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

Polarization-Dependent Elliptical and Rectangular Mie Voids

偏振相关的椭圆和矩形米氏空洞

Arslan, Serkan; Sulejman, Shaban B; Klein, Sebastian; Haehner, Jonathan; Schwab, Julian; Ludescher, Dominik; Wesemann, Lukas; Roberts, Ann; Giessen, Harald; Hentschel, Mario

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

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

KDM2A基因的新生变异会导致综合征性神经发育障碍。

Anderson Eric N, Drukewitz Stephan, Kour Sukhleen, Chimata Anuradha V, Rajan Deepa S, Schönnagel Senta, Stals Karen L, Donnelly Deirdre, O'Sullivan Siobhan, Mantovani John F, Tan Tiong Y, Stark Zornitza, Zacher Pia, Chatron Nicolas, Monin Pauline, Drunat Severine, Vial Yoann, Latypova Xenia, Levy Jonathan, Verloes Alain, Carter Jennefer N, Bonner Devon E, Shankar Suma P, Bernstein Jonathan A, Cohen Julie S, Comi Anne, Carere Deanna Alexis, Dyer Lisa M, Mullegama Sureni V, Sanchez-Lara Pedro A, Grand Katheryn, Kim Hyung-Goo, Ben-Mahmoud Afif, Gospe Sidney M Jr, Belles Rebecca S, Bellus Gary, Lichtenbelt Klaske D, Oegema Renske, Rauch Anita, Ivanovski Ivan, Mau-Them Frederic Tran, Garde Aurore, Rabin Rachel, Pappas John, Bley Annette E, Bredow Janna, Wagner Timo, Decker Eva, Bergmann Carsten, Domenach Louis, Margot Henri, Lemke Johannes R, Abou Jamra Rami, Hentschel Julia, Mefford Heather, Singh Amit, Pandey Udai Bhan, Platzer Konrad

Sea urchin eggs contain a plastid-derived structure that contributes to their development

海胆卵含有质体衍生的结构,这种结构有助于它们的发育。

Carrier, Tyler J; Rufino-Navarro, Andrés; Knoop, Thorben; Repnik, Urska; Caraballo-Rodríguez, Andrés Mauricio; Needham, David M; Bang, Corinna; Franzenburg, Sören; Bramkamp, Marc; Rath, Willi; Biastoch, Arne; Hernández, José Carlos; Hentschel, Ute

Seed-Mediated Synthesis of NiPt-Alloy-Tipped CdSe/CdS Nanocrystals for Photocatalysis

以种子介导法合成NiPt合金尖端CdSe/CdS纳米晶用于光催化

Dittmar, Mareike; Voß, Julia; Hentschel, Sebastian; Klemeyer, Lars; Koziej, Dorota; Bonatz, Dennis; Ruhmlieb, Charlotte; Kipp, Tobias; Mews, Alf

NOD-like receptor repertoire in the chromosome-level genome of the demosponge Dysidea avara (Schmidt, 1862)

海绵动物 Dysidea avara (Schmidt, 1862) 染色体基因组中的 NOD 样受体库

Koutsouveli, Vasiliki; Torres-Oliva, Montserrat; Marulanda-Gomez, Angela M; Franke, Andre; Fuß, Janina; Schmitz, Ruth A; Hentschel, Ute; Reusch, Thorsten B H; Pita, Lucía

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

Who Am I? Eyebrow Follicles Minimize Donor-Derived DNA for Germline Testing After Hematopoietic Stem Cell Transplantation

我是谁?眉毛毛囊可最大限度减少造血干细胞移植后生殖系检测中供体来源的DNA

Mertens, Matthias; Sadlo, Mona; Kühl, Jörn-Sven; Metzeler, Klaus; Zschenderlein, Louisa; Edelmann, Jeanett; Lehmann, Claudia; Thull, Sarah; Karakaya, Mert; Velmans, Clara; Tumewu, Theresa; Böhme, Matthias; Klötzer, Christina; Weigert, Anne; Vucinic, Vladan; Hentschel, Julia; Mertens, Mareike

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