Id4 and FABP7 are preferentially expressed in cells with astrocytic features in oligodendrogliomas and oligoastrocytomas

por Liang, Yu, Bollen, Andrew W, Nicholas, M Kelly, Gupta, Nalin
Publicado 2005

Nuclear FABP7 immunoreactivity is preferentially expressed in infiltrative glioma and is associated with poor prognosis in EGFR-overexpressing glioblastoma

por Liang, Yu, Bollen, Andrew W, Aldape, Ken D, Gupta, Nalin
Publicado 2006

Systemic and Craniospinal Rosai Dorfman Disease with Intraparenchymal, Intramedullary and Leptomeningeal Disease

por Li, Yi, Sloan, Emily, Bollen, Andrew, Solomon, David, Theodosopoulos, Philip, Cha, Soonmee
Publicado 2021

Case Report: Neuroblastoma-Like Schwannoma in a Domestic Short-Haired Cat

por Chen, Vivian S., Bollen, Andrew W., Marco-Salazar, Paola, Higgins, Robert J., Sisó, Sílvia
Publicado 2022

Clinical Utility of LC3 and p62 Immunohistochemistry in Diagnosis of Drug-Induced Autophagic Vacuolar Myopathies: A Case-Control Study

por Lee, Han S., Daniels, Brianne H., Salas, Eduardo, Bollen, Andrew W., Debnath, Jayanta, Margeta, Marta
Publicado 2012

Endothelial Rbpj deletion normalizes Notch4-induced brain arteriovenous malformation in mice

por Nielsen, Corinne M., Zhang, Xuetao, Raygor, Kunal, Wang, Shaoxun, Bollen, Andrew W., Wang, Rong A.
Publicado 2022

Adult-onset central nervous system hemophagocytic lymphohistiocytosis: a case report

por Pastula, Daniel M., Burish, Mark, Reis, Gerald F., Bollen, Andrew, Cha, Soonmee, Ralph, Jeffrey, Douglas, Vanja C.
Publicado 2015

Human Neurobrucellosis with Intracerebral Granuloma Caused by a Marine Mammal Brucella spp.

por Sohn, Annette H., Probert, Will S., Glaser, Carol A., Gupta, Nalin, Bollen, Andrew W., Wong, Jane D., Grace, Elizabeth M., McDonald, William C.
Publicado 2003

Somatic mosaic SOX10 indel mutations underlie a form of segmental schwannomatosis

por Terry, Merryl, Gupta, Rohit, Ravindranathan, Ajay, Wu, Jasper, Chan, Emily, Bollen, Andrew W., Chang, Susan M., Berger, Mitchel S., Jacques, Line, Solomon, David A.
Publicado 2023

Familial melanoma-astrocytoma syndrome: synchronous diffuse astrocytoma and pleomorphic xanthoastrocytoma in a patient with germline CDKN2A/B deletion and a significant family hist...

por Chan, Andrew K., Han, Seunggu J., Choy, Winward, Beleford, Daniah, Aghi, Manish K., Berger, Mitchel S., Shieh, Joseph T., Bollen, Andrew W., Perry, Arie, Phillips, Joanna J., Butowski, Nicholas, Solomon, David A.
Publicado 2017

Successful Treatment of Balamuthia mandrillaris Granulomatous Amebic Encephalitis with Nitroxoline

por Spottiswoode, Natasha, Pet, Douglas, Kim, Annie, Gruenberg, Katherine, Shah, Maulik, Ramachandran, Amrutha, Laurie, Matthew T., Zia, Maham, Fouassier, Camille, Boutros, Christine L., Lu, Rufei, Zhang, Yueyuan, Servellita, Venice, Bollen, Andrew, Chiu, Charles Y., Wilson, Michael R., Valdivia, Liza, DeRisi, Joseph L.
Publicado 2023

Diagnosing Balamuthia mandrillaris Encephalitis With Metagenomic Deep Sequencing

por Wilson, Michael R., Shanbhag, Niraj M., Reid, Michael J., Singhal, Neel S., Gelfand, Jeffrey M., Sample, Hannah A., Benkli, Barlas, O'Donovan, Brian D., Ali, Ibne K.M., Keating, M. Kelly, Dunnebacke, Thelma H., Wood, Matthew D., Bollen, Andrew, DeRisi, Joseph L.
Publicado 2015

Genome-Wide Association Analysis Identifies a Mutation in the Thiamine Transporter 2 (SLC19A3) Gene Associated with Alaskan Husky Encephalopathy

por Vernau, Karen M., Runstadler, Jonathan A., Brown, Emily A., Cameron, Jessie M., Huson, Heather J., Higgins, Robert J., Ackerley, Cameron, Sturges, Beverly K., Dickinson, Peter J., Puschner, Birgit, Giulivi, Cecilia, Shelton, G. Diane, Robinson, Brian H., DiMauro, Salvatore, Bollen, Andrew W., Bannasch, Danika L.
Publicado 2013

Multiplatform Molecular Profiling Reveals Epigenomic Intratumor Heterogeneity in Ependymoma

por Liu, S. John, Magill, Stephen T., Vasudevan, Harish N., Hilz, Stephanie, Villanueva-Meyer, Javier E., Lastella, Sydney, Daggubati, Vikas, Spatz, Jordan, Choudhury, Abrar, Orr, Brent A., Demaree, Benjamin, Seo, Kyounghee, Ferris, Sean P., Abate, Adam R., Oberheim Bush, Nancy Ann, Bollen, Andrew W., McDermott, Michael W., Costello, Joseph F., Raleigh, David R.
Publicado 2020

Clinical, radiologic, and genetic characteristics of histone H3 K27M-mutant diffuse midline gliomas in adults

por Schulte, Jessica D, Buerki, Robin A, Lapointe, Sarah, Molinaro, Annette M, Zhang, Yalan, Villanueva-Meyer, Javier E, Perry, Arie, Phillips, Joanna J, Tihan, Tarik, Bollen, Andrew W, Pekmezci, Melike, Butowski, Nicholas, Oberheim Bush, Nancy Ann, Taylor, Jennie W, Chang, Susan M, Theodosopoulos, Philip, Aghi, Manish K, Hervey-Jumper, Shawn L, Berger, Mitchel S, Solomon, David A, Clarke, Jennifer L
Publicado 2020

A genetically distinct pediatric subtype of primary CNS large B-cell lymphoma is associated with favorable clinical outcome

por Güney, Ekin, Lucas, Calixto-Hope G., Qi, Zhongxia, Yu, Jingwei, Zhang, Ruth, Ohgami, Robert S., Rubenstein, James L., Boué, Daniel R., Schafernak, Kristian, Wertheim, Gerald B., Dahiya, Sonika, Giulino-Roth, Lisa, Attarbaschi, Andishe, Barth, Matthew J., Kothari, Shalin, Abla, Oussama, Cohen, Adam L., Mendez, Joe S., Bollen, Andrew, Perry, Arie, Tihan, Tarik, Pekmezci, Melike, Solomon, David A., Wen, Kwun Wah
Publicado 2022

Molecular profiling identifies at least 3 distinct types of posttransplant lymphoproliferative disorder involving the CNS

por Guney, Ekin, Lucas, Calixto-Hope G., Singh, Kunwar, Pekmezci, Melike, Fernandez-Pol, Sebastian, Mirchia, Kanish, Toland, Angus, Vogel, Hannes, Bannykh, Serguei, Schafernak, Kristian T., Alexandrescu, Sanda, Mobley, Bret C., Powell, Suzanne, Davidson, Christian J., Neltner, Janna, Boué, Daniel R., Hattab, Eyas, Ferris, Sean P., Ohgami, Robert S., Rubenstein, James L., Bollen, Andrew W., Tihan, Tarik, Perry, Arie, Solomon, David A., Wen, Kwun Wah
Publicado 2023

The genetic landscape of ganglioglioma

por Pekmezci, Melike, Villanueva-Meyer, Javier E., Goode, Benjamin, Van Ziffle, Jessica, Onodera, Courtney, Grenert, James P., Bastian, Boris C., Chamyan, Gabriel, Maher, Ossama M., Khatib, Ziad, Kleinschmidt-DeMasters, Bette K., Samuel, David, Mueller, Sabine, Banerjee, Anuradha, Clarke, Jennifer L., Cooney, Tabitha, Torkildson, Joseph, Gupta, Nalin, Theodosopoulos, Philip, Chang, Edward F., Berger, Mitchel, Bollen, Andrew W., Perry, Arie, Tihan, Tarik, Solomon, David A.
Publicado 2018

A recurrent kinase domain mutation in PRKCA defines chordoid glioma of the third ventricle

por Goode, Benjamin, Mondal, Gourish, Hyun, Michael, Ruiz, Diego Garrido, Lin, Yu-Hsiu, Van Ziffle, Jessica, Joseph, Nancy M., Onodera, Courtney, Talevich, Eric, Grenert, James P., Hewedi, Iman H., Snuderl, Matija, Brat, Daniel J., Kleinschmidt-DeMasters, Bette K., Rodriguez, Fausto J., Louis, David N., Yong, William H., Lopes, M. Beatriz, Rosenblum, Marc K., Butowski, Nicholas, Tihan, Tarik, Bollen, Andrew W., Phillips, Joanna J., Wiita, Arun P., Yeh, Iwei, Jacobson, Matthew P., Bastian, Boris C., Perry, Arie, Solomon, David A.
Publicado 2018

Prospective genomically guided identification of “early/evolving” and “undersampled” IDH-wildtype glioblastoma leads to improved clinical outcomes

por Zhang, Yalan, Lucas, Calixto-Hope G, Young, Jacob S, Morshed, Ramin A, McCoy, Lucie, Oberheim Bush, Nancy Ann, Taylor, Jennie W, Daras, Mariza, Butowski, Nicholas A, Villanueva-Meyer, Javier E, Cha, Soonmee, Wrensch, Margaret, Wiencke, John K, Lee, Julieann C, Pekmezci, Melike, Phillips, Joanna J, Perry, Arie, Bollen, Andrew W, Aghi, Manish K, Theodosopoulos, Philip, Chang, Edward F, Hervey-Jumper, Shawn L, Berger, Mitchel S, Clarke, Jennifer L, Chang, Susan M, Molinaro, Annette M, Solomon, David A
Publicado 2022