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

Winter Temperature Affects Fatty Acid Composition and Gene Expression, but Not Fat Content and Survival in a Northern Population of a Range-Expanding Spider

冬季气温影响脂肪酸组成和基因表达，但不影响北方一种正在扩张分布范围的蜘蛛种群的脂肪含量和存活率。

期刊:Ecology and Evolution
影响因子:2.3
doi:10.1002/ece3.72507
Ortiz-Movliav, Carolina; Wolz, Marina; Klockmann, Michael; Kuss, Andreas Walter; Jensen, Lars Riff; Jensen, Corinna; Wacker, Alexander; Uhl, Gabriele B
代谢
发表日期：2025
文献求助 收藏

The C-Mannosylome of Human Induced Pluripotent Stem Cells Implies a Role for ADAMTS16 C-Mannosylation in Eye Development

人类诱导性多能干细胞的 C-甘露糖基化暗示 ADAMTS16 C-甘露糖基化在眼部发育中发挥作用

期刊:Molecular & Cellular Proteomics
影响因子:6.1
doi:10.1016/j.mcpro.2021.100092
Karsten Cirksena, Hermann J Hütte, Aleksandra Shcherbakova, Thomas Thumberger, Roman Sakson, Stefan Weiss, Lars Riff Jensen, Alina Friedrich, Daniel Todt, Andreas W Kuss, Thomas Ruppert, Joachim Wittbrodt, Hans Bakker, Falk F R Buettner
发育与干细胞
干细胞
发表日期：2021
文献求助 收藏

Identification of RELN variant p.(Ser2486Gly) in an Iranian family with ankylosing spondylitis; the first association of RELN and AS

在伊朗一个强直性脊柱炎家族中鉴定出RELN基因变异p.(Ser2486Gly)；这是RELN基因与强直性脊柱炎的首次关联。

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-020-0573-4
Garshasbi, Masoud; Mahmoudi, Mahdi; Razmara, Ehsan; Vojdanian, Mahdi; Aslani, Saeed; Farhadi, Elham; Jensen, Lars Riff; Arzaghi, Seyed Masoud; Poursani, Shiva; Bitaraf, Amirreza; Eidi, Milad; Gharehdaghi, Elika Esmaeilzadeh; Kuss, Andreas Walter; Jamshidi, Ahmadreza
强直性脊柱炎
免疫/内分泌
发表日期：2020
文献求助 收藏

A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation

离子型谷氨酸受体 6 基因 (GRIK2) 缺陷与常染色体隐性智力障碍有关

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1086/521275
Mohammad Mahdi Motazacker, Benjamin Rainer Rost, Tim Hucho, Masoud Garshasbi, Kimia Kahrizi, Reinhard Ullmann, Seyedeh Sedigheh Abedini, Sahar Esmaeeli Nieh, Saeid Hosseini Amini, Chandan Goswami, Andreas Tzschach, Lars Riff Jensen, Dietmar Schmitz, Hans Hilger Ropers, Hossein Najmabadi, Andreas Wal
信号转导
发表日期：2007
文献求助 收藏

Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation

JARID1C 基因突变与转录调控和染色质重塑有关，会导致 X 连锁智力障碍

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1086/427563
Lars Riff Jensen, Marion Amende, Ulf Gurok, Bettina Moser, Verena Gimmel, Andreas Tzschach, Andreas R Janecke, Gholamali Tariverdian, Jamel Chelly, Jean-Pierre Fryns, Hilde Van Esch, Tjitske Kleefstra, Ben Hamel, Claude Moraine, Jozef Gecz, Gillian Turner, Richard Reinhardt, Vera M Kalscheuer, Hans-
信号转导
发表日期：2005
文献求助 收藏

Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males

MECP2区域的重复是男性严重智力低下和进行性神经系统症状的常见原因。

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1086/444549
Van Esch, Hilde; Bauters, Marijke; Ignatius, Jaakko; Jansen, Mieke; Raynaud, Martine; Hollanders, Karen; Lugtenberg, Dorien; Bienvenu, Thierry; Jensen, Lars Riff; Gecz, Jozef; Moraine, Claude; Marynen, Peter; Fryns, Jean-Pierre; Froyen, Guy
MECP2
发表日期：2005
文献求助 收藏