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

Asymmetric Desymmetrizing Sulfonylation of Diarylmethanes via Peptidyl-Cu(I)-Catalysis with Remote Stereocontrol

利用肽基-Cu(I)催化实现二芳基甲烷的不对称去对称磺酰化反应及其远程立体控制

Um, Hyun-Suk; Miller, Scott J

Neuronal mitochondrial disaggregase CLPB ameliorates Huntington's disease pathology in mice

神经元线粒体解聚酶CLPB可改善小鼠亨廷顿病病理

Kim, Hyeonho; Hyun, Gaeun; Kim, Seunghye; Yu, Changmo; Hong, Young-Gi; Yu, Jihyeon; Bae, Sangsu; Rhee, Hyun-Woo; Ko, Jaewon; Um, Ji Won

Development of New IL-1R Antagonists with Improved Anti-inflammatory Efficacy

开发具有更高抗炎功效的新型IL-1R拮抗剂

Mooseok Kang,Ae-Ree Lee,Hyeji Jung,Gyubin Jang,Byeongchan Kim,Sung-Hyun Yoon,Je-Wook Yu,Jaewon Ko,Ji Won Um,Iksoo Chang

An automated plasma-based proteotyping immunoassay for APOE ε4 zygosity classification in Alzheimer's disease

一种基于血浆的自动化蛋白质组学免疫分析方法,用于阿尔茨海默病中APOE ε4基因型分类

Levin, Scott; Engel, Brian; Carlson, Corey; Hinson, Jeremiah; Holland, Mark; Figdore, Dan; Lim, Hyun Kook; Tiers, Laurent; Bhatt, Kinal; Schlichtmann, Ben; Hoffmann, Katie; Bae, Ye Eun; Szabo, Miklos; Lehmann, Sylvain; Um, Yoo Hyun; Algeciras-Schimnich, Alicia

Autism-associated ARHGEF9 variants impair GABAergic synapses and ultrasonic communication by reducing gephyrin phosphorylation.

与自闭症相关的 ARHGEF9 变异体通过减少 gephyrin 磷酸化来损害 GABA 能突触和超声波通讯。

Jung Hyeji, Kim Byeongchan, Jang Gyubin, Lee Hyojung, Kim Younghye, Kim Hyeonho, Lee Hea Ji, Kim Dongwook, Yang Yeji, Jeong Woo Chan, Kim Seungjoon, Han Ah-Reum, Kim Ho Min, Papadopoulos Theofilos, Durand Benjamin, Francannet Christine, Piton Amélie, Kim Jin Young, Ko Jaewon, Um Ji Won

HIFU-triggered burst release of gallic acid from gelatin/polyvinyl pyrrolidone hydrogel network crosslinked with magnesium gallate MOF

高强度聚焦超声(HIFU)触发的没食子酸从明胶/聚乙烯吡咯烷酮水凝胶网络中突释,该水凝胶网络与没食子酸镁金属有机框架(MOF)交联。

Sridharan, Badrinathan; Lee, Cho Eun; Kim, Daehun; Park, Jin Hyeong; Um, Wooram; Nam, Seung Yun; Kang, Juhyun; Lim, Hae Gyun

Ellagic Acid Alleviates Abnormal Fat Reduction by Activating the RXRβ-PPARγ Pathways in a CT26 Tumour-Induced Cachexia Mouse Model

鞣花酸通过激活CT26肿瘤诱导的恶病质小鼠模型中的RXRβ-PPARγ通路来缓解异常脂肪减少

Park, Woo Yong; Kim, Beomsu; Song, Gahee; Kim, Sang Hee; Kim, Jin-Hyung; Park, Ja Yeon; Jung, Se Jin; Jiao, Wenjun; Han, Jisoo; Kong, Taekyoung; Ahn, Kwang Seok; Kwak, Hyun Jeong; Um, Jae-Young

Genetic risk factors modulate the association between physical activity and colorectal cancer

遗传风险因素会影响体力活动与结直肠癌之间的关联。

Peoples, Anita R; Obón-Santacana, Mireia; Kim, Andre E; Kawaguchi, Eric S; Fu, Yubo; Qu, Conghui; Moratalla-Navarro, Ferran; Morrison, John; Lin, Yi; Arndt, Volker; Berndt, Sonja I; Bien, Stephanie A; Bishop, D Timothy; Bouras, Emmanouil; Brenner, Hermann; Buchanan, Daniel D; Campbell, Peter T; Chan, Andrew T; Chang-Claude, Jenny; Conti, David V; Corley, Douglas Ac; Devall, Matthew A; Dimou, Niki; Drew, David A; Gruber, Stephen B; Gunter, Marc J; Harlid, Sophia; Harrison, Tabitha A; Hoffmeister, Michael; Hsu, Li; Huyghe, Jeroen R; Keku, Temitope O; Kundaje, Anshul; Lewinger, Juan Pablo; Li, Li; Lynch, Brigid M; Le Marchand, Loic; Martín, Vicente; Murphy, Neil; Newton, Christina C; Ogino, Shuji; Hardikar, Sheetal; Ose, Jennifer; Pai, Rish K; Palmer, Julie R; Papadimitriou, Nikos; Pardamean, Bens; Pellatt, Andrew J; Pinchev, Mila; Platz, Elizabeth A; Potter, John D; Rennert, Gad; Ruiz-Narvaez, Edward A; Sakoda, Lori C; Schoen, Robert E; Shcherbina, Anna; Stern, Mariana C; Su, Yu-Ru; Thomas, Claire E; Tian, Yu; Tsilidis, Konstantinos K; Um, Caroline Y; van Duijnhoven, Franzel J B; Van Guelpen, Bethany; Visvanathan, Kala; Wang, Jun; White, Emily; Wolk, Alicja; Woods, Michael O; Wu, Anna H; Ulrich, Cornelia M; Peters, Ulrike; Gauderman, W James; Moreno, Victor

Bazedoxifene reverses sexually dimorphic autistic-like abnormalities in biallelic MDGA1-mutant mice.

巴泽多昔芬可逆转双等位基因 MDGA1 突变小鼠的性二态性自闭症样异常。

Kim Seungjoon, Kim Hyeonho, Pelayo Javier Porta, Alvarez Sara, Jang Gyubin, Kim Jinhu, Kim Byeongchan, Hoelscher Victoria M, Calleja-Pérez Beatriz, Jung Hyunsu, Yang Yeji, Lee Hea Ji, Lee Jihae, Kim Seoyeon, de la Peña Mar Jiménez, Lee Yelin, Kim Sohye, Han Ah-Reum, Lee Dong Sun, Ji Sangho, Yu Wookyung, Kim Ho Min, An Joon-Yong, Oh Won Chan, Kwon Seok-Kyu, Kim Jin Young, Um Ji Won, Fernández-Jaén Alberto, Ko Jaewon

MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathy

MDGA2纯合功能缺失变异会导致发育性和癫痫性脑病。

Morsy, Heba; Kim, Hyeonho; Jang, Gyubin; Zaki, Maha S; Severino, Mariasavina; Abdelrazek, Ibrahim M; Hussien, Haytham; Self, Eleanor; Albaradie, Raidah Saleem; Bakur, Khadijah; Firoozfar, Zahra; Efthymiou, Stephanie; Noureldeen, Mahmoud M; Nabil, Amira; Alvi, Javeria Raza; Molavi, Fateme; Alavi, Shahryar; Alibakhshi, Reza; Topcu, Vehap; Mancilar, Hanifenur; Uctepe, Eyyup; Yesilyurt, Ahmet; Aldhalaan, Hesham; Showki Tous, Ehab Salah; Alhaddad, Bader; Elbendary, Hasnaa M; Scardamaglia, Annarita; Murphy, David; Yépez, Vicente A; Gagneur, Julien; Omar, Tarek I; Abd Elmaksoud, Marwa; Vandrovocova, Jana; Abdalla, Ebtessam; Reilly, Mary M; Sultan, Tipu; Alkuraya, Fowzan S; Gleeson, Joseph G; Um, Ji Won; Houlden, Henry; Ko, Jaewon; Maroofian, Reza