Intracellular Ca(2+) Stores and Ca(2+) Influx Are Both Required for BDNF to Rapidly Increase Quantal Vesicular Transmitter Release

por Amaral, Michelle D., Pozzo-Miller, Lucas
Publicado 2012

The Blossoming of Technology for the Analysis of Complex Aroma Bouquets—A Review on Flavour and Odorant Multidimensional and Comprehensive Gas Chromatography Applications

por Amaral, Michelle S.S., Marriott, Philip J.
Publicado 2019

Lipase-catalysed changes in essential oils revealed by comprehensive two-dimensional gas chromatography

por Amaral, Michelle S. S., Hearn, Milton T. W., Marriott, Philip J.
Publicado 2023

Using the Uganda National Panel Survey to analyze the effect of staple food consumption on undernourishment in Ugandan children

por Amaral, Michelle M., Herrin, William E., Gulere, Grace Bulenzi
Publicado 2017

Cross-sectional imaging of the torso reveals occult injuries in asymptomatic blunt trauma patients

por Roberts, Gregory J., Jacobson, Lewis E., Amaral, Michelle M., Jensen, Courtney D., Cooke, Louis, Schultz, Jacqueline F., Kinstedt, Alexander J., Saxe, Jonathan M.
Publicado 2020

Pharmacogenetic Predictors of Cannabidiol Response and Tolerability in Treatment‐Resistant Epilepsy

por Davis, Brittney H., Beasley, T. Mark, Amaral, Michelle, Szaflarski, Jerzy P., Gaston, Tyler, Perry Grayson, Leslie, Standaert, David G, Bebin, E. Martina, Limdi, Nita A.
Publicado 2021

Contributions of rare and common variation to early-onset and atypical dementia risk

por Wright, Carter A., Taylor, Jared W., Cochran, Meagan, Lawlor, James M.J., Moyers, Belle A., Amaral, Michelle D., Bonnstetter, Zachary T., Carter, Princess, Solomon, Veronika, Myers, Richard M., Love, Marissa Natelson, Geldmacher, David S., Cooper, Sara J., Roberson, Erik D., Cochran, J. Nicholas
Publicado 2023

Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities

por Snijders Blok, Lot, Vino, Arianna, den Hoed, Joery, Underhill, Hunter R., Monteil, Danielle, Li, Hong, Reynoso Santos, Francis Jeshira, Chung, Wendy K., Amaral, Michelle D., Schnur, Rhonda E., Santiago-Sim, Teresa, Si, Yue, Brunner, Han G., Kleefstra, Tjitske, Fisher, Simon E.
Publicado 2020

Contributions of rare and common variation to early-onset and atypical dementia risk

por Wright, Carter A., Taylor, Jared W., Cochran, Meagan, Lawlor, James M.J., Moyers, Belle A., Amaral, Michelle D., Bonnstetter, Zachary T., Carter, Princess, Solomon, Veronika, Myers, Richard M., Love, Marissa Natelson, Geldmacher, David S., Cooper, Sara J., Roberson, Erik D., Cochran, J. Nicholas
Publicado 2023

Genomic sequencing identifies secondary findings in a cohort of parent study participants

por Thompson, Michelle L., Finnila, Candice R., Bowling, Kevin M., Brothers, Kyle B., Neu, Matthew B., Amaral, Michelle D., Hiatt, Susan M., East, Kelly M., Gray, David E., Lawlor, James M.J., Kelley, Whitley V., Lose, Edward J., Rich, Carla A., Simmons, Shirley, Levy, Shawn E., Myers, Richard M., Barsh, Gregory S., Bebin, E. Martina, Cooper, Gregory M.
Publicado 2018

Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles

por Cochran, J. Nicholas, McKinley, Emily C., Cochran, Meagan, Amaral, Michelle D., Moyers, Bryan A., Lasseigne, Brittany N., Gray, David E., Lawlor, James M.J., Prokop, Jeremy W., Geier, Ethan G., Holt, James M., Thompson, Michelle L., Newberry, J. Scott, Yokoyama, Jennifer S., Worthey, Elizabeth A., Geldmacher, David S., Love, Marissa Natelson, Cooper, Gregory M., Myers, Richard M., Roberson, Erik D.
Publicado 2019

Genomic diagnosis for children with intellectual disability and/or developmental delay

por Bowling, Kevin M., Thompson, Michelle L., Amaral, Michelle D., Finnila, Candice R., Hiatt, Susan M., Engel, Krysta L., Cochran, J. Nicholas, Brothers, Kyle B., East, Kelly M., Gray, David E., Kelley, Whitley V., Lamb, Neil E., Lose, Edward J., Rich, Carla A., Simmons, Shirley, Whittle, Jana S., Weaver, Benjamin T., Nesmith, Amy S., Myers, Richard M., Barsh, Gregory S., Bebin, E. Martina, Cooper, Gregory M.
Publicado 2017

SYT1-associated neurodevelopmental disorder: a case series

por Baker, Kate, Gordon, Sarah L, Melland, Holly, Bumbak, Fabian, Scott, Daniel J, Jiang, Tess J, Owen, David, Turner, Bradley J, Boyd, Stewart G, Rossi, Mari, Al-Raqad, Mohammed, Elpeleg, Orly, Peck, Dawn, Mancini, Grazia M S, Wilke, Martina, Zollino, Marcella, Marangi, Giuseppe, Weigand, Heike, Borggraefe, Ingo, Haack, Tobias, Stark, Zornitza, Sadedin, Simon, Tan, Tiong Yang, Jiang, Yunyun, Gibbs, Richard A, Ellingwood, Sara, Amaral, Michelle, Kelley, Whitley, Kurian, Manju A, Cousin, Michael A, Raymond, F Lucy
Publicado 2018

Parents’ Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit

por Lemke, Amy A., Thompson, Michelle L., Gimpel, Emily C., McNamara, Katelyn C., Rich, Carla A., Finnila, Candice R., Cochran, Meagan E., Lawlor, James M. J., East, Kelly M., Bowling, Kevin M., Latner, Donald R., Hiatt, Susan M., Amaral, Michelle D., Kelley, Whitley V., Greve, Veronica, Gray, David E., Felker, Stephanie A., Meddaugh, Hannah, Cannon, Ashley, Luedecke, Amanda, Jackson, Kelly E., Hendon, Laura G., Janani, Hillary M., Johnston, Marla, Merin, Lee Ann, Deans, Sarah L., Tuura, Carly, Hughes, Trent, Williams, Heather, Laborde, Kelly, Neu, Matthew B., Patrick-Esteve, Jessica, Hurst, Anna C. E., Kirmse, Brian M., Savich, Renate, Spedale, Steven B., Knight, Sara J., Barsh, Gregory S., Korf, Bruce R., Cooper, Gregory M., Brothers, Kyle B.
Publicado 2023