The PKC-β selective inhibitor, Enzastaurin, impairs memory in middle-aged rats

por Willeman, Mari N., Mennenga, Sarah E., Siniard, Ashley L., Corneveaux, Jason J., De Both, Matt, Hewitt, Lauren T., Tsang, Candy W. S., Caselli, Jason, Braden, B. Blair, Bimonte-Nelson, Heather A., Huentelman, Matthew J.
Publicado 2018

Hippocampal Transcriptomic Profiles: Subfield Vulnerability to Age and Cognitive Impairment

por Ianov, Lara, De Both, Matt, Chawla, Monica K., Rani, Asha, Kennedy, Andrew J., Piras, Ignazio, Day, Jeremy J., Siniard, Ashley, Kumar, Ashok, Sweatt, J. David, Barnes, Carol A., Huentelman, Matthew J., Foster, Thomas C.
Publicado 2017

Association of SNPs in EGR3 and ARC with Schizophrenia Supports a Biological Pathway for Schizophrenia Risk

por Huentelman, Matthew J., Muppana, Leela, Corneveaux, Jason J., Dinu, Valentin, Pruzin, Jeremy J., Reiman, Rebecca, Borish, Cassie N., De Both, Matt, Ahmed, Amber, Todorov, Alexandre, Cloninger, C. Robert, Zhang, Rui, Ma, Jie, Gallitano, Amelia L.
Publicado 2015

A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome

por Schrauwen, Isabelle, Szelinger, Szabolcs, Siniard, Ashley L., Kurdoglu, Ahmet, Corneveaux, Jason J., Malenica, Ivana, Richholt, Ryan, Van Camp, Guy, De Both, Matt, Swaminathan, Shanker, Turk, Mari, Ramsey, Keri, Craig, David W., Narayanan, Vinodh, Huentelman, Matthew J.
Publicado 2015

Family SES Is Associated with the Gut Microbiome in Infants and Children

por Lewis, Candace R., Bonham, Kevin S., McCann, Shelley Hoeft, Volpe, Alexandra R., D’Sa, Viren, Naymik, Marcus, De Both, Matt D., Huentelman, Matthew J., Lemery-Chalfant, Kathryn, Highlander, Sarah K., Deoni, Sean C. L., Klepac-Ceraj, Vanja
Publicado 2021

Extracellular circular RNA profiles in plasma and urine of healthy, male college athletes

por Hutchins, Elizabeth, Reiman, Rebecca, Winarta, Joseph, Beecroft, Taylor, Richholt, Ryan, De Both, Matt, Shahbander, Khalouk, Carlson, Elizabeth, Janss, Alex, Siniard, Ashley, Balak, Chris, Bruhns, Ryan, Whitsett, Timothy G., McCoy, Roger, Anastasi, Matthew, Allen, April, Churas, Brian, Huentelman, Matthew, Van Keuren-Jensen, Kendall
Publicado 2021

A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia

por Moskowitz, Abby M., Belnap, Newell, Siniard, Ashley L., Szelinger, Szabolcs, Claasen, Ana M., Richholt, Ryan F., De Both, Matt, Corneveaux, Jason J., Balak, Chris, Piras, Ignazio S., Russell, Megan, Courtright, Amanda L., Rangasamy, Sampath, Ramsey, Keri, Craig, David W., Narayanan, Vinodh, Huentelman, Matt J., Schrauwen, Isabelle
Publicado 2016

Case Report: Novel mutations in TBC1D24 are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disabilit...

por Banuelos, Erika, Ramsey, Keri, Belnap, Newell, Krishnan, Malavika, Balak, Chris, Szelinger, Szabolcs, Siniard, Ashley L., Russell, Megan, Richholt, Ryan, De Both, Matt, Piras, Ignazio, Naymik, Marcus, Claasen, Ana M., Rangasamy, Sampathkumar, Huentelman, Matthew J., Craig, David W., Campeau, Philippe M., Narayanan, Vinodh, Schrauwen, Isabelle
Publicado 2017