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

Mutational scanning reveals oncogenic CTNNB1 mutations have diverse effects on signaling

突变扫描揭示致癌性CTNNB1突变对信号传导具有多种影响

Krishna, Anagha; Meynert, Alison; Dolt, Karamjit Singh; Kelder, Martijn; Mesropian, Agavni; Ewing, Ailith; Brouwers, Conny; Claassens, Jill Wc; Linssen, Margot M; Sheraz, Shahida; Taylor, Gillian Ca; Gautier, Philippe; Ferrer-Vaquer, Anna; Grimes, Graeme; Becher, Hannes; Silk, Ryan; Gris-Oliver, Albert; Pinyol, Roser; Semple, Colin A; Kendall, Timothy J; Bird, Thomas Graham; Hadjantonakis, Anna-Katerina; Marsh, Joseph A; Llovet, Josep M; Hohenstein, Peter; Wood, Andrew J; Ozdemir, Derya D

A high-fidelity microfluidic platform reveals retrograde propagation as the main mechanism of α-Synuclein spread in human neurons.

高保真微流控平台揭示了逆行传播是α-突触核蛋白在人类神经元中扩散的主要机制

Vroman Rozan, de Lichtervelde Lorenzo, Singh Dolt Karamjit, Robertson Graham, Kriek Marco, Barbato Michela, Cholewa-Waclaw Justyna, Kunath Tilo, Downey Patrick, Zagnoni Michele

Glycine-to-aspartic acid mutation at codon 51 in Snca disrupts the synaptic localisation of α-synuclein and enhances its propensity for synucleinopathy.

Snca 基因第 51 位密码子上的甘氨酸突变为天冬氨酸,破坏了 α-突触核蛋白的突触定位,并增强了其发生突触核蛋白病的倾向

West Stephen, Natalwala Ammar, Singh Dolt Karamjit, Lamont Douglas J, McMillan Melanie, Luk Kelvin, Mashimo Tomoji, Kunath Tilo

Diagnostic Reassessment of a Historical Case of Atypical Heparin-Induced Thrombocytopenia: Between Spontaneous Heparin-Induced Thrombocytopenia and a Vaccine-Induced Immune Thrombotic Thrombocytopenia-Like Syndrome

对一例非典型肝素诱导血小板减少症历史病例的诊断再评估:介于自发性肝素诱导血小板减少症和疫苗诱导的免疫性血栓性血小板减少症样综合征之间

Wimmer, Jordan; Kirscher, Solène; Dolt, Manon; Herb, Agathe; Pierre, Léa; Grunebaum, Lélia; Feugeas, Olivier; Sattler, Laurent; Desprez, Dominique

Redundancy of p75NTR neurotrophin receptor function in development, growth and fertility in the rat

p75NTR 神经营养因子受体功能冗余在大鼠发育、生长和生育中的作用

Stephen Meek, Karamjit Singh-Dolt, Linda Sutherland, Matthew G F Sharp, Jorge Del-Pozo, David Walker, Tom Burdon

In vivo18F-DOPA PET imaging identifies a dopaminergic deficit in a rat model with a G51D α-synuclein mutation

体内18F-DOPA PET 成像可识别 G51D α-突触核蛋白突变大鼠模型中的多巴胺能缺陷

Victoria Morley, Karamjit Singh Dolt, Carlos J Alcaide-Corral, Tashfeen Walton, Christophe Lucatelli, Tomoji Mashimo, Adriana A S Tavares, Tilo Kunath

Midbrain organoids with an SNCA gene triplication model key features of synucleinopathy

具有SNCA基因三倍体模型的脑类器官是突触核蛋白病的关键特征

Nguyen-Vi Mohamed,Julien Sirois,Janani Ramamurthy,Meghna Mathur,Paula Lépine,Eric Deneault,Gilles Maussion,Michael Nicouleau,Carol X-Q Chen,Narges Abdian,Vincent Soubannier,Eddie Cai,Harris Nami,Rhalena A Thomas,Dingke Wen,Mahdieh Tabatabaei,Lenore K Beitel,Karamjit Singh Dolt,Jason Karamchandani,Jo Anne Stratton,Tilo Kunath,Edward A Fon,Thomas M Durcan

Alpha synuclein aggregation drives ferroptosis: an interplay of iron, calcium and lipid peroxidation

α-突触核蛋白聚集驱动铁死亡:铁、钙和脂质过氧化的相互作用

Plamena R Angelova #,Minee L Choi #,Alexey V Berezhnov ,Mathew H Horrocks ,Craig D Hughes,Suman De ,Margarida Rodrigues ,Ratsuda Yapom,Daniel Little ,Karamjit S Dolt,Tilo Kunath,Michael J Devine,Paul Gissen ,Mikhail S Shchepinov,Sergiy Sylantyev,Evgeny V Pavlov,David Klenerman ,Andrey Y Abramov ,Sonia Gandhi

α-Synuclein-Confocal Nanoscanning (ASYN-CONA), a Bead-Based Assay for Detecting Early-Stage α-Synuclein Aggregation

α-突触核蛋白共聚焦纳米扫描 (ASYN-CONA),一种基于珠子的检测早期 α-突触核蛋白聚集的检测方法

Irene Pérez-Pi, David A Evans, Mathew H Horrocks, Nhan T Pham, Karamjit S Dolt, Joanna Koszela, Tilo Kunath, Manfred Auer

Engineering synucleinopathy-resistant human dopaminergic neurons by CRISPR-mediated deletion of the SNCA gene

通过 CRISPR 介导的 SNCA 基因删除来设计抗突触核蛋白病的人类多巴胺能神经元

Yixi Chen, Karamjit Singh Dolt, Marco Kriek, Terry Baker, Patrick Downey, Nicola J Drummond, Maurice A Canham, Ammar Natalwala, Susan Rosser, Tilo Kunath