檢索結果 - Lin, Jimmy C

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

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Novel somatic mutations in heterotrimeric G proteins in melanoma 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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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