The strengths of the genetic approach to understanding neural systems development and function: Ray Guillery's synthesis

por LaMantia, Anthony‐Samuel
Publicado 2018

Why Does the Face Predict the Brain? Neural Crest Induction, Craniofacial Morphogenesis, and Neural Circuit Development

por LaMantia, Anthony-Samuel
Publicado 2020

In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?

por Motahari, Zahra, Moody, Sally Ann, Maynard, Thomas Michael, LaMantia, Anthony-Samuel
Publicado 2019

Disrupted Coordination of Hypoglossal Motor Control in a Mouse Model of Pediatric Dysphagia in DiGeorge/22q11.2 Deletion Syndrome

por Wang, Xin, Popratiloff, Anastas, Motahari, Zahra, LaMantia, Anthony-Samuel, Mendelowitz, David
Publicado 2020

Aberrant early growth of individual trigeminal sensory and motor axons in a series of mouse genetic models of 22q11.2 deletion syndrome

por Motahari, Zahra, Maynard, Thomas M, Popratiloff, Anastas, Moody, Sally A, LaMantia, Anthony-S
Publicado 2020

Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome

por Karpinski, Beverly A., Maynard, Thomas M., Fralish, Matthew S., Nuwayhid, Samer, Zohn, Irene E., Moody, Sally A., LaMantia, Anthony-S.
Publicado 2014

Ranbp1 modulates morphogenesis of the craniofacial midline in mouse models of 22q11.2 deletion syndrome

por Paronett, Elizabeth M, Bryan, Corey A, Maynard, Megan E, Goroff, Julia A, Meechan, Daniel W, LaMantia, Anthony-Samuel, Maynard, Thomas M
Publicado 2023

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

Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome

por Maynard, Thomas M, Horvath, Anelia, P Bernot, James, Karpinski, Beverly A, Tavares, Andre L P, Shah, Ankita, Zheng, Qianqian, Spurr, Liam, Olender, Jacqueline, Moody, Sally A, Fraser, Claire M, LaMantia, Anthony-S, Lee, Norman H
Publicado 2020

Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome

por Maynard, Thomas M, Horvath, Anelia, Bernot, James P, Karpinski, Beverly A, Tavares, Andre L P, Shah, Ankita, Zheng, Qianqian, Spurr, Liam, Olender, Jacqueline, Moody, Sally A, Fraser, Claire M, LaMantia, Anthony-S, Lee, Norman H
Publicado 2020

3.2 PARVALBUMIN INTERNEURON IMPAIRMENT INDUCED BY OXIDATIVE STRESS AS A COMMON PATHOLOGICAL MECHANISM IN ANIMAL MODELS OF SCHIZOPHRENIA

por Cabungcal, Jan Harry, Steullet, Pascal, Coyle, Joseph, Didriksen, Michael, Gill, Kathryn, Grace, Anthony, Takao, Hensch, LaMantia, Anthony, Lindemann, Lothar, Maynard, Thomas, Meyer, Urs, Morishita, Hirofumi, O’Donnell, Patricio, Puhl, Matthew, Cuenod, Michel, Do, Kim Q
Publicado 2018

Developmental and Degenerative Features in a Complicated Spastic Paraplegia

por Manzini, M Chiara, Rajab, Anna, Maynard, Thomas M, Mochida, Ganeshwaran H, Tan, Wen-Hann, Nasir, Ramzi, Hill, R Sean, Gleason, Danielle, Al Saffar, Muna, Partlow, Jennifer N, Barry, Brenda J, Vernon, Mike, LaMantia, Anthony-Samuel, Walsh, Christopher A
Publicado 2010