Cd248 Structure

CD248 CD248 molecule endosialin

CD248 enhances tissue factor procoagulant function promoting arterial

CD248 enhanced the interaction between ITGB1 and ECM proteins A

CD248 is a membranefacilitated binding partner for the orphan protein

CD248 Cleaved Form in Human Colorectal Cancer Stroma Implications for

Frontiers CD248 induces PDL1 expression on cancerassociated

Blocking CD248 molecules in perivascular stromal cells of patients with

Frontiers CD248 induces PDL1 expression on cancerassociated

Interference in melanoma CD248 function reduces vascular mimicry and

CD248 Wikipedia

Frontiers Pancancer analysis identified CD248 as a potential target

TGFinduced suppression of CD248 is mediated via canonical signaling

CD248 is a membranefacilitated binding partner for the orphan protein

Frontiers CD248 induces PDL1 expression on cancerassociated

The pericyte and stromal cell marker CD248 endosialin is required for

It takes two to tango Tissue factor and CD248

CD248 induces a maladaptive unfolded protein response in diabetic

Panel a Typical CD248 staining patterns in the fibrotic lung in a

CD248 is upregulated in MCTinduced primary pulmonary arterial smooth

CD248 Polyclonal Antibody Invitrogen PA584090

The WGCNA and enrichment analysis of CD248 coexpressed genes A The

Regulation of CD248 in cancer cells A B Wehi231 A and A20 B

Cd248 disruption reduced infiltration and profibrotic phenotype

Cell surface and intracellular distribution of CD248 in tumor cells and

The Diagnostic and Immunotherapeutic Value of CD248 in Renal Cell

Knockdown of CD248 inhibited migration and invasion of OS cells in

Phenotype of pericytes in wildtype and CD248 knockout skeletal muscle

Targeting fibroblast CD248 attenuates CCL17expressing macrophages and

CD248 induces a maladaptive unfolded protein response in diabetic

CD248 promotes NOX4 expression through NF‐κB activation. A and B, (A ...

