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

Gene targeting as a therapeutic avenue in diseases mediated by the complement alternative pathway

基因靶向治疗作为治疗补体旁路途径介导疾病的一种途径。

Dreismann, Anna K; Hallam, Thomas M; Tam, Lawrence Cs; Nguyen, Calvin V; Hughes, Jane P; Ellis, Scott; Harris, Claire L

C3 Glomerulopathy and Related Disorders in Children: Etiology-Phenotype Correlation and Outcomes

儿童C3肾小球病及相关疾病:病因-表型相关性及预后

Wong, Edwin K S; Marchbank, Kevin J; Lomax-Browne, Hannah; Pappworth, Isabel Y; Denton, Harriet; Cooke, Katie; Ward, Sophie; McLoughlin, Amy-Claire; Richardson, Grant; Wilson, Valerie; Harris, Claire L; Morgan, B Paul; Hakobyan, Svetlana; McAlinden, Paul; Gale, Daniel P; Maxwell, Heather; Christian, Martin; Malcomson, Roger; Goodship, Timothy H J; Marks, Stephen D; Pickering, Matthew C; Kavanagh, David; Cook, H Terence; Johnson, Sally A

Long-term outcomes and response to treatment in diacylglycerol kinase epsilon nephropathy

二酰甘油激酶ε肾病的长期预后和治疗反应

Brocklebank, Vicky; Kumar, Gurinder; Howie, Alexander J; Chandar, Jayanthi; Milford, David V; Craze, Janet; Evans, Jonathan; Finlay, Eric; Freundlich, Michael; Gale, Daniel P; Inward, Carol; Mraz, Martin; Jones, Caroline; Wong, William; Marks, Stephen D; Connolly, John; Corner, Bronte M; Smith-Jackson, Kate; Walsh, Patrick R; Marchbank, Kevin J; Harris, Claire L; Wilson, Valerie; Wong, Edwin K S; Malina, Michal; Johnson, Sally; Sheerin, Neil S; Kavanagh, David

Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2

STAT2基因纯合种系突变导致严重的I型干扰素病和不受控制的干扰素信号传导。

Duncan, Christopher J A; Thompson, Benjamin J; Chen, Rui; Rice, Gillian I; Gothe, Florian; Young, Dan F; Lovell, Simon C; Shuttleworth, Victoria G; Brocklebank, Vicky; Corner, Bronte; Skelton, Andrew J; Bondet, Vincent; Coxhead, Jonathan; Duffy, Darragh; Fourrage, Cecile; Livingston, John H; Pavaine, Julija; Cheesman, Edmund; Bitetti, Stephania; Grainger, Angela; Acres, Meghan; Innes, Barbara A; Mikulasova, Aneta; Sun, Ruyue; Hussain, Rafiqul; Wright, Ronnie; Wynn, Robert; Zarhrate, Mohammed; Zeef, Leo A H; Wood, Katrina; Hughes, Stephen M; Harris, Claire L; Engelhardt, Karin R; Crow, Yanick J; Randall, Richard E; Kavanagh, David; Hambleton, Sophie; Briggs, Tracy A

Expanding horizons in complement drug discovery: challenges and emerging strategies

拓展补体药物研发的视野:挑战与新兴策略

Harris, Claire L

A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H-Related 3 Gene in Atypical Hemolytic Uremic Syndrome

非典型溶血性尿毒综合征中补体激活调节因子簇的从头缺失导致混合补体因子H/补体因子H相关3基因的产生

Challis, Rachel C; Araujo, Geisilaine S R; Wong, Edwin K S; Anderson, Holly E; Awan, Atif; Dorman, Anthony M; Waldron, Mary; Wilson, Valerie; Brocklebank, Vicky; Strain, Lisa; Morgan, B Paul; Harris, Claire L; Marchbank, Kevin J; Goodship, Timothy H J; Kavanagh, David

Complement, a target for therapy in inflammatory and degenerative diseases

补体是炎症性和退行性疾病的治疗靶点

Morgan, B Paul; Harris, Claire L

An anticomplement agent that homes to the damaged brain and promotes recovery after traumatic brain injury in mice

一种能靶向受损脑组织并促进小鼠创伤性脑损伤后恢复的抗补体剂

Ruseva, Marieta M; Ramaglia, Valeria; Morgan, B Paul; Harris, Claire L

Functional analysis of a complement polymorphism (rs17611) associated with rheumatoid arthritis

与类风湿性关节炎相关的补体多态性(rs17611)的功能分析

Giles, Joanna L; Choy, Ernest; van den Berg, Carmen; Morgan, B Paul; Harris, Claire L

Complement activation in multiple sclerosis plaques: an immunohistochemical analysis

多发性硬化斑块中补体激活:免疫组织化学分析

Ingram, Gillian; Loveless, Sam; Howell, Owain W; Hakobyan, Svetlana; Dancey, Bethan; Harris, Claire L; Robertson, Neil P; Neal, James W; Morgan, B Paul