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

Gene augmentation therapy treats mature mice with complete congenital stationary night blindness (cCSNB), improving retinal function and visual acuity

基因增强疗法可治疗患有完全性先天性静止性夜盲症(cCSNB)的成年小鼠,改善其视网膜功能和视力。

Hasan, Nazarul; Attaway, Cecilia A; Di Paolo, Mattia; McCall, Maureen A; Gregg, Ronald G

Domain-specific functions of LRIT3 in synaptic assembly and retinal signal transmission

LRIT3在突触组装和视网膜信号传递中的特定功能

Hasan, Nazarul; Gregg, Ronald G

RHO1-2 meganuclease gene editing targets human P23H rhodopsin-induced retinitis pigmentosa to rejuvenate rods and maintain cones.

RHO1-2 巨核酸酶基因编辑靶向人类 P23H 视紫红质诱导的视网膜色素变性,以恢复视杆细胞活力并维持视锥细胞功能。

Jalligampala Archana, Young Jacob M, Feist Jack, Wang Wei, Barone Francesca, Alston David C, Fransen James W, Jaikumar Gita, Kamboj Kautuk, Mooreman Caitlin, Nash Stephen, Noel Jennifer M, Pangeni Gobinda, Prestigiacomo Joseph C, Sahu Bhubanananda, Turner Caitlin, Kaplan Henry J, Green Jonathan A, Wells Kevin D, Bartsevich Victor V, Chatterton Jon E, Davis Mara, Evans Kathryn S, Lape Janel, Lewis Whitney C, van de Beek Rebecca, Viles Kristi D, Jantz Derek, Gregg Ronald G, Smith Jeff, McCall Maureen A

Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness

玻璃体内注射一种新型AAV载体靶向ON双极细胞,可恢复完全性先天性静止性夜盲症小鼠模型的视觉功能。

Scalabrino, Miranda L; Boye, Sanford L; Fransen, Kathryn M H; Noel, Jennifer M; Dyka, Frank M; Min, Seok Hong; Ruan, Qing; De Leeuw, Charles N; Simpson, Elizabeth M; Gregg, Ronald G; McCall, Maureen A; Peachey, Neal S; Boye, Shannon E

Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness

鉴定出一种新的突变等位基因 Grm6(nob7),该基因与完全性先天性静止性夜盲症有关

Qian, Haohua; Ji, Rui; Gregg, Ronald G; Peachey, Neal S

GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness

GPR179是双极细胞去极化功能所必需的,并且在常染色体隐性遗传的完全性先天性静止性夜盲症中发生突变。

Peachey, Neal S; Ray, Thomas A; Florijn, Ralph; Rowe, Lucy B; Sjoerdsma, Trijntje; Contreras-Alcantara, Susana; Baba, Kenkichi; Tosini, Gianluca; Pozdeyev, Nikita; Iuvone, P Michael; Bojang, Pasano Jr; Pearring, Jillian N; Simonsz, Huibert Jan; van Genderen, Maria; Birch, David G; Traboulsi, Elias I; Dorfman, Allison; Lopez, Irma; Ren, Huanan; Goldberg, Andrew F X; Nishina, Patsy M; Lachapelle, Pierre; McCall, Maureen A; Koenekoop, Robert K; Bergen, Arthur A B; Kamermans, Maarten; Gregg, Ronald G

Topological analysis of small leucine-rich repeat proteoglycan nyctalopin

富含亮氨酸重复序列的小蛋白聚糖夜光蛋白的拓扑分析

Bojang, Pasano Jr; Gregg, Ronald G

rnaset2 mutant zebrafish model familial cystic leukoencephalopathy and reveal a role for RNase T2 in degrading ribosomal RNA.

rnaset2 突变斑马鱼模型可诱发家族性囊性白质脑病,并揭示 RNase T2 在降解核糖体 RNA 中的作用

Haud Noémie, Kara Firat, Diekmann Simone, Henneke Marco, Willer Jason R, Hillwig Melissa S, Gregg Ronald G, Macintosh Gustavo C, Gärtner Jutta, Alia A, Hurlstone Adam F L

Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma

斑马鱼 lrp2 基因突变会导致成年期发病的眼部疾病,该疾病可模拟近视和其他青光眼风险因素。

Veth, Kerry N; Willer, Jason R; Collery, Ross F; Gray, Matthew P; Willer, Gregory B; Wagner, Daniel S; Mullins, Mary C; Udvadia, Ava J; Smith, Richard S; John, Simon W M; Gregg, Ronald G; Link, Brian A

Distribution of voltage gated calcium channel β subunits in the mouse retina.

小鼠视网膜中电压门控钙通道β亚基的分布

Ball Sherry L, McEnery Maureen W, Yunker Anne Marie R, Shin Hee-Sup, Gregg Ronald G