检索结果 - Kasai, Yumi

Drosophila as a tool for personalized medicine: a primer 由 Kasai, Yumi, Cagan, Ross

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Specification of the Drosophila CNS Midline Cell Lineage: Direct Control of Single-Minded Transcription by Dorsal/Ventral Patterning Genes 由 Kasai, Yumi, Stahl, Stephanie, Crews, Stephen

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PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data 由 Chen, Ken, McLellan, Michael D., Ding, Li, Wendl, Michael C., Kasai, Yumi, Wilson, Richard K., Mardis, Elaine R.

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Analytical validation of whole exome and whole genome sequencing for clinical applications 由 Linderman, Michael D, Brandt, Tracy, Edelmann, Lisa, Jabado, Omar, Kasai, Yumi, Kornreich, Ruth, Mahajan, Milind, Shah, Hardik, Kasarskis, Andrew, Schadt, Eric E

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Frequency of the Cholesteryl Ester Storage Disease Common LIPA E8SJM Mutation (c.894G>A) in Various Racial and Ethnic Groups 由 Scott, Stuart A., Liu, Benny, Nazarenko, Irina, Martis, Suparna, Kozlitina, Julia, Yang, Yao, Ramirez, Charina, Kasai, Yumi, Hyatt, Tommy, Peter, Inga, Desnick, Robert J.

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Integrated Genomic Analysis Implicates Haploinsufficiency of Multiple Chromosome 5q31.2 Genes in De Novo Myelodysplastic Syndromes Pathogenesis 由 Graubert, Timothy A., Payton, Michelle A., Shao, Jin, Walgren, Richard A., Monahan, Ryan S., Frater, John L., Walshauser, Mark A., Martin, Mike G., Kasai, Yumi, Walter, Matthew J.

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Comprehensive Genetic Variant Discovery in the Surfactant Protein B Gene 由 Hamvas, Aaron, Wegner, Daniel J., Carlson, Christopher S., Bergmann, Kelly R., Trusgnich, Michelle A., Fulton, Lucinda, Kasai, Yumi, An, Ping, Mardis, Elaine R., Wilson, Richard K., Cole, F. Sessions

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Novel MEK1 Mutation Identified by Mutational Analysis of Epidermal Growth Factor Receptor Signaling Pathway Genes in Lung Adenocarcinoma 由 Marks, Jenifer L., Gong, Yixuan, Chitale, Dhananjay, Golas, Ben, McLellan, Michael D., Kasai, Yumi, Ding, Li, Mardis, Elaine R., Wilson, Richard K., Solit, David, Levine, Ross, Michel, Kathrin, Thomas, Roman K., Rusch, Valerie W., Ladanyi, Marc, Pao, William

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Mutational Analysis of EGFR and Related Signaling Pathway Genes in Lung Adenocarcinomas Identifies a Novel Somatic Kinase Domain Mutation in FGFR4 由 Marks, Jenifer L., McLellan, Michael D., Zakowski, Maureen F., Lash, Alex E., Kasai, Yumi, Broderick, Stephen, Sarkaria, Inderpal S., Pham, DuyKhanh, Singh, Bhuvanesh, Miner, Tracie L., Fewell, Ginger A., Fulton, Lucinda L., Mardis, Elaine R., Wilson, Richard K., Kris, Mark G., Rusch, Valerie W., Varmus, Harold, Pao, William

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Identification of a novel RASD1 somatic mutation in a USP8-mutated corticotroph adenoma 由 Uzilov, Andrew V., Cheesman, Khadeen C., Fink, Marc Y., Newman, Leah C., Pandya, Chetanya, Lalazar, Yelena, Hefti, Marco, Fowkes, Mary, Deikus, Gintaras, Lau, Chun Yee, Moe, Aye S., Kinoshita, Yayoi, Kasai, Yumi, Zweig, Micol, Gupta, Arpeta, Starcevic, Daniela, Mahajan, Milind, Schadt, Eric E., Post, Kalmon D., Donovan, Michael J., Sebra, Robert, Chen, Rong, Geer, Eliza B.

