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Number of items: 3.

Jenewein, Tina and Kanner, Scott A. and Bauer, Daniel and Hertel, Brigitte and Colecraft, Henry M. and Moroni, Anna and Thiel, Gerhard and Kauferstein, Silke (2020):
The mutation L69P in the PAS domain of the hERG potassium channel results in LQTS by trafficking deficiency.
In: Channels (Austin, Tex.), (1), 14. pp. 163-174, ISSN 1933-6969,
DOI: 10.1080/19336950.2020.1751522,
[Article]

Porro, Alessandro and Saponaro, Andrea and Gasparri, Federica and Bauer, Daniel and Gross, Christine and Pisoni, Matteo and Abbandonato, Gerardo and Hamacher, Kay and Santoro, Bina and Thiel, Gerhard and Moroni, Anna (2019):
The HCN domain couples voltage gating and cAMP response in Hyperpolarization-activated Cyclic Nucleotide-gated channels.
In: eLife, 8pp. e49672, ISSN 2050-084X,
DOI: 10.7554/eLife.49672,
[Article]

Marini, Carla and Porro, Alessandro and Rastetter, Agnès and Dalle, Carine and Rivolta, Ilaria and Bauer, Daniel and Oegema, Renske and Nava, Caroline and Parrini, Elena and Mei, Davide and Mercer, Catherine and Dhamija, Radhika and Chambers, Chelsea and Coubes, Christine and Thévenon, Julien and Kuentz, Paul and Julia, Sophie and Pasquier, Laurent and Dubourg, Christèle and Carré, Wilfrid and Rosati, Anna and Melani, Federico and Pisano, Tiziana and Giardino, Maria and Innes, A Micheil and Alembik, Yves and Scheidecker, Sophie and Santos, Manuela and Figueiroa, Sonia and Garrido, Cristina and Fusco, Carlo and Frattini, Daniele and Spagnoli, Carlotta and Binda, Anna and Granata, Tiziana and Ragona, Francesca and Freri, Elena and Franceschetti, Silvana and Canafoglia, Laura and Castellotti, Barbara and Gellera, Cinzia and Milanesi, Raffaella and Mancardi, Maria Margherita and Clark, Damien R. and Kok, Fernando and Helbig, Katherine L. and Ichikawa, Shoji and Sadler, Laurie and Neupauerová, Jana and Laššuthova, Petra and Šterbová, Katalin and Laridon, Annick and Brilstra, Eva and Koeleman, Bobby and Lemke, Johannes R. and Zara, Federico and Striano, Pasquale and Soblet, Julie and Smits, Guillaume and Deconinck, Nicolas and Barbuti, Andrea and DiFrancesco, Dario and LeGuern, Eric and Guerrini, Renzo and Santoro, Bina and Hamacher, Kay and Thiel, Gerhard and Moroni, Anna and DiFrancesco, Jacopo C. and Depienne, Christel (2018):
HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond.
In: Brain : a journal of neurology, 141 (11), pp. 3160-3178, ISSN 1460-2156,
[Article]

This list was generated on Sat May 23 00:36:34 2020 CEST.