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

Distinct metabolic profiles associated with autism spectrum disorder versus cancer in individuals with germline PTEN mutations.

携带生殖系 PTEN 突变的个体中,自闭症谱系障碍与癌症相关的代谢特征存在显著差异

Yehia Lamis, Ni Ying, Sadler Tammy, Frazier Thomas W, Eng Charis

Selective deletion of MyD88 signaling in α-SMA positive cells ameliorates experimental intestinal fibrosis via post-transcriptional regulation

选择性敲除α-SMA阳性细胞中的MyD88信号通路可通过转录后调控改善实验性肠道纤维化。

Zhao, Shuai; Dejanovic, Dina; Yao, Peng; Bhilocha, Shardul; Sadler, Tammy; Schirbel, Anja; West, Gail; Doyon, Genevieve; Lopez, Rocio; Mao, Ren; Kurada, Satya; El Ouali, Sara; Grassl, Guntram; Fox, Paul L; Cruise, Michael; Worthley, Daniel L; de la Motte, Carol; Fiocchi, Claudio; Rieder, Florian

Distinct Alterations in Tricarboxylic Acid Cycle Metabolites Associate with Cancer and Autism Phenotypes in Cowden Syndrome and Bannayan-Riley-Ruvalcaba Syndrome

考登综合征和班纳扬-赖利-鲁瓦尔卡巴综合征中三羧酸循环代谢物的独特改变与癌症和自闭症表型相关

Yehia, Lamis; Ni, Ying; Feng, Fang; Seyfi, Marilyn; Sadler, Tammy; Frazier, Thomas W; Eng, Charis

Mutual Regulation of TLR/NLR and CEACAM1 in the Intestinal Microvasculature: Implications for IBD Pathogenesis and Therapy

肠道微血管中TLR/NLR和CEACAM1的相互调控:对炎症性肠病发病机制和治疗的意义

Schirbel, Anja; Rebert, Nancy; Sadler, Tammy; West, Gail; Rieder, Florian; Wagener, Christoph; Horst, Andrea; Sturm, Andreas; de la Motte, Carol; Fiocchi, Claudio

Genome-wide analysis of DNA methylation and gene expression defines molecular characteristics of Crohn's disease-associated fibrosis

全基因组DNA甲基化和基因表达分析揭示了克罗恩病相关纤维化的分子特征

Sadler, Tammy; Bhasin, Jeffrey M; Xu, Yaomin; Barnholz-Sloan, Jill; Chen, Yanwen; Ting, Angela H; Stylianou, Eleni

Inflammation-induced endothelial-to-mesenchymal transition: a novel mechanism of intestinal fibrosis

炎症诱导的内皮-间质转化:肠道纤维化的一种新机制

Rieder, Florian; Kessler, Sean P; West, Gail A; Bhilocha, Shardul; de la Motte, Carol; Sadler, Tammy M; Gopalan, Banu; Stylianou, Eleni; Fiocchi, Claudio

Germline mutations and variants in the succinate dehydrogenase genes in Cowden and Cowden-like syndromes

考登综合征和考登样综合征中琥珀酸脱氢酶基因的种系突变和变异

Ni, Ying; Zbuk, Kevin M; Sadler, Tammy; Patocs, Attila; Lobo, Glenn; Edelman, Emily; Platzer, Petra; Orloff, Mohammed S; Waite, Kristin A; Eng, Charis