CD248 promotes NOX4 expression through NFB activation A and B A

Knockdown of CD248 inhibited the metastasis of OS cells in vivo A

CD248 expression in skin of patients with systemic sclerosis SSc a

Targeting fibroblast CD248 attenuates CCL17expressing macrophages and

Frontiers Pancancer analysis identified CD248 as a potential target

Cell surface and intracellular distribution of CD248 in tumor cells and

Loss of Cd248 changed blood vessel functions in LLCderived tumors A

CD248 is expressed in human and mouse osteoblasts but not osteoclasts

Frontiers Pancancer analysis identified CD248 as a potential target

Frontiers CD248 induces PDL1 expression on cancerassociated

CD248 was involved in multiple cell adhesion and migration pathways

CD248 regulates PDGFBBinduced signal pathways and promotes a PDGF

CD248 Cleaved Form in Human Colorectal Cancer Stroma Implications for

CD248 enhanced the interaction between ITGB1 and ECM proteins A

CD248 expression in stromal cells in vitro from human and mouse liver

CD248 was highly expressed in OS tissues and was correlated with

CD248 expression in stromal cells in vitro from human and mouse liver

Interference in melanoma CD248 function reduces vascular mimicry and

Immunofluorescent staining and digital analysis of CD248 expression

Expression of CD248 by mesenchymal cells in response to cytokines and

Antibodydrug conjugates targeting CD248 inhibits liver fibrosis

Frontiers Pancancer analysis identified CD248 as a potential target

CD248 Wikipedia

Subcellular CD248 The Human Protein Atlas

CD248 promotes insulin resistance by binding to the insulin receptor

Frontiers Pancancer analysis identified CD248 as a potential target

Specific loss of adipocyte CD248 improves metabolic health via reduced

CD248 enhances tissue factor procoagulant function promoting arterial

CD248 was involved in multiple cell adhesion and migration pathways

The role of CD248 in RCC progression A B CD248 overexpression in

CD248 is a specific biomarker for CAFs A Correlation analysis

TGFmediated suppression of CD248 via ALK5 is specific A B MEF

Frontiers CD248 induces PDL1 expression on cancerassociated

CD248 A therapeutic target in cancer and fibrotic diseases Oncotarget

Ctype lectin domain group 14 proteins in vascular biology cancer and

Frontiers Cd248a and Cd248b in zebrafish participate in innate immune

Linking myofibroblast generation and microvascular alteration The role

Projects HPH Lab

PDF CD248 Reviewing its Role in Health and Disease

CD248

Inflammatory Mesenchymal Stem Cells Express Abundant MembraneBound and

Role of tumor endothelial marker 1 EndosialinCD248 lectinlike

CD248

Nat Cardiovasc ResCD248

Frontiers CD248 CancerAssociated Fibroblasts A Novel Prognostic

Subcellular localization of Cd248a Cd248b and truncated Cd248b in

基于生物活性 siRNA 的脂质体通过恢复 CD248+ TSPCs 的干性促进骨质疏松小鼠的肌腱骨愈合,Advanced Science ...

siRNA CD248 TSPCs Advanced Science

Inflammatory CD248 activated fibroblasts are a potential therapeutic

Inflammatory Mesenchymal Stem Cells Express Abundant MembraneBound and

Targeting the activated microenvironment with endosialin CD248

CD248CD8 T lymphocytes suppress pathological vascular remodeling in

Frontiers Cd248a and Cd248b in zebrafish participate in innate immune

Coexpression of CD248 OPN and SERPINE1 in human lung cancerassociated

Figure 510 from Exploring the role of CD248endosialinTEM1 on

CD248expressing cancerassociated fibroblasts induce nonsmall cell

Frontiers CD248 CancerAssociated Fibroblasts A Novel Prognostic

文献分享---单细胞分辨率下心脏纤维化的动态分子图谱显示心脏成纤维细胞中的CD248与免疫细胞相互作用（Stereo-seq）-腾讯云开发者 ...

CD248Stereoseq

Induction of SMA in human pericytes and suppression effects of

CD248 A therapeutic target in cancer and fibrotic diseases Oncotarget

Targeting the activated microenvironment with endosialin CD248

Deciphering the Dysregulating IGF1SP1CD248 Pathway in Fibroblast

CD248expressing cancerassociated fibroblasts induce epithelial

Nat Cardiovasc Res｜揭示CD248+成纤维细胞介导的成纤维-免疫交互在心脏纤维化中的重要作用 - 企业动态 - 丁香通

Nat Cardiovasc ResCD248

CD248targeted BBIRT cell therapy against lateactivated fibroblasts

CD248CD8 T lymphocytes suppress pathological vascular remodeling in

IL8 from CD248expressing cancerassociated fibroblasts generates

Frontiers CD248 CancerAssociated Fibroblasts A Novel Prognostic

谢峻/徐清波教授团队《自然·通讯》：开发靶向CD248的BBIR-T细胞免疫疗法精准清除心肌梗死后延迟活化的成纤维细胞亚群-MedSci.cn

CD248BBIRTMedScicn

CD248

Targeting the activated microenvironment with endosialin CD248

Frontiers Stromal cells support the survival of human primary chronic

Nat Cardiovasc Res 浙江大学胡新央团队揭示CD248+成纤维细胞介导的成纤维-免疫交互在心脏纤维化中的重要作用-MedSci.cn

Nat Cardiovasc Res CD248MedScicn

CD248Stereoseq

CD248CD8 T lymphocytes suppress pathological vascular remodeling in

Targeting the activated microenvironment with endosialin CD248

Targeting endosialinCD248 through antibodymediated internalization

Targeting the activated microenvironment with endosialin CD248

Figure 1 from EndosialinCD248 may be a potential therapeutic target to

Frontiers CD248 CancerAssociated Fibroblasts A Novel Prognostic

Figure 1 from CD248 A therapeutic target in cancer and fibrotic

Corrigendum to CD248 induces a maladaptive unfolded protein response

CD248 A therapeutic target in cancer and fibrotic diseases Oncotarget

Nat Cardiovasc ResCD248

IL8 from CD248expressing cancerassociated fibroblasts generates

Nat Cardiovasc ResCD248

Corrigendum to CD248 induces a maladaptive unfolded protein response

Antibodydrug conjugates targeting CD248 myofibroblasts effectively

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