Molecular alterations in areas generating fast ripples in an animal model of temporal lobe epilepsy

Por Winden, Kellen D., Bragin, Anatol, Engel, Jerome, Geschwind, Dan H.
Publicado no Neurobiol Dis (2015)

Stroke in Primary Hyperoxaluria Type I

Por Rao, Neal M., Yallapragada, Anil, Winden, Kellen D., Saver, Jeffrey, Liebeskind, David S.
Publicado em 2013

A Systems Level, Functional Genomics Analysis of Chronic Epilepsy

Por Winden, Kellen D., Karsten, Stanislav L., Bragin, Anatol, Kudo, Lili C., Gehman, Lauren, Ruidera, Josephine, Geschwind, Daniel H., Engel, Jerome
Publicado em 2011

The organization of the transcriptional network in specific neuronal classes

Por Winden, Kellen D, Oldham, Michael C, Mirnics, Karoly, Ebert, Philip J, Swan, Christo H, Levitt, Pat, Rubenstein, John L, Horvath, Steve, Geschwind, Daniel H
Publicado em 2009

Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex

Por Ercan, Ebru, Han, Juliette M., Di Nardo, Alessia, Winden, Kellen, Han, Min-Joon, Hoyo, Leonie, Saffari, Afshin, Leask, Andrew, Geschwind, Daniel H., Sahin, Mustafa
Publicado no J Exp Med (2017)

Human-Specific Transcriptional Regulation of CNS Development Genes by FOXP2

Por Konopka, Genevieve, Bomar, Jamee M., Winden, Kellen, Coppola, Giovanni, Jonsson, Zophonias O., Gao, Fuying, Peng, Sophia, Preuss, Todd M., Wohlschlegel, James A., Geschwind, Daniel H.
Publicado em 2009

Substrate Sequence Influences γ-Secretase Modulator Activity, Role of the Transmembrane Domain of the Amyloid Precursor Protein

Por Sagi, Sarah A., Lessard, Christian B., Winden, Kellen D., Maruyama, Hiroko, Koo, Jeremy C., Weggen, Sascha, Kukar, Thomas L., Golde, Todd E., Koo, Edward H.
Publicado em 2011

Human-specific transcriptional networks in the brain

Por Konopka, Genevieve, Friedrich, Tara, Davis-Turak, Jeremy, Winden, Kellen, Oldham, Michael C., Gao, Fuying, Chen, Leslie, Wang, Guang-Zhong, Luo, Rui, Preuss, Todd M., Geschwind, Daniel H.
Publicado em 2012

Functional Genomic Analyses Identify Pathways Dysregulated by Progranulin Deficiency Implicating Wnt Signaling

Por Rosen, Ezra Y., Wexler, Eric M., Versano, Revital, Coppola, Giovanni, Gao, Fuying, Winden, Kellen D., Oldham, Michael C., Martens, Lauren Herl, Zhou, Ping, Farese, Robert V., Geschwind, Daniel H.
Publicado em 2011

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities and core autism-related deficits

Por Peñagarikano, Olga, Abrahams, Brett S., Herman, Edward I., Winden, Kellen C., Gdalyahu, Amos, Dong, Hongmei, Sonnenblick, Lisa I., Gruver, Robin, Almajano, Joel, Bragin, Anatol, Golshani, Peyman, Trachtenberg, Joshua T., Peles, Elior, Geschwind, Daniel H.
Publicado em 2011