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

Pre-Pulse Inhibition of an escape response in adult fruit fly, Drosophila melanogaster

成年果蝇(Drosophila melanogaster)逃避反应的预脉冲抑制

Viragh, Erika; Asztalos, Lenke; Fenckova, Michaela; Szlanka, Tamas; Gyorgypal, Zoltan; Kovacs, Karoly; IntHout, Joanna; Cizek, Pavel; Konda, Mihaly; Konda-Szucs, Emanuela; Zvara, Agnes; Biro, Judit; Csapo, Eniko; Lukacsovich, Tamas; Steinbach, Gabor; Hegedus, Zoltan; Puskas, Laszlo; Schenck, Annette; Asztalos, Zoltan

Intellectual disability-associated disruption of O-GlcNAc cycling impairs habituation learning in Drosophila

智力障碍相关的 O-GlcNAc 循环紊乱会损害果蝇的习惯化学习能力

Fenckova, Michaela; Muha, Villo; Mariappa, Daniel; Catinozzi, Marica; Czajewski, Ignacy; Blok, Laura E R; Ferenbach, Andrew T; Storkebaum, Erik; Schenck, Annette; van Aalten, Daan M F

The epigenetic regulator G9a attenuates stress-induced resistance and metabolic transcriptional programs across different stressors and species

表观遗传调控因子G9a能够减弱不同胁迫因子和物种的应激诱导抗性和代谢转录程序。

Riahi, Human; Fenckova, Michaela; Goruk, Kayla J; Schenck, Annette; Kramer, Jamie M

O-GlcNAcase contributes to cognitive function in Drosophila.

O-GlcNAcase 有助于果蝇的认知功能

Muha Villo, Fenckova Michaela, Ferenbach Andrew T, Catinozzi Marica, Eidhof Ilse, Storkebaum Erik, Schenck Annette, van Aalten Daan M F

Habituation Learning Is a Widely Affected Mechanism in Drosophila Models of Intellectual Disability and Autism Spectrum Disorders

习惯化学习是果蝇智力障碍和自闭症谱系障碍模型中普遍受影响的机制

Fenckova, Michaela; Blok, Laura E R; Asztalos, Lenke; Goodman, David P; Cizek, Pavel; Singgih, Euginia L; Glennon, Jeffrey C; IntHout, Joanna; Zweier, Christiane; Eichler, Evan E; von Reyn, Catherine R; Bernier, Raphael A; Asztalos, Zoltan; Schenck, Annette

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

靶向测序鉴定出91个与自闭症和发育障碍相关的神经发育障碍风险基因

Stessman, Holly A F; Xiong, Bo; Coe, Bradley P; Wang, Tianyun; Hoekzema, Kendra; Fenckova, Michaela; Kvarnung, Malin; Gerdts, Jennifer; Trinh, Sandy; Cosemans, Nele; Vives, Laura; Lin, Janice; Turner, Tychele N; Santen, Gijs; Ruivenkamp, Claudia; Kriek, Marjolein; van Haeringen, Arie; Aten, Emmelien; Friend, Kathryn; Liebelt, Jan; Barnett, Christopher; Haan, Eric; Shaw, Marie; Gecz, Jozef; Anderlid, Britt-Marie; Nordgren, Ann; Lindstrand, Anna; Schwartz, Charles; Kooy, R Frank; Vandeweyer, Geert; Helsmoortel, Celine; Romano, Corrado; Alberti, Antonino; Vinci, Mirella; Avola, Emanuela; Giusto, Stefania; Courchesne, Eric; Pramparo, Tiziano; Pierce, Karen; Nalabolu, Srinivasa; Amaral, David G; Scheffer, Ingrid E; Delatycki, Martin B; Lockhart, Paul J; Hormozdiari, Fereydoun; Harich, Benjamin; Castells-Nobau, Anna; Xia, Kun; Peeters, Hilde; Nordenskjöld, Magnus; Schenck, Annette; Bernier, Raphael A; Eichler, Evan E

Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder

组蛋白甲基转移酶EHMT1和KMT2C的功能趋同与智力障碍和自闭症谱系障碍有关

Koemans, Tom S; Kleefstra, Tjitske; Chubak, Melissa C; Stone, Max H; Reijnders, Margot R F; de Munnik, Sonja; Willemsen, Marjolein H; Fenckova, Michaela; Stumpel, Connie T R M; Bok, Levinus A; Sifuentes Saenz, Margarita; Byerly, Kyna A; Baughn, Linda B; Stegmann, Alexander P A; Pfundt, Rolph; Zhou, Huiqing; van Bokhoven, Hans; Schenck, Annette; Kramer, Jamie M

Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders

POGZ功能紊乱与智力障碍和自闭症谱系障碍相关

Stessman, Holly A F; Willemsen, Marjolein H; Fenckova, Michaela; Penn, Osnat; Hoischen, Alexander; Xiong, Bo; Wang, Tianyun; Hoekzema, Kendra; Vives, Laura; Vogel, Ida; Brunner, Han G; van der Burgt, Ineke; Ockeloen, Charlotte W; Schuurs-Hoeijmakers, Janneke H; Klein Wassink-Ruiter, Jolien S; Stumpel, Connie; Stevens, Servi J C; Vles, Hans S; Marcelis, Carlo M; van Bokhoven, Hans; Cantagrel, Vincent; Colleaux, Laurence; Nicouleau, Michael; Lyonnet, Stanislas; Bernier, Raphael A; Gerdts, Jennifer; Coe, Bradley P; Romano, Corrado; Alberti, Antonino; Grillo, Lucia; Scuderi, Carmela; Nordenskjöld, Magnus; Kvarnung, Malin; Guo, Hui; Xia, Kun; Piton, Amélie; Gerard, Bénédicte; Genevieve, David; Delobel, Bruno; Lehalle, Daphne; Perrin, Laurence; Prieur, Fabienne; Thevenon, Julien; Gecz, Jozef; Shaw, Marie; Pfundt, Rolph; Keren, Boris; Jacquette, Aurelia; Schenck, Annette; Eichler, Evan E; Kleefstra, Tjitske

Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules

系统表型组学分析将智力障碍中发生的基因突变分解为生物学上连贯的模块

Kochinke, Korinna; Zweier, Christiane; Nijhof, Bonnie; Fenckova, Michaela; Cizek, Pavel; Honti, Frank; Keerthikumar, Shivakumar; Oortveld, Merel A W; Kleefstra, Tjitske; Kramer, Jamie M; Webber, Caleb; Huynen, Martijn A; Schenck, Annette

De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila

WAC基因的新生功能丧失突变会导致果蝇出现可识别的智力障碍综合征和学习缺陷。

Lugtenberg, Dorien; Reijnders, Margot R F; Fenckova, Michaela; Bijlsma, Emilia K; Bernier, Raphael; van Bon, Bregje W M; Smeets, Eric; Vulto-van Silfhout, Anneke T; Bosch, Danielle; Eichler, Evan E; Mefford, Heather C; Carvill, Gemma L; Bongers, Ernie M H F; Schuurs-Hoeijmakers, Janneke Hm; Ruivenkamp, Claudia A; Santen, Gijs W E; van den Maagdenberg, Arn M J M; Peeters-Scholte, Cacha M P C D; Kuenen, Sabine; Verstreken, Patrik; Pfundt, Rolph; Yntema, Helger G; de Vries, Petra F; Veltman, Joris A; Hoischen, Alexander; Gilissen, Christian; de Vries, Bert B A; Schenck, Annette; Kleefstra, Tjitske; Vissers, Lisenka E L M