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

Molecular basis of CXC chemokine receptor 3 ligand multispecificity

CXC趋化因子受体3配体多特异性的分子基础

Bouyssou, Alexandre; Sun, Dawei; Zhou, Tricia; Smith, Shannon; Ho, Hoangdung; Johnson, Matthew; Azumaya, Caleigh; Noreng, Sigrid; Liu, Peter; Ti, Shu; Joshi, Prajakta; Tam, Christine; Yang, Ying; Janezic, Eric; Comps-Agrar, Laëtitia; Masureel, Matthieu

Methane by the Numbers: The Need for Clear and Comparable Methane Intensity Metrics

甲烷数据解读:亟需清晰且可比较的甲烷强度指标

Johnson, Matthew R; Conrad, Bradley M; Zimmerle, Daniel J; Kleinberg, Robert L

Loss of function variants in the primate-specific gene ZNF808 cause neonatal, transient and adult-onset diabetes

灵长类特异性基因 ZNF808 的功能缺失变异会导致新生儿糖尿病、暂时性糖尿病和成人发病型糖尿病。

Russ-Silsby, James; Colclough, Kevin; Johnson, Matthew B; Wakeling, Matthew N; Owens, Nick D L; Amaratunga, Shenali A; Flanagan, Sarah E; Patel, Kashyap A; Hattersley, Andrew T; De Franco, Elisa

Psilocybin or Nicotine Patch for Smoking Cessation: A Pilot Randomized Clinical Trial

用于戒烟的裸盖菇素或尼古丁贴片:一项初步随机临床试验

Johnson, Matthew W; Naudé, Gideon P; Hendricks, Peter S; Garcia-Romeu, Albert

Longitudinal changes in haemoglobin, iron stores, and inflammatory markers following surgery and in critical illness: an analysis from the Practical Anaemia Bundle for Sustained Blood Recovery randomised clinical trial

手术和危重疾病后血红蛋白、铁储备和炎症标志物的纵向变化:来自持续血液恢复实用贫血治疗方案随机临床试验的分析

Warner, Matthew A; Hanson, Andrew C; Johnson, Matthew L; Go, Ronald S; Gajic, Ognjen; Schulte, Phillip J; Kor, Daryl J; Serra, Marion; Kalfa, Theodosia A; Blanc, Lionel

Bi-allelic variants in the non-protein-coding minor spliceosome components RNU6ATAC and RNU4ATAC cause syndromic monogenic autoimmune diabetes

非蛋白质编码的次要剪接体组分 RNU6ATAC 和 RNU4ATAC 的双等位基因变异会导致综合征型单基因自身免疫性糖尿病

Johnson, Matthew B; Russ-Silsby, James; Blair, Paul A; Govier, Molly; Bonfield, Georgia; Domingo-Vila, Clara; Wakeling, Matthew N; Oram, Richard A; Flanagan, Sarah E; Tree, Timothy I M; Patel, Kashyap A; Hattersley, Andrew T; De Franco, Elisa

Biallelic Pathogenic Variants in IL2RA Cause Neonatal-Onset Monogenic Autoimmune Diabetes

IL2RA基因的双等位致病变异导致新生儿期发病的单基因自身免疫性糖尿病

Bonfield, Georgia; Russ-Silsby, James; Ramchand, Suraj; Luckett, Amber M; Wakeling, Matthew N; Kulkarni, Abhishek; Nagesh, V Sri; Deeb, Asma; Ravikumar, K G; Nguyen, Phuong T K; Hattersley, Andrew T; Oram, Richard A; Flanagan, Sarah E; De Franco, Elisa; Johnson, Matthew B

The versatile world of cumulene chemistry

累烯化学的多元世界

Pareek, Abhishek; Qiu, Yu; Johnson, Matthew A; Tykwinski, Rik R; Gaweł, Przemysław

Adenine base editor for knockout of proteins: A practical guide from design to analysis with updated MultiEditRbatch

用于蛋白质敲除的腺嘌呤碱基编辑器:从设计到分析的实用指南(含更新版 MultiEditRbatch)

Eaton, Ella J; Wick, Bryce J; Chacón, Jeremy S; Wang, Amy J; Kluesner, Mitchell; Barnes, Jackson T; Kar, Bibekananda; Wang, Minjing; Johnson, Matthew J; Skeate, Joseph G; Webber, Beau R; Moriarity, Branden S

Unconventional Lysine-Type Lipid Assemblies Enable Efficient Antisense Oligonucleotide Delivery with Distinct Structural Features

非常规赖氨酸型脂质组装体具有独特的结构特征,可实现高效的反义寡核苷酸递送。

He, Jieyan; Shatz-Binder, Whitney; Robles, Alexandra; Zang, Nanzhi; Jia, Wei; Sahai, Sakura; Johnson, Matthew C; Li, Jing; Yen, Chun-Wan; Takeoka, Shinji