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Identification of somatic JAK1 mutations in patients with acute myeloid leukemia 由 Xiang, Zhifu, Zhao, Yu, Mitaksov, Vesselin, Fremont, Daved H., Kasai, Yumi, Molitoris, AnnaLynn, Ries, Rhonda E., Miner, Tracie L., McLellan, Michael D., DiPersio, John F., Link, Daniel C., Payton, Jacqueline E., Graubert, Timothy A., Watson, Mark, Shannon, William, Heath, Sharon E., Nagarajan, Rakesh, Mardis, Elaine R., Wilson, Richard K., Ley, Timothy J., Tomasson, Michael H.

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Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia 由 Tomasson, Michael H., Xiang, Zhifu, Walgren, Richard, Zhao, Yu, Kasai, Yumi, Miner, Tracie, Ries, Rhonda E., Lubman, Olga, Fremont, Daved H., McLellan, Michael D., Payton, Jacqueline E., Westervelt, Peter, DiPersio, John F., Link, Daniel C., Walter, Matthew J., Graubert, Timothy A., Watson, Mark, Baty, Jack, Heath, Sharon, Shannon, William D., Nagarajan, Rakesh, Bloomfield, Clara D., Mardis, Elaine R., Wilson, Richard K., Ley, Timothy J.

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Insights into beta cell regeneration for diabetes via integration of molecular landscapes in human insulinomas 由 Wang, Huan, Bender, Aaron, Wang, Peng, Karakose, Esra, Inabnet, William B., Libutti, Steven K., Arnold, Andrew, Lambertini, Luca, Stang, Micheal, Chen, Herbert, Kasai, Yumi, Mahajan, Milind, Kinoshita, Yayoi, Fernandez-Ranvier, Gustavo, Becker, Thomas C., Takane, Karen K., Walker, Laura A., Saul, Shira, Chen, Rong, Scott, Donald K., Ferrer, Jorge, Antipin, Yevgeniy, Donovan, Michael, Uzilov, Andrew V., Reva, Boris, Schadt, Eric E., Losic, Bojan, Argmann, Carmen, Stewart, Andrew F.

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Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia 由 Link, Daniel C., Kunter, Ghada, Kasai, Yumi, Zhao, Yu, Miner, Tracie, McLellan, Michael D., Ries, Rhonda E., Kapur, Deepak, Nagarajan, Rakesh, Dale, David C., Bolyard, Audrey Anna, Boxer, Laurence A., Welte, Karl, Zeidler, Cornelia, Donadieu, Jean, Bellanné-Chantelot, Christine, Vardiman, James W., Caligiuri, Michael A., Bloomfield, Clara D., DiPersio, John F., Tomasson, Michael H., Graubert, Timothy A., Westervelt, Peter, Watson, Mark, Shannon, William, Baty, Jack, Mardis, Elaine R., Wilson, Richard K., Ley, Timothy J.

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Development and clinical application of an integrative genomic approach to personalized cancer therapy 由 Uzilov, Andrew V., Ding, Wei, Fink, Marc Y., Antipin, Yevgeniy, Brohl, Andrew S., Davis, Claire, Lau, Chun Yee, Pandya, Chetanya, Shah, Hardik, Kasai, Yumi, Powell, James, Micchelli, Mark, Castellanos, Rafael, Zhang, Zhongyang, Linderman, Michael, Kinoshita, Yayoi, Zweig, Micol, Raustad, Katie, Cheung, Kakit, Castillo, Diane, Wooten, Melissa, Bourzgui, Imane, Newman, Leah C., Deikus, Gintaras, Mathew, Bino, Zhu, Jun, Glicksberg, Benjamin S., Moe, Aye S., Liao, Jun, Edelmann, Lisa, Dudley, Joel T., Maki, Robert G., Kasarskis, Andrew, Holcombe, Randall F., Mahajan, Milind, Hao, Ke, Reva, Boris, Longtine, Janina, Starcevic, Daniela, Sebra, Robert, Donovan, Michael J., Li, Shuyu, Schadt, Eric E., Chen, Rong

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