The Atypical Stimulant and Nootropic Modafinil Interacts with the Dopamine Transporter in a Different Manner than Classical Cocaine-Like Inhibitors

por Schmitt, Kyle C., Reith, Maarten E. A.
Publicado 2011

Correction: The Atypical Stimulant and Nootropic Modafinil Interacts with the Dopamine Transporter in a Different Manner than Classical Cocaine-Like Inhibitors

por Schmitt, Kyle C., Reith, Maarten E. A.
Publicado 2012

Structural Modifications of Neuroprotective Anti-Parkinsonian (−)-N6-(2-(4-(Biphenyl-4-yl)piperazin-1-yl)-ethyl)-N6-propyl-4,5,6,7-tetrahydrobenzo[d]thiazole-2,6-diamine (D-264): A...

por Modi, Gyan, Antonio, Tamara, Reith, Maarten, Dutta, Aloke
Publicado 2014

Overview of the structure and function of the dopamine transporter and its protein interactions

por Nepal, Binod, Das, Sanjay, Reith, Maarten E., Kortagere, Sandhya
Publicado 2023

Pharmacological and Behavioral Characterization of D-473, an Orally Active Triple Reuptake Inhibitor Targeting Dopamine, Serotonin and Norepinephrine Transporters

por Dutta, Aloke K., Santra, Soumava, Sharma, Horrick, Voshavar, Chandrashekhar, Xu, Liping, Mabrouk, Omar, Antonio, Tamara, Reith, Maarten E. A.
Publicado 2014

SLC6 transporter oligomerization

por Jayaraman, Kumaresan, Das, Anand K., Luethi, Dino, Szöllősi, Dániel, Schütz, Gerhard J., Reith, Maarten E. A., Sitte, Harald H., Stockner, Thomas
Publicado 2020

The dopamine transporter gene SLC6A3: multidisease risks

por Reith, Maarten E. A., Kortagere, Sandhya, Wiers, Corinde E., Sun, Hui, Kurian, Manju A., Galli, Aurelio, Volkow, Nora D., Lin, Zhicheng
Publicado 2021

Effect of Iboga Alkaloids on µ-Opioid Receptor-Coupled G Protein Activation

por Antonio, Tamara, Childers, Steven R., Rothman, Richard B., Dersch, Christina M., King, Christine, Kuehne, Martin, Bornmann, William G., Eshleman, Amy J., Janowsky, Aaron, Simon, Eric R., Reith, Maarten E. A., Alper, Kenneth
Publicado 2013

Insulin enhances striatal dopamine release by activating cholinergic interneurons and thereby signals reward

por Stouffer, Melissa A., Woods, Catherine A., Patel, Jyoti C., Lee, Christian R., Witkovsky, Paul, Bao, Li, Machold, Robert P., Jones, Kymry T., de Vaca, Soledad Cabeza, Reith, Maarten E. A., Carr, Kenneth D., Rice, Margaret E.
Publicado 2015

Design, Synthesis, and Structure–Activity Relationship Studies of a Series of [4-(4-Carboxamidobutyl)]-1-arylpiperazines: Insights into Structural Features Contributing to Dopamine...

por Ananthan, Subramaniam, Saini, Surendra K., Zhou, Guangyan, Hobrath, Judith V., Padmalayam, Indira, Zhai, Ling, Bostwick, J. Robert, Antonio, Tamara, Reith, Maarten E. A., McDowell, Shea, Cho, Eunie, McAleer, Leah, Taylor, Michelle, Luedtke, Robert R.
Publicado 2014

Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood

por Ng, Joanne, Zhen, Juan, Meyer, Esther, Erreger, Kevin, Li, Yan, Kakar, Naseebullah, Ahmad, Jamil, Thiele, Holger, Kubisch, Christian, Rider, Nicholas L., Holmes Morton, D., Strauss, Kevin A., Puffenberger, Erik G., D’Agnano, Daniela, Anikster, Yair, Carducci, Claudia, Hyland, Keith, Rotstein, Michael, Leuzzi, Vincenzo, Borck, Guntram, Reith, Maarten E. A., Kurian, Manju A.
Publicado 2014

Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study

por Kurian, Manju A, Li, Yan, Zhen, Juan, Meyer, Esther, Hai, Nebula, Christen, Hans-Jürgen, Hoffmann, Georg F, Jardine, Philip, von Moers, Arpad, Mordekar, Santosh R, O'Callaghan, Finbar, Wassmer, Evangeline, Wraige, Elizabeth, Dietrich, Christa, Lewis, Timothy, Hyland, Keith, Heales, Simon JR, Sanger, Terence, Gissen, Paul, Assmann, Birgit E, Reith, Maarten EA, Maher, Eamonn R
Publicado 2010

Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures

por Stödberg, Tommy, McTague, Amy, Ruiz, Arnaud J., Hirata, Hiromi, Zhen, Juan, Long, Philip, Farabella, Irene, Meyer, Esther, Kawahara, Atsuo, Vassallo, Grace, Stivaros, Stavros M., Bjursell, Magnus K., Stranneheim, Henrik, Tigerschiöld, Stephanie, Persson, Bengt, Bangash, Iftikhar, Das, Krishna, Hughes, Deborah, Lesko, Nicole, Lundeberg, Joakim, Scott, Rod C., Poduri, Annapurna, Scheffer, Ingrid E., Smith, Holly, Gissen, Paul, Schorge, Stephanie, Reith, Maarten E. A., Topf, Maya, Kullmann, Dimitri M., Harvey, Robert J., Wedell, Anna, Kurian, Manju A.
Publicado 2015

MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia

por Reid, Kimberley M., Spaull, Robert, Salian, Smrithi, Barwick, Katy, Meyer, Esther, Zhen, Juan, Hirata, Hiromi, Sheipouri, Diba, Benkerroum, Hind, Gorman, Kathleen M., Papandreou, Apostolos, Simpson, Michael A., Hirano, Yoshinobu, Farabella, Irene, Topf, Maya, Grozeva, Detelina, Carss, Keren, Smith, Martin, Pall, Hardev, Lunt, Peter, De Gressi, Susanna, Kamsteeg, Erik‐Jan, Haack, Tobias B., Carr, Lucinda, Guerreiro, Rita, Bras, Jose, Maher, Eamonn R., Scott, Richard H., Vandenberg, Robert J., Raymond, F. Lucy, Chong, Wui K., Sudhakar, Sniya, Mankad, Kshitij, Reith, Maarten E., Campeau, Philippe M., Harvey, Robert J., Kurian, Manju A.
Publicado 2022