Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Alycen Harney"'
Autor:
Sarah Jeanfavre, Kerry A. Pierce, Eitan Hoch, Alina Ainbinder, Suzanne B.R. Jacobs, Federico Centeno-Cruz, Courtney Dennis, Karen Gelinas-Roa, Amy Deik, Lorena Orozco, Patricia Glover, Kevin Bullock, Jesse Krejci, Francisco Barajas-Olmos, Anthony N. Hollenberg, Jose C. Florez, Carlos Zerrweck, Liping Zhao, Clary B. Clish, Eric S. Lander, Jinyoung Choi, Alycen Harney, Victor Rusu
SUMMARYGenetic variation at the SLC16A11 locus contributes to the disproportionate impact of type 2 diabetes (T2D) on Latino populations. We recently demonstrated that T2D risk variants reduce SLC16A11 liver expression and function of MCT11, the mono
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe176c8174e9997c0a00611592c8eb5f
https://doi.org/10.1101/2021.09.08.459307
https://doi.org/10.1101/2021.09.08.459307
Autor:
Garrett Garborcauskas, Alycen Harney, Hesam Dashti, Anne E. Carpenter, Miriam S. Udler, Elizabeth McGonagle, Aaron Leong, Hannah Ebert, Josée Dupuis, Maria Kost-Alimova, Cecilia M. Lindgren, Sierra Harken, Giacomo Deodato, Hans Hauner, Beth A. Cimini, Suzanne B.R. Jacobs, Josep M. Mercader, Saskia Reibe-Pal, Jose C. Florez, Adam Stefek, Samantha Laber, David R. Stirling, Gregory P. Way, Nasa Sinnott-Armstrong, Katherine Figueroa, Julius Honecker, Alham Saadat, Alina Ainbinder, Virtudes Calabuig, Melina Claussnitzer, Yixin Zhang, Sophie Strobel
SummaryA primary obstacle in translating genetics and genomics data into therapeutic strategies is elucidating the cellular programs affected by genetic variants and genes associated with human diseases. Broadly applicable high-throughput, unbiased a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16e99c4f7b03bd908d4d964e2603077b
https://doi.org/10.1101/2021.07.17.452050
https://doi.org/10.1101/2021.07.17.452050