未登录

D

Deeksha Prasad

l v prasad eye institute

H指数:9

被引数:191

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Comparative analysis of ocular surface restoration following different techniques of allogeneic limbal transplantation in a rabbit model of limbal stem cell deficiency

不同同种异体角膜缘移植技术在兔角膜缘干细胞缺乏模型中眼表修复的比较分析

Scientific Reports

IF3.9

2026-07-300

OA

Proteomic mapping of human Tenon's fascia reveals its biomimetic potential for corneal stromal extracellular matrix reconstruction

Experimental Eye Research

IF2.7

2025-12-300

PRE

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

评估高渗性和炎症应激对人类角膜上皮细胞的独立及联合效应

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

IF4.7

2025-10-010

PRE

Developing a model for aqueous deficient dry eye secondary to periglandular cicatrizing conjunctivitis*

开发继发于腺周瘢痕性结膜炎的水液缺乏性干眼模型 *

EXPERIMENTAL EYE RESEARCH

IF2.7

2024-07-011

PRE

Neutrophil-driven and interleukin-36γ-associated ocular surface inflammation in chronic Stevens-Johnson syndrome

IF12

2024-04-292

OAAI

Human cornea-derived extracellular matrix hydrogel for prevention of post-traumatic corneal scarring: A translational approach

人角膜来源的细胞外基质水凝胶预防外伤后角膜瘢痕形成: 一种转化方法

ACTA BIOMATERIALIA

IF9.6

2023-11-0110

OAAI

Development and validation of a reliable rabbit model of limbal stem cell deficiency by mechanical debridement using an ophthalmic burr

EXPERIMENTAL EYE RESEARCH

IF2.7

2023-11-010

PRE

identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy (vol 17, 361, 2022)

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2023-06-290

OAAI

Expansion and characterization of human limbus-derived stromal/mesenchymal stem cells in xeno-free medium for therapeutic applications

STEM CELL RESEARCH & THERAPY

IF7.3

2023-04-156

OAAI

Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy

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

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2022-09-174

OAAI

Differential expression of tear film cytokines in Stevens-Johnson syndrome patients and comparative review of literature

SCIENTIFIC REPORTS

IF3.9

2021-09-168

OAAI