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收藏分享 收藏 分享 收藏 Recovery of the full in vivo firing range in post-lesion surviving DA SN neurons associated with Kv4.3-mediated pacemaker plasticity与Kv4.3介导的起搏器可塑性相关的，损伤后存活的黑质致密部DA神经元恢复完整的在体放电范围
Kovacheva, Lora; Shin, Josef; Zaldivar-Diez, Josefa; Mankel, Johanna; Farassat, Navid; Costa, Kaue Machado; Thakur, Poonam; Obeso, Jose A.; Roeper, Jochen; Ding, Jun 分享 收藏 分享 收藏 分享 收藏 The human channel gating-modifying A749G CACNA1D (Cav1.3) variant induces a neurodevelopmental syndrome-like phenotype in mice人类通道门控修饰A749G CACNA1D (Cav1.3) 变体在小鼠中诱导神经发育综合征样表型Ortner, Nadine J.; Sah, Anupam; Paradiso, Enrica; Shin, Josef; Stojanovic, Strahinja; Hammer, Niklas; Haritonova, Maria; Hofer, Nadja T.; Marcantoni, Andrea; Guarina, Laura; Tuluc, Petronel; Theiner, Tamara; Pitterl, Florian; Ebner, Karl; Oberacher, Herbert; Carbone, Emilio; Stefanova, Nadia; Ferraguti, Francesco; Singewald, Nicolas; Roeper, Jochen; Striessnig, Joerg 分享 收藏 Cav1.3 calcium channels are full-range linear amplifiers of firing frequencies in lateral DA SN neuronsCav1.3钙通道是侧向DA SN神经元放电频率的全范围线性放大器Shin, Josef; Kovacheva, Lora; Thomas, Dominique; Stojanovic, Strahinja; Knowlton, Christopher J.; Mankel, Johanna; Boehm, Johannes; Farassat, Navid; Paladini, Carlos; Striessnig, Joerg; Canavier, Carmen C.; Geisslinger, Gerd; Roeper, Jochen 分享 收藏 分享 收藏 Developmental HCN channelopathy results in decreased neural progenitor proliferation and microcephaly in mice发育性HCN通道病导致小鼠神经祖细胞增殖减少和小头畸形Schlusche, Anna Katharina; Vay, Sabine Ulrike; Kleinenkuhnen, Niklas; Sandke, Steffi; Campos-Martin, Rafael; Florio, Marta; Huttner, Wieland; Tresch, Achim; Roeper, Jochen; Rueger, Maria Adele; Jakovcevski, Igor; Stockebrand, Malte; Isbrandt, Dirk 分享 收藏 分享 收藏 α-Synuclein-induced Kv4 channelopathy in mouse vagal motoneurons drives nonmotor parkinsonian symptomsChiu, Wei-Hua; Kovacheva, Lora; Musgrove, Ruth E.; Arien-Zakay, Hadar; Koprich, James B.; Brotchie, Jonathan M.; Yaka, Rami; Ben-Zvi, Danny; Hanani, Menachem; Roeper, Jochen; Goldberg, Joshua A. 分享 收藏 分享 收藏 分享 收藏 Inhibition of histone deacetylation rescues phenotype in a mouse model of Birk-Barel intellectual disability syndrome抑制组蛋白去乙酰化可挽救birk-barel智力障碍综合征小鼠模型的表型Cooper, Alexis; Butto, Tamer; Hammer, Niklas; Jagannath, Somanath; Fend-Guella, Desiree Lucia; Akhtar, Junaid; Radyushkin, Konstantin; Lesage, Florian; Winter, Jennifer; Strand, Susanne; Roeper, Jochen; Zechner, Ulrich; Schweiger, Susann 分享 收藏 An ER Assembly Line of AMPA-Receptors Controls Excitatory Neurotransmission and Its PlasticitySchwenk, Jochen; Boudkkazi, Sami; Kocylowski, Maciej K.; Brechet, Aline; Zolles, Gerd; Bus, Thorsten; Costa, Kaue; Kollewe, Astrid; Jordan, Johannes; Bank, Julia; Bildl, Wolfgang; Sprengel, Rolf; Kulik, Akos; Roeper, Jochen; Schulte, Uwe; Fakler, Bernd 分享 收藏 In vivo functional diversity of midbrain dopamine neurons within identified axonal projectionsFarassat, Navid; Costa, Kaue Machado; Stojanovic, Strahinja; Albert, Stefan; Kovacheva, Lora; Shin, Josef; Egger, Richard; Somayaji, Mahalakshmi; Duvarci, Sevil; Schneider, Gaby; Roeper, Jochen 分享 收藏 分享 收藏 分享 收藏 分享 收藏 
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