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

On variants and disease-causing mutations: Case studies of a SEMA4A variant identified in inherited blindness

关于变异和致病突变:遗传性失明中发现的SEMA4A变异的案例研究

Bryant, Laura; Lozynska, Olga; Han, Grace; Morgan, Jessica I W; Gai, Xiaowu; Maguire, Albert M; Aleman, Tomas; Bennett, Jean

Prescreening whole exome sequencing results from patients with retinal degeneration for variants in genes associated with retinal degeneration

对视网膜变性患者的全外显子组测序结果进行预筛选,以寻找与视网膜变性相关的基因变异

Bryant, Laura; Lozynska, Olga; Maguire, Albert M; Aleman, Tomas S; Bennett, Jean

Drug discovery for Duchenne muscular dystrophy via utrophin promoter activation screening.

通过肌营养不良蛋白启动子激活筛选发现杜氏肌营养不良症的药物

Moorwood Catherine, Lozynska Olga, Suri Neha, Napper Andrew D, Diamond Scott L, Khurana Tejvir S

C. elegans dysferlin homolog fer-1 is expressed in muscle, and fer-1 mutations initiate altered gene expression of muscle enriched genes

秀丽隐杆线虫的dysferlin同源物fer-1在肌肉中表达,fer-1突变会引发肌肉富集基因的表达改变。

Krajacic, Predrag; Hermanowski, Jane; Lozynska, Olga; Khurana, Tejvir S; Lamitina, Todd

Ets-2 repressor factor silences extrasynaptic utrophin by N-box mediated repression in skeletal muscle

Ets-2抑制因子通过N-box介导的抑制作用沉默骨骼肌中的突触外肌营养不良蛋白。

Perkins, Kelly J; Basu, Utpal; Budak, Murat T; Ketterer, Caroline; Baby, Santhosh M; Lozynska, Olga; Lunde, John A; Jasmin, Bernard J; Rubinstein, Neal A; Khurana, Tejvir S

Heregulin-induced epigenetic regulation of the utrophin-A promoter

赫格林诱导的肌营养不良蛋白A启动子的表观遗传调控

Basu, Utpal; Gyrd-Hansen, Mads; Baby, Santhosh M; Lozynska, Olga; Krag, Thomas O B; Jensen, Claus J; Frödin, Morten; Khurana, Tejvir S

QSulf1 remodels the 6-O sulfation states of cell surface heparan sulfate proteoglycans to promote Wnt signaling

QSulf1 重塑细胞表面硫酸乙酰肝素蛋白聚糖的 6-O 硫酸化状态,从而促进 Wnt 信号传导。

Ai, Xingbin; Do, Anh-Tri; Lozynska, Olga; Kusche-Gullberg, Marion; Lindahl, Ulf; Emerson, Charles P Jr