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

Oronasal mucosal melanoma is defined by two transcriptional subtypes in humans and dogs with implications for diagnosis and therapy

人类和犬的口鼻黏膜黑色素瘤根据两种转录亚型进行定义,这对诊断和治疗具有重要意义。

Kelly L Bowlt Blacklock ,Kevin Donnelly ,Yuting Lu ,Jorge Del Pozo ,Laura Glendinning ,Gerry Polton ,Laura Selmic ,Jean-Benoit Tanis ,David Killick ,Maciej Parys ,Joanna S Morris ,Inge Breathnach ,Stefano Zago ,Sara M Gould ,Darren J Shaw ,Michael S Tivers ,Davide Malucelli ,Ana Marques ,Katarzyna Purzycka ,Matteo Cantatore ,Marie E Mathers ,Mark Stares ,Alison Meynert ,E Elizabeth Patton

Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules

纤毛病患者的变异揭示了TUBB4B在轴丝微管中的细胞器特异性功能

Daniel O Dodd # ,Sabrina Mechaussier # ,Patricia L Yeyati ,Fraser McPhie ,Jacob R Anderson ,Chen Jing Khoo ,Amelia Shoemark ,Deepesh K Gupta ,Thomas Attard ,Maimoona A Zariwala ,Marie Legendre ,Diana Bracht ,Julia Wallmeier ,Miao Gui ,Mahmoud R Fassad ,David A Parry ,Peter A Tennant ,Alison Meynert ,Gabrielle Wheway ,Lucas Fares-Taie ,Holly A Black ,Rana Mitri-Frangieh ,Catherine Faucon ,Josseline Kaplan ,Mitali Patel ,Lisa McKie ,Roly Megaw ,Christos Gatsogiannis ,Mai A Mohamed ,Stuart Aitken ,Philippe Gautier ,Finn R Reinholt ,Robert A Hirst ,Chris O'Callaghan ,Ketil Heimdal ,Mathieu Bottier ,Estelle Escudier ,Suzanne Crowley ,Maria Descartes ,Ethylin W Jabs ,Priti Kenia ,Jeanne Amiel ,Giacomo Maria Bacci ,Claudia Calogero ,Viviana Palazzo ,Lucia Tiberi ,Ulrike Blümlein ,Andrew Rogers ,Jennifer A Wambach ,Daniel J Wegner ,Anne B Fulton ,Margaret Kenna ,Margaret Rosenfeld ,Ingrid A Holm ,Alan Quigley ,Emma A Hall ,Laura C Murphy ,Diane M Cassidy ,Alex von Kriegsheim ,Laurent Pasquier ,Marlène S Murris ,James D Chalmers ,Claire Hogg ,Kenneth A Macleod ,Don S Urquhart ,Stefan Unger ,Timothy J Aitman ,Serge Amselem ,Margaret W Leigh ,Michael R Knowles ,Heymut Omran ,Hannah M Mitchison ,Alan Brown ,Joseph A Marsh ,Julie P I Welburn ,Shih-Chieh Ti ,Amjad Horani ,Jean-Michel Rozet ,Isabelle Perrault ,Pleasantine Mill

Control of endothelial cell function and arteriogenesis by MEG3:EZH2 epigenetic regulation of integrin expression

MEG3:EZH2 表观遗传调控整合素表达控制内皮细胞功能和动脉生成

Hywel Dunn-Davies, Tatiana Dudnakova, Antonella Nogara, Julie Rodor, Anita C Thomas, Elisa Parish, Philippe Gautier, Alison Meynert, Igor Ulitsky, Paolo Madeddu, Andrea Caporali, Andrew Baker, David Tollervey, Tijana Mitić

Rapid evolution of colistin resistance in a bioreactor model of infection of Klebsiella pneumoniae

肺炎克雷伯菌感染生物反应器模型中粘菌素耐药性的快速演变

Juan-Carlos Jiménez-Castellanos, Bartlomiej Waclaw, Alison Meynert, Sean P McAteer, Thamarai Schneiders

Toll-like receptor 2 orchestrates a tumor suppressor response in non-small cell lung cancer

Toll样受体2在非小细胞肺癌中协调肿瘤抑制反应

Fraser R Millar ,Adam Pennycuick ,Morwenna Muir ,Andrea Quintanilla ,Priya Hari ,Elisabeth Freyer ,Philippe Gautier ,Alison Meynert ,Graeme Grimes ,Carla Salomo Coll ,Sofia Zdral ,Stella Victorelli ,Vitor H Teixeira ,John Connelly ,João F Passos ,Marian A Ros ,William A H Wallace ,Margaret C Frame ,Andrew H Sims ,Luke Boulter ,Sam M Janes ,Simon Wilkinson ,Juan Carlos Acosta

Robust Genetic Analysis of the X-Linked Anophthalmic (Ie) Mouse

连锁无眼畸形 (Ie) 小鼠的稳健遗传分析

Brianda A Hernandez-Moran, Andrew S Papanastasiou, David Parry, Alison Meynert, Philippe Gautier, Graeme Grimes, Ian R Adams, Violeta Trejo-Reveles, Hemant Bengani, Margaret Keighren, Ian J Jackson, David J Adams, David R FitzPatrick, Joe Rainger

ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy

ITPase 缺乏会导致 Martsolf 样综合征,并伴有致命的婴儿扩张型心肌病

Mark T Handley, Kaalak Reddy, Jimi Wills, Elisabeth Rosser, Archith Kamath, Mihail Halachev, Gavin Falkous, Denise Williams, Phillip Cox, Alison Meynert, Eleanor S Raymond, Harris Morrison, Stephen Brown, Emma Allan, Irene Aligianis, Andrew P Jackson, Bernard H Ramsahoye, Alex von Kriegsheim, Robert

Heterochromatin delays CRISPR-Cas9 mutagenesis but does not influence the outcome of mutagenic DNA repair

异染色质延迟 CRISPR-Cas9 诱变,但不影响诱变 DNA 修复的结果

Eirini M Kallimasioti-Pazi, Keerthi Thelakkad Chathoth, Gillian C Taylor, Alison Meynert, Tracy Ballinger, Martijn J E Kelder, Sébastien Lalevée, Ildem Sanli, Robert Feil, Andrew J Wood

Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects

YAP1 杂合功能丧失突变可导致孤立性或综合征性视神经裂隙闭合缺陷

Kathleen A Williamson, Joe Rainger, James A B Floyd, Morad Ansari, Alison Meynert, Kishan V Aldridge, Jacqueline K Rainger, Carl A Anderson, Anthony T Moore, Matthew E Hurles, Angus Clarke, Veronica van Heyningen, Alain Verloes, Martin S Taylor, Andrew O M Wilkie; UK10K Consortium; David R Fitzpatri