Search Results - "VAKA, Dedeepya"

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    Organ Size Control Is Dominant over Rb Family Inactivation to Restrict Proliferation In Vivo by Ehmer, Ursula, Zmoos, Anne-Flore, Auerbach, Raymond K., Vaka, Dedeepya, Butte, Atul J., Kay, Mark A., Sage, Julien

    Published in Cell reports (Cambridge) (24-07-2014)
    “…In mammals, a cell’s decision to divide is thought to be under the control of the Rb/E2F pathway. We previously found that inactivation of the Rb family of…”
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    Lymphangiocrine signals are required for proper intestinal repair after cytotoxic injury by Palikuqi, Brisa, Rispal, Jérémie, Reyes, Efren A., Vaka, Dedeepya, Boffelli, Dario, Klein, Ophir

    Published in Cell stem cell (04-08-2022)
    “…The intestinal epithelium undergoes continuous renewal and has an exceptional capacity to regenerate after injury. Maintenance and proliferation of intestinal…”
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    Tissue signals imprint ILC2 identity with anticipatory function by Ricardo-Gonzalez, Roberto R., Van Dyken, Steven J., Schneider, Christoph, Lee, Jinwoo, Nussbaum, Jesse C., Liang, Hong-Erh, Vaka, Dedeepya, Eckalbar, Walter L., Molofsky, Ari B., Erle, David J., Locksley, Richard M.

    Published in Nature immunology (01-10-2018)
    “…Group 2 innate lymphoid cells (ILC2s) are distributed systemically and produce type 2 cytokines in response to a variety of stimuli, including the epithelial…”
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    Comprehensive genomic profiles of small cell lung cancer by George, Julie, Lim, Jing Shan, Jang, Se Jin, Cun, Yupeng, Ozretić, Luka, Kong, Gu, Leenders, Frauke, Lu, Xin, Fernández-Cuesta, Lynnette, Bosco, Graziella, Müller, Christian, Dahmen, Ilona, Jahchan, Nadine S., Park, Kwon-Sik, Yang, Dian, Karnezis, Anthony N., Vaka, Dedeepya, Torres, Angela, Wang, Maia Segura, Korbel, Jan O., Menon, Roopika, Chun, Sung-Min, Kim, Deokhoon, Wilkerson, Matt, Hayes, Neil, Engelmann, David, Pützer, Brigitte, Bos, Marc, Michels, Sebastian, Vlasic, Ignacija, Seidel, Danila, Pinther, Berit, Schaub, Philipp, Becker, Christian, Altmüller, Janine, Yokota, Jun, Kohno, Takashi, Iwakawa, Reika, Tsuta, Koji, Noguchi, Masayuki, Muley, Thomas, Hoffmann, Hans, Schnabel, Philipp A., Petersen, Iver, Chen, Yuan, Soltermann, Alex, Tischler, Verena, Choi, Chang-min, Kim, Yong-Hee, Massion, Pierre P., Zou, Yong, Jovanovic, Dragana, Kontic, Milica, Wright, Gavin M., Russell, Prudence A., Solomon, Benjamin, Koch, