Search Results - Lin, Jimmy C

Delving into somatic variation in sporadic melanoma by Walia, Vijay, Mu, Euphemia W., Lin, Jimmy C., Samuels, Yardena

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Novel somatic mutations in heterotrimeric G proteins in melanoma by Cárdenas-Navia, L Isabel, Cruz, Pedro, Lin, Jimmy C, Rosenberg, Steven A, Samuels, Yardena

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Clinical applications of next generation sequencing in cancer: from panels, to exomes, to genomes by Shen, Tony, Pajaro-Van de Stadt, Stefan Hans, Yeat, Nai Chien, Lin, Jimmy C.-H.

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Comparative exome sequencing of metastatic lesions provides insights into the mutational progression of melanoma by Gartner, Jared J, Davis, Sean, Wei, Xiaomu, Lin, Jimmy C, Trivedi, Niraj S, Teer, Jamie K, Meltzer, Paul S, Rosenberg, Steven A, Samuels, Yardena

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Analysis of the Tyrosine Kinome in Melanoma Reveals Recurrent Mutations in ERBB4 by Prickett, Todd D., Agrawal, Neena S., Wei, Xiaomu, Yates, Kristin E., Lin, Jimmy C., Wunderlich, John, Cronin, Julia C., Cruz, Pedro, Rosenberg, Steven A., Samuels, Yardena

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Analysis of the Disintegrin-metalloproteinases Family Reveals ADAM29 and ADAM7 Are Often Mutated in Melanoma by Wei, Xiaomu, Moncada-Pazos, Angela, Cal, Santiago, Soria-Valles, Clara, Gartner, Jared, Rudloff, Udo, Lin, Jimmy C., Rosenberg, Steven A., López-Otín, Carlos, Samuels, Yardena

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Mutational and Functional Analysis of the Tumor-Suppressor PTPRD in Human Melanoma by Walia, Vijay, Prickett, Todd D., Kim, Jung-Sik, Gartner, Jared J., Lin, Jimmy C., Zhou, Ming, Rosenberg, Steven A., Elble, Randolph C., Solomon, David A., Waldman, Todd, Samuels, Yardena

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Mining Exomic Sequencing Data to Identify Mutated Antigens Recognized by Adoptively Transferred Tumor-reactive T cells by Robbins, Paul F., Lu, Yong-Chen, El-Gamil, Mona, Li, Yong F., Gross, Colin, Gartner, Jared, Lin, Jimmy C., Teer, Jamie K., Cliften, Paul, Tycksen, Eric, Samuels, Yardena, Rosenberg, Steven A.

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Mutational and Functional Analysis Reveals ADAMTS18 Metalloproteinase as a Novel Oncogene in Melanoma by Wei, Xiaomu, Prickett, Todd D., Viloria, Cristina G., Molinolo, Alfredo, Lin, Jimmy C., Cardenas-Navia, Isabel, Cruz, Pedro, Rosenberg, Steven A., Davies, Michael A., Gershenwald, Jeffrey E., López-Otín, Carlos, Samuels, Yardena

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Exome sequencing identifies GRIN2A as frequently mutated in melanoma by Wei, Xiaomu, Walia, Vijay, Lin, Jimmy C, Teer, Jamie K, Prickett, Todd D, Gartner, Jared, Davis, Sean, Stemke-Hale, Katherine, Davies, Michael A, Gershenwald, Jeffrey E, Robinson, William, Robinson, Steven, Rosenberg, Steven A, Samuels, Yardena

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Frequent Mutations in the MITF Pathway in Melanoma by Cronin, Julia C., Wunderlich, John, Loftus, Stacie K., Prickett, Todd D., Wei, Xiaomu, Ridd, Katie, Vemula, Swapna, Burrell, Allison S., Agrawal, Neena S., Lin, Jimmy C., Banister, Carolyn E., Buckhaults, Phillip, Rosenberg, Steven A., Bastian, Boris C., Pavan, William J., Samuels, Yardena

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Exon capture analysis of G protein-coupled receptors identifies activating mutations in GRM3 in melanoma by Prickett, Todd D, Wei, Xiaomu, Cardenas-Navia, Isabel, Teer, Jamie K, Lin, Jimmy C, Walia, Vijay, Gartner, Jared, Jiang, Jiji, Cherukuri, Praveen F, Molinolo, Alfredo, Davies, Michael A, Gershenwald, Jeffrey E, Stemke-Hale, Katherine, Rosenberg, Steven A, Margulies, Elliott H, Samuels, Yardena

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Organization for rare diseases India (ORDI) – addressing the challenges and opportunities for the Indian rare diseases' community by RAJASIMHA, HARSHA KARUR, SHIROL, PRASANNAKUMAR BASAYYA, RAMAMOORTHY, PREVEEN, HEGDE, MADHURI, BARDE, SANGEETA, CHANDRU, VIJAY, RAVINANDAN, M. E., RAMCHANDRAN, RAMANI, HALDAR, KASTURI, LIN, JIMMY C., BABAR, IMRAN A., GIRISHA, KATTA M., SRINIVASAN, SUDHA, NAVANEETHAM, DURAISWAMY, BATTU, RAJANI, DEVARAKONDA, RAJASHREE, KINI, USHA, VIJAYACHANDRA, KINNIMULKI, VERMA, ISHWAR C.

