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

Fractal Dimension of High-Risk Neuroblastoma Vascularity in MRI Is Associated with Chemotherapy Response and Event-Free Survival

MRI中高危神经母细胞瘤血管分布的分形维数与化疗反应和无事件生存期相关

Michallek, Florian; Dewey, Marc; Hero, Barbara; Hauptmann, Kathrin; Veldhoen, Simon; Paulsen, Verena; Astrahantseff, Kathy; Deubzer, Hedwig E; Simon, Thorsten; Eggert, Angelika; Thole-Kliesch, Theresa M

YAP1 Enhances Mesenchymal-Type Gene Expression in Human Adrenergic-Type Neuroblastoma Cells

YAP1增强人肾上腺素能型神经母细胞瘤细胞中间充质型基因的表达

Ludwig, Marius; Ahrens, Kerstin; Winkler, Annika; Wünschel, Jasmin; Ruka, Peris; Lodrini, Marco; Hertwig, Falk; Castelli, Sveva; Thole-Kliesch, Theresa M; Hollander, Jan F; Fuchs, Steffen; Künkele, Annette; Jens, Marvin; Mamlouk, Soulafa; Warmann, Steven W; Astrahantseff, Kathy; Eggert, Angelika; Schulte, Johannes H; Szymansky, Annabell; Deubzer, Hedwig E

Normozoospermic men in infertile couples: Potential benefit of early medical diagnostic procedures

精子数量正常的男性在不育夫妇中:早期医学诊断程序的潜在益处

Bier, Simone; Wolff, Anton; Zitzmann, Michael; Kliesch, Sabine

Fertility Preservation for Patients with Malignant Disease. Guideline of the DGGG, OEGGG and SGGG (S2k-Level, AWMF Registry No. 015/082, May 2025)

恶性肿瘤患者的生育力保存。DGGG、OEGGG 和 SGGG 指南(S2k 级别,AWMF 注册号 015/082,2025 年 5 月)

Lotz, Laura; Kliesch, Sabine; Baston-Buest, Dunja; Schüring, Andreas; Balcerek, Magdalena; Bartsch, Brigitta; Baumann, René; Beckmann, Matthias; Behringer, Karolin; Borgmann-Staudt, Anja; Böttcher, Bettina; Corradini, Stefanie; Cremer, Wolfgang; Dinkel, Andreas; Diesch-Furlanetto, Tamara; Frenz, Stefanie; Germeyer, Ariane; Goeckenjan, Maren; Hepp, Vera; Hetzer, Franc; Jarisch, Andrea; Kentenich, Heribert; Knuth, Ulrich A; Korell, Matthias; Köhn, Frank-Michael; Bender-Liebenthron, Jana; Lindel, Katja; Leszinski, Gloria Sarah; Lux, Michael; Meißner, Julia; Micke, Oliver; Müller, Alexander; Nawroth, Frank; Nordhoff, Verena; Oppelt, Patricia; Reisch, Nicole; Reiser, Elisabeth; Reschke, Felix; Rink, Andreas; Sahi, Alexander; Sänger, Nicole; Soave, Armin; Roxana, Schwab; Sigg, Christian; Sikora, Meike; Tauchert, Sascha; Thorn, Petra; Weberschock, Tobias; Wimberger, Pauline; Wischmann, Tewes; Würstlein, Rachel; von Wolff, Michael; Dittrich, Ralf

NXT2 is a key component of the RNA nuclear export factor complex in the human testis and essential for spermatogenesis

NXT2是人类睾丸中RNA核输出因子复合物的关键组成部分,对精子发生至关重要。

Ann-Kristin Dicke,Ammar Ahmedani,Lin Ma,Leonie Herrmann,Godfried W van der Heijden,Sophie A Koser,Claudia Krallmann,Oguzhan Kalyon,Miguel J Xavier,Joris A Veltman,Sabine Kliesch,Nina Neuhaus,Noora Kotaja,Frank Tüttelmann #,Birgit Stallmeyer #

Functional and clinical insights into nuclear receptor variants for advancing precision diagnostics in male infertility.

核受体变异体的功能和临床见解,以推进男性不育症的精准诊断

Gaikwad Avinash S, Wyrwoll Margot J, Koser Sophie A, Emich Jana, Kuß Johanna, Aravina Mariya, Krallmann Claudia, Gromoll Jörg, Kliesch Sabine, Laurentino Sandra, Stallmeyer Birgit, Friedrich Corinna, Tüttelmann Frank

Genotype-specific differences in infertile men due to loss-of-function variants in M1AP or ZZS genes

由于M1AP或ZZS基因功能缺失变异导致的男性不育存在基因型特异性差异

Nadja Rotte ,Jessica E M Dunleavy ,Michelle D Runkel ,Lina Bosse ,Daniela Fietz ,Adrian Pilatz ,Johanna Kuss ,Ann-Kristin Dicke ,Sofia B Winge ,Sara Di Persio ,Christian Ruckert ,Verena Nordhoff ,Hans-Christian Schuppe ,Kristian Almstrup ,Sabine Kliesch ,Nina Neuhaus ,Birgit Stallmeyer ,Moira K O'Bryan ,Frank Tüttelmann ,Corinna Friedrich

Unraveling a Subgroup of Men With Unexplained Male Infertility-Men With Normogonadotropic Nonobstructive Azoospermia

揭示不明原因男性不育症的一个亚群——正常促性腺激素性非梗阻性无精子症患者

Schwarzkopf, Vanessa; Wistuba, Joachim; Sandhowe-Klaverkamp, Reinhild; Kliesch, Sabine; Gromoll, Jörg; Schubert, Maria

Towards a kingdom of reproductive life - the core sperm proteome

迈向生殖生命王国——精子核心蛋白质组

Pini, Taylor; Nixon, Brett; Karr, Timothy L; Teperino, Raffaele; Sanz-Moreno, Adrián; da Silva-Buttkus, Patricia; Tüttelmann, Frank; Kliesch, Sabine; Gailus-Durner, Valérie; Fuchs, Helmut; Marschall, Susan; Hrabě de Angelis, Martin; Skerrett-Byrne, David A

Clinical syndromes linked to biallelic germline variants in MCM8 and MCM9

与MCM8和MCM9基因双等位基因种系变异相关的临床综合征

Helderman, Noah C; Yang, Ting; Palles, Claire; Terlouw, Diantha; Mei, Hailiang; Vorderman, Ruben H P; Cats, Davy; Díaz-Gay, Marcos; Jongmans, Marjolijn C J; Ramdien, Ashwin; van de Beek, Irma; Eleveld, Thomas F; Green, Andrew; Hes, Frederik J; van den Heuvel-Eibrink, Marry M; Van Der Kelen, Annelore; Kliesch, Sabine; Kuiper, Roland P; Lakeman, Inge M M; Lashley, Lisa E E L O; Looijenga, Leendert H J; Oud, Manon S; Steingröver, Johanna; Tenenbaum-Rakover, Yardena; Tops, Carli M; Tüttelmann, Frank; de Voer, Richarda M; Westra, Dineke; Wyrwoll, Margot J; Golubicki, Mariano; Antelo, Marina; Bonjoch, Laia; Terradas, Mariona; Valle, Laura; Alexandrov, Ludmil B; Morreau, Hans; van Wezel, Tom; Castellví-Bel, Sergi; Goldberg, Yael; Nielsen, Maartje