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

Uncovering genetic mechanisms of kidney aging through transcriptomics, genomics, and epigenomics

通过转录组学、基因组学和表观基因组学揭示肾脏衰老的遗传机制

Rowland, Joshua; Akbarov, Artur; Eales, James; Xu, Xiaoguang; Dormer, John P; Guo, Hui; Denniff, Matthew; Jiang, Xiao; Ranjzad, Parisa; Nazgiewicz, Alicja; Prestes, Priscilla Ribeiro; Antczak, Andrzej; Szulinska, Monika; Wise, Ingrid A; Zukowska-Szczechowska, Ewa; Bogdanski, Pawel; Woolf, Adrian S; Samani, Nilesh J; Charchar, Fadi J; Tomaszewski, Maciej

Congenital Disorders of the Human Urinary Tract: Recent Insights From Genetic and Molecular Studies

人类泌尿系统先天性疾病:来自遗传学和分子生物学研究的最新见解

Woolf, Adrian S; Lopes, Filipa M; Ranjzad, Parisa; Roberts, Neil A

Measures of kidney function by minimally invasive techniques correlate with histological glomerular damage in SCID mice with adriamycin-induced nephropathy

在阿霉素诱导肾病的SCID小鼠中,采用微创技术测量的肾功能与肾小球组织学损伤相关。

Scarfe, Lauren; Rak-Raszewska, Aleksandra; Geraci, Stefania; Darssan, Darsy; Sharkey, Jack; Huang, Jiaguo; Burton, Neal C; Mason, David; Ranjzad, Parisa; Kenny, Simon; Gretz, Norbert; Lévy, Raphaël; Kevin Park, B; García-Fiñana, Marta; Woolf, Adrian S; Murray, Patricia; Wilm, Bettina

Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome.

毒蕈碱乙酰胆碱受体 M3 突变导致膀胱疾病和类似腹壁皱褶综合征

Weber Stefanie, Thiele Holger, Mir Sevgi, Toliat Mohammad Reza, Sozeri Betül, Reutter Heiko, Draaken Markus, Ludwig Michael, Altmüller Janine, Frommolt Peter, Stuart Helen M, Ranjzad Parisa, Hanley Neil A, Jennings Rachel, Newman William G, Wilcox Duncan T, Thiel Uwe, Schlingmann Karl Peter, Beetz Rolf, Hoyer Peter F, Konrad Martin, Schaefer Franz, Nürnberg Peter, Woolf Adrian S

Development of viral vectors for use in cardiovascular gene therapy

开发用于心血管基因治疗的病毒载体

Williams, Paul D; Ranjzad, Parisa; Kakar, Salik J; Kingston, Paul A