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

Screening for psychotrauma related symptomatology: Greek adaptation and validation of the Global Psychotrauma Screen

心理创伤相关症状筛查:全球心理创伤筛查的希腊语版改编与验证

Anastassiou-Hadjicharalambous, Xenia; Syros, Ioannis; Charalampidou, Pavlina; Frewen, Paul; Jernslett, Maria; Evgeniou, Eleftheria; Miliaraki, Christina; Papathanasiou, Eleni; Olff, Miranda; Hoeber, Chris

Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy

NCDN基因的单等位基因和双等位基因变异会导致神经发育迟缓、智力障碍和癫痫。

Fatima, Ambrin; Hoeber, Jan; Schuster, Jens; Koshimizu, Eriko; Maya-Gonzalez, Carolina; Keren, Boris; Mignot, Cyril; Akram, Talia; Ali, Zafar; Miyatake, Satoko; Tanigawa, Junpei; Koike, Takayoshi; Kato, Mitsuhiro; Murakami, Yoshiko; Abdullah, Uzma; Ali, Muhammad Akhtar; Fadoul, Rein; Laan, Loora; Castillejo-López, Casimiro; Liik, Maarika; Jin, Zhe; Birnir, Bryndis; Matsumoto, Naomichi; Baig, Shahid M; Klar, Joakim; Dahl, Niklas

ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function

ZEB2单倍体不足的Mowat-Wilson综合征诱导多能干细胞表现出GABA能转录调控和功能紊乱

Schuster, Jens; Klar, Joakim; Khalfallah, Ayda; Laan, Loora; Hoeber, Jan; Fatima, Ambrin; Sequeira, Velin Marita; Jin, Zhe; Korol, Sergiy V; Huss, Mikael; Nordgren, Ann; Anderlid, Britt Marie; Gallant, Caroline; Birnir, Bryndis; Dahl, Niklas

The Royal Canadian Mounted Police (RCMP) Study: protocol for a prospective investigation of mental health risk and resilience factors

加拿大皇家骑警(RCMP)研究:心理健康风险和韧性因素前瞻性调查方案

Carleton, R Nicholas; Krätzig, Gregory P; Sauer-Zavala, Shannon; Neary, J Patrick; Lix, Lisa M; Fletcher, Amber J; Afifi, Tracie O; Brunet, Alain; Martin, Ron; Hamelin, Karen S; Teckchandani, Taylor A; Jamshidi, Laleh; Maguire, Kirby Q; Gerhard, David; McCarron, Michelle; Hoeber, Orland; Jones, Nicholas A; Stewart, Sherry H; Keane, Terence M; Sareen, Jitender; Dobson, Keith; Asmundson, Gordon J G

Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy

NCDN 中的单等位基因和双等位基因变异会导致神经发育迟缓、智力障碍和癫痫

Ambrin Fatima, Jan Hoeber, Jens Schuster, Eriko Koshimizu, Carolina Maya-Gonzalez, Boris Keren, Cyril Mignot, Talia Akram, Zafar Ali, Satoko Miyatake, Junpei Tanigawa, Takayoshi Koike, Mitsuhiro Kato, Yoshiko Murakami, Uzma Abdullah, Muhammad Akhtar Ali, Rein Fadoul, Loora Laan, Casimiro Castillejo-

Site-Dependent Relationships Between Fungal Community Composition, Plant Genotypic Diversity and Environmental Drivers in a Salix Biomass System

柳树生物质系统中真菌群落组成、植物基因型多样性和环境驱动因素之间的地点依赖性关系

Hoeber, Stefanie; Baum, Christel; Weih, Martin; Manzoni, Stefano; Fransson, Petra

LGG-33. ISOMORPHIC DIFFUSE GLIOMA HAS RECURRENT GENE FUSIONS OF MYBL1 OR MYB AND CAN BE DISTINGUISHED FROM OTHER MYB/MYBL1 ALTERED GLIOMAS BASED ON A DISTINCT MORPHOLOGY AND DNA METHYLATION PROFILE

LGG-33。同形弥漫性胶质瘤具有MYBL1或MYB基因的复发性融合,可根据其独特的形态学和DNA甲基化谱与其他MYB/MYBL1改变的胶质瘤相鉴别。

Braune, Katarina; Wäldchen, Mandy; Raile, Klemens; Hahn, Sigrid; Ubben, Tebbe; Römer, Susanne; Hoeber, Daniela; Reibel, Nora Johanna; Launspach, Michael; Blankenstein, Oliver; Bührer, Christoph; Sill, Martin; Sahm, Felix; Schrimpf, Daniel; Capper, David; Pfister, Stefan M; von Deimling, Andreas; Jones, David T W; Fangusaro, Jason; Witt, Olas; Driever, Pablo Hernaiz; Bag, Asim; de Blank, Peter; Kadom, Nadja; Kilburn, Lindsay; Lober, Robert; Robison, Nathan; Fisher, Michael; Packer, Roger; Poussaint, Tina Young; Papusha, Ludmila; Avula, Shivaram; Brandes, Alba; Bouffet, Eric; Bowers, Daniel; Artemov, Anton; Chintagumpala, Murali; Zurakowski, David; van den Bent, Martin; Bison, Brigitte; Yeom, Kristen; Taal, Walter; Warren, Katherine; Masliah-Planchon, Julien; Girard, Elodie; Euskirchen, Philipp; Bourneix, Christine; Lequin, Delphine; Blanluet, Maud; Aillaud, Jean-Baptiste; Doz, Francois; Bourdeaut, Franck; Delattre, Olivier; Djirackor, Luna; Halldorsson, Skarphedinn; Sandberg, Cecilie; Euskirchen, Philipp; Skaga, Erlend; Kulesskiy, Evgeny; Wennerberg, Krister; Langmoen, Iver; Vik-Mo, Einar; Hagel, Christian; Sloman, Veronika; Mynarek, Martin; Petrasch, Katharina; Obrecht, Denise; Deinlein, Frank; Schmid, Renate; von Bueren, André O; Friedrich, Carsten; Juhnke, B Ole; Gerber, Nicolas U; Kwiecien, Robert; Girschick, Hermann; Höller, Alexandra; Zapf, Antonia; von Hoff, Katja; Rutkowski, Stefan; Goto, Hiroaki; Geoerger, Birgit; DuBois, Steven G; Grilley-Olson, Juneko E; van Tilburg, Cornelis M; Schulte, Johannes; Kang, Hyoung Jin; Tahara, Makoto; Boni, Valentina; Perreault, Sebastien; Capra, Michael; Reeves, John A; Brega, Nicoletta; Childs, Barrett H; Laetsch, Theodore W; Ziegler, David S; Doz, François; Ng, Chia Huan; Obrecht, Denise; Buntine, Molly; Wells, Olivia; Campbell, Martin A; Bhatia, Kanika; Sullivan, Michael; Williams, Molly; Quang, Dong Anh Khuong; Kinross, Kathryn; White, Christine; Algar, Elizabeth; Witt, Hendrik; Schuller, Ulrich; Mynarek, Martin; Pietsch, Torsten; Gerber, Nicolas U; Benesch, Martin; Warmuth-Metz, Monika; Kortmann, Rolf; Bison, Brigitte; Taylor, Michael D; Ramaswamy, Vijay; Rutkowski, Stefan; Pfister, Stefan M; Jones, David T W; Gottardo, Nicholas G; Von Hoff, Katja; Pajtler, Kristian W; Hansford, Jordan R; Sturm, Dominik; Sahm, Felix; Andreiuolo, Felipe; Capper, David; Gessi, Marco; Rode, Agata; Bison, Brigitte; Hirsch, Steffen; Gerber, Nicolas U; Gottardo, Nicholas G; Kramm, Christof M; Rutkowski, Stefan; von Deimling, Andreas; Pietsch, Torsten; Pfister, Stefan M; Jones, David T W; Wefers, Annika K; Stichel, Damian; Schrimpf, Daniel; Sahm, Felix; von Deimling, Andreas; Blumcke, Ingmar; Jones, David T W; Capper, David

Empty mesoporous silica particles significantly delay disease progression and extend survival in a mouse model of ALS

空介孔二氧化硅颗粒显著延缓了 ALS 小鼠模型的病情进展并延长了生存期

Marcel F Leyton-Jaimes, Patrik Ivert, Jan Hoeber, Yilin Han, Adam Feiler, Chunfang Zhou, Stanislava Pankratova, Varda Shoshan-Barmatz, Adrian Israelson, Elena N Kozlova

DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors

唐氏综合征衍生的神经 iPSC 中的 DNA 甲基化变化揭示了 ZNF 和 HOX3 转录因子家族的共同失调

Loora Laan, Joakim Klar, Maria Sobol, Jan Hoeber, Mansoureh Shahsavani, Malin Kele, Ambrin Fatima, Muhammad Zakaria, Göran Annerén, Anna Falk, Jens Schuster, Niklas Dahl

A VDAC1-Derived N-Terminal Peptide Inhibits Mutant SOD1-VDAC1 Interactions and Toxicity in the SOD1 Model of ALS

VDAC1衍生的N端肽可抑制SOD1突变体ALS模型中SOD1-VDAC1的相互作用及其毒性。

Shteinfer-Kuzmine, Anna; Argueti, Shirel; Gupta, Rajeev; Shvil, Neta; Abu-Hamad, Salah; Gropper, Yael; Hoeber, Jan; Magrì, Andrea; Messina, Angela; Kozlova, Elena N; Shoshan-Barmatz, Varda; Israelson, Adrian