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

The exploration of glucocorticoid pathway based on disease severity in COVID-19 patients

基于COVID-19患者疾病严重程度的糖皮质激素通路探索

Aliska, Gestina; Putra, Andani Eka; Anggrainy, Fenty; Lailani, Mutia

Production of Exopolysaccharides and İndole Acetic Acid (IAA) by Rhizobacteria and Their Potential against Drought Stress in Upland Rice

根际细菌胞外多糖和吲哚乙酸(IAA)的产生及其在旱稻抗旱胁迫中的应用潜力

Linda, Tetty Marta; Aliska, Jusinta; Feronika, Nita; Melisa, Ineiga; Juliantari, Erwina

The role of the glucocorticoid receptor and its impact on steroid response in moderate-severe COVID-19 patients

糖皮质激素受体的作用及其对中重度 COVID-19 患者类固醇反应的影响

Aliska, Gestina; Nafrialdi, Nafrialdi; Lie, Khie Chen; Setiabudy, Rianto; Putra, Andani Eka; Widyahening, Indah Suci; Harahap, Alida Roswita

A Carboxy-terminal Smarcb1 Point Mutation Induces Hydrocephalus Formation and Affects AP-1 and Neuronal Signalling Pathways in Mice

羧基末端 Smarcb1 点突变诱导小鼠脑积水形成并影响 AP-1 和神经信号通路

Aliska K Brugmans #, Carolin Walter #, Natalia Moreno, Carolin Göbel, Dörthe Holdhof, Flavia W de Faria, Marc Hotfilder, Daniela Jeising, Michael C Frühwald, Boris V Skryabin, Timofey S Rozhdestvensky, Lydia Wachsmuth, Cornelius Faber, Martin Dugas, Julian Varghese, Ulrich Schüller, Thomas K Albert,

SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2

SOX7 缺陷通过影响心内膜-间质转化以及 Wnt4 和 Bmp2 的表达,导致室间隔缺损。

Hernández-García, Andrés; Pendleton, Katherine E; Kim, Sangbae; Li, Yumei; Kim, Bum J; Zaveri, Hitisha P; Jordan, Valerie K; Berry, Aliska M; Ljungberg, M Cecilia; Chen, Rui; Lanz, Rainer B; Scott, Daryl A

Appendicitis among Patients Admitted to the Department of Surgery of a Tertiary Care Centre: A Descriptive Cross-sectional Study

一家三级医疗中心外科收治的阑尾炎患者:一项描述性横断面研究

Deo, Kishor Kumar; Yogi, Prajwala; Niroula, Aliska; Maharjan, Sujata

Remarkable Recovery in a Patient with Lethal Dose Paraquat Poisoning: A Case Report

百草枯中毒致死剂量患者奇迹般康复:病例报告

Adhikari, Nishob; Chapagain, Nibedita; Acharya, Rajat; Pokhrel, Anil; Niroula, Aliska

Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency

阐明一种与PAX5单倍体不足相关的新型神经发育综合征

Gofin, Yoel; Wang, Tianyun; Gillentine, Madelyn A; Scott, Tiana M; Berry, Aliska M; Azamian, Mahshid S; Genetti, Casie; Agrawal, Pankaj B; Picker, Jonathan; Wojcik, Monica H; Delgado, Mauricio R; Lynch, Sally A; Scherer, Stephen W; Howe, Jennifer L; Bacino, Carlos A; DiTroia, Stephanie; VanNoy, Grace E; O'Donnell-Luria, Anne; Lalani, Seema R; Graf, William D; Rosenfeld, Jill A; Eichler, Evan E; Earl, Rachel K; Scott, Daryl A

Underlying genetic etiologies of congenital diaphragmatic hernia

先天性膈疝的潜在遗传病因

Scott, Daryl A; Gofin, Yoel; Berry, Aliska M; Adams, April D

Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data

利用DECIPHER数据识别先天性膈疝附加症(CDH+)的表型扩展

Hardcastle, Amy; Berry, Aliska M; Campbell, Ian M; Zhao, Xiaonan; Liu, Pengfei; Gerard, Amanda E; Rosenfeld, Jill A; Sisoudiya, Saumya D; Hernandez-Garcia, Andres; Loddo, Sara; Di Tommaso, Silvia; Novelli, Antonio; Dentici, Maria L; Capolino, Rossella; Digilio, Maria C; Graziani, Ludovico; Rustad, Cecilie F; Neas, Katherine; Ferrero, Giovanni B; Brusco, Alfredo; Di Gregorio, Eleonora; Wellesley, Diana; Beneteau, Claire; Joubert, Madeleine; Van Den Bogaert, Kris; Boogaerts, Anneleen; McMullan, Dominic J; Dean, John; Giuffrida, Maria G; Bernardini, Laura; Varghese, Vinod; Shannon, Nora L; Harrison, Rachel E; Lam, Wayne W K; McKee, Shane; Turnpenny, Peter D; Cole, Trevor; Morton, Jenny; Eason, Jacqueline; Jones, Marilyn C; Hall, Rebecca; Wright, Michael; Horridge, Karen; Shaw, Chad A; Chung, Wendy K; Scott, Daryl A