Novel and Functional Norepinephrine Transporter Protein Variants Identified in Attention-Deficit Hyperactivity Disorder

Por Hahn, Maureen K., Steele, Angela, Couch, R. Steven, Stein, Mark A., Krueger, Jessica J.
Publicado em 2009

Functional Coding Variation in the Presynaptic Dopamine Transporter Associated with Neuropsychiatric Disorders Drives Enhanced Motivation and Context-Dependent Impulsivity in Mice

Por Davis, Gwynne L., Stewart, Adele, Stanwood, Gregg D., Gowrishankar, Raajaram, Hahn, Maureen K., Blakely, Randy D.
Publicado no Behav Brain Res (2017)

Extracellular Norepinephrine Clearance by the Norepinephrine Transporter Is Required for Skeletal Homeostasis

Por Ma, Yun, Krueger, Jessica J., Redmon, Sara N., Uppuganti, Sasidhar, Nyman, Jeffry S., Hahn, Maureen K., Elefteriou, Florent
Publicado em 2013

Genetic targeting of the amphetamine and methylphenidate-sensitive dopamine transporter: On the path to an animal model of attention-deficit hyperactivity disorder

Por Mergy, Marc A., Gowrishankar, Raajaram, Davis, Gwynne L., Jessen, Tammy N., Wright, Jane, Stanwood, Gregg D., Hahn, Maureen K., Blakely, Randy D.
Publicado em 2013

Genetic Variation in the Presynaptic Norepinephrine Transporter is Associated with Blood Pressure Responses to Exercise in Healthy Humans

Por Kohli, Utkarsh, Hahn, Maureen K., English, Brett A., Sofowora, Gbenga G., Muszkat, Mordechai, Li, Chun, Blakely, Randy D., Stein, C. Michael, Kurnik, Daniel
Publicado em 2011

Choline transporter gene variation is associated with attention-deficit hyperactivity disorder

Por English, Brett A., Hahn, Maureen K., Gizer, Ian R., Mazei-Robison, Michelle, Steele, Angela, Kurnik, Daniel M., Stein, Mark A., Waldman, Irwin D., Blakely, Randy D.
Publicado em 2009

Genetic variation in alpha(2)-adrenoreceptors and heart rate recovery after exercise

Por Kohli, Utkarsh, Diedrich, André, Kannankeril, Prince J., Muszkat, Mordechai, Sofowora, Gbenga G., Hahn, Maureen K., English, Brett A., Blakely, Randy D., Stein, C. Michael, Kurnik, Daniel
Publicado no Physiol Genomics (2015)

The rare DAT coding variant Val559 perturbs DA neuron function, changes behavior, and alters in vivo responses to psychostimulants

Por Mergy, Marc A., Gowrishankar, Raajaram, Gresch, Paul J., Gantz, Stephanie C., Williams, John, Davis, Gwynne L., Wheeler, C. Austin, Stanwood, Gregg D., Hahn, Maureen K., Blakely, Randy D.
Publicado no Proc Natl Acad Sci U S A (2014)

Norepinephrine transporter variant A457P knock-in mice display key features of human postural orthostatic tachycardia syndrome

Por Shirey-Rice, Jana K., Klar, Rebecca, Fentress, Hugh M., Redmon, Sarah N., Sabb, Tiffany R., Krueger, Jessica J., Wallace, Nathan M., Appalsamy, Martin, Finney, Charlene, Lonce, Suzanna, Diedrich, André, Hahn, Maureen K.
Publicado em 2013

A polymorphism in the norepinephrine transporter gene alters promoter activity and is associated with attention-deficit hyperactivity disorder

Por Kim, Chun-Hyung, Hahn, Maureen K., Joung, Yoosook, Anderson, Susan L., Steele, Angela H., Mazei-Robinson, Michelle S., Gizer, Ian, Teicher, Martin H., Cohen, Bruce M., Robertson, David, Waldman, Irwin D., Blakely, Randy D., Kim, Kwang-Soo
Publicado em 2006