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

Inhibition of Adipocyte Lipolysis Reduces Liver Injury in a Mouse Model of Ischemia Reperfusion Injury

抑制脂肪细胞脂解作用可减轻小鼠缺血再灌注损伤模型中的肝损伤

Liss, Kim H H; Goldman, Samantha; He, Mai; Shew, Trevor M; Ferguson, Daniel; Finck, Brian N

A case of autoimmune hepatitis in a patient with inflammatory bowel disease and significant lymphadenopathy in the porta hepatis

一例患有炎症性肠病和肝门部明显淋巴结肿大的自身免疫性肝炎病例

Malamet, Benjamin J; Joerger, Shannon; Caudill, Karen; He, Mai; Genere, Juan Reyes; Stoll, Janis

Enhanced Activities of OCT4 and SOX2 Promote Epigenetic Reprogramming by Shortening G1 Phase.

OCT4 和 SOX2 活性增强通过缩短 G1 期促进表观遗传重编程

Guo Lin, Lin Jiechun, Ren Qiwen, Sun Hao, Wu Yanhua, Ge Haofei, Wu Xiaolan, Lin Lihui, Liang Lining, Li Changpeng, Liu He, Mai Yuangbang, Chu Shilong, Liu Jiadong, Liu Jing, Chen Jiekai, Pei Duanqing, Zheng Hui

Excited-State Engineering toward Accelerated Reverse Intersystem Crossing in Diindolocarbazole-Embedded Multiple-Resonance Emitters for High-Performance Blue OLEDs

利用激发态工程加速二吲哚咔唑嵌入式多共振发光体中的反向系间窜越,实现高性能蓝色OLED

Wang, Shuxin; Zhou, Jianping; Jin, Jibiao; Jiang, He; Mai, Minqiang; Duan, Lian; Zhang, Xinping; Wong, Wai-Yeung

A Critical Role for the Mitochondrial Pyruvate Carrier in Hepatic Stellate Cell Activation.

线粒体丙酮酸载体在肝星状细胞活化中的关键作用

Habibi Mohammad, Ferguson Daniel, Eichler Sophie J, Chan Mandy M, Fu Christina, Pietka Terri A, Bredemeyer Andrea L, LaPoint Andrew, Shew Trevor M, He Mai, Liss Kim H H, Lutkewitte Andrew J, Cho Kevin, Schilling Joel D, Patti Gary J, Finck Brian N

Diagnostic alignment to optimize inter-rater reliability among lung transplant pathologists

诊断一致性旨在优化肺移植病理学家之间的评分者间信度

Pavlisko, Elizabeth N; Neely, Megan L; Wikenheiser-Brokamp, Kathryn A; Fishbein, Gregory A; Litzky, Leslie; Farver, Carol F; Pal, Prodipto; He, Mai; Illei, Peter B; Deshpande, Charuhas; Robien, Mark A; Kirchner, Jerry; Frankel, Courtney W; Lang, Jason E; Belperio, John A; Palmer, Scott M; Sweet, Stuart C

Compound heterozygous missense and intronic variants in B9D1 contribute to a recurrent Meckel syndrome pedigree

B9D1基因中的复合杂合错义变异和内含子变异导致了复发性梅克尔综合征家系

Jing, Huining; Xu, Bocheng; Wang, Hao; Liu, Shanling; Wang, He; Mai, Jingqun; Yao, Wencong; Zhang, Zhu

Atypical Presentation of IARS1-Related Disorder: Expanding the Phenotype and Genotype

IARS1相关疾病的非典型表现:扩展表型和基因型

Wongkittichote, Parith; Jonatzke, Kira E; Hyde, Benjamin T; Peterson, Lance W; He, Mai; McKinstry, Robert C; Antonellis, Anthony; Shinawi, Marwan

Noninvasive Markers of Inflammation and Protein Loss Augment Diagnosis of Pediatric Celiac Disease

无创性炎症和蛋白质丢失标志物有助于诊断儿童乳糜泻

Sutton, Kimberly A; He, Mai; Ma, Changqing; Liu, Ta-Chiang; Faubion, William A; Hoffmann, Julie; Linneman, Laura; Rodriguez, Cynthia; Holtz, Lori R

A Case of Congenital Nephrotic Syndrome with Crescents Caused by a Novel Compound Heterozygous Pairing of NPHS1 Genetic Variants

一例由NPHS1基因变异的新型复合杂合配对引起的先天性肾病综合征伴新月体形成病例报告

Goodman, Kyle N; Puapatanakul, Pongpratch; Barton, Kevin T; He, Mai; Miner, Jeffrey H; Gaut, Joseph P