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Somatic mutations in MAP3K5 attenuate its pro-apoptotic function in melanoma through increased binding to Thioredoxin by Prickett, Todd D., Zerlanko, Brad, Gartner, Jared J., Parker, Stephen C. J., Dutton-Regester, Ken, Lin, Jimmy C., Teer, Jamie K., Wei, Xiaomu, Jiang, Jiji, Chen, Guo, Davies, Michael A., Gershenwald, Jeffrey E., Robinson, William, Robinson, Steven, Hayward, Nicholas K., Rosenberg, Steven, A., Margulies, Elliott H., Samuels, Yardena

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Multi-Dimensional Omics for Precision Therapy of Children and Adolescent Young Adults with Relapsed and Refractory Cancer: Report from Pediatric Oncology Branch, NCI by Chang, Wendy, Brohl, Andrew S., Patidar, Rajesh, Sindiri, Sivasish, Shern, Jack F., Wei, Jun S., Song, Young K., Yohe, Marielle E., Gryder, Berkley, Zhang, Shile, Calzone, Kathleen A., Shivaprasad, Nityashree, Wen, Xinyu, Badgett, Thomas C., Miettinen, Markku, Hartman, Kip R., League-Pascual, James C., Trahair, Toby N., Widemann, Brigitte C., Merchant, Melinda S., Kaplan, Rosandra N., Lin, Jimmy C., Khan, Javed

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RGS7 is recurrently mutated in melanoma and promotes migration and invasion of human cancer cells by Qutob, Nouar, Masuho, Ikuo, Alon, Michal, Emmanuel, Rafi, Cohen, Isadora, Di Pizio, Antonella, Madore, Jason, Elkahloun, Abdel, Ziv, Tamar, Levy, Ronen, Gartner, Jared J., Hill, Victoria K., Lin, Jimmy C., Hevroni, Yael, Greenberg, Polina, Brodezki, Alexandra, Rosenberg, Steven A., Kosloff, Mickey, Hayward, Nicholas K., Admon, Arie, Niv, Masha Y., Scolyer, Richard A., Martemyanov, Kirill A., Samuels, Yardena

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Author Correction: RGS7 is recurrently mutated in melanoma and promotes migration and invasion of human cancer cells by Qutob, Nouar, Masuho, Ikuo, Alon, Michal, Emmanuel, Rafi, Cohen, Isadora, Di Pizio, Antonella, Madore, Jason, Elkahloun, Abdel, Ziv, Tamar, Levy, Ronen, Gartner, Jared J., Hill, Victoria K., Lin, Jimmy C., Hevroni, Yael, Greenberg, Polina, Brodezki, Alexandra, Rosenberg, Steven A., Kosloff, Mickey, Hayward, Nicholas K., Admon, Arie, Niv, Masha Y., Scolyer, Richard A., Martemyanov, Kirill A., Samuels, Yardena

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Integrated analysis of homozygous deletions, focal amplifications, and sequence alterations in breast and colorectal cancers by Leary, Rebecca J., Lin, Jimmy C., Cummins, Jordan, Boca, Simina, Wood, Laura D., Parsons, D. Williams, Jones, Siân, Sjöblom, Tobias, Park, Ben-Ho, Parsons, Ramon, Willis, Joseph, Dawson, Dawn, Willson, James K. V., Nikolskaya, Tatiana, Nikolsky, Yuri, Kopelovich, Levy, Papadopoulos, Nick, Pennacchio, Len A., Wang, Tian-Li, Markowitz, Sanford D., Parmigiani, Giovanni, Kinzler, Kenneth W., Vogelstein, Bert, Velculescu, Victor E.

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Analysis of the matrix metalloproteinase family reveals that MMP8 is often mutated in melanoma by Palavalli, Lavanya H, Prickett, Todd D, Wunderlich, John R, Wei, Xiaomu, Burrell, Allison S, Porter-Gill, Patricia, Davis, Sean, Wang, Chenwei, Cronin, Julia C, Agrawal, Neena S, Lin, Jimmy C, Westbroek, Wendy, Hoogstraten-Miller, Shelley, Molinolo, Alfredo A, Fetsch, Patricia, Filie, Armando C, O’Connell, Michael P, Banister, Carolyn E, Howard, Jason D, Buckhaults, Phillip, Weeraratna, Ashani T, Brody, Lawrence C, Rosenberg, Steven A, Samuels, Yardena

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Recurrent inactivating RASA2 mutations in melanoma by Arafeh, Rand, Qutob, Nouar, Emmanuel, Rafi, Keren-Paz, Alona, Madore, Jason, Elkahloun, Abdel, Wilmott, James S., Gartner, Jared J., Di Pizio, Antonella, Winograd-Katz, Sabina, Sindiri, Sivasish, Rotkopf, Ron, Dutton-Regester, Ken, Johansson, Peter, Pritchard, Antonia, Waddell, Nicola, Hill, Victoria K., Lin, Jimmy C., Hevroni, Yael, Rosenberg, Steven A., Khan, Javed, Ben-Dor, Shifra, Niv, Masha Y., Ulitsky, Igor, Mann, Graham J, Scolyer, Richard A., Hayward, Nicholas K., Samuels, Yardena

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