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

Tubule-Specific Compensatory Responses to Cpt1a Deletion in Aged Mice.

老年小鼠中 Cpt1a 缺失引起的肾小管特异性补偿反应

Funk Steven D, Kern Justin T, Viquez Olga M, Sulvaran-Guel Elizabeth, Koenitzer Jeffrey R, Feola Kyle C, Blum Jacob S, Zent Roy, Humphreys Benjamin D, Huen Sarah C, Gewin Leslie S

A deletion in the N-terminal polymerizing domain of laminin β2 is a new mouse model of chronic nephrotic syndrome

层粘连蛋白β2 N端聚合结构域的缺失是慢性肾病综合征的一种新的小鼠模型。

Funk, Steven D; Bayer, Raymond H; McKee, Karen K; Okada, Kazushi; Nishimune, Hiroshi; Yurchenco, Peter D; Miner, Jeffrey H

Pathogenicity of a Human Laminin β2 Mutation Revealed in Models of Alport Syndrome

在阿尔波特综合征模型中揭示人类层粘连蛋白β2突变的致病性

Funk, Steven D; Bayer, Raymond H; Malone, Andrew F; McKee, Karen K; Yurchenco, Peter D; Miner, Jeffrey H

Alport syndrome and Pierson syndrome: Diseases of the glomerular basement membrane

阿尔波特综合征和皮尔森综合征:肾小球基底膜疾病

Funk, Steven D; Lin, Meei-Hua; Miner, Jeffrey H

EphA2 Expression Regulates Inflammation and Fibroproliferative Remodeling in Atherosclerosis

EphA2表达调控动脉粥样硬化中的炎症和纤维增生性重塑

Finney, Alexandra C; Funk, Steven D; Green, Jonette M; Yurdagul, Arif Jr; Rana, Mohammad Atif; Pistorius, Rebecca; Henry, Miriam; Yurochko, Andrew; Pattillo, Christopher B; Traylor, James G; Chen, Jin; Woolard, Matthew D; Kevil, Christopher G; Orr, A Wayne

Muscular dystrophy meets protein biochemistry, the mother of invention

肌肉萎缩症与蛋白质生物化学相遇,发明之母

Funk, Steven D; Miner, Jeffrey H

Functional assessment of a novel COL4A5 splice region variant and immunostaining of plucked hair follicles as an alternative method of diagnosis in X-linked Alport syndrome

对一种新型 COL4A5 剪接区变异体进行功能评估,并采用拔取毛囊进行免疫染色,作为 X 连锁 Alport 综合征的替代诊断方法。

Malone, Andrew F; Funk, Steven D; Alhamad, Tarek; Miner, Jeffrey H