Ngā hua rapu - Lin, Jimmy C

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

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