SHIP2相关文献与解析，生知库 | 链接生命科学的每一步

Ramos, Ana Raquel; Bregni, Giacomo; Gillet, Nadia; Ando, Kunie; Bodart, Cyril; Vercauteren Drubbel, Alizée; Descampe, Louison; Moresi, Fabiana; Bisteau, Xavier; Verheye, Quentin; Pirard, Sheleya; Erneux, Christophe; Beck, Benjamin

肿瘤

PLK1

肿瘤免疫

NCAM1-SHIP2 axis upon recognizing microbes inhibits the expressions of inflammatory factors through P38-H3K4me and P38-NF-κB pathways in oyster

牡蛎中NCAM1-SHIP2轴在识别微生物后，通过P38-H3K4me和P38-NF-κB通路抑制炎症因子的表达。

期刊:Cell Communication and Signaling

影响因子:8.9

doi:10.1186/s12964-025-02087-1

Sun, Jiejie; Shi, Xiangqi; Wang, Mengjia; He, Muchun; Yang, Wenwen; Song, Linsheng

Differential activation of the inositol 5-phosphatase SHIP2 by EGF and insulin signaling pathways.

EGF 和胰岛素信号通路对肌醇 5-磷酸酶 SHIP2 的差异性激活。

期刊:Journal of Biological Chemistry

影响因子:3.9

doi:10.1016/j.jbc.2025.110275

TangNaikang Formula Alleviates Podocyte Injury in Diabetic Nephropathy by Modulating the SHIP2/PI3K/AKT Pathway.

唐乃康方通过调节SHIP2/PI3K/AKT通路减轻糖尿病肾病中的足细胞损伤。

期刊:Journal of Diabetes Research

影响因子:3.4

doi:10.1155/jdr/6568591

Yang Tao, Huang Yongxin, Li Wenjing, Qin Lingling, Wu You, Wu Lili, Liu Tonghua

Upregulation of SHIP2 Participates in the Development of Breast Cancer via Promoting Wnt/β-Catenin Signaling [Retraction]

SHIP2 上调通过促进 Wnt/β-catenin 信号通路参与乳腺癌的发生发展 [撤稿]

期刊:Oncotargets and Therapy

影响因子:2.8

doi:10.2147/OTT.S558484

The Functional Roles of the Src Homology 2 Domain-Containing Inositol 5-Phosphatases SHIP1 and SHIP2 in the Pathogenesis of Human Diseases

含有Src同源性2结构域的肌醇5-磷酸酶SHIP1和SHIP2在人类疾病发病机制中的功能作用

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms25105254

Müller, Spike Murphy; Jücker, Manfred

Discovery of aurones bearing two amine functionalities as SHIP2 inhibitors with insulin-sensitizing effect in rat myotubes

发现具有两个胺基官能团的橙酮作为 SHIP2 抑制剂，对大鼠肌管具有胰岛素增敏作用

期刊:RSC Medicinal Chemistry

影响因子:4.1

doi:10.1039/d3md00360d

Phei Ching Lim, Beow Keat Yap, Yi Juin Tay, Nur Aziah Hanapi, Siti Rafidah Yusof, Chong-Yew Lee

LINC01468 drives NAFLD-HCC progression through CUL4A-linked degradation of SHIP2

LINC01468 通过 CUL4A 介导的 SHIP2 降解促进 NAFLD-HCC 的进展

期刊:Cell Death Discovery

影响因子:7

doi:10.1038/s41420-022-01234-8

Wang, Hongquan; Wang, Yan; Lai, Shihui; Zhao, Liang; Liu, Wenhui; Liu, Shiqian; Chen, Haiqiang; Wang, Jinhua; Du, Guanhua; Tang, Bo

Structural Insights into the Binding Propensity of Human SHIP2 SH2 to Oncogenic CagA Isoforms from Helicobacter pylori

人类SHIP2 SH2与幽门螺杆菌致癌CagA亚型结合倾向的结构解析

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms231911299

Wang, Zi; Shan, Yubao; Wang, Ru; Zhou, Heng; Hu, Rui; Li, Ying; Zhu, Jiang; Yang, Yunhuang; Liu, Maili

Targeting SHIP1 and SHIP2 in Cancer

靶向SHIP1和SHIP2治疗癌症

期刊:Cancers

影响因子:4.4

doi:10.3390/cancers13040890

Pedicone, Chiara; Meyer, Shea T; Chisholm, John D; Kerr, William G

SHIP2-PLK1 crosstalk promotes sensitivity to dual inhibition in esophageal squamous cell carcinoma

SHIP2-PLK1 相互作用促进食管鳞状细胞癌对双重抑制的敏感性

NCAM1-SHIP2 axis upon recognizing microbes inhibits the expressions of inflammatory factors through P38-H3K4me and P38-NF-κB pathways in oyster

牡蛎中NCAM1-SHIP2轴在识别微生物后，通过P38-H3K4me和P38-NF-κB通路抑制炎症因子的表达。

Differential activation of the inositol 5-phosphatase SHIP2 by EGF and insulin signaling pathways.

EGF 和胰岛素信号通路对肌醇 5-磷酸酶 SHIP2 的差异性激活。

TangNaikang Formula Alleviates Podocyte Injury in Diabetic Nephropathy by Modulating the SHIP2/PI3K/AKT Pathway.

唐乃康方通过调节SHIP2/PI3K/AKT通路减轻糖尿病肾病中的足细胞损伤。

Upregulation of SHIP2 Participates in the Development of Breast Cancer via Promoting Wnt/β-Catenin Signaling [Retraction]

SHIP2 上调通过促进 Wnt/β-catenin 信号通路参与乳腺癌的发生发展 [撤稿]

The Functional Roles of the Src Homology 2 Domain-Containing Inositol 5-Phosphatases SHIP1 and SHIP2 in the Pathogenesis of Human Diseases

含有Src同源性2结构域的肌醇5-磷酸酶SHIP1和SHIP2在人类疾病发病机制中的功能作用

Discovery of aurones bearing two amine functionalities as SHIP2 inhibitors with insulin-sensitizing effect in rat myotubes

发现具有两个胺基官能团的橙酮作为 SHIP2 抑制剂，对大鼠肌管具有胰岛素增敏作用

LINC01468 drives NAFLD-HCC progression through CUL4A-linked degradation of SHIP2

LINC01468 通过 CUL4A 介导的 SHIP2 降解促进 NAFLD-HCC 的进展

Structural Insights into the Binding Propensity of Human SHIP2 SH2 to Oncogenic CagA Isoforms from Helicobacter pylori

人类SHIP2 SH2与幽门螺杆菌致癌CagA亚型结合倾向的结构解析

Targeting SHIP1 and SHIP2 in Cancer

靶向SHIP1和SHIP2治疗癌症