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

A microphysiological human mini-bladder reveals urine-urothelium interplay in tissue resilience and UPEC recurrence in urinary tract infections.

微生理学的人类迷你膀胱揭示了尿液与尿路上皮在组织弹性和尿路感染中 UPEC 复发方面的相互作用。

Paduthol Gauri, Nikolaev Mikhail, Sharma Kunal, Blanc Jérôme, Tomasek Kathrin, Schlunke Léa Ivana Esméralda, Borgeat Valentin, Ambrosini Giovanna, Kolotuev Irina, Clerc-Rosset Stéphanie, Gjorevski Nikolche, Knott Graham W, Lütolf Matthias P, Thacker Vivek V, McKinney John D

Nasal Rhinomyiasis Caused by Cochliomyia hominivorax Complicated by a Parapharyngeal Abscess: A Case Report

由人鼻蝇(Cochliomyia hominivorax)引起的鼻肌病并发咽旁脓肿:病例报告

Megchún Hernández, Mauricio; Espinoza Pérez, Eleasib Alejandro Sr; García Chong, Néstor Rodolfo M; Ralda Gómez, Helen Ariadne; Diaz-Haaz, Diego Ivan

Simultaneous CRISPR screening and spatial transcriptomics reveal intracellular, intercellular, and functional transcriptional circuits

同步CRISPR筛选和空间转录组学揭示细胞内、细胞间和功能性转录回路

Loϊc Binan ,Aiping Jiang ,Serwah A Danquah ,Vera Valakh ,Brooke Simonton ,Jon Bezney ,Robert T Manguso ,Kathleen B Yates ,Ralda Nehme ,Brian Cleary ,Samouil L Farhi

Combining phenomics with transcriptomics reveals cell-type-specific morphological and molecular signatures of the 22q11.2 deletion.

将表型组学与转录组学相结合,揭示了 22q11.2 缺失的细胞类型特异性形态和分子特征

Tegtmeyer Matthew, Liyanage Dhara, Han Yu, Hebert Kathryn B, Pei Ruifan, Way Gregory P, Ryder Pearl V, Hawes Derek, Tromans-Coia Callum, Cimini Beth A, Carpenter Anne E, Singh Shantanu, Nehme Ralda

An integrative systems-biology approach defines mechanisms of Alzheimer's disease neurodegeneration

整合系统生物学方法阐明了阿尔茨海默病神经退行性变的机制。

Matthew J Leventhal ,Camila A Zanella ,Byunguk Kang ,Jiajie Peng ,David Gritsch ,Zhixiang Liao ,Hassan Bukhari ,Tao Wang ,Ping-Chieh Pao ,Serwah Danquah ,Joseph Benetatos ,Ralda Nehme ,Samouil Farhi ,Li-Huei Tsai ,Xianjun Dong ,Clemens R Scherzer ,Mel B Feany ,Ernest Fraenkel

βIV spectrin abundancy, cellular distribution and sensitivity to AKT/GSK3 regulation in schizophrenia.

精神分裂症中βIV谱蛋白的丰度、细胞分布及对AKT/GSK3调控的敏感性

Di Re Jessica, Marini Michela, Hussain Syed Ibrar, Singh Aditya K, Venkatesh Akshaya, Alshammari Musaad A, Alshammari Tahani K, Hamoud Abdul-Rizaq Ali, Imami Ali Sajid, Haghighijoo Zahra, Fularcyzk Nickolas, Stertz Laura, Hawes Derek, Mosebarger Angela, Jernigan Jordan, Chaljub Claire, Nehme Ralda, Walss-Bass Consuelo, Schulmann Anton, Vawter Marquis P, McCullumsmith Robert, Damoiseaux Robert D, Limon Agenor, Labate Demetrio, Wells Michael F, Laezza Fernanda

Postnatal Zika and Dengue Infection and their Effects on Neurodevelopment Among Children Living in Rural Guatemala

危地马拉农村地区儿童出生后寨卡病毒和登革热感染及其对神经发育的影响

Asturias, Edwin J; Connery, Amy K; Olson, Daniel; Lamb, Molly M; Paniagua-Avila, Alejandra; Anderson, Evan J; Focht, Chris; Colbert, Alison M; Natrajan, Muktha; Waggoner, Jesse J; Scherer, Erin; Calvimontes, D Mirella; Bolaños, Guillermo A; Bauer, Desirée; Arroyave, Paola; Hernández, Sara; Martinez, Maria A; Ralda, Aida V; Rojop, Neudy; Barrios, Edgar E; Chacon, Andrea; Dempsey, Walla; Tomashek, Kay M; Keitel, Wendy A; El Sahly, Hana M; Muñoz, Flor M

Modified Marionette lip-split incision for bucco-gingival cancer

改良型木偶唇裂切口治疗颊龈癌

Illescas Ralda, Monica Maria; Tsao, Chung-Kan; Lin, Ta-Chun; Young, Chi-Kuang; Hu, Yu-Feng; Liao, Chun-Ta; Kang, Chung-Jan; Huang, Shiang-Fu

A foundational neuronal protein network model unifying multimodal genetic, transcriptional, and proteomic perturbations in schizophrenia

一个基础性的神经元蛋白网络模型,统一了精神分裂症中多模态的遗传、转录和蛋白质组扰动

Pintacuda, Greta; Hsu, Yu-Han H; Páleníková, Petra; Dubonyte, Ugne; Fornelos, Nadine; Chen, Miao; Mena, Daya; Biagini, Julia C; Botts, Travis; Martorana, Makayla; Rebelo, Danzel; Ching, Joshua K T; Crouse, Ethan; Gebre, Hilena; Adiconis, Xian; Haywood, Nathan; Simmons, Sean; Weïwer, Michel; Hawes, Derek; Pietilainen, Olli; Werge, Thomas; Li, Ka Wan; Smit, August B; Kirkeby, Agnete; Levin, Joshua Z; Nehme, Ralda; Lage, Kasper

Gene editing in "cell villages" enables exploring disease-relevant mutations in many genetic backgrounds

在“细胞村”中进行基因编辑,可以探索多种遗传背景下与疾病相关的突变。

Battaglia, Rachel A; Bolshakova, Sonia; Mazureac, Ilinca; Liyanage, Dhara; Pettinari, Noah; Johnson, Autumn; Crouse, Ethan; Habib, Sartaj; Flessas, Isabel; Nadig, Ajay; Hawes, Derek; Tegtmeyer, Matthew; Becker, Caroline; Ghosh, Sulagna; Genovese, Giulio; Hogan, Marina; Maglieri, Adrianna; Barrett, Lindy E; Daheron, Laurence; McCarroll, Steven A; Nehme, Ralda