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

AgileMultiIdeogram: Rapid Identification and Visualization of Autozygous Regions Using Illumina Short-Read Sequencing Data

AgileMultiIdeogram:利用Illumina短读测序数据快速识别和可视化纯合区域

Watson, Christopher M; Lascelles, Carolina; Raynor, Morag; Elpidorou, Marilena; Hany, Ummey; Crinnion, Laura; Johnson, Colin A; Sheridan, Eamonn; Markham, Alexander F; Poulter, James A; Bonthron, David T; Carr, Ian M

A Single Short 'Tone Burst' Results in Optimal Drug Delivery to Tumours Using Ultrasound-Triggered Therapeutic Microbubbles

利用超声触发的治疗性微泡,单次短促的“脉冲串”可实现向肿瘤的最佳药物递送

Ingram, Nicola; McVeigh, Laura E; Abou-Saleh, Radwa H; Batchelor, Damien V B; Loadman, Paul M; McLaughlan, James R; Markham, Alexander F; Evans, Stephen D; Coletta, P Louise

Ultrasound-triggered therapeutic microbubbles enhance the efficacy of cytotoxic drugs by increasing circulation and tumor drug accumulation and limiting bioavailability and toxicity in normal tissues

超声触发的治疗性微泡通过增加循环和肿瘤药物蓄积,并限制正常组织中的生物利用度和毒性,从而增强细胞毒性药物的疗效。

Ingram, Nicola; McVeigh, Laura E; Abou-Saleh, Radwa H; Maynard, Juliana; Peyman, Sally A; McLaughlan, James R; Fairclough, Michael; Marston, Gemma; Valleley, Elizabeth M A; Jimenez-Macias, Jorge L; Charalambous, Antonia; Townley, William; Haddrick, Malcolm; Wierzbicki, Antonia; Wright, Alexander; Volpato, Milène; Simpson, Peter B; Treanor, Darren E; Thomson, Neil H; Loadman, Paul M; Bushby, Richard J; Johnson, Benjamin R G; Jones, Pamela F; Evans, J Anthony; Freear, Steven; Markham, Alexander F; Evans, Stephen D; Coletta, P Louise

CD105 is a prognostic marker and valid endothelial target for microbubble platforms in cholangiocarcinoma.

CD105 是胆管癌中微泡平台的预后标志物和有效的内皮靶点

Nair Amit, Ingram Nicola, Verghese Eldo T, Wijetunga Imeshi, Markham Alexander F, Wyatt Judy, Prasad K Rajendra, Coletta P Louise

Sub-Nanometer Thick Gold Nanosheets as Highly Efficient Catalysts

亚纳米级厚度的金纳米片作为高效催化剂

Ye, Sunjie; Brown, Andy P; Stammers, Ashley C; Thomson, Neil H; Wen, Jin; Roach, Lucien; Bushby, Richard J; Coletta, Patricia Louise; Critchley, Kevin; Connell, Simon D; Markham, Alexander F; Brydson, Rik; Evans, Stephen D

Characterization and Genomic Localization of a SMAD4 Processed Pseudogene

SMAD4加工假基因的特征分析和基因组定位

Watson, Christopher M; Camm, Nick; Crinnion, Laura A; Antanaviciute, Agne; Adlard, Julian; Markham, Alexander F; Carr, Ian M; Charlton, Ruth; Bonthron, David T

A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain development

α8微管蛋白敲除小鼠模型表明,该基因可能在精子发生中发挥作用,但在大脑发育中则不然。

Diggle, Christine P; Martinez-Garay, Isabel; Molnar, Zoltan; Brinkworth, Martin H; White, Ed; Fowler, Ewan; Hughes, Ruth; Hayward, Bruce E; Carr, Ian M; Watson, Christopher M; Crinnion, Laura; Asipu, Aruna; Woodman, Ben; Coletta, P Louise; Markham, Alexander F; Dear, T Neil; Bonthron, David T; Peckham, Michelle; Morrison, Ewan E; Sheridan, Eamonn

Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy

TSPAN12基因突变导致常染色体显性遗传性家族性渗出性玻璃体视网膜病变

Poulter, James A; Ali, Manir; Gilmour, David F; Rice, Aine; Kondo, Hiroyuki; Hayashi, Kenshi; Mackey, David A; Kearns, Lisa S; Ruddle, Jonathan B; Craig, Jamie E; Pierce, Eric A; Downey, Louise M; Mohamed, Moin D; Markham, Alexander F; Inglehearn, Chris F; Toomes, Carmel

Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy

PDE10A基因的双等位基因突变导致纹状体PDE10A缺失,并引发婴儿期发病的多动症。

Diggle, Christine P; Sukoff Rizzo, Stacey J; Popiolek, Michael; Hinttala, Reetta; Schülke, Jan-Philip; Kurian, Manju A; Carr, Ian M; Markham, Alexander F; Bonthron, David T; Watson, Christopher; Sharif, Saghira Malik; Reinhart, Veronica; James, Larry C; Vanase-Frawley, Michelle A; Charych, Erik; Allen, Melanie; Harms, John; Schmidt, Christopher J; Ng, Joanne; Pysden, Karen; Strick, Christine; Vieira, Päivi; Mankinen, Katariina; Kokkonen, Hannaleena; Kallioinen, Matti; Sormunen, Raija; Rinne, Juha O; Johansson, Jarkko; Alakurtti, Kati; Huilaja, Laura; Hurskainen, Tiina; Tasanen, Kaisa; Anttila, Eija; Marques, Tiago Reis; Howes, Oliver; Politis, Marius; Fahiminiya, Somayyeh; Nguyen, Khanh Q; Majewski, Jacek; Uusimaa, Johanna; Sheridan, Eamonn; Brandon, Nicholas J

Rapid Detection of Rare Deleterious Variants by Next Generation Sequencing with Optional Microarray SNP Genotype Data

利用下一代测序技术结合可选的微阵列SNP基因型数据快速检测罕见有害变异

Watson, Christopher M; Crinnion, Laura A; Gurgel-Gianetti, Juliana; Harrison, Sally M; Daly, Catherine; Antanavicuite, Agne; Lascelles, Carolina; Markham, Alexander F; Pena, Sergio D J; Bonthron, David T; Carr, Ian M