2. BMP6 as the candidate target gene ofmiR- 124-3p in cells with the ‘seed sequence’ in the 3’UTR.
Article Snippet: TBST containing 5% non-fat dry milk (Merck, Darmstadt, Germany) was used to block the membranes for 60 min.
Techniques: Sequencing
Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
Article Title: A MicroRNA-124 Polymorphism is Associated with Fracture Healing via Modulating BMP6 Expression.
doi: 10.1159/000475570
Figure Lengend Snippet: Fig. 4. The correlation between the expression level of miR-124-3p and BMP6 mRNA.
Article Snippet: TBST containing 5% non-fat dry milk (Merck, Darmstadt, Germany) was used to block the membranes for 60 min.
Techniques: Expressing
Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
Article Title: A MicroRNA-124 Polymorphism is Associated with Fracture Healing via Modulating BMP6 Expression.
doi: 10.1159/000475570
Figure Lengend Snippet: Fig. 5. The expression of BMP6 mRNA (Fig. 5A) and protein (Fig. 5B) decreased in GG group compared with GC and CC group (** P<0.01 compared with the control).
Article Snippet: TBST containing 5% non-fat dry milk (Merck, Darmstadt, Germany) was used to block the membranes for 60 min.
Techniques: Expressing, Control
Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
Article Title: A MicroRNA-124 Polymorphism is Associated with Fracture Healing via Modulating BMP6 Expression.
doi: 10.1159/000475570
Figure Lengend Snippet: Fig. 3. Luciferase activity reporter assay was conducted to verify BMP6 as the direct target gene of miR-124-3p (** P<0.01 compared with the control).
Article Snippet: TBST containing 5% non-fat dry milk (Merck, Darmstadt, Germany) was used to block the membranes for 60 min.
Techniques: Luciferase, Activity Assay, Reporter Assay, Control
Journal: Journal of Assisted Reproduction and Genetics
Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis
doi: 10.1007/s10815-024-03377-2
Figure Lengend Snippet: The combinations of transfected plasmids
Article Snippet:
Techniques: Transfection, Plasmid Preparation
Journal: Journal of Assisted Reproduction and Genetics
Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis
doi: 10.1007/s10815-024-03377-2
Figure Lengend Snippet: Primers used for quantitative real-time polymerase chain reaction
Article Snippet:
Techniques: Sequencing
Journal: Journal of Assisted Reproduction and Genetics
Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis
doi: 10.1007/s10815-024-03377-2
Figure Lengend Snippet: Antibody information
Article Snippet:
Techniques:
Journal: Journal of Assisted Reproduction and Genetics
Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis
doi: 10.1007/s10815-024-03377-2
Figure Lengend Snippet: Comparison of the expression levels of BMAL1 and BMP6 in human OGCs between PCOS and control groups. A, B BMAL1 and BMP6 mRNA levels between PCOS and control groups. C–E BMAL1 and BMP6 protein levels between PCOS and control groups. F Correlations between the mRNA expression levels of BMP6 and BMAL1 in OGCs. * P < 0.05, ** P < 0.01, and *** P < 0.001
Article Snippet:
Techniques: Comparison, Expressing, Control
Journal: Journal of Assisted Reproduction and Genetics
Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis
doi: 10.1007/s10815-024-03377-2
Figure Lengend Snippet: The mRNA levels of BMAL1 and BMP6 in OGCs are correlated with ART outcomes of patients. Spearman’s correlation analyses were used to investigate the correlation between the mRNA levels of BMAL1 and the number of retrieved oocytes ( A ), 2PN fertilized oocytes ( B ), available embryos ( C ), and high-quality embryos ( D ). Spearman’s correlation analyses were used to investigate the correlation between the mRNA levels of BMP6 and the number of retrieved oocytes ( E ), 2PN fertilized oocytes ( F ), available embryos ( G ), and high-quality embryos ( H )
Article Snippet:
Techniques:
Journal: Journal of Assisted Reproduction and Genetics
Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis
doi: 10.1007/s10815-024-03377-2
Figure Lengend Snippet: BMP6 is a downstream target of BMAL1. A Predicted binding site and mutated binding site of BMAL1 in the promoter of BMP6[created with figdraw.com]. B Direct interaction between BMAL1 and BMP6 detected by the dual-luciferase assay. * P < 0.05, ** P < 0.01, and *** P < 0.001
Article Snippet:
Techniques: Binding Assay, Luciferase
Journal: Journal of Assisted Reproduction and Genetics
Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis
doi: 10.1007/s10815-024-03377-2
Figure Lengend Snippet: The impact of BMAL1 on the expression of BMP6 in KGN cells. A, B Expression levels of BMAL1 and BMP6 mRNA in KGN cells after transfection. C, D Expression levels of BMP6 protein in KGN cells after transfection. OE, overexpression; NC, negative control. * P < 0.05, ** P < 0.01, and *** P < 0.001
Article Snippet:
Techniques: Expressing, Transfection, Over Expression, Negative Control
Journal: Biology of Reproduction
Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells
doi: 10.1093/biolre/ioz108
Figure Lengend Snippet: BMP6 upregulates the expression of CTGF in hGL cells. A and B, SVOG cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (A) or 6 h (B), and the mRNA (A) and protein (B) levels of CTGF were examined using RT-qPCR and western blotting, respectively. C and D, SVOG cells were treated with vehicle control or 30 ng/ml of BMP6 for 1, 3, 6, 12, or 24 h, and the mRNA (C) and protein (D) levels of CTGF were examined using RT-qPCR and western blotting, respectively. E and F, Primary hGL cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (E) or 6 h (F), and the mRNA (E) and protein (F) levels of CTGF were examined using RT-qPCR and Western blot, respectively. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05). B6, BMP6; Ctrl, control; hGL, primary human granulosa lutein.
Article Snippet: Antibodies and reagents
Techniques: Expressing, Quantitative RT-PCR, Western Blot
Journal: Biology of Reproduction
Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells
doi: 10.1093/biolre/ioz108
Figure Lengend Snippet: BMP6 does not affect the expression of CYR61 in hGL cells. (A and B) SVOG cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (A) or 6 h (B), and the mRNA (A) and protein (B) levels of CYR61 were examined using RT-qPCR and western blotting, respectively. (C and D) SVOG cells were treated with vehicle control or 30 ng/ml of BMP6 for 1, 3, 6, 12, or 24 h, and the mRNA (C) and protein (D) levels of CYR61 were examined using RT-qPCR and western blotting, respectively. (E and F) Primary hGL cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (E) or 6 h (F), and the mRNA (E) and protein (F) levels of CYR61 were examined using RT-qPCR and western blotting, respectively. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05).
Article Snippet: Antibodies and reagents
Techniques: Expressing, Quantitative RT-PCR, Western Blot
Journal: Biology of Reproduction
Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells
doi: 10.1093/biolre/ioz108
Figure Lengend Snippet: BMP6 induces the phosphorylation of SMAD1/5/8 in SVOG cells. (A) SVOG cells were treated with a vehicle control or 30 ng/ml of BMP6 for 20, 40, or 60 min, and the phosphorylated protein levels of SMAD1/5/8 were examined using western blotting. (B) SVOG cells were pretreated with a vehicle control (DMSO), 5 μM dorsomorphin, or 5 μM DMH-1 for 60 min, and then treated with 30 ng/ml BMP6 for an additional 40 min. The phosphorylated protein levels of SMAD1/5/8 were examined using western blotting. (C) SVOG cells were treated with a vehicle control or 30 ng/ml BMP6 for 40 min, fixed in 4% paraformaldehyde in PBS, and examined for phosphorylated SMAD1/5/8 (red) and nuclear (DAPI in blue) immunofluorescence. (D) SVOG cells were treated with a vehicle control, 30 ng/ml of BMP6 (for 20, 40, or 60 min) or 5 ng/ml of TGF-β1 (for 20 min as a positive control) and the phosphorylated protein levels of SMAD2 and SMAD3 were examined using western blotting. (E) SVOG cells were pretreated with a vehicle control (DMSO), 5 μM dorsomorphin, or 5 μM DMH-1 for 60 min, and then treated with 30 ng/ml BMP6 for an additional 40 min. The phosphorylated protein levels of SMAD2 and SMAD3 were examined using western blotting. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05).
Article Snippet: Antibodies and reagents
Techniques: Western Blot, Immunofluorescence, Positive Control
Journal: Biology of Reproduction
Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells
doi: 10.1093/biolre/ioz108
Figure Lengend Snippet: ALK2 or ALK3 is required for the BMP6-induced upregulation of CTGF expression in SVOG cells. (A and B) SVOG cells were pretreated with a vehicle control (DMSO), 5 μM dorsomorphin, or 5 μM DMH-1 for 60 min, and then treated with 30 ng/ml BMP6 for an additional 3 h (A) and 6 h (B), and the mRNA (A) and protein (B) levels of CTGF were examined using RT-qPCR and western blot, respectively. (C and D) SVOG cells were pretreated with a vehicle control (DMSO) or 5 μM SB431542 for 60 min, and then treated with 30 ng/ml BMP6 for an additional 3 h (C) and 6 h (D), and the mRNA (A) and protein (B) levels of CTGF were examined using RT-qPCR and western blot, respectively. (E and F) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl), 25 nM of ALK2 siRNA (siALK2), 25 nM of ALK3 siRNA (siALK3), or 25 nM of siALK2 combined with 25 nM of siALK3, followed by treatment with vehicle control or 30 ng/ml of BMP6 for 40 min (E) and 3 h (F). The phosphorylated protein levels of SMAD1/5/8 (E) and mRNA levels of CTGF were examined using western blotting and RT-qPCR, respectively. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05). ALK, activin receptor-like kinase.
Article Snippet: Antibodies and reagents
Techniques: Expressing, Quantitative RT-PCR, Western Blot, Transfection
Journal: Biology of Reproduction
Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells
doi: 10.1093/biolre/ioz108
Figure Lengend Snippet: SMAD-dependent signaling pathway is required for the BMP6-induced stimulation of CTGF in SVOG cells. (A) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of SMAD4 siRNA (siSMAD4), followed by treatment with vehicle control or 30 ng/ml of BMP6 for 3 h. The mRNA levels of SMAD4 and CTGF were examined using RT-qPCR. (B) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of SMAD4 siRNA (siSMAD4) followed by treatment with vehicle control or 30 ng/ml of BMP6 for 6 h. The protein levels of CTGF and SMAD4 were examined using western blotting. (C) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of SMAD4 siRNA (siSMAD4), followed by treatment with vehicle control or 30 ng/ml of BMP6 for 3 h. The mRNA levels of SMAD4 and CYR61 were examined using RT-qPCR. (D) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of SMAD4 siRNA (siSMAD4) followed by treatment with vehicle control or 30 ng/ml of BMP6 for 6 h. The protein levels of CYR61 and SMAD4 were examined using western blotting. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05).
Article Snippet: Antibodies and reagents
Techniques: Transfection, Quantitative RT-PCR, Western Blot
Journal: Biology of Reproduction
Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells
doi: 10.1093/biolre/ioz108
Figure Lengend Snippet: CTGF mediates the BMP6-induced up-regulation of LOX expression in SVOG cells. SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of CTGF siRNA (siCTGF), followed by treatment with vehicle control or 30 ng/ml of BMP6 for 3 h. The mRNA levels of CTGF and LOX were examined using RT-qPCR. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05). LOX, lysyl oxidase.
Article Snippet: Antibodies and reagents
Techniques: Expressing, Transfection, Quantitative RT-PCR
Journal: Biology of Reproduction
Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells
doi: 10.1093/biolre/ioz108
Figure Lengend Snippet: Proposed model for the effect of BMP6 on the expression levels CTGF and LOX in human granulosa-lutein cells. BMP6 binds to a complex containing type I (ALK2 and ALK3) and II receptors leading to the phosphorylation/activation of receptor-regulated SMAD (SMAD1/5/8), which binds to the common SMAD (SMAD4). This complex then translocates into the nucleus to promote the transcription of CTGF. The up-regulation of CTGF subsequently contributes to the increase in LOX expression in human granulosa-lutein cells.
Article Snippet: Antibodies and reagents
Techniques: Expressing, Activation Assay
Journal: The EMBO journal
Article Title: Self-organized developmental patterning and differentiation in cerebral organoids
doi: 10.15252/embj.201694700
Figure Lengend Snippet: Antibodies used in the study
Article Snippet:
Techniques: