Current understanding of epigenetics in atopic dermatitis

por Schmidt, Alina D., de Guzman Strong, Cristina
Publicado 2021

Selective sweep for an enhancer involucrin allele identifies skin barrier adaptation out of Africa

por Mathyer, Mary Elizabeth, Brettmann, Erin A., Schmidt, Alina D., Goodwin, Zane A., Oh, Inez Y., Quiggle, Ashley M., Tycksen, Eric, Ramakrishnan, Natasha, Matkovich, Scot J., Guttman-Yassky, Emma, Edwards, John R., de Guzman Strong, Cristina
Publicado 2021

A human mitofusin 2 mutation can cause mitophagic cardiomyopathy

por Franco, Antonietta, Li, Jiajia, Kelly, Daniel P, Hershberger, Ray E, Marian, Ali J, Lewis, Renate M, Song, Moshi, Dang, Xiawei, Schmidt, Alina D, Mathyer, Mary E, Edwards, John R, Strong, Cristina de Guzman, Dorn, Gerald W
Publicado 2023

A Novel Bone Morphogenetic Protein 2 Mutant Mouse, nBmp2NLS(tm), Displays Impaired Intracellular Ca(2+) Handling in Skeletal Muscle

por Bridgewater, Laura C., Mayo, Jaime L., Evanson, Bradley G., Whitt, Megan E., Dean, Spencer A., Yates, Joshua D., Holden, Devin N., Schmidt, Alina D., Fox, Christopher L., Dhunghel, Saroj, Steed, Kevin S., Adam, Michael M., Nichols, Caitlin A., Loganathan, Sampath K., Barrow, Jeffery R., Hancock, Chad R.
Publicado 2013

Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samples

por Barnell, Erica K., Ronning, Peter, Campbell, Katie M., Krysiak, Kilannin, Ainscough, Benjamin J., Sheta, Lana M., Pema, Shahil P., Schmidt, Alina D., Richters, Megan, Cotto, Kelsy C., Danos, Arpad M., Ramirez, Cody, Skidmore, Zachary L., Spies, Nicholas C., Hundal, Jasreet, Sediqzad, Malik S., Kunisaki, Jason, Gomez, Felicia, Trani, Lee, Matlock, Matthew, Wagner, Alex H., Swamidass, S. Joshua, Griffith, Malachi, Griffith, Obi L.
Publicado 2018