Deficits in early neural tube identity found in CHARGE syndrome

por Haldipur, Parthiv, Millen, Kathleen J
Publicado 2013

Hippocampal granule cell dispersion: a non-specific finding in pediatric patients with no history of seizures

por Roy, Achira, Millen, Kathleen J., Kapur, Raj P.
Publicado 2020

Neonatal subarachnoid hemorrhage disrupts multiple aspects of cerebellar development

por Butler, David F., Skibo, Jonathan, Traudt, Christopher M., Millen, Kathleen J.
Publicado 2023

Looking at Cerebellar Malformations through Text-Mined Interactomes of Mice and Humans

por Iossifov, Ivan, Rodriguez-Esteban, Raul, Mayzus, Ilya, Millen, Kathleen J., Rzhetsky, Andrey
Publicado 2009

Genetic Variation and Population Substructure in Outbred CD-1 Mice: Implications for Genome-Wide Association Studies

por Aldinger, Kimberly A., Sokoloff, Greta, Rosenberg, David M., Palmer, Abraham A., Millen, Kathleen J.
Publicado 2009

Systemic glycerol decreases neonatal rabbit brain and cerebellar growth independent of intraventricular hemorrhage

por Traudt, Christopher M, McPherson, Ron J, Studholme, Colin, Millen, Kathleen J, Juul, Sandra E
Publicado 2013

Foxc1 dependent mesenchymal signalling drives embryonic cerebellar growth

por Haldipur, Parthiv, Gillies, Gwendolyn S, Janson, Olivia K, Chizhikov, Victor V, Mithal, Divakar S, Miller, Richard J, Millen, Kathleen J
Publicado 2014

Sensory and spinal inhibitory dorsal midline crossing is independent of Robo3

por Comer, John D., Pan, Fong Cheng, Willet, Spencer G., Haldipur, Parthiv, Millen, Kathleen J., Wright, Christopher V. E., Kaltschmidt, Julia A.
Publicado 2015

Intermediate progenitors support migration of neural stem cells into dentate gyrus outer neurogenic niches

por Nelson, Branden R, Hodge, Rebecca D, Daza, Ray AM, Tripathi, Prem Prakash, Arnold, Sebastian J, Millen, Kathleen J, Hevner, Robert F
Publicado 2020

Non-synaptic Cell-Autonomous Mechanisms Underlie Neuronal Hyperactivity in a Genetic Model of PIK3CA-Driven Intractable Epilepsy

por Roy, Achira, Han, Victor Z., Bard, Angela M., Wehle, Devin T., Smith, Stephen E. P., Ramirez, Jan-Marino, Kalume, Franck, Millen, Kathleen J.
Publicado 2021

PI3K-Yap activity drives cortical gyrification and hydrocephalus in mice

por Roy, Achira, Murphy, Rory M, Deng, Mei, MacDonald, James W, Bammler, Theo K, Aldinger, Kimberly A, Glass, Ian A, Millen, Kathleen J
Publicado 2019

Early dorsomedial tissue interactions regulate gyrification of distal neocortex

por Chizhikov, Victor V., Iskusnykh, Igor Y., Steshina, Ekaterina Y., Fattakhov, Nikolai, Lindgren, Anne G., Shetty, Ashwin S., Roy, Achira, Tole, Shubha, Millen, Kathleen J.
Publicado 2019

Phenotypic outcomes in Mouse and Human Foxc1 dependent Dandy-Walker cerebellar malformation suggest shared mechanisms

por Haldipur, Parthiv, Dang, Derek, Aldinger, Kimberly A, Janson, Olivia K, Guimiot, Fabien, Adle-Biasette, Homa, Dobyns, William B, Siebert, Joseph R, Russo, Rosa, Millen, Kathleen J
Publicado 2017

Mouse models of human PIK3CA-related brain overgrowth have acutely treatable epilepsy

por Roy, Achira, Skibo, Jonathan, Kalume, Franck, Ni, Jing, Rankin, Sherri, Lu, Yiling, Dobyns, William B, Mills, Gordon B, Zhao, Jean J, Baker, Suzanne J, Millen, Kathleen J
Publicado 2015

MDB-21. THE OTX2-REGULATED ALTERNATIVE SPLICING LANDSCAPE CONTROLS DIFFERENTIATION AND RECONSTITUTES THE DEVELOPMENTAL ORIGINS OF GROUP 3 MEDULLOBLASTOMA

por Saulnier, Olivier, Zagozewski, Jamie, Liang, Lisa, Hendrikse, Liam D, Gordon, Victor, Aldinger, Kimberly A, Haldipur, Parthiv, Borlase, Stephanie, Coudiere-Morrison, Ludivine, Layug, Paul, Cai, Ting, Porter, Christopher J, Richard, Stephane, Doble, Brad W, Millen, Kathleen J, Taylor, Michael D, Werbowetski-Ogilvie, Tamra E
Publicado 2023

Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria

por Sajan, Samin A., Fernandez, Liliana, Nieh, Sahar Esmaeeli, Rider, Eric, Bukshpun, Polina, Wakahiro, Mari, Christian, Susan L., Rivière, Jean-Baptiste, Sullivan, Christopher T., Sudi, Jyotsna, Herriges, Michael J., Paciorkowski, Alexander R., Barkovich, A. James, Glessner, Joseph T., Millen, Kathleen J., Hakonarson, Hakon, Dobyns, William B., Sherr, Elliott H.
Publicado 2013

Spiny mice activate unique transcriptional programs after severe kidney injury regenerating organ function without fibrosis

por Okamura, Daryl M., Brewer, Chris M., Wakenight, Paul, Bahrami, Nadia, Bernardi, Kristina, Tran, Amy, Olson, Jill, Shi, Xiaogang, Yeh, Szu-Ying, Piliponsky, Adrian, Collins, Sarah J., Nguyen, Elizabeth D., Timms, Andrew E., MacDonald, James W., Bammler, Theo K., Nelson, Branden R., Millen, Kathleen J., Beier, David R., Majesky, Mark W.
Publicado 2021

GENOME REPORT: Chromosome-scale genome assembly of the African spiny mouse (Acomys cahirinus)

por Nguyen, Elizabeth Dong, Fard, Vahid Nikoonejad, Kim, Bernard Y., Collins, Sarah, Galey, Miranda, Nelson, Branden R., Wakenight, Paul, Gable, Simone M., McKenna, Aaron, Bammler, Theo K., MacDonald, Jim, Okamura, Daryl M., Shendure, Jay, Beier, David R., Ramirez, Jan Marino, Majesky, Mark W., Millen, Kathleen J., Tollis, Marc, Miller, Danny E.
Publicado 2023

Genome Report: chromosome-scale genome assembly of the African spiny mouse (Acomys cahirinus)

por Nguyen, Elizabeth Dong, Fard, Vahid Nikoonejad, Kim, Bernard Y, Collins, Sarah, Galey, Miranda, Nelson, Branden R, Wakenight, Paul, Gable, Simone M, McKenna, Aaron, Bammler, Theo K, MacDonald, Jim, Okamura, Daryl M, Shendure, Jay, Beier, David R, Ramirez, Jan Marino, Majesky, Mark W, Millen, Kathleen J, Tollis, Marc, Miller, Danny E
Publicado 2023

A Novel Intergenic ETnII-β Insertion Mutation Causes Multiple Malformations in Polypodia Mice

por Lehoczky, Jessica A., Thomas, Peedikayil E., Patrie, Kevin M., Owens, Kailey M., Villarreal, Lisa M., Galbraith, Kenneth, Washburn, Joe, Johnson, Craig N., Gavino, Bryant, Borowsky, Alexander D., Millen, Kathleen J., Wakenight, Paul, Law, William, Van Keuren, Margaret L., Gavrilina, Galina, Hughes, Elizabeth D., Saunders, Thomas L., Brihn, Lesil, Nadeau, Joseph H., Innis, Jeffrey W.
Publicado 2013