日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

HNF4A P2 isoform alleviates kidney fibrosis by inhibiting dedifferentiation of proximal tubular cells through JAG1/NOTCH signaling

HNF4A P2亚型通过JAG1/NOTCH信号通路抑制近端肾小管细胞去分化,从而减轻肾纤维化。

Jiang, Guiya; Lu, Xun; Cao, Rui; Zhang, Houliang; Gao, Yue; Lu, Kai; Zhang, Lei; Zhang, Guangyuan; Wu, Jianping; Xu, Bin; Zhong, Jian; Sun, Jin; Chen, Ming; Chen, Shuqiu

RNA‑binding protein DAZAP1 promotes gastric cancer metastasis by enhancing NOTCH1 and JAG1 mRNA stability.

RNA结合蛋白DAZAP1通过增强NOTCH1和JAG1 mRNA的稳定性来促进胃癌转移。

Peng Siyang, Chen Yidong, Wu Jieke, Huang Xiaodong, Hong Linjie, Xie Yanci, Lei Yuting, Wei Xiangyang, Yang Ping, Zhang Jieming, Yang Qiong, Liu Guangnan, Li Aimin, Liu Side, Li Jiaying, Dai Weiyu, Hu Yanfeng, Wang Jing, Xiong Jing, Wang Jide

Improved functional JAG1 and NOTCH2 variant testing in patients with clinical or suspected Alagille syndrome using new low-Notch activity cells

利用新型低Notch活性细胞,改进对临床诊断或疑似阿拉吉尔综合征患者的JAG1和NOTCH2功能变异检测。

Buhl, Nicole; Pfister, Eva-Doreen; Oliveira, Daniel V; Turetti, Fabio; Lurz, Eberhard; Baumann, Ulrich; Di Donato, Nataliya; Illig, Thomas; Skawran, Britta; Andersson, Emma R; Mašek, Jan; Stalke, Amelie

JAG1 expression in papillary thyroid cancer stem-like cells predicts poor prognosis and implicates angiogenesis

乳头状甲状腺癌干细胞样细胞中JAG1的表达预示着不良预后,并与血管生成有关。

Yoshida-Minato, Riho; Horie, Tetsuhiro; Aga, Mitsuharu; Sakamoto, Takuya; Inujima, Akiko; Nakamura, Yuka; Yasumoto, Kazuo; Ishigaki, Yasuhito; Miwa, Takaki; Shiga, Hideaki

A patient with Alagille syndrome had a novel JAG1 gene mutation

一名患有阿拉吉勒综合征的患者携带一种新的JAG1基因突变。

Peng, Ziting; Chen, Yao; Zhang, Li; Shi, Tongdong; Wang, Na

Synapsin III promotes neuronal-like transdifferentiation of glioblastoma stem cells by disrupting JAG1-Notch1 interaction

突触蛋白III通过破坏JAG1-Notch1相互作用促进胶质母细胞瘤干细胞向神经元样转分化。

Deng, Yilin; Yuan, Zheng; Jin, Xiong; Wang, Zekun; Gong, Rui; Ren, Shuai; Park, Jong Bae; Shi, Bingyang; Yin, Jinlong

Muscle-specific increased expression of JAG1 improves the skeletal muscle phenotype in dystrophin-deficient mice

肌肉特异性增加JAG1表达可改善肌营养不良蛋白缺陷小鼠的骨骼肌表型。

de Souza Leite, Felipe; Lambert, Matthias R; Zhang, Tracy Yuanfan; Conner, James R; Paulo, Joao A; Oliveira, Sheldon Furtado; Guha Thakurta, Sanjukta; Bowles, Jennifer; Gussoni, Emanuela; Gygi, Steven P; Widrick, Jeffrey J; Kunkel, Louis M

Phenotypic Divergence of JAG1- and NOTCH2-Associated Alagille Syndrome & Disease-Specific NOTCH2 Variant Classification Guidelines

JAG1 和 NOTCH2 相关阿拉吉尔综合征的表型差异及疾病特异性 NOTCH2 变异分类指南

Vandriel, Shannon M; Li, Li-Ting; She, Huiyu; Wang, Jian-She; Loomes, Kathleen M; Piccoli, David A; Jankowska, Irena; Czubkowski, Piotr; Gliwicz-Miedzińska, Dorota; D'Antiga, Lorenzo; Nicastro, Emanuele; Lacaille, Florence; Debray, Dominique; Sokal, Étienne M; Demaret, Tanguy; Fawaz, Rima L; Nastasio, Silvia; Kim, Kyung Mo; Oh, Seak Hee; Fischler, Björn; Arnell, Henrik; Larson-Nath, Catherine; Hardikar, Winita; Shankar, Sahana; Sundaram, Shikha S; Chaidez, Alexander; Bulut, Pinar; Calvo, Pier Luigi; Kasahara, Mureo; Blondet, Niviann; Lurz, Eberhard; Kavallar, Anna-Maria; Gonzales, Emmanuel M; Jacquemin, Emmanuel; Bouligand, Jérôme; Ebel, Noelle H; Feinstein, Jeffrey A; Siew, Susan M; Stormon, Michael O; Karpen, Saul J; Romero, Rene; Jensen, M Kyle; Jaramillo, Catalina; Squires, James E; Bedoyan, Sarah M; Kelly, Deirdre A; Hartley, Jane; Verkade, Henkjan J; Lee, Way Seah; Lertudomphonwanit, Chatmanee; Fischer, Ryan T; Lin, Henry C; Rock, Nathalie; Mozer-Glassberg, Yael; Roberts, Amin J; Evans, Helen M; Karnsakul, Wikrom; Nebbia, Gabriella; Wolters, Victorien M; Valentino, Pamela L; Bernabeu, Jesus Quintero; Aqul, Amal A; Arikan, Cigdem; Tamara, María Legarda; Busoms, Cristina Molera; Sandahl, Thomas Damgaard; Indolfi, Giuseppe; Zizzo, Andréanne N; Zellos, Aglaia; Quiros-Tejeira, Ruben E; Santos-Silva, Ermelinda; Schwarz, Kathleen B; Brecelj, Jernej; Sanchez, Maria Camila; Cavalieri, Maria Lorena; Tzivinikos, Christos; Wiecek, Sabina; Eshun, John; Kerkar, Nanda; Mujawar, Quais; Önal, Zerrin; Gonçalves, Cristina; Garcia, Jennifer; Alam, Seema; Jimenez-Rivera, Carolina; Bujanda, Luis; Thompson, Richard J; Hansen, Bettina E; Spinner, Nancy B; Gilbert, Melissa A; Kamath, Binita M

Alagille syndrome due to a novel JAG1 mutation in a Chinese pediatric patient: A case report.

中国儿童患者因新型 JAG1 基因突变而患上阿拉吉勒综合征:病例报告。

Zhang Zongdan, Zhang Xuezu, He Chuangfeng

Generation of induced pluripotent stem cell lines TRNDi037-A and TRNDi038-A from two patients with Alagille syndrome carrying heterozygous JAG1 mutations

从两名携带杂合JAG1突变的阿拉吉勒综合征患者中生成诱导多能干细胞系TRNDi037-A和TRNDi038-A

Elena F Evans ,Guibin Chen ,Ivan Pavlinov ,Xiuli Huang ,Kaari Linask ,Chengyu Liu ,Alexander Rodriguez Lopez ,Melissa A Gilbert ,Nancy B Spinner ,Steven Rodemse ,Karsten Baumgärtele ,Catherine Z Chen ,Jizhong Zou ,Wei Zheng