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

Correction: Heparanase inhibition as a systemic approach to protect the endothelial glycocalyx and prevent microvascular complications in diabetes

更正:肝素酶抑制剂作为一种系统性方法,可保护内皮糖萼并预防糖尿病微血管并发症。

Gamez, Monica; E Elhegni, Hesham; Fawaz, Sarah; Ho Ho, Kwan; W Campbell, Neill; A Copland, David; L Onions, Karen; J Butler, Matthew; J Wasson, Elizabeth; Crompton, Michael; D Ramnath, Raina; Qiu, Yan; Yamaguchi, Yu; P Arkill, Kenton; O Bates, David; E Turnbull, Jeremy; V Zubkova, Olga; I Welsh, Gavin; Atan, Denize; C Satchell, Simon; R Foster, Rebecca

T cell phenotype in paediatric heart transplant recipients

儿童心脏移植接受者的 T 细胞表型

Konstantinos Mengrelis, Filip Kucera, Nadia Shahid, Eleanor Watt, Susan Ross, Ching-In Lau, Stuart Adams, Kimberly Gilmour, Dietmar Pils, Tessa Crompton, Michael Burch, E Graham Davies

The Epidemiology of Otosclerosis in a British Cohort

英国人群中耳硬化症的流行病学研究

Crompton, Michael; Cadge, Barbara A; Ziff, Joanna L; Mowat, Andrew J; Nash, Robert; Lavy, Jeremy A; Powell, Harry R F; Aldren, Christopher P; Saeed, Shakeel R; Dawson, Sally J

A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.

Nischarin 基因突变通过 LIMK1 和 NF-κB 通路引起中耳炎

Crompton Michael, Purnell Tom, Tyrer Hayley E, Parker Andrew, Ball Greg, Hardisty-Hughes Rachel E, Gale Richard, Williams Debbie, Dean Charlotte H, Simon Michelle M, Mallon Ann-Marie, Wells Sara, Bhutta Mahmood F, Burton Martin J, Tateossian Hilda, Brown Steve D M

Mutations and altered expression of SERPINF1 in patients with familial otosclerosis

家族性耳硬化症患者中SERPINF1的突变和表达改变

Ziff, Joanna L; Crompton, Michael; Powell, Harry R F; Lavy, Jeremy A; Aldren, Christopher P; Steel, Karen P; Saeed, Shakeel R; Dawson, Sally J