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

Development of a Highly Sensitive ELISA for Detecting Antibodies Against a Novel Variant Avian Reovirus Based on Dual σC and σB Antigens

基于双重σC和σB抗原开发用于检测新型禽呼肠孤病毒变异株抗体的高灵敏度ELISA

Beilina, Alexandra; Park, Jae-Hyeon; Landeck, Natalie; Chia, Ruth; Ding, Jinhui; Reed, Xylena; Bailey, Hannah; Kim, Changyoun; Kaganovich, Alice; Acri, Dominic J; Brooks, Janet; Mann, Alexandra; Zaghloul, Kareem A; Marsan, Elise; Raphael Gibbs, J; DeCasien, Alex; Cookson, Mark R; Zhao, Fuxi; Zhou, Wanyi; Yuan, Yilin; Peng, Qiuyun; Wang, Weibin; Cao, Weisheng

Inflammatory signaling differentially changes chromatin accessibility and gene expression of the PD- associated kinase LRRK2 between human and mice.

炎症信号对人类和小鼠的帕金森病相关激酶 LRRK2 的染色质可及性和基因表达的影响存在差异。

Beilina Alexandra, Park Jae-Hyeon, Landeck Natalie, Chia Ruth, Ding Jinhui, Reed Xylena, Bailey Hannah, Kim Changyoun, Kaganovich Alice, Acri Dominic J, Brooks Janet, Mann Alexandra, Zaghloul Kareem A, Marsan Elise, Gibbs J Raphael, DeCasien Alex, Cookson Mark R

Association of a common genetic variant with Parkinson's disease is mediated by microglia

常见基因变异与帕金森病之间的关联是由小胶质细胞介导的。

Langston, Rebekah G; Beilina, Alexandra; Reed, Xylena; Kaganovich, Alice; Singleton, Andrew B; Blauwendraat, Cornelis; Gibbs, J Raphael; Cookson, Mark R

Correction: Mutations in LRRK2 linked to Parkinson disease sequester Rab8a to damaged lysosomes and regulate transferrin-mediated iron uptake in microglia

更正:与帕金森病相关的LRRK2基因突变会将Rab8a隔离到受损的溶酶体中,并调节小胶质细胞中转铁蛋白介导的铁摄取。

Mamais, Adamantios; Kluss, Jillian H; Bonet-Ponce, Luis; Landeck, Natalie; Langston, Rebekah G; Smith, Nathan; Beilina, Alexandra; Kaganovich, Alice; Ghosh, Manik C; Pellegrini, Laura; Kumaran, Ravindran; Papazoglou, Ioannis; Heaton, George R; Harvey, Kirsten; Bandopadhyay, Rina; Maio, Nunziata; Kim, Changyoun; LaVoie, Matthew J; Gershlick, David C; Cookson, Mark R

LRRK2 mediates microglial neurotoxicity via NFATc2 in rodent models of synucleinopathies

在突触核蛋白病啮齿动物模型中,LRRK2 通过 NFATc2 介导小胶质细胞神经毒性

Kim, Changyoun; Beilina, Alexandria; Smith, Nathan; Li, Yan; Kim, Minhyung; Kumaran, Ravindran; Kaganovich, Alice; Mamais, Adamantios; Adame, Anthony; Iba, Michiyo; Kwon, Somin; Lee, Won-Jae; Shin, Soo-Jean; Rissman, Robert A; You, Sungyong; Lee, Seung-Jae; Singleton, Andrew B; Cookson, Mark R; Masliah, Eliezer

Differences in Stability, Activity and Mutation Effects Between Human and Mouse Leucine-Rich Repeat Kinase 2

人类和小鼠富亮氨酸重复激酶2在稳定性、活性和突变效应方面的差异

Langston, Rebekah G; Rudenko, Iakov N; Kumaran, Ravindran; Hauser, David N; Kaganovich, Alice; Ponce, Luis Bonet; Mamais, Adamantios; Ndukwe, Kelechi; Dillman, Allissa A; Al-Saif, Amr M; Beilina, Aleksandra; Cookson, Mark R

Molecular changes in the absence of severe pathology in the pulvinar in dementia with Lewy bodies

路易体痴呆患者丘脑枕核在无严重病理改变的情况下发生分子改变

Erskine, Daniel; Ding, Jinhui; Thomas, Alan J; Kaganovich, Alice; Khundakar, Ahmad A; Hanson, Peter S; Taylor, John-Paul; McKeith, Ian G; Attems, Johannes; Cookson, Mark R; Morris, Christopher M

Hexokinase activity is required for recruitment of parkin to depolarized mitochondria

己糖激酶活性是帕金蛋白募集到去极化线粒体所必需的。

McCoy, Melissa K; Kaganovich, Alice; Rudenko, Iakov N; Ding, Jinhui; Cookson, Mark R

The G2385R variant of leucine-rich repeat kinase 2 associated with Parkinson's disease is a partial loss-of-function mutation.

与帕金森病相关的富亮氨酸重复激酶 2 的 G2385R 变体是一种部分功能丧失突变

Rudenko Iakov N, Kaganovich Alice, Hauser David N, Beylina Aleksandra, Chia Ruth, Ding Jinhui, Maric Dragan, Jaffe Howard, Cookson Mark R

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

C9ORF72基因中六核苷酸重复序列的扩增是9p21染色体连锁的ALS-FTD的病因。

Renton, Alan E; Majounie, Elisa; Waite, Adrian; Simón-Sánchez, Javier; Rollinson, Sara; Gibbs, J Raphael; Schymick, Jennifer C; Laaksovirta, Hannu; van Swieten, John C; Myllykangas, Liisa; Kalimo, Hannu; Paetau, Anders; Abramzon, Yevgeniya; Remes, Anne M; Kaganovich, Alice; Scholz, Sonja W; Duckworth, Jamie; Ding, Jinhui; Harmer, Daniel W; Hernandez, Dena G; Johnson, Janel O; Mok, Kin; Ryten, Mina; Trabzuni, Danyah; Guerreiro, Rita J; Orrell, Richard W; Neal, James; Murray, Alex; Pearson, Justin; Jansen, Iris E; Sondervan, David; Seelaar, Harro; Blake, Derek; Young, Kate; Halliwell, Nicola; Callister, Janis Bennion; Toulson, Greg; Richardson, Anna; Gerhard, Alex; Snowden, Julie; Mann, David; Neary, David; Nalls, Michael A; Peuralinna, Terhi; Jansson, Lilja; Isoviita, Veli-Matti; Kaivorinne, Anna-Lotta; Hölttä-Vuori, Maarit; Ikonen, Elina; Sulkava, Raimo; Benatar, Michael; Wuu, Joanne; Chiò, Adriano; Restagno, Gabriella; Borghero, Giuseppe; Sabatelli, Mario; Heckerman, David; Rogaeva, Ekaterina; Zinman, Lorne; Rothstein, Jeffrey D; Sendtner, Michael; Drepper, Carsten; Eichler, Evan E; Alkan, Can; Abdullaev, Ziedulla; Pack, Svetlana D; Dutra, Amalia; Pak, Evgenia; Hardy, John; Singleton, Andrew; Williams, Nigel M; Heutink, Peter; Pickering-Brown, Stuart; Morris, Huw R; Tienari, Pentti J; Traynor, Bryan J