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

Baseline and innate immune response characterization of a Zfp30 knockout mouse strain

Zfp30基因敲除小鼠品系的基础免疫反应和先天免疫反应特征分析

Laudermilk, Lucas T; Tovar, Adelaide; Homstad, Alison K; Thomas, Joseph M; McFadden, Kathryn M; Tune, Miriya K; Cowley, Dale O; Mock, Jason R; Ideraabdullah, Folami; Kelada, Samir N P

A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS

Wilms 肿瘤 1 基因的一种新的错义突变导致常染色体显性遗传性局灶节段性肾小球硬化症 (FSGS)。

Hall, Gentzon; Gbadegesin, Rasheed A; Lavin, Peter; Wu, Guanghong; Liu, Yangfan; Oh, Edwin C; Wang, Liming; Spurney, Robert F; Eckel, Jason; Lindsey, Thomas; Homstad, Alison; Malone, Andrew F; Phelan, Paul J; Shaw, Andrey; Howell, David N; Conlon, Peter J; Katsanis, Nicholas; Winn, Michelle P

HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome

HLA-DQA1 和 PLCG2 是儿童期发病的类固醇敏感性肾病综合征的候选风险基因位点

Gbadegesin, Rasheed A; Adeyemo, Adebowale; Webb, Nicholas J A; Greenbaum, Larry A; Abeyagunawardena, Asiri; Thalgahagoda, Shenal; Kale, Arundhati; Gipson, Debbie; Srivastava, Tarak; Lin, Jen-Jar; Chand, Deepa; Hunley, Tracy E; Brophy, Patrick D; Bagga, Arvind; Sinha, Aditi; Rheault, Michelle N; Ghali, Joanna; Nicholls, Kathy; Abraham, Elizabeth; Janjua, Halima S; Omoloja, Abiodun; Barletta, Gina-Marie; Cai, Yi; Milford, David D; O'Brien, Catherine; Awan, Atif; Belostotsky, Vladimir; Smoyer, William E; Homstad, Alison; Hall, Gentzon; Wu, Guanghong; Nagaraj, Shashi; Wigfall, Delbert; Foreman, John; Winn, Michelle P

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

罕见的遗传性 COL4A3/COL4A4 变异可能被误诊为家族性局灶节段性肾小球硬化症。

Malone, Andrew F; Phelan, Paul J; Hall, Gentzon; Cetincelik, Umran; Homstad, Alison; Alonso, Andrea S; Jiang, Ruiji; Lindsey, Thomas B; Wu, Guanghong; Sparks, Matthew A; Smith, Stephen R; Webb, Nicholas J A; Kalra, Philip A; Adeyemo, Adebowale A; Shaw, Andrey S; Conlon, Peter J; Jennette, J Charles; Howell, David N; Winn, Michelle P; Gbadegesin, Rasheed A

Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS

编码 F-肌动蛋白结合蛋白 anillin 的基因突变会导致 FSGS

Rasheed A Gbadegesin, Gentzon Hall, Adebowale Adeyemo, Nils Hanke, Irini Tossidou, James Burchette, Guanghong Wu, Alison Homstad, Matthew A Sparks, Jose Gomez, Ruiji Jiang, Andrea Alonso, Peter Lavin, Peter Conlon, Ron Korstanje, M Christine Stander, Ghaidan Shamsan, Moumita Barua, Robert Spurney, P

TNXB mutations can cause vesicoureteral reflux

TNXB 突变可导致膀胱输尿管反流

Rasheed A Gbadegesin, Patrick D Brophy, Adebowale Adeyemo, Gentzon Hall, Indra R Gupta, David Hains, Bartlomeij Bartkowiak, C Egla Rabinovich, Settara Chandrasekharappa, Alison Homstad, Katherine Westreich, Guanghong Wu, Yutao Liu, Danniele Holanda, Jason Clarke, Peter Lavin, Angelica Selim, Sara Mi

Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis

散发性和遗传性局灶节段性肾小球硬化症患者中具有表达变异的反向formin 2突变

Gbadegesin, Rasheed A; Lavin, Peter J; Hall, Gentzon; Bartkowiak, Bartlomiej; Homstad, Alison; Jiang, Ruiji; Wu, Guanghong; Byrd, Alison; Lynn, Kelvin; Wolfish, Norman; Ottati, Carolina; Stevens, Paul; Howell, David; Conlon, Peter; Winn, Michelle P

TRPC6 enhances angiotensin II-induced albuminuria

TRPC6 增强血管紧张素 II 诱导的蛋白尿

Eckel, Jason; Lavin, Peter J; Finch, Elizabeth A; Mukerji, Nirvan; Burch, Jarrett; Gbadegesin, Rasheed; Wu, Guanghong; Bowling, Brandy; Byrd, Alison; Hall, Gentzon; Sparks, Matthew; Zhang, Zhu Shan; Homstad, Alison; Barisoni, Laura; Birbaumer, Lutz; Rosenberg, Paul; Winn, Michelle P

A new locus for familial FSGS on chromosome 2p

2p染色体上发现一个新的家族性FSGS基因位点

Gbadegesin, Rasheed; Lavin, Peter; Janssens, Louis; Bartkowiak, Bartlomiej; Homstad, Alison; Wu, Guanghong; Bowling, Brandy; Eckel, Jason; Potocky, Chris; Abbott, Diana; Conlon, Peter; Scott, William K; Howell, David; Hauser, Elizabeth; Winn, Michelle P