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

Assessing the Independent and Combined Effects of Hyperosmolarity and Inflammatory Stress on Human Corneal Epithelial Cells.

评估高渗和炎症应激对人角膜上皮细胞的独立和联合影响。

期刊:Investigative Ophthalmology & Visual Science
影响因子:4.7
doi:10.1167/iovs.66.13.47
Prasad Deeksha, Siddiqui Mohammad Gufran, Dar Mahi Al Ahmad, Sonar Rohini, Singh Swati, Donthineni Pragnya Rao, Basu Sayan, Singh Vivek
Human
细胞生物学
上皮细胞
炎症
发表日期：2025
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Comparative assessment of structural and tear film alterations in rabbit meibomian gland dysfunction models using chemical and electrocauterization techniques.

采用化学和电灼技术对兔睑板腺功能障碍模型的结构和泪膜变化进行比较评估

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-025-06923-9
Prasad Deeksha, Jakati Saumya, Bokara Kiran Kumar, Basu Sayan, Singh Vivek, Donthineni Pragnya Rao
其它
Rabbit
发表日期：2025
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Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy

更正：对印度先天性遗传性内皮营养不良家族性和散发性病例中SLC4A11变异谱的鉴定和计算机分析

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-023-02791-6
Salman, Mohd; Verma, Anshuman; Chaurasia, Sunita; Prasad, Deeksha; Kannabiran, Chitra; Singh, Vivek; Ramappa, Muralidhar
SLC4A1
发表日期：2023
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A review of rabbit models of meibomian gland dysfunction and scope for translational research

对兔睑板腺功能障碍模型及其转化研究前景的综述

期刊:Indian Journal of Ophthalmology
影响因子:1.8
doi:10.4103/IJO.IJO_2815_22
Prasad, Deeksha; Salman, Mohd; Reddy, A Aniruth; Jaffet, Jilu; Sahoo, Abhishek; Jakati, Saumya; Bokara, Kiran Kumar; Singh, Swati; Basu, Sayan; Singh, Vivek; Donthineni, Pragnya Rao
发表日期：2023
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Optimization and evaluation of tear protein elution from Schirmer's strips in dry eye disease

干眼症中泪液蛋白从泪液试纸中洗脱的优化和评价

期刊:Indian Journal of Ophthalmology
影响因子:1.8
doi:10.4103/IJO.IJO_2774_22
Koduri, Madhuri Amulya; Prasad, Deeksha; Pingali, Tejaswini; Singh, Vijay Kumar; Shanbhag, Swapna S; Basu, Sayan; Singh, Vivek
干眼症
发表日期：2023
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Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy

对印度家族性和散发性先天性遗传性内皮营养不良病例中SLC4A11变异谱的鉴定和计算机分析

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-022-02521-4
Salman, Mohd; Verma, Anshuman; Chaurasia, Sunita; Prasad, Deeksha; Kannabiran, Chitra; Singh, Vivek; Ramappa, Muralidhar
SLC4A1
发表日期：2022
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