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

Insulin Induces Outer Blood-Retinal Barrier Disruption via Downregulation of Claudin-19

胰岛素通过下调 Claudin-19 诱导外血视网膜屏障破坏

Hernandez, Karen R; Pollock, Lana M; Rodriguez, Aidan D; Lohr, M F; Matsuoka, Ryota L; Anand-Apte, Bela

Photoreceptor regeneration occurs normally in microglia-deficient irf8 mutant zebrafish following acute retinal damage

在小胶质细胞缺陷型irf8突变斑马鱼中,急性视网膜损伤后感光细胞再生正常发生。

Song, Ping; Parsana, Dhwani; Singh, Rupesh; Pollock, Lana M; Anand-Apte, Bela; Perkins, Brian D

Primary cilia are present on endothelial cells of the hyaloid vasculature but are not required for the development of the blood-retinal barrier

初级纤毛存在于玻璃体血管的内皮细胞上,但并非血视网膜屏障发育所必需。

Pollock, Lana M; Perkins, Brian; Anand-Apte, Bela

Supervillin Is a Component of the Hair Cell's Cuticular Plate and the Head Plates of Organ of Corti Supporting Cells

超级绒毛蛋白是毛细胞角质层板和科尔蒂氏器头部板支持细胞的组成部分。

Pollock, Lana M; Gupta, Nilay; Chen, Xi; Luna, Elizabeth J; McDermott, Brian M Jr

ACF7 is a hair-bundle antecedent, positioned to integrate cuticular plate actin and somatic tubulin.

ACF7 是毛束前体,定位于整合角质板肌动蛋白和体细胞微管蛋白

Antonellis Patrick J, Pollock Lana M, Chou Shih-Wei, Hassan Ahmed, Geng Ruishuang, Chen Xi, Fuchs Elaine, Alagramam Kumar N, Auer Manfred, McDermott Brian M Jr

Sequencing of candidate chromosome instability genes in endometrial cancers reveals somatic mutations in ESCO1, CHTF18, and MRE11A.

对子宫内膜癌中候选染色体不稳定性基因进行测序,发现 ESCO1、CHTF18 和 MRE11A 存在体细胞突变

Price Jessica C, Pollock Lana M, Rudd Meghan L, Fogoros Sarah K, Mohamed Hassan, Hanigan Christin L, Le Gallo Matthieu, Zhang Suiyuan, Cruz Pedro, Cherukuri Praveen F, Hansen Nancy F, McManus Kirk J, Godwin Andrew K, Sgroi Dennis C, Mullikin James C, Merino Maria J, Hieter Philip, Bell Daphne W

Mutations in KARS, encoding lysyl-tRNA synthetase, cause autosomal-recessive nonsyndromic hearing impairment DFNB89

编码赖氨酰tRNA合成酶的KARS基因突变会导致常染色体隐性遗传的非综合征性听力障碍DFNB89。

Santos-Cortez, Regie Lyn P; Lee, Kwanghyuk; Azeem, Zahid; Antonellis, Patrick J; Pollock, Lana M; Khan, Saadullah; Irfanullah; Andrade-Elizondo, Paula B; Chiu, Ilene; Adams, Mark D; Basit, Sulman; Smith, Joshua D; Nickerson, Deborah A; McDermott, Brian M Jr; Ahmad, Wasim; Leal, Suzanne M

Predisposition to cancer caused by genetic and functional defects of mammalian Atad5.

哺乳动物 Atad5 的遗传和功能缺陷导致癌症易感性

Bell Daphne W, Sikdar Nilabja, Lee Kyoo-Young, Price Jessica C, Chatterjee Raghunath, Park Hee-Dong, Fox Jennifer, Ishiai Masamichi, Rudd Meghan L, Pollock Lana M, Fogoros Sarah K, Mohamed Hassan, Hanigan Christin L, Zhang Suiyuan, Cruz Pedro, Renaud Gabriel, Hansen Nancy F, Cherukuri Praveen F, Borate Bhavesh, McManus Kirk J, Stoepel Jan, Sipahimalani Payal, Godwin Andrew K, Sgroi Dennis C, Merino Maria J, Elliot Gene, Elkahloun Abdel, Vinson Charles, Takata Minoru, Mullikin James C, Wolfsberg Tyra G, Hieter Philip, Lim Dae-Sik, Myung Kyungjae

Fascin 2b is a component of stereocilia that lengthens actin-based protrusions

Fascin 2b 是立体纤毛的组成部分,可延长基于肌动蛋白的突起。

Chou, Shih-Wei; Hwang, Philsang; Gomez, Gustavo; Fernando, Carol A; West, Megan C; Pollock, Lana M; Lin-Jones, Jennifer; Burnside, Beth; McDermott, Brian M Jr