Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome

por Karpinski, Beverly A., Maynard, Thomas M., Bryan, Corey A., Yitsege, Gelila, Horvath, Anelia, Lee, Norman H., Moody, Sally A., LaMantia, Anthony-Samuel
Publicado 2021

Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome

por Welby, Lauren, Caudill, Hailey, Yitsege, Gelila, Hamad, Ali, Bunyak, Filiz, Zohn, Irene E., Maynard, Thomas, LaMantia, Anthony-Samuel, Mendelowitz, David, Lever, Teresa E.
Publicado 2020

Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome

por Yitsege, Gelila, Stokes, Bethany A., Sabatino, Julia A., Sugrue, Kelsey F., Banyai, Gabor, Paronett, Elizabeth M., Karpinski, Beverly A., Maynard, Thomas M., LaMantia, Anthony‐S., Zohn, Irene E.
Publicado 2020