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

ZFP148 is a transcriptional repressor of cytolytic effector CD8(+) T cell differentiation

ZFP148是细胞溶解效应CD8(+) T细胞分化的转录抑制因子

Xiao, Tong; Chen, Xingyu; Song, No-Joon; Brown, Ryan J; Ma, Anjun; Mandula, Jay K; Yousif, Amir; Wang, Yi; Le, Minh Quynh May; Li, Jianying; Gao, Fengxia; Weaver, Bella; Chen, Heng-Yi; Lay, Fang-Yun; Sundi, Debasish; Velegraki, Maria; Weltge, Payton; Merchant, Juanita L; Rubinstein, Mark P; Oestreich, Kenneth J; Lio, Chan-Wang Jerry; Ghoneim, Hazem E; Li, Xue; Theodorescu, Dan; Xin, Gang; Ma, Qin; Cui, Weiguo; Li, Zihai

Cognitive Impairment and Chemoendocrine vs Endocrine Therapy in Pre- and Postmenopausal Women: A Secondary Analysis of the RxPONDER Randomized Clinical Trial

认知障碍与绝经前和绝经后妇女的化学内分泌治疗与内分泌治疗:RxPONDER随机临床试验的二次分析

Kang, Irene M; Forschmiedt, Jamie K; Loch, Michelle M; Lew, Danika L; Barlow, William E; Gralow, Julie R; Meric-Bernstam, Funda; Albain, Kathy S; Hayes, Daniel F; Lin, Nancy U; Perez, Edith A; Goldstein, Lori J; Rastogi, Priya; Schott, Anne F; Baehner, Rick; Sharma, Priyanka; Tripathy, Debasish; Pusztai, Lajos; Hortobagyi, Gabriel N; Kalinsky, Kevin; Henry, N Lynn

Age-related macular degeneration and cerebral amyloid angiopathy have similar pathologies from cholesterol-APOE-amyloid-β-complement mediated inflammation

年龄相关性黄斑变性和脑淀粉样血管病具有相似的病理机制,均源于胆固醇-APOE-β淀粉样蛋白-补体介导的炎症反应。

Stuard Sambhariya, Whitney; Bowes Rickman, Catherine; D'Amore, Patricia A; Corradetti, Giulia; Hageman, Gregory S; Howell, Gareth R; Marola, Olivia J; Phatnani, Hemali; Philp, Nancy J; Sinha, Debasish; Toomey, Christopher B; Stone, Faith; Eberhart, Charles; Handa, James T

STING activation induces polarized cytokine secretion of IFN-β and IL-17A promoting photoreceptor death and choroidal disruption in age-related macular degeneration.

STING 激活诱导极化的细胞因子 IFN-β 和 IL-17A 分泌,促进与年龄相关的黄斑变性中的感光细胞死亡和脉络膜破坏。

Huang Chao, Babu Vishnu Suresh, Bammidi Sridhar, Arnold Jakob N, Ebeling Martin, Widmer Gabriella, Strassburger Pamela, Lazendic Mirjana, Grüner Sabine, Koester Janis, Dutta Puja, Hose Stacey, Singh Sonali, Gautam Pooja, Lad Eleonora M, Westenskow Peter D, Kutsyr Oksana, Csaky Karl G, Ghosh Sayan, Sripathi Srinivasa R, Proia Alan D, Flores-Bellver Miguel, Sinha Debasish, Feenstra Derrick

Long term outcomes of the Indian childhood cancer survivorship (C2S) cohort: a multicentre study (2016-2024)

印度儿童癌症幸存者(C2S)队列的长期结果:一项多中心研究(2016-2024 年)

Seth, Rachna; Kapoor, Gauri; Moulik, Nirmalya Roy; Kaushik, Prakruthi; Verma, Nishant; Mahajan, Amita; T, Priyakumari; Radhakrishnan, Nita; Raj, Revathi; Singh, Amitabh; Sharma, Sujata; Radhakrishnan, Venkatraman; Rani, Sirishia; Bhattacharyya, Parthasarathi; Krishnan, Yamini; Mandal, Piali; Rahiman, Emine A; Jain, Prachi; Sahoo, Debasish; Mohapatra, Debabrata; Das, Gargi; Gupta, Vineeta; Singh, Gurpreet; Kakkar, Shruti; Singh, Anuj; Prabhakar, Prashant; Kumar Ar, Arun; Meena, Jagdish Prasad; Gupta, Aditya Kumar; Malhotra, Payal; Kumar, Chandan; Didel, Siyaram; Arora, Shilpa Khanna; Patil, Veerendra; Prakash, Anand; Kanvinde, Purva; Prasad, Maya; Chandra, Jagdish; Kurkure, Purna; Arora, Ramandeep

Variants in MTNAP1 underlie a neurodegenerative disorder by impairing mitochondrial stability.

MTNAP1基因的变异会损害线粒体稳定性,从而导致神经退行性疾病。

Kumar Abhishek, Saha Smita, Nasir Nazim, Gaurav Vishal, Mathuria Yogendra Pratap, Gupta Shailesh Kumar, Ranjan Akash, Ghosh Debasish Kumar

Obstructive sleep apnea a synergistic health risk in type 2 diabetes mellitus: a cross-sectional analytical study using STOP-BANG questionnaire in a tertiary care teaching hospital of Eastern Odisha

阻塞性睡眠呼吸暂停是2型糖尿病的协同健康风险:一项在奥里萨邦东部一家三级教学医院使用STOP-BANG问卷进行的横断面分析研究

Goyal, Prateek; Bose, Manika; Mishra, Srimannarayan; Mishra, Tapaswini; Misra, Debasish; Mangaraj, Swayamsidha

Efficacy of Family-based Interventions in Addressing Substance Use Disorders: A Systematic Review on Randomized Controlled Trials

家庭干预在解决物质使用障碍方面的疗效:随机对照试验的系统评价

Aswathy P V; Junaid K P; Ghosh, Abhishek; Basu, Debasish; Sharma, Suresh K; Pillai, Renjith R

Embracing innovations and upholding excellence in pharmacology

拥抱创新,坚持药理学领域的卓越标准

Bezbaruah, Babul Kumar; Hota, Debasish

A Novel SLC9A3R1 Mutation as a Rare Cause of Infantile Hypercalcemia

一种新的SLC9A3R1突变是婴儿高钙血症的罕见病因

Ravi Kumar, Padala; Biswas, Ankeet; Dash, Deepak K; Patro, Debasish; Madhav Reddy, D Sai