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

Human genomic DNA is widely interspersed with i-motif structures

人类基因组DNA中广泛散布着i-基序结构。

Cristian David Peña Martinez ,Mahdi Zeraati ,Romain Rouet ,Ohan Mazigi ,Jake Y Henry ,Brian Gloss ,Jessica A Kretzmann ,Cameron W Evans ,Emanuela Ruggiero ,Irene Zanin ,Maja Marušič ,Janez Plavec ,Sara N Richter ,Tracy M Bryan ,Nicole M Smith ,Marcel E Dinger ,Sarah Kummerfeld ,Daniel Christ

Protocol for the production and purification of an i-Motif-specific nanobody

i-Motif 特异性纳米抗体的生产和纯化方案

Mahdi Zeraati, Samuel E Ross, Behnaz Aghaei, Alvaro González Rajal, Cecile King, Marcel E Dinger

Different types of disease-causing noncoding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disability

连锁智力障碍家族中基因组和基因表达分析揭示的不同类型的致病非编码变异

Michael J Field, Raman Kumar, Anna Hackett, Sayaka Kayumi, Cheryl A Shoubridge, Lisa J Ewans, Atma M Ivancevic, Tracy Dudding-Byth, Renée Carroll, Thessa Kroes, Alison E Gardner, Patricia Sullivan, Thuong T Ha, Charles E Schwartz, Mark J Cowley, Marcel E Dinger, Elizabeth E Palmer, Louise Christie, 

Denisovan, modern human and mouse TNFAIP3 alleles tune A20 phosphorylation and immunity

丹尼索瓦人、现代人类和小鼠 TNFAIP3 等位基因调节 A20 磷酸化和免疫力

Nathan W Zammit #, Owen M Siggs #, Paul E Gray, Keisuke Horikawa, David B Langley, Stacey N Walters, Stephen R Daley, Claudia Loetsch, Joanna Warren, Jin Yan Yap, Daniele Cultrone, Amanda Russell, Elisabeth K Malle, Jeanette E Villanueva, Mark J Cowley, Velimir Gayevskiy, Marcel E Dinger, Robert Bri

Mouse Model of Mutated in Colorectal Cancer Gene Deletion Reveals Novel Pathways in Inflammation and Cancer

结直肠癌基因缺失突变小鼠模型揭示炎症和癌症的新途径

Nicola Currey, Zeenat Jahan, C Elizabeth Caldon, Phuong N Tran, Fahad Benthani, Penelope De Lacavalerie, Daniel L Roden, Brian S Gloss, Claudia Campos, Elaine G Bean, Amanda Bullman, Saskia Reibe-Pal, Marcel E Dinger, Mark A Febbraio, Stephen J Clarke, Jane E Dahlstrom, Maija R J Kohonen-Corish

A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures

轻微的PUM1基因突变与成人发病型共济失调有关,而单倍体不足则会导致发育迟缓和癫痫发作。

Vincenzo A Gennarino ,Elizabeth E Palmer ,Laura M McDonell ,Li Wang ,Carolyn J Adamski ,Amanda Koire ,Lauren See ,Chun-An Chen ,Christian P Schaaf ,Jill A Rosenfeld ,Jessica A Panzer ,Ute Moog ,Shuang Hao ,Ann Bye ,Edwin P Kirk ,Pawel Stankiewicz ,Amy M Breman ,Arran McBride ,Tejaswi Kandula ,Holly A Dubbs ,Rebecca Macintosh ,Michael Cardamone ,Ying Zhu ,Kevin Ying ,Kerith-Rae Dias ,Megan T Cho ,Lindsay B Henderson ,Berivan Baskin ,Paula Morris ,Jiang Tao ,Mark J Cowley ,Marcel E Dinger ,Tony Roscioli ,Oana Caluseriu ,Oksana Suchowersky ,Rani K Sachdev ,Olivier Lichtarge ,Jianrong Tang ,Kym M Boycott ,J Lloyd Holder Jr ,Huda Y Zoghbi

Expanding the spectrum of PEX16 mutations and novel insights into disease mechanisms

扩大 PEX16 突变范围并深入了解疾病机制

Kishore R Kumar, Gautam Wali, Ryan L Davis, Amali C Mallawaarachchi, Elizabeth E Palmer, Velimir Gayevskiy, Andre E Minoche, David Veivers, Marcel E Dinger, Alan Mackay-Sim, Mark J Cowley, Carolyn M Sue

CCR6 Defines Memory B Cell Precursors in Mouse and Human Germinal Centers, Revealing Light-Zone Location and Predominant Low Antigen Affinity

CCR6 定义小鼠和人类生发中心中的记忆 B 细胞前体,揭示亮区位置和主要的低抗原亲和力

Dan Suan, Nike J Kräutler, Jesper L V Maag, Danyal Butt, Katherine Bourne, Jana R Hermes, Danielle T Avery, Clara Young, Aaron Statham, Michael Elliott, Marcel E Dinger, Antony Basten, Stuart G Tangye, Robert Brink

The long non-coding RNA NEAT1 is responsive to neuronal activity and is associated with hyperexcitability states

长链非编码RNA NEAT1对神经元活动有反应,并与过度兴奋状态相关。

Guy Barry,James A Briggs,Do Won Hwang,Sam P Nayler,Patrick R J Fortuna,Nicky Jonkhout,Fabien Dachet,Jesper L V Maag,Pieter Mestdagh,Erin M Singh,Lotta Avesson,Dominik C Kaczorowski,Ezgi Ozturk,Nigel C Jones,Irina Vetter,Luis Arriola-Martinez,Jianfei Hu,Gloria R Franco,Victoria M Warn,Andrew Gong,Marcel E Dinger,Frank Rigo,Leonard Lipovich,Margaret J Morris,Terence J O'Brien,Dong Soo Lee,Jeffrey A Loeb,Seth Blackshaw,John S Mattick,Ernst J Wolvetang

RNA-seq reveals more consistent reference genes for gene expression studies in human non-melanoma skin cancers

RNA 测序揭示了更一致的参考基因,可用于研究人类非黑色素瘤皮肤癌的基因表达

Van L T Hoang #, Lisa N Tom #, Xiu-Cheng Quek #, Jean-Marie Tan, Elizabeth J Payne, Lynlee L Lin, Sudipta Sinnya, Anthony P Raphael, Duncan Lambie, Ian H Frazer, Marcel E Dinger, H Peter Soyer, Tarl W Prow