历年文献基因敲除小鼠_转基因小鼠定制

                            
                            Divergent Roles of C/EBPβ Isoforms LAP and LIP in Shaping T Cell Dysfunction and Tumor Progression in Triple-Negative Breast Cancer
                        

产品名称：C57BL/6

研究领域：肿瘤免疫

发表年份：2025 发表杂志：FASEB JOURNAL

                            
                            Preclinical evaluation of STSA-1002, a novel human and rhesus monkeys cross-reactive monoclonal antibody targeting C5a, in acute respiratory distress syndrome models
                        

产品名称：hC5

研究领域：补体靶向免疫

发表年份：2025 发表杂志：INTERNATIONAL IMMUNOPHARMACOLOGY

                            
                            Mitochondrial calcium uniporter promotes MSU crystal-induced inflammation through inducing mitochondrial Ca2+ overload and ubiquitination of SIRT5 protein
                        

产品名称：Mcu-KO

研究领域：风湿免疫

发表年份：2025 发表杂志：ARTHRITIS RESEARCH & THERAPY

                            
                            Deletion of SH2D5 alleviates epileptic seizures and NMDAR expression via autophagic degradation of STAT1
                        

产品名称：Sh2d5-Flox

研究领域：神经系统疾病

发表年份：2025 发表杂志：JCI Insight

                            
                            Bilirubin Degradation by Hypochlorous Acid: Identification of Products and Their Formation Ex Vivo and In Vivo
                        

产品名称：C57BL/6

研究领域：胆红素; 生物标志物

发表年份：2025 发表杂志：ChemistrySelect

                            
                            Shank3 oligomerization governs material properties of the postsynaptic density condensate and synaptic plasticity
                        

产品名称：Shank3-M1718E

研究领域：突触可塑性

发表年份：2025 发表杂志：CELL

                            
                            Biomimetic nanoimmunotherapy boosts spatiotemporal PANoptosis and reshapes desmoplastic tumor microenvironment
                        

产品名称：BALB/c, BALB/c-nu; C57BL/6

研究领域：肿瘤及肿瘤免疫

发表年份：2025 发表杂志：Cell Reports Medicine

                            
                            Deconjugating taurocholic acid with Bifidobacterium to mitigate obesity-driven cancer progression by restoring CD8+ T-cell infiltration
                        

产品名称：Hepa1-6-luc

研究领域：肿瘤及肿瘤免疫

发表年份：2025 发表杂志：npj Biofilms and Microbiomes

                            
                            Dual Keap1-Dependent Actions of Pubescenoside A Against Ulcerative Colitis: Promoting DDX5 Ubiquitination Degradation and Nrf2 Nuclear Translocation to Suppress Inflammation
                        

产品名称：Keap1-Flox

研究领域：炎症性肠病

发表年份：2025 发表杂志：FREE RADICAL BIOLOGY AND MEDICINE

                            
                            Myofibroblast-transformed MSCs promote osteoclastogenesis via mitochondrial transfer in ORNJ
                        

产品名称：R26-CAG-LSL-tdTomato

研究领域：罕见病

发表年份：2025 发表杂志：MATERIALS & DESIGN

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Divergent Roles of C/EBPβ Isoforms LAP and LIP in Shaping T Cell Dysfunction and Tumor Progression in Triple-Negative Breast Cancer

Preclinical evaluation of STSA-1002, a novel human and rhesus monkeys cross-reactive monoclonal antibody targeting C5a, in acute respiratory distress syndrome models

Mitochondrial calcium uniporter promotes MSU crystal-induced inflammation through inducing mitochondrial Ca2+ overload and ubiquitination of SIRT5 protein

Deletion of SH2D5 alleviates epileptic seizures and NMDAR expression via autophagic degradation of STAT1

Bilirubin Degradation by Hypochlorous Acid: Identification of Products and Their Formation Ex Vivo and In Vivo

Shank3 oligomerization governs material properties of the postsynaptic density condensate and synaptic plasticity

Biomimetic nanoimmunotherapy boosts spatiotemporal PANoptosis and reshapes desmoplastic tumor microenvironment

Deconjugating taurocholic acid with Bifidobacterium to mitigate obesity-driven cancer progression by restoring CD8+ T-cell infiltration

Dual Keap1-Dependent Actions of Pubescenoside A Against Ulcerative Colitis: Promoting DDX5 Ubiquitination Degradation and Nrf2 Nuclear Translocation to Suppress Inflammation

Myofibroblast-transformed MSCs promote osteoclastogenesis via mitochondrial transfer in ORNJ

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