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

Dysregulation of protein SUMOylation networks in Huntington's disease R6/2 mouse striatum.

亨廷顿病 R6/2 小鼠纹状体中蛋白质 SUMO 化网络失调

Kachemov Marketta, Vaibhav Vineet, Smith Charlene, Sundararaman Niveda, Heath Marie, Pendlebury Devon F, Matlock Andrea, Lau Alice, Morozko Eva, Lim Ryan G, Reidling Jack, Steffan Joan S, Van Eyk Jennifer E, Thompson Leslie M

In-Situ Optimization of an Optoelectronic Reservoir Computer with Digital Delayed Feedback

基于数字延迟反馈的光电储层计算机的原位优化

Morozko, Fyodor; Watad, Shadad; Naser, Amir; Calà Lesina, Antonio; Novitsky, Andrey; Karabchevsky, Alina

Taperin bundles F-actin at stereocilia pivot points enabling optimal lifelong mechanosensitivity.

Taperin 将 F-肌动蛋白束固定在立体纤毛的枢轴点,从而实现最佳的终生机械敏感性

Belyantseva Inna A, Liu Chang, Dragich Abigail K, Miyoshi Takushi, Inagaki Sayaka, Imtiaz Ayesha, Tona Risa, Zuluaga-Osorio Karen Sofia, Hadi Shadan, Wilson Elizabeth, Morozko Eva, Olszewski Rafal, Yousaf Rizwan, Sokolova Yuliya, Riordan Gavin P, Aston S Andrew, Rehman Atteeq U, Fenollar Ferrer Cristina, Wisniewski Jan, Gu Shoujun, Nayak Gowri, Goodyear Richard J, Li Jinan, Krey Jocelyn F, Wafa Talah, Faridi Rabia, Adadey Samuel Mawuli, Drummond Meghan, Perrin Benjamin, Winkler Dennis C, Starost Matthew F, Cheng Hui, Fitzgerald Tracy, Richardson Guy P, Dong Lijin, Barr-Gillespie Peter G, Hoa Michael, Frolenkov Gregory I, Friedman Thomas B, Zhao Bo

On-chip beam rotators, adiabatic mode converters, and waveplates through low-loss waveguides with variable cross-sections

通过具有可变横截面的低损耗波导实现片上光束旋转器、绝热模式转换器和波片

Sun, Bangshan; Morozko, Fyodor; Salter, Patrick S; Moser, Simon; Pong, Zhikai; Patel, Raj B; Walmsley, Ian A; Wang, Mohan; Hazan, Adir; Barré, Nicolas; Jesacher, Alexander; Fells, Julian; He, Chao; Katiyi, Aviad; Tian, Zhen-Nan; Karabchevsky, Alina; Booth, Martin J

PIAS1 modulates striatal transcription, DNA damage repair, and SUMOylation with relevance to Huntington's disease

PIAS1 调节纹状体转录、DNA 损伤修复和 SUMO 化,与亨廷顿氏病相关

Eva L Morozko, Charlene Smith-Geater, Alejandro Mas Monteys, Subrata Pradhan, Ryan G Lim, Peter Langfelder, Marketta Kachemov, Jayesh A Kulkarni, Josh Zaifman, Austin Hill, Jennifer T Stocksdale, Pieter R Cullis, Jie Wu, Joseph Ochaba, Ricardo Miramontes, Anirban Chakraborty, Tapas K Hazra, Alice La

Longitudinal Biochemical Assay Analysis of Mutant Huntingtin Exon 1 Protein in R6/2 Mice

R6/2小鼠突变型亨廷顿蛋白外显子1的纵向生化测定分析

Eva L Morozko, Joseph Ochaba, Sarah J Hernandez, Alice Lau, Isabella Sanchez, Iliana Orellana, Lexi Kopan, Joshua Crapser, Janet H Duong, Julia Overman, Silvia Yeung, Joan S Steffan, Jack Reidling, Leslie M Thompson

Mutant Huntingtin Disrupts the Nuclear Pore Complex

突变的亨廷顿蛋白破坏了核孔复合体

Jonathan C Grima, J Gavin Daigle, Nicolas Arbez, Kathleen C Cunningham, Ke Zhang, Joseph Ochaba, Charlene Geater, Eva Morozko, Jennifer Stocksdale, Jenna C Glatzer, Jacqueline T Pham, Ishrat Ahmed, Qi Peng, Harsh Wadhwa, Olga Pletnikova, Juan C Troncoso, Wenzhen Duan, Solomon H Snyder, Laura P W Ran

Harnessing molecular motors for nanoscale pulldown in live cells

利用分子马达在活细胞中实现纳米级下拉

Jonathan E Bird, Melanie Barzik, Meghan C Drummond, Daniel C Sutton, Spencer M Goodman, Eva L Morozko, Stacey M Cole, Alexandra K Boukhvalova, Jennifer Skidmore, Diana Syam, Elizabeth A Wilson, Tracy Fitzgerald, Atteeq U Rehman, Donna M Martin, Erich T Boger, Inna A Belyantseva, Thomas B Friedman

ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells

ILDR1基因敲除小鼠是人类耳聋DFNB42的模型,其三细胞紧密连接的结构异常以及听觉毛细胞的退化是其特征。

Morozko, Eva L; Nishio, Ayako; Ingham, Neil J; Chandra, Rashmi; Fitzgerald, Tracy; Martelletti, Elisa; Borck, Guntram; Wilson, Elizabeth; Riordan, Gavin P; Wangemann, Philine; Forge, Andrew; Steel, Karen P; Liddle, Rodger A; Friedman, Thomas B; Belyantseva, Inna A