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

Loss of histone macroH2A1.1 causes kidney abnormalities secondary to a change in nutrient metabolization.

组蛋白macroH2A1.1的缺失会导致营养代谢改变,进而引起肾脏异常。

Winkler René, Comas-Armangué Gemma, Corujo David, Sanz-Moreno Adrián, Calzada-Wack Julia, Bhattacharya Shubhra Ashish, Rathkolb Birgit, Dragano Nathalia Romanelli Vicente, Qiao Colina X, Chiodi Valentina, Filipescu Dan, Park Dylan H, Domenici Maria Rosaria, Kirigin Callaú Valentina, Gerlini Raffaele, Rozman Jan, Klein-Rodewald Tanja, Aguilar-Pimentel Antonio, Becker Lore, Seisenberger Claudia, Marschall Susan, Fuchs Helmut, Gailus-Durner Valérie, Bernstein Emily, Vinciguerra Manlio, Oberdoerffer Philipp, Hrabě de Angelis Martin, Teperino Raffaele, Buschbeck Marcus

Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita.

小鼠中 Ten1 的缺失会导致端粒缩短,并模拟人类先天性角化不良症

Sanz-Moreno Adrián, Becker Lore, Xie Kan, da Silva-Buttkus Patricia, Dragano Nathalia R V, Aguilar-Pimentel Antonio, Amarie Oana V, Calzada-Wack Julia, Kraiger Markus, Leuchtenberger Stefanie, Seisenberger Claudia, Marschall Susan, Rathkolb Birgit, Scifo Enzo, Liu Ting, Thanabalasingam Anoja, Sanchez-Vazquez Raul, Martinez Paula, Blasco Maria A, Savage Sharon A, Fuchs Helmut, Ehninger Dan, Gailus-Durner Valérie, de Angelis Martin Hrabê

Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

转录因子 FOXD2 功能障碍与肾脏和泌尿道综合征性先天性异常 (CAKUT) 的关系

Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, Julia Calzada-Wack, Yong Li, Nurit Assia Batzir, Seha Saygılı, Vera Wimmers, Gwang-Jin Kim, Marialena Chrysanthou, Zeineb Bakey, Efrat Sofrin-Drucker, Markus Kraiger, Adrián Sanz-Moreno, Oana V Amarie, Birgit Rathkolb, Tanja Klein-Rodewald, L

X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes

X染色体连锁缺失Crossfirre、Firre和Dxz4基因在体内揭示了多种表型以及对常染色体的组合效应

Tim P Hasenbein # ,Sarah Hoelzl # ,Zachary D Smith ,Chiara Gerhardinger ,Marion O C Gonner ,Antonio Aguilar-Pimentel ,Oana V Amarie ,Lore Becker ,Julia Calzada-Wack ,Nathalia R V Dragano ,Patricia da Silva-Buttkus ,Lillian Garrett ,Sabine M Hölter ,Markus Kraiger ,Manuela A Östereicher ,Birgit Rathkolb ,Adrián Sanz-Moreno ,Nadine Spielmann ,Wolfgang Wurst ,Valerie Gailus-Durner ,Helmut Fuchs ,Martin Hrabě de Angelis ,Alexander Meissner ,Stefan Engelhardt ,John L Rinn ,Daniel Andergassen

Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria

从甲基丙二酸尿症小鼠模型了解能量平衡失调

Marie Lucienne, Raffaele Gerlini, Birgit Rathkolb, Julia Calzada-Wack, Patrick Forny, Stephan Wueest, Andres Kaech, Florian Traversi, Merima Forny, Céline Bürer, Antonio Aguilar-Pimentel, Martin Irmler, Johannes Beckers, Sven Sauer, Stefan Kölker, Joseph P Dewulf, Guido T Bommer, Daniel Hoces, Valer

Knockout mouse models as a resource for the study of rare diseases

基因敲除小鼠模型作为罕见病研究的资源

da Silva-Buttkus, Patricia; Spielmann, Nadine; Klein-Rodewald, Tanja; Schütt, Christine; Aguilar-Pimentel, Antonio; Amarie, Oana V; Becker, Lore; Calzada-Wack, Julia; Garrett, Lillian; Gerlini, Raffaele; Kraiger, Markus; Leuchtenberger, Stefanie; Östereicher, Manuela A; Rathkolb, Birgit; Sanz-Moreno, Adrián; Stöger, Claudia; Hölter, Sabine M; Seisenberger, Claudia; Marschall, Susan; Fuchs, Helmut; Gailus-Durner, Valerie; Hrabě de Angelis, Martin

Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

FOXD2 功能障碍与肾脏和泌尿道综合征性先天性异常 (CAKUT) 的关系

Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, Julia Calzada-Wack, Yong Li, Seha Saygılı, Vera Wimmers, Gwang-Jin Kim, Marialena Chrysanthou, Zeineb Bakey, Markus Kraiger, Adrián Sanz-Moreno, Oana V Amarie, Birgit Rathkolb, Tanja Klein-Rodewald, Lillian Garrett, Sabine M Hölter, Claudia S

GPR101 loss promotes insulin resistance and diet-induced obesity risk.

GPR101 缺失会促进胰岛素抵抗和饮食诱导的肥胖风险

Garrett Lillian, Irmler Martin, Baljuls Angela, Rathkolb Birgit, Dragano Nathalia, Gerlini Raffaele, Sanz-Moreno Adrián, Aguilar-Pimentel Antonio, Becker Lore, Kraiger Markus, Reithmeir Rosa, Beckers Johannes, Calzada-Wack Julia, Wurst Wolfgang, Fuchs Helmut, Gailus-Durner Valerie, Zimmermann Tina, Hölter Sabine M, de Angelis Martin Hrabě

Mass spectrometry-based draft of the mouse proteome

基于质谱的小鼠蛋白质组草图

Piero Giansanti #, Patroklos Samaras #, Yangyang Bian #, Chen Meng, Andrea Coluccio, Martin Frejno, Hannah Jakubowsky, Sophie Dobiasch, Rashmi R Hazarika, Julia Rechenberger, Julia Calzada-Wack, Johannes Krumm, Sebastian Mueller, Chien-Yun Lee, Nicole Wimberger, Ludwig Lautenbacher, Zonera Hassan, Y

Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice

深度表型分析和生命轨迹揭示了长寿调节剂对 C57BL/6J 小鼠衰老过程的影响有限

Kan Xie, Helmut Fuchs, Enzo Scifo, Dan Liu, Ahmad Aziz, Juan Antonio Aguilar-Pimentel, Oana Veronica Amarie, Lore Becker, Patricia da Silva-Buttkus, Julia Calzada-Wack, Yi-Li Cho, Yushuang Deng, A Cole Edwards, Lillian Garrett, Christina Georgopoulou, Raffaele Gerlini, Sabine M Hölter, Tanja Klein-R