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

HP1β recruits RING1A to ubiquitinate histone H2A for BRCA1-mediated resection of double-stand breaks.

HP1β 招募 RING1A 泛素化组蛋白 H2A,以介导 BRCA1 介导的双链断裂切除。

Charaka Vijaya, Pandita Raj K, Tsai Chi-Lin, Wang Xiaoyan, Chakraborty Sharmista, Ramos Kenneth S, Nandi Sandhik, Leonard Fransisca, Singh Vipin, Sarkar Partha S, Hunt Clayton R, Tainer John A, Das Chandrima, Pandita Tej K

Huntingtin preserves mitochondrial genome integrity in neurons, which is impaired in Huntington's disease.

亨廷顿蛋白能够维持神经元中线粒体基因组的完整性,而亨廷顿病会损害这种完整性

Pradhan Subrata, Gaikwad Sagar, Tsai Chi-Lin, Smith Charlene, Zhang Nan, Bush Keegan, Chakraborty Anirban, Yuan Subo, Choudhary Sanjeev, Keene C Dirk, Ellerby Lisa M, Hazra Tapas K, La Spada Albert R, Wairkar Yogesh P, Ashizawa Tatsuo, Tainer John A, Pandita Tej K, Thompson Leslie M, Sarkar Partha S

Correction: The Role of the Mammalian DNA End-processing Enzyme Polynucleotide Kinase 3'-Phosphatase in Spinocerebellar Ataxia Type 3 Pathogenesis

更正:哺乳动物DNA末端加工酶多核苷酸激酶3'-磷酸酶在脊髓小脑性共济失调3型发病机制中的作用

Chatterjee, Arpita; Saha, Saikat; Chakraborty, Anirban; Silva-Fernandes, Anabela; Mandal, Santi M; Neves-Carvalho, Andreia; Liu, Yongping; Pandita, Raj K; Hegde, Muralidhar L; Hegde, Pavana M; Boldogh, Istvan; Ashizawa, Tetsuo; Koeppen, Arnulf H; Pandita, Tej K; Maciel, Patricia; Sarkar, Partha S; Hazra, Tapas K

Chromatin remodeler BRG1 recruits huntingtin to repair DNA double-strand breaks in neurons

染色质重塑因子BRG1招募亨廷顿蛋白修复神经元中的DNA双链断裂

Pradhan, Subrata; Bush, Keegan; Zhang, Nan; Pandita, Raj K; Tsai, Chi-Lin; Smith, Charlene; Pandlebury, Devon F; Gaikwad, Sagar; Leonard, Francis; Nie, Linghui; Tao, Annie; Russell, William; Yuan, Subo; Choudhary, Sanjeev; Ramos, Kenneth S; Elferink, Cornelis; Wairkar, Yogesh P; Tainer, John A; Thompson, Leslie M; Pandita, Tej K; Sarkar, Partha S

Polyglutamine Expansion in Huntingtin and Mechanism of DNA Damage Repair Defects in Huntington's Disease

亨廷顿蛋白中的多聚谷氨酰胺扩增及亨廷顿病DNA损伤修复缺陷机制

Pradhan, Subrata; Gao, Rui; Bush, Keegan; Zhang, Nan; Wairkar, Yogesh P; Sarkar, Partha S

Editorial: Neurodegeneration: From Disease Mechanism to Therapeutic Advancement

社论:神经退行性疾病:从疾病机制到治疗进展

Sarkar, Partha S; Meola, Giovanni; Zhang, Nan

Deficiency in classical nonhomologous end-joining-mediated repair of transcribed genes is linked to SCA3 pathogenesis

转录基因经典非同源末端连接介导的修复缺陷与SCA3发病机制相关。

Chakraborty, Anirban; Tapryal, Nisha; Venkova, Tatiana; Mitra, Joy; Vasquez, Velmarini; Sarker, Altaf H; Duarte-Silva, Sara; Huai, Weihan; Ashizawa, Tetsuo; Ghosh, Gourisankar; Maciel, Patricia; Sarkar, Partha S; Hegde, Muralidhar L; Chen, Xu; Hazra, Tapas K

Ethanol suppresses PGC-1α expression by interfering with the cAMP-CREB pathway in neuronal cells

乙醇通过干扰神经元细胞中的cAMP-CREB通路来抑制PGC-1α的表达。

Liu, Zilong; Liu, Yongping; Gao, Rui; Li, Haixia; Dunn, Tiffany; Wu, Ping; Smith, Robert G; Sarkar, Partha S; Fang, Xiang

Purkinje cell loss is the major brain pathology of spinocerebellar ataxia type 10

浦肯野细胞丢失是10型脊髓小脑性共济失调的主要脑部病理改变。

Xia, Guangbin; McFarland, Karen N; Wang, Kang; Sarkar, Partha S; Yachnis, Anthony T; Ashizawa, Tetsuo

Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability

重复中断对脊髓小脑性共济失调10型扩增和重复不稳定性产生的矛盾影响

McFarland, Karen N; Liu, Jilin; Landrian, Ivette; Gao, Rui; Sarkar, Partha S; Raskin, Salmo; Moscovich, Mariana; Gatto, Emilia M; Teive, Hélio A G; Ochoa, Adriana; Rasmussen, Astrid; Ashizawa, Tetsuo