Three Phases of DiGeorge/22q11 Deletion Syndrome Pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes

Por Meechan, D.W., Maynard, T.M., Tucker, E.S., LaMantia, A-S.
Publicado em 2010

When Half Is Not Enough: Gene Expression and Dosage in the 22q11 Deletion Syndrome

Por Meechan, D. W., Maynard, T. M., Gopalakrishna, D., Wu, Y., LaMantia, A.-S.
Publicado no Gene Expr (2018)

Cognitive Ability is Associated with Altered Medial Frontal Cortical Circuits in the LgDel Mouse Model of 22q11.2DS

Por Meechan, D.W., Rutz, H.L.H., Fralish, M.S., Maynard, T.M., Rothblat, L.A., LaMantia, A.-S.
Publicado no Cereb Cortex (2015)

Mitochondral localization and function of a subset of 22q11 Deletion Syndrome candidate genes

Por Maynard, T. M., Meechan, D. W., Dudevoir, M. L., Gopalakrishna, D., Peters, A. Z., Heindel, C. C., Sugimoto, T. J., Wu, Y., Lieberman, J. A., LaMantia, A.-S.
Publicado em 2008

Specific mesenchymal/epithelial induction of olfactory receptor, vomeronasal, and gonadotropin-releasing hormone (GnRH) neurons

Por Rawson, N.E, Lischka, F. W., Yee, K.K., Peters, A.Z., Tucker, E.S., Meechan, D.W., Zirlinger, M., Maynard, T.M., Burd, G.B., Dulac, C., Pevny, L., LaMantia, A-S.
Publicado em 2010