Loss of Ptf1a Leads to a Widespread Cell-Fate Misspecification in the Brainstem, Affecting the Development of Somatosensory and Viscerosensory Nuclei

Por Iskusnykh, Igor Y., Steshina, Ekaterina Y., Chizhikov, Victor V.
Publicado no J Neurosci (2016)

Transformation of the cerebellum into more ventral brainstem fates causes cerebellar agenesis in the absence of Ptf1a function

Por Millen, Kathleen J., Steshina, Ekaterina Y., Iskusnykh, Igor Y., Chizhikov, Victor V.
Publicado em 2014

Overlapping Function of Lmx1a and Lmx1b in Anterior Hindbrain Roof Plate Formation and Cerebellar Growth

Por Mishima, Yuriko, Lindgren, Anne G., Chizhikov, Victor V., Johnson, Randy L., Millen, Kathleen J.
Publicado em 2009

Phenotypic and genetic analysis of the cerebellar mutant tmgc26, a new ENU-induced ROR-alpha allele

Por Swanson, Douglas, Steshina, Ekaterina Y., Wakenight, Paul, Aldinger, Kimberly A., Goldowitz, Daniel, Millen, Kathleen J., Chizhikov, Victor V.
Publicado em 2010

Multiple developmental programs are altered by loss of Zic1 and Zic4 to cause Dandy-Walker malformation cerebellar pathogenesis

Por Blank, Marissa C., Grinberg, Inessa, Aryee, Emmanuel, Laliberte, Christine, Chizhikov, Victor V., Henkelman, R. Mark, Millen, Kathleen J.
Publicado em 2011

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 no eLife (2014)

The spontaneous ataxic mouse mutant tippy is characterized by a novel Purkinje cell morphogenesis and degeneration phenotype

Por Shih, Evelyn K., Sekerková, Gabriella, Ohtsuki, Gen, Aldinger, Kimberly A., Chizhikov, Victor V., Hansel, Christian, Mugnaini, Enrico, Millen, Kathleen J.
Publicado no Cerebellum (2015)

Lmx1a regulates fates and location of cells originating from the cerebellar rhombic lip and telencephalic cortical hem

Por Chizhikov, Victor V., Lindgren, Anne G., Mishima, Yuriko, Roberts, Richard W., Aldinger, Kimberly A., Miesegaes, George R., Currle, D. Spencer, Monuki, Edwin S., Millen, Kathleen J.
Publicado em 2010

FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation

Por Aldinger, Kimberly A, Lehmann, Ordan J, Hudgins, Louanne, Chizhikov, Victor V, Bassuk, Alexander G, Ades, Lesley C, Krantz, Ian D, Dobyns, William B, Millen, Kathleen J
Publicado em 2009

Active medulloblastoma enhancers reveal subgroup-specific cellular origins

Por Lin, Charles Y., Erkek, Serap, Tong, Yiai, Yin, Linlin, Federation, Alexander J., Zapatka, Marc, Haldipur, Parthiv, Kawauchi, Daisuke, Risch, Thomas, Warnatz, Hans-Jörg, Worst, Barbara C., Ju, Bensheng, Orr, Brent A., Zeid, Rhamy, Polaski, Donald R., Segura-Wang, Maia, Waszak, Sebastian M., Jones, David T.W., Kool, Marcel, Hovestadt, Volker, Buchhalter, Ivo, Sieber, Laura, Johann, Pascal, Chavez, Lukas, Gröschel, Stefan, Ryzhova, Marina, Korshunov, Andrey, Chen, Wenbiao, Chizhikov, Victor V., Millen, Kathleen J., Amstislavskiy, Vyacheslav, Lehrach, Hans, Yaspo, Marie-Laure, Eils, Roland, Lichter, Peter, Korbel, Jan O., Pfister, Stefan M., Bradner, James E., Northcott, Paul A.
Publicado no Nature (2016)

The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes

Por Curry, Cynthia J, Rosenfeld, Jill A, Grant, Erica, Gripp, Karen W, Anderson, Carol, Aylsworth, Arthur S, Ben Saad, Taha, Chizhikov, Victor V, Dybose, Giedre, Fagerberg, Christina, Falco, Michelle, Fels, Christina, Fichera, Marco, Graakjaer, Jesper, Greco, Donatella, Hair, Jennifer, Hopkins, Elizabeth, Huggins, Marlene, Ladda, Roger, Li, Chumei, Moeschler, John, Nowaczyk, Malgorzata JM, Ozmore, Jillian R, Reitano, Santina, Romano, Corrado, Roos, Laura, Schnur, Rhonda E, Sell, Susan, Suwannarat, Pim, Svaneby, Dea, Szybowska, Marta, Tarnopolsky, Mark, Tervo, Raymond, Tsai, Anne Chun-Hui, Tucker, Megan, Vallee, Stephanie, Wheeler, Ferrin C, Zand, Dina J, Barkovich, A James, Aradhya, Swaroop, Shaffer, Lisa G, Dobyns, William B
Publicado no Am J Med Genet A (2013)