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

Weight loss with GLP-1 medicines does not result in a disproportionate loss of muscle mass or function in obese mice and humans

使用 GLP-1 药物减轻体重不会导致肥胖小鼠和人类的肌肉质量或功能不成比例地丧失。

Langer, Henning Tim; Gilmore, Natalie K; Hayden, Christopher M T; Roux, Julien; Bariohay, Bruno; Rouquet, Thaïs; Awada, Manar; Marcotorchino, Julie; Bournot, Lorrine; Nunn, Elizabeth; Titchenell, Paul M; Liskiewicz, Daniela; Müller, Timo D; Anyiam, Oluwaseun; Atherton, Philip J; Idris, Iskandar; Hentschel, Andreas; Roos, Andreas; Haritonow, Natalie; Norman, Kristina; Müller-Werdan, Ursula; Baar, Keith

Brachio-cervical inflammatory myopathy: multilevel clinical, histopathological and multi-omic analyses of a syndrome variably associated with systemic sclerosis

臂颈炎症性肌病:对一种与系统性硬化症有不同程度关联的综合征进行多层次的临床、组织病理学和多组学分析

Kleefeld, Felix; Teran Gamboa, Joanna; Pinal-Fernandez, Iago; Preusse, Corinna; Nelke, Christopher; Goebel, Hans-Hilmar; Mensch, Alexander; Mossakowski, Agata; Miah, Mohi-Uddin; Diaz-Manera, Jordi; Torchia, Eleonora; Bortolani, Sara; Hentschel, Andreas; Funke, Andreas; Souvannanorath, Sarah; Authier, François-Jérôme; Malfatti, Edoardo; Gehrig, Johannes; Mammen, Andrew L; Casal-Dominguez, Maria; De Winter, Jonathan; De Ridder, Willem; Ruck, Tobias; Schneider, Udo; Roos, Andreas; Gallardo, Eduard; Tasca, Giorgio; Stenzel, Werner

Proteomic profiles in inclusion body myositis and polymyositis with mitochondrial pathology

包涵体肌炎和伴有线粒体病理的多发性肌炎的蛋白质组学特征

Kleefeld, Felix; Schroeter, Christina B; Abdennebi, Donya; Dobelmann, Vera; Walli, Sara; Roos, Andreas; Distler, Ute; Tenzer, Stefan; Bopp, Tobias; Quint, Paula; Schmitt, Linda-Isabell; Leo, Markus; Hagenacker, Tim; Pinal-Fernandez, Iago; Casal-Dominguez, Maria; Mammen, Andrew L; Preuße, Corinna; Maggi, Lorenzo; Mensch, Alexander; Meuth, Sven G; Stenzel, Werner; Ruck, Tobias; Nelke, Christopher

Mitochondrial energetic failure underlies FLVCR1-related sensory neuropathy.

线粒体能量衰竭是 FLVCR1 相关感觉神经病变的根本原因。

Bertino Francesca, Zanin Venturini Diletta Isabella, Grasso Eleonora, Kopecka Joanna, Salio Chiara, Gnutti Barbara, Basnet Ram Manohar, Bellini Stefania, Mignani Luca, Zhao Boxun, Kleefeld Felix, Hentschel Andreas, Magnani Francesca, Fiorito Veronica, Abalai Raluca Elena, Metani Livia, Allocco Anna Lucia, Petrillo Sara, De Giorgio Francesco, Ammirata Giorgia, Salsano Ettore, Pareyson Davide, di Rocco Maja, Abicht Angela, McCourt Emily, Horvath Rita, Kölbel Heike, Larson Austin, Roos Andreas, Yu Timothy W, Finazzi Dario, Riganti Chiara, Tolosano Emanuela, Chiabrando Deborah

Exploring molecular signatures in PURA syndrome using muscle proteomics and serum biomarkers

利用肌肉蛋白质组学和血清生物标志物探索PURA综合征的分子特征

Mroczek, Magdalena; Preusse, Corinna; Hentschel, Andreas; Chrościńska-Krawczyk, Magdalena; Bielak, Michał; Sobolewska, Adela; Della Marina, Adela; Hila, Anisa; Iyadurai, Stanley; Kraft, Florian; Chetty, Venkatesh Kumar; Muhmann, David; Ruck, Tobias; Goebel, Hans-Hilmar; Schara-Schmidt, Ulrike; Dobelmann, Vera; Thakur, Basant Kumar; Stenzel, Werner; Roos, Andreas

Unveiling FLNC variants: iPSC-derived myogenic cells as a model to study disease mechanisms

揭示FLNC变体:iPSC衍生的成肌细胞作为研究疾病机制的模型

Daya, Nassam M; Schänzer, Anne; Hentschel, Andreas; Kienitz, Marie-Cecile; Sellung, Dominik; Suedkamp, Nicolina; Krause, Karsten; Kinold, Jaqueline C; Volke, Leon; Schreiner, Anja; Schlierbach, Hanna; Nelke, Christopher; Kleefeld, Felix; Guettsches, Anne-Katrin; Zaehres, Holm; Ruck, Tobias; Mavrommatis, Lampros; Roos, Andreas; Vorgerd, Matthias

XUV fluorescence as a probe of interatomic coulombic decay of resonantly excited He nanodroplets

利用极紫外荧光探测共振激发氦纳米液滴的原子间库仑衰变

Sishodia, Keshav; Ltaief, Ltaief Ben; Scheel, Niklas; Földes, István B; Roos, Andreas Hult; Albrecht, Martin; Staněk, Matyáš; Jurkovičová, Lucie; Hort, Ondrej; Nejdl, Jaroslav; García-Alfonso, Ernesto; Halberstadt, Nadine; Andreasson, Jakob; Klimešová, Eva; Krikunova, Maria; Krishnan, Sivarama; Heidenreich, Andreas; Mudrich, Marcel

Myopathy With Exercise-Induced Intolerance due to Novel Biallelic Variants in OBSCN-A Clinical, Morphological and Molecular Analysis

由OBSCN-A基因新型双等位基因变异引起的运动诱发性肌病:临床、形态学和分子分析

Krämer-Best, Heidrun H; Reis, Marlen C; Hentschel, Andreas; Weiß, Michaela; Schaiter, Alexander; Böhm, Klaus-Dieter; Roos, Andreas; Nolte, Dagmar; Schänzer, Anne

The p.(Leu97Ile) variant expands the genetic landscape of NEFL-associated Charcot-Marie-tooth neuropathies

p.(Leu97Ile)变异扩展了NEFL相关夏科-马里-图斯神经病的遗传图谱

Oeztuerk, Menekse; Walli, Sara; Muhmann, David; Choueiri, Catherine; Dobelmann, Vera; Abicht, Angela; Leube, Barbara; Schara-Schmidt, Ulrike; Meuth, Sven G; Horvath, Rita; Lochmueller, Hanns; Roos, Andreas; Ruck, Tobias

Clinical, morphological, and molecular characterization of patients with X-linked myopathy with excessive autophagy (XMEA).

对患有过度自噬的 X 连锁肌病 (XMEA) 的患者进行临床、形态学和分子特征分析。

Merlet Angèle N, Lacène Emmanuelle, Nelson Isabelle, Brochier Guy, Labasse Clémence, Chanut Anais, Madelaine Angeline, Beuvin Maud, Bonne Gisèle, Féasson Léonard, Minot Marie-Christine, Noury Jean-Baptiste, Fradin Mélanie, Savarese Marco, Fernández-Eulate Gorka, Behin Anthony, Stojkovic Tanya, Hentschel Andreas, Marcorelles Pascale, Roos Andreas, Evangelista Teresinha