Proteasome activator 28γ (PA28γ) allosterically activates trypsin-like proteolysis by binding to the α-ring of the 20S proteasome

por Thomas, Taylor A., Smith, David M.
Publicado 2022

Structure, Function, and Allosteric Regulation of the 20S Proteasome by the 11S/PA28 Family of Proteasome Activators

por Thomas, Taylor, Salcedo-Tacuma, David, Smith, David M.
Publicado 2023

Case report and literature review of popliteal artery entrapment syndrome

por Skeik, Nedaa, Thomas, Taylor M, Engstrom, Bjorn I, Alexander, Jason Q
Publicado 2015

Estimating the Prevalence and Genetic Risk Mechanisms of ARFID in a Large Autism Cohort

por Koomar, Tanner, Thomas, Taylor R., Pottschmidt, Natalie R., Lutter, Michael, Michaelson, Jacob J.
Publicado 2021

Coping and Mental Health in Early Adolescence during COVID-19

por Hussong, Andrea M., Midgette, Allegra J., Thomas, Taylor E., Coffman, Jennifer L., Cho, Su
Publicado 2021

Clinical autism subscales have common genetic liabilities that are heritable, pleiotropic, and generalizable to the general population

por Thomas, Taylor R., Koomar, Tanner, Casten, Lucas G., Tener, Ashton J., Bahl, Ethan, Michaelson, Jacob J.
Publicado 2022

COVID-19 Life Events Spill-Over on Family Functioning and Adolescent Adjustment

por Hussong, Andrea M., Midgette, Allegra J., Richards, Adrianna N., Petrie, Rachel C., Coffman, Jennifer L., Thomas, Taylor E.
Publicado 2022

Inhibition of mTOR Pathway by Rapamycin Reduces Brain Damage in Rats Subjected to Transient Forebrain Ischemia

por Yang, Xiao, Hei, Changhun, Liu, Ping, Song, Yaozu, Thomas, Taylor, Tshimanga, Sylvie, Wang, Feng, Niu, Jianguo, Sun, Tao, Li, P. Andy
Publicado 2015

Community attitudes on genetic research of gender identity, sexual orientation, and mental health

por Thomas, Taylor R., Hofammann, Dabney, McKenna, Brooke G., I. R. van der Miesen, Anna, Stokes, Mark A., Daniolos, Peter, Michaelson, Jacob J.
Publicado 2020

Genetic and morphological estimates of androgen exposure predict social deficits in multiple neurodevelopmental disorder cohorts

por McKenna, Brooke G., Huang, Yongchao, Vervier, Kévin, Hofammann, Dabney, Cafferata, Mary, Al-Momani, Seima, Lowenthal, Florencia, Zhang, Angela, Koh, Jin-Young, Thenuwara, Savantha, Brueggeman, Leo, Bahl, Ethan, Koomar, Tanner, Pottschmidt, Natalie, Kalmus, Taylor, Casten, Lucas, Thomas, Taylor R., Michaelson, Jacob J.
Publicado 2021

Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes

por Zhou, Xueya, Feliciano, Pamela, Shu, Chang, Wang, Tianyun, Astrovskaya, Irina, Hall, Jacob B., Obiajulu, Joseph U., Wright, Jessica R., Murali, Shwetha C., Xu, Simon Xuming, Brueggeman, Leo, Thomas, Taylor R., Marchenko, Olena, Fleisch, Christopher, Barns, Sarah D., Snyder, LeeAnne Green, Han, Bing, Chang, Timothy S., Turner, Tychele N., Harvey, William T., Nishida, Andrew, O’Roak, Brian J., Geschwind, Daniel H., Michaelson, Jacob J., Volfovsky, Natalia, Eichler, Evan E., Shen, Yufeng, Chung, Wendy K.
Publicado 2022