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

Maternal smoking DNA methylation risk score associated with health outcomes in offspring of European and South Asian ancestry

母亲吸烟与DNA甲基化风险评分相关的欧洲和南亚裔后代健康结果

Deng, Wei Q; Cawte, Nathan; Campbell, Natalie; Azab, Sandi M; de Souza, Russell J; Lamri, Amel; Morrison, Katherine M; Atkinson, Stephanie A; Subbarao, Padmaja; Turvey, Stuart E; Moraes, Theo J; Teo, Koon K; Mandhane, Piush J; Azad, Meghan B; Simons, Elinor; Paré, Guillaume; Anand, Sonia S

Consistent cord blood DNA methylation signatures of gestational age between South Asian and white European cohorts

南亚人群和欧洲白人人群脐带血DNA甲基化特征与孕龄的一致性

Deng, Wei Q; Pigeyre, Marie; Azab, Sandi M; Wilson, Samantha L; Campbell, Natalie; Cawte, Nathan; Morrison, Katherine M; Atkinson, Stephanie A; Subbarao, Padmaja; Turvey, Stuart E; Moraes, Theo J; Mandhane, Piush; Azad, Meghan B; Simons, Elinor; Pare, Guillaume; Anand, Sonia S

Genetic screening for anticancer genes highlights FBLN5 as a synthetic lethal partner of MYC

抗癌基因的基因筛查发现FBLN5是MYC的合成致死伴侣。

Motasim Masood #,Qize Ding #,Adam D Cawte,David S Rueda,Stefan W Grimm,Ernesto Yagüe,Mona El-Bahrawy

GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia

血液线粒体DNA拷贝数的全基因组关联研究(GWAS)和外显子组关联研究(ExWAS)鉴定出71个基因位点,并揭示了其在痴呆症中的潜在因果作用。

Chong, Michael; Mohammadi-Shemirani, Pedrum; Perrot, Nicolas; Nelson, Walter; Morton, Robert; Narula, Sukrit; Lali, Ricky; Khan, Irfan; Khan, Mohammad; Judge, Conor; Machipisa, Tafadzwa; Cawte, Nathan; O'Donnell, Martin; Pigeyre, Marie; Akhabir, Loubna; Paré, Guillaume

Live cell imaging of single RNA molecules with fluorogenic Mango II arrays

利用荧光 Mango II 阵列对单个 RNA 分子进行活细胞成像

Adam D Cawte, Peter J Unrau, David S Rueda

Fluorogenic RNA Mango aptamers for imaging small non-coding RNAs in mammalian cells

荧光 RNA Mango 适体用于对哺乳动物细胞中的小非编码 RNA 进行成像

Alexis Autour, Sunny C Y Jeng, Adam D Cawte, Amir Abdolahzadeh, Angela Galli, Shanker S S Panchapakesan, David Rueda, Michael Ryckelynck, Peter J Unrau

A common mechanism by which type 2A von Willebrand disease mutations enhance ADAMTS13 proteolysis revealed with a von Willebrand factor A2 domain FRET construct

利用冯·维勒布兰德因子 A2 结构域 FRET 构建体揭示 2A 型冯·维勒布兰德病突变增强 ADAMTS13 蛋白水解的常见机制

Christopher J Lynch, Adam D Cawte, Carolyn M Millar, David Rueda, David A Lane

An endemic neurological disorder in tribal Australian aborigines

澳大利亚土著部落的一种地方性神经系统疾病

Kiloh, L G; Lethlean, A K; Morgan, G; Cawte, J E; Harris, M

Still dissolving discs?

还在溶解光盘吗?

Cawte, E C