Ameloblastoma: A Review of Recent Molecular Pathogenetic Discoveries

Por Brown, Noah A., Betz, Bryan L.
Publicado no Biomark Cancer (2015)

In Vivo Imatinib Sensitivity in a Patient With GI Stromal Tumor Bearing a PDGFRA Deletion DIM842-844

Por Fanta, Paul T., Sicklick, Jason K., Betz, Bryan L., Peterson, Michael R.
Publicado no J Clin Oncol (2015)

Cutaneous Syncytial Myoepithelioma: A Recently Described Neoplasm Which May Mimic Nevoid Melanoma and Epithelioid Sarcoma

Por Alomari, Ahmed K., Brown, Noah, Andea, Aleodor, Betz, Bryan L., Patel, Rajiv M.
Publicado no J Cutan Pathol (2017)

The EGFR T790M mutation is acquired through AICDA-mediated deamination of 5-methylcytosine following TKI treatment in lung cancer.

Por Kadi, Najwa El, Wang, Luo, Davis, April, Korkaya, Hasan, Cooke, Alexander, Vadnala, Varun, Brown, Noah A., Betz, Bryan L., Cascalho, Marilia, Kalemkerian, Gregory P., Hassan, Khaled A.
Publicado no Cancer Res (2018)

Gemcitabine Plus Radiation Therapy for High Grade Glioma: Long-term Results of a Phase I Dose-Escalation Study

Por Kim, Michelle M., Camelo-Piragua, Sandra, Schipper, Matthew, Tao, Yebin, Normolle, Daniel, Junck, Larry, Mammoser, Aaron, Betz, Bryan L., Cao, Yue, Kim, Christopher J, Heth, Jason, Sagher, Oren, Lawrence, Theodore S, Tsien, Christina I
Publicado no Int J Radiat Oncol Biol Phys (2015)

Brainstem Low-Grade Gliomas in Children—Excellent Outcomes With Multimodality Therapy

Por Upadhyaya, Santhosh A., Koschmann, Carl, Muraszko, Karin, Venneti, Sriram, Garton, Hugh J., Hamstra, Daniel A., Maher, Cormac O., Betz, Bryan L., Brown, Noah A., Wahl, Daniel, Weigelin, Helmut C., DuRoss, Kathleen E., Leonard, Annette S., Robertson, Patricia L.
Publicado no J Child Neurol (2016)

High frequency targetable EGFR mutations in sinonasal squamous cell carcinomas arising from inverted sinonasal papilloma

Por Udager, Aaron M., Rolland, Delphine C.M., McHugh, Jonathan B., Betz, Bryan L., Murga-Zamalloa, Carlos, Carey, Thomas E., Marentette, Lawrence J., Hermsen, Mario A., DuRoss, Kathleen E., Lim, Megan S., Elenitoba-Johnson, Kojo S. J., Brown, Noah A.
Publicado no Cancer Res (2015)

Whole-genome sequencing identifies recurrent somatic NOTCH2 mutations in splenic marginal zone lymphoma

Por Kiel, Mark J., Velusamy, Thirunavukkarasu, Betz, Bryan L., Zhao, Lili, Weigelin, Helmut G., Chiang, Mark Y., Huebner-Chan, David R., Bailey, Nathanael G., Yang, David T., Bhagat, Govind, Miranda, Roberto N., Bahler, David W., Medeiros, L. Jeffrey, Lim, Megan S., Elenitoba-Johnson, Kojo S.J.
Publicado em 2012

Integrated genomic sequencing reveals mutational landscape of T-cell prolymphocytic leukemia

Por Kiel, Mark J., Velusamy, Thirunavukkarasu, Rolland, Delphine, Sahasrabuddhe, Anagh A., Chung, Fuzon, Bailey, Nathanael G., Schrader, Alexandra, Li, Bo, Li, Jun Z., Ozel, Ayse B., Betz, Bryan L., Miranda, Roberto N., Medeiros, L. Jeffrey, Zhao, Lili, Herling, Marco, Lim, Megan S., Elenitoba-Johnson, Kojo S. J.
Publicado em 2014

Genomic analyses reveal recurrent mutations in epigenetic modifiers and the JAK–STAT pathway in Sézary syndrome

Por Kiel, Mark J., Sahasrabuddhe, Anagh A., Rolland, Delphine C. M., Velusamy, Thirunavukkarasu, Chung, Fuzon, Schaller, Matthew, Bailey, Nathanael G., Betz, Bryan L., Miranda, Roberto N., Porcu, Pierluigi, Byrd, John C., Jeffrey Medeiros, L., Kunkel, Steven L., Bahler, David W., Lim, Megan S., Elenitoba-Johnson, Kojo S. J.
Publicado no Nat Commun (2015)

Development and Validation of a Scalable Next-Generation Sequencing System for Assessing Relevant Somatic Variants in Solid Tumors()()

Por Hovelson, Daniel H., McDaniel, Andrew S., Cani, Andi K., Johnson, Bryan, Rhodes, Kate, Williams, Paul D., Bandla, Santhoshi, Bien, Geoffrey, Choppa, Paul, Hyland, Fiona, Gottimukkala, Rajesh, Liu, Guoying, Manivannan, Manimozhi, Schageman, Jeoffrey, Ballesteros-Villagrana, Efren, Grasso, Catherine S., Quist, Michael J., Yadati, Venkata, Amin, Anmol, Siddiqui, Javed, Betz, Bryan L., Knudsen, Karen E., Cooney, Kathleen A., Feng, Felix Y., Roh, Michael H., Nelson, Peter S., Liu, Chia-Jen, Beer, David G., Wyngaard, Peter, Chinnaiyan, Arul M., Sadis, Seth, Rhodes, Daniel R., Tomlins, Scott A.
Publicado no Neoplasia (2015)