Lipid rafts control P2X3 receptor distribution and function in trigeminal sensory neurons of a transgenic migraine mouse model

Por Gnanasekaran, Aswini, Sundukova, Mayya, van den Maagdenberg, Arn MJM, Fabbretti, Elsa, Nistri, Andrea
Publicado em 2011

Epigenetic mechanisms in migraine: a promising avenue?

Por Eising, Else, A Datson, Nicole, van den Maagdenberg, Arn MJM, Ferrari, Michel D
Publicado em 2013

Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in Ca(V)2.1 knockin migraine mice

Por Vecchia, Dania, Tottene, Angelita, van den Maagdenberg, Arn M.J.M., Pietrobon, Daniela
Publicado em 2014

Abnormal cortical synaptic transmission in Ca(V)2.1 knockin mice with the S218L missense mutation which causes a severe familial hemiplegic migraine syndrome in humans

Por Vecchia, Dania, Tottene, Angelita, van den Maagdenberg, Arn M.J.M., Pietrobon, Daniela
Publicado no Front Cell Neurosci (2015)

Inefficient constitutive inhibition of P2X3 receptors by brain natriuretic peptide system contributes to sensitization of trigeminal sensory neurons in a genetic mouse model of fam...

Por Marchenkova, Anna, Vilotti, Sandra, Ntamati, Niels, van den Maagdenberg, Arn MJM, Nistri, Andrea
Publicado no Mol Pain (2016)

Functional crosstalk in culture between macrophages and trigeminal sensory neurons of a mouse genetic model of migraine

Por Franceschini, Alessia, Nair, Asha, Bele, Tanja, van den Maagdenberg, Arn MJM, Nistri, Andrea, Fabbretti, Elsa
Publicado em 2012

In silico phenotyping via co-training for improved phenotype prediction from genotype

Por Roqueiro, Damian, Witteveen, Menno J., Anttila, Verneri, Terwindt, Gisela M., van den Maagdenberg, Arn M.J.M., Borgwardt, Karsten
Publicado no Bioinformatics (2015)

Familial hemiplegic migraine Ca(V)2.1 channel mutation R192Q enhances ATP-gated P2X(3 )receptor activity of mouse sensory ganglion neurons mediating trigeminal pain

Por Nair, Asha, Simonetti, Manuela, Birsa, Nicol, Ferrari, Michel D, van den Maagdenberg, Arn MJM, Giniatullin, Rashid, Nistri, Andrea, Fabbretti, Elsa
Publicado em 2010

Mutated Ca(V)2.1 channels dysregulate CASK/P2X3 signaling in mouse trigeminal sensory neurons of R192Q Cacna1a knock-in mice

Por Gnanasekaran, Aswini, Bele, Tanja, Hullugundi, Swathi, Simonetti, Manuela, Ferrari, Michael D, van den Maagdenberg, Arn MJM, Nistri, Andrea, Fabbretti, Elsa
Publicado no Mol Pain (2013)

The first knockin mouse model of episodic ataxia type 2

Por Rose, Samuel J., Kriener, Lisa H., Heinzer, Ann K., Fan, Xueliang, Raike, Robert S., van den Maagdenberg, Arn M.J.M., Hess, Ellen J.
Publicado em 2014

Differential Cerebellar GABA(A) Receptor Expression in Mice with Mutations in Ca(V)2.1 (P/Q-type) Calcium Channels

Por Kaja, Simon, Payne, Andrew J., Nielsen, Elsebet Ø., Thompson, Christopher L., van den Maagdenberg, Arn M.J.M., Koulen, Peter, Snutch, Terrance P.
Publicado no Neuroscience (2015)

Gain of Function in FHM-1 Ca(v)2.1 Knock-In Mice Is Related to the Shape of the Action Potential

Por Inchauspe, Carlota González, Urbano, Francisco J., Di Guilmi, Mariano N., Forsythe, Ian D., Ferrari, Michel D., van den Maagdenberg, Arn M.J.M., Uchitel, Osvaldo D.
Publicado em 2010

Synaptic Gain-of-Function Effects of Mutant Ca(v)2.1 Channels in a Mouse Model of Familial Hemiplegic Migraine Are Due to Increased Basal [Ca(2+)](i)

Por Di Guilmi, Mariano N., Wang, Tiantian, Inchauspe, Carlota Gonzalez, Forsythe, Ian D., Ferrari, Michel D., van den Maagdenberg, Arn M.J.M., Borst, J. Gerard G., Uchitel, Osvaldo D.
Publicado em 2014

Migraine Mutations Impair Hippocampal Learning Despite Enhanced Long-Term Potentiation

Por Dilekoz, Ergin, Houben, Thijs, Eikermann-Haerter, Katharina, Balkaya, Mustafa, Lenselink, A. Mariette, Whalen, Michael J., Spijker, Sabine, Ferrari, Michel D., van den Maagdenberg, Arn M.J.M., Ayata, Cenk
Publicado no J Neurosci (2015)

Genetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1

Por Eikermann-Haerter, Katharina, Dileköz, Ergin, Kudo, Chiho, Savitz, Sean I., Waeber, Christian, Baum, Michael J., Ferrari, Michel D., van den Maagdenberg, Arn M.J.M., Moskowitz, Michael A., Ayata, Cenk
Publicado em 2008

Spreading depolarizations increase delayed brain injury in a rat model of subarachnoid hemorrhage

Por Hamming, Arend M, Wermer, Marieke JH, Umesh Rudrapatna, S, Lanier, Christian, van Os, Hine JA, van den Bergh, Walter M, Ferrari, Michel D, van der Toorn, Annette, van den Maagdenberg, Arn MJM, Stowe, Ann M, Dijkhuizen, Rick M
Publicado no J Cereb Blood Flow Metab (2015)

Mutations in the human GlyT2 gene define a presynaptic component of human startle disease

Por Rees, Mark I., Harvey, Kirsten, Pearce, Brian R., Chung, Seo-Kyung, Duguid, Ian C., Thomas, Philip, Beatty, Sarah, Graham, Gail E., Armstrong, Linlea, Shiang, Rita, Abbott, Kim J., Zuberi, Sameer M., Stephenson, John B.P., Owen, Michael J., Tijssen, Marina A.J., van den Maagdenberg, Arn M.J.M., Smart, Trevor G., Supplisson, Stéphane, Harvey, Robert J.
Publicado em 2006

Meta-analysis of genome-wide association for migraine in six population-based European cohorts

Por Ligthart, Lannie, de Vries, Boukje, Smith, Albert V, Ikram, M Arfan, Amin, Najaf, Hottenga, Jouke-Jan, Koelewijn, Stephany C, Kattenberg, V Mathijs, de Moor, Marleen HM, Janssens, A Cecile JW, Aulchenko, Yurii S, Oostra, Ben A, de Geus, Eco JC, Smit, Johannes H, Zitman, Frans G, Uitterlinden, André G, Hofman, Albert, Willemsen, Gonneke, Nyholt, Dale R, Montgomery, Grant W, Terwindt, Gisela M, Gudnason, Vilmundur, Penninx, Brenda WJH, Breteler, Monique, Ferrari, Michel D, Launer, Lenore J, van Duijn, Cornelia M, van den Maagdenberg, Arn MJM, Boomsma, Dorret I
Publicado em 2011

A high-density association screen of 155 ion transport genes for involvement with common migraine

Por Nyholt, Dale R., LaForge, K. Steven, Kallela, Mikko, Alakurtti, Kirsi, Anttila, Verneri, Färkkilä, Markus, Hämaläinen, Eija, Kaprio, Jaakko, Kaunisto, Mari A., Heath, Andrew C., Montgomery, Grant W., Göbel, Hartmut, Todt, Unda, Ferrari, Michel D., Launer, Lenore J., Frants, Rune R., Terwindt, Gisela M., de Vries, Boukje, Verschuren, W.M. Monique, Brand, Jan, Freilinger, Tobias, Pfaffenrath, Volker, Straube, Andreas, Ballinger, Dennis G., Zhan, Yiping, Daly, Mark J., Cox, David R., Dichgans, Martin, van den Maagdenberg, Arn M.J.M., Kubisch, Christian, Martin, Nicholas G., Wessman, Maija, Peltonen, Leena, Palotie, Aarno
Publicado em 2008

Migraine without aura: genome-wide association analysis identifies several novel susceptibility

Por de Vries, Boukje, Freilinger, Tobias, Anttila, Verneri, Malik, Rainer, Kallela, Mikko, Terwindt, Gisela M, Pozo-Rosich, Patricia, Winsvold, Bendik, Nyholt, Dale R, van Oosterhout, Willebrordus PJ, Artto, Ville, Todt, Unda, Hämäläinen, Eija, Fernández-Morales, Jèssica, Louter, Mark A, Kaunisto, Mari A, Schoenen, Jean, Raitakari, Olli, Lehtimäki, Terho, Vila-Pueyo, Marta, Göbel, Hartmut, Wichmann, Erich, Sintas, Cèlia, Uitterlinden, Andre G, Hofman, Albert, Rivadeneira, Fernando, Heinze, Axel, Tronvik, Erling, van Duijn, Cornelia M, Kaprio, Jaakko, Cormand, Bru, Wessman, Maija, Frants, Rune R, Meitinger, Thomas, Müller-Myhsok, Bertram, Zwart, John-Anker, Färkkilä, Markus, Macaya, Alfons, Ferrari, Michel D, Kubisch, Christian, Palotie, Aarno, Dichgans, Martin, van den Maagdenberg, Arn MJM
Publicado em 2013