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

The AudioGene Translational Dashboard for Diagnosing Autosomal Dominant Nonsyndromic Hearing Loss: Phenotypic Data Visualization and Analysis Study

AudioGene转化应用平台在诊断常染色体显性非综合征型听力损失中的应用:表型数据可视化和分析研究

DeSollar, Benjamin; Schaefer, Nathan; Walls, Daniel; Odell, Amanda M; Booth, Kevin T A; Azaiez, Hela; Schnieders, Michael; Smith, Richard J H; Braun, Terry; Casavant, Thomas

Factor H-related 1 and heparan sulfate architecture contribute to complement dysregulation in C3 glomerulopathy.

因子 H 相关 1 和硫酸乙酰肝素结构导致 C3 肾小球病中的补体失调

Slagle Amanda K, Ghiringhelli Borsa Nicolo, Wang Kai, Taylor Amanda O, Meyer Nicole C, Jones Michael B, Walls William D, Nelson Angela F M, Roberts Sarah M, Sun Mingyao, Goicoechea de Jorge Elena, Rodriguez de Cordoba Santiago, Jalal Diana I, Nester Carla M, Zhang Yuzhou, Smith Richard J H

Acquired drivers of C3 glomerulopathy

获得性C3肾小球病驱动因素

Welsh, Seth J; Zhang, Yuzhou; Smith, Richard J H

Investigation of GSDME results in the identification of the first pathogenic synonymous variants and genotype-phenotype correlations

对 GSDME 的研究结果发现了首批致病性同义变异和基因型-表型相关性。

Chin, Joseph J; Walls, W Daniel; Wang, Kai; Odell, Amanda M; Kolbe, Diana L; Booth, Kevin T A; Azaiez, Hela; Smith, Richard J H

Pregnancy outcomes in C3 glomerulopathy: a retrospective review

C3肾小球病患者的妊娠结局:一项回顾性研究

Fergus, Lauren O; Waldman, Meryl; Hall, Monica D; Vining, Lynn; Hall, Jillian; Liu, Tina; Zhang, Yuzhou; Walker, Patrick J; Smith, Richard J H; Nester, Carla M

Correction: Pregnancy outcomes in C3 glomerulopathy: a retrospective review

更正:C3肾小球病患者的妊娠结局:一项回顾性研究

Fergus, Lauren O; Waldman, Meryl; Hall, Monica D; Vining, Lynn; Hall, Jillian; Liu, Tina; Zhang, Yuzhou; Walker, Patrick J; Smith, Richard J H; Nester, Carla M

Outcomes from the International Society of Nephrology Hemolytic Uremic Syndromes International Forum

国际肾脏病学会溶血性尿毒综合征国际论坛成果

Kavanagh, David; Ardissino, Gianluigi; Brocklebank, Vicky; Bouwmeester, Romy N; Bagga, Arvind; Ter Heine, Rob; Johnson, Sally; Licht, Christoph; Ma, Alison L T; Noris, Marina; Praga, Manuel; Rondeau, Eric; Sinha, Aditi; Smith, Richard J H; Sheerin, Neil S; Trimarchi, H; Wetzels, Jack F M; Vivarelli, Marina; Van de Kar, Nicole C A J; Greenbaum, Larry A

Renin and renin blockade have no role in complement activity.

肾素和肾素阻断剂对补体活性没有作用

Zhang Yuzhou, Martin Bertha, Spies M Ashley, Roberts Sarah M, Nott Joel, Goodfellow Renee X, Nelson Angela F M, Blain Samantha J, Redondo Elena, Nester Carla M, Smith Richard J H

Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working Group

推进肾脏疾病基因检测:国家肾脏基金会工作组报告

Franceschini, Nora; Feldman, David L; Berg, Jonathan S; Besse, Whitney; Chang, Alexander R; Dahl, Neera K; Gbadegesin, Rasheed; Pollak, Martin R; Rasouly, Hila Milo; Smith, Richard J H; Winkler, Cheryl A; Gharavi, Ali G

Functional evaluation of rare variants in complement factor I using a minigene assay

利用微基因检测对补体因子 I 的罕见变异进行功能评估

Donelson, Cobey J H; Ghiringhelli Borsa, Nicolo; Taylor, Amanda O; Smith, Richard J H; Zhang, Yuzhou