Résultats de la recherche - Löhr, Heiko
- Résultat(s) 1 - 9 résultats de 9
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1
A Mutation in cnot8, Component of the Ccr4-Not Complex Regulating Transcript Stability, Affects Expression Levels of Developmental Regulators and Reveals a Role of Fgf3 in Developm... par Koch, Peter, Löhr, Heiko B., Driever, Wolfgang
Publié 2014Texte -
2
Sim1a and Arnt2 contribute to hypothalamo-spinal axon guidance by regulating Robo2 activity via a Robo3-dependent mechanism par Schweitzer, Jörn, Löhr, Heiko, Bonkowsky, Joshua L., Hübscher, Katrin, Driever, Wolfgang
Publié 2013Texte -
3
Direct and indirect roles of Fgf3 and Fgf10 in innervation and vascularisation of the vertebrate hypothalamic neurohypophysis par Liu, Fang, Pogoda, Hans-Martin, Pearson, Caroline Alayne, Ohyama, Kyoji, Löhr, Heiko, Hammerschmidt, Matthias, Placzek, Marysia
Publié 2013Texte -
4
Direct activation of chordoblasts by retinoic acid is required for segmented centra mineralization during zebrafish spine development par Pogoda, Hans-Martin, Riedl-Quinkertz, Iris, Löhr, Heiko, Waxman, Joshua S., Dale, Rodney M., Topczewski, Jacek, Schulte-Merker, Stefan, Hammerschmidt, Matthias
Publié 2018Texte -
5
An Ultraconserved Brain-specific Enhancer within ADGRL3 (LPHN3) Underpins ADHD Susceptibility par Martinez, Ariel F., Abe, Yu, Hong, Sungkook, Molyneux, Kevin, Yarnell, David, Löhr, Heiko, Driever, Wolfgang, Acosta, Maria T., Arcos-Burgos, Mauricio, Muenke, Maximilian
Publié 2016Texte -
6
Hypothalamic Pomc neurons innervate the spinal cord and modulate the excitability of premotor circuits par Reinoß, Philip, Ciglieri, Elisa, Minere, Marielle, Bremser, Stephan, Klein, Andreas, Löhr, Heiko, Fuller, Patrick M., Büschges, Ansgar, Kloppenburg, Peter, Fenselau, Henning, Hammerschmidt, Matthias
Publié 2020Texte -
7
Diet-Induced Growth Is Regulated via Acquired Leptin Resistance and Engages a Pomc-Somatostatin-Growth Hormone Circuit par Löhr, Heiko, Hess, Simon, Pereira, Mafalda M.A., Reinoß, Philip, Leibold, Sandra, Schenkel, Christel, Wunderlich, Claudia M., Kloppenburg, Peter, Brüning, Jens C., Hammerschmidt, Matthias
Publié 2018Texte -
8
Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function par Mendoza-Ferreira, Natalia, Coutelier, Marie, Janzen, Eva, Hosseinibarkooie, Seyyedmohsen, Löhr, Heiko, Schneider, Svenja, Milbradt, Janine, Karakaya, Mert, Riessland, Markus, Pichlo, Christian, Torres-Benito, Laura, Singleton, Andrew, Zuchner, Stephan, Brice, Alexis, Durr, Alexandra, Hammerschmidt, Matthias, Stevanin, Giovanni, Wirth, Brunhilde
Publié 2018Texte -
9
Neurocalcin Delta Suppression Protects against Spinal Muscular Atrophy in Humans and across Species by Restoring Impaired Endocytosis par Riessland, Markus, Kaczmarek, Anna, Schneider, Svenja, Swoboda, Kathryn J., Löhr, Heiko, Bradler, Cathleen, Grysko, Vanessa, Dimitriadi, Maria, Hosseinibarkooie, Seyyedmohsen, Torres-Benito, Laura, Peters, Miriam, Upadhyay, Aaradhita, Biglari, Nasim, Kröber, Sandra, Hölker, Irmgard, Garbes, Lutz, Gilissen, Christian, Hoischen, Alexander, Nürnberg, Gudrun, Nürnberg, Peter, Walter, Michael, Rigo, Frank, Bennett, C. Frank, Kye, Min Jeong, Hart, Anne C., Hammerschmidt, Matthias, Kloppenburg, Peter, Wirth, Brunhilde
Publié 2017Texte