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

HIPRO: A High-Efficiency, Hypoxia-Induced Protocol for Generation of Photoreceptors in Retinal Organoids from Mouse Pluripotent Stem Cells.

HIPRO:一种利用小鼠多能干细胞在视网膜类器官中高效生成低氧诱导光感受器的方案

Chen Holly Y, Kelley Ryan A, Swaroop Anand

Phenotypic conservation in patients with X-linked retinitis pigmentosa caused by RPGR mutations

由RPGR基因突变引起的X连锁视网膜色素变性患者的表型保守性

Zahid, Sarwar; Khan, Naheed; Branham, Kari; Othman, Mohammad; Karoukis, Athanasios J; Sharma, Nisha; Moncrief, Ashley; Mahmood, Mahdi N; Sieving, Paul A; Swaroop, Anand; Heckenlively, John R; Jayasundera, Thiran

Transcriptome analysis and molecular signature of human retinal pigment epithelium

人类视网膜色素上皮的转录组分析和分子特征

N V Strunnikova, A Maminishkis, J J Barb, F Wang, C Zhi, Y Sergeev, W Chen, A O Edwards, D Stambolian, G Abecasis, A Swaroop, P J Munson, S S Miller

Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome

Chd7 缺陷小鼠的神经干细胞增殖和嗅觉缺陷表明人类 CHARGE 综合征的嗅觉减退机制

W S Layman, D P McEwen, L A Beyer, S R Lalani, S D Fernbach, E Oh, A Swaroop, C C Hegg, Y Raphael, J R Martens, D M Martin

RPGR-containing protein complexes in syndromic and non-syndromic retinal degeneration due to ciliary dysfunction

睫状体功能障碍引起的综合征性和非综合征性视网膜变性中含有RPGR的蛋白复合物

Murga-Zamalloa, Carlos A; Swaroop, Anand; Khanna, Hemant

Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function

隐性NRL突变与色素性视网膜变性呈团块状且蓝锥细胞功能相对保留的患者相关

Nishiguchi, Koji M; Friedman, James S; Sandberg, Michael A; Swaroop, Anand; Berson, Eliot L; Dryja, Thaddeus P

Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosa

北美一组患有X连锁视网膜色素变性的家族中RP2基因的蛋白质截短突变

Mears, A J; Gieser, L; Yan, D; Chen, C; Fahrner, S; Hiriyanna, S; Fujita, R; Jacobson, S G; Sieving, P A; Swaroop, A

Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa

在20%的X连锁视网膜色素变性家族中发现了RPGR基因突变谱

Buraczynska, M; Wu, W; Fujita, R; Buraczynska, K; Phelps, E; Andréasson, S; Bennett, J; Birch, D G; Fishman, G A; Hoffman, D R; Inana, G; Jacobson, S G; Musarella, M A; Sieving, P A; Swaroop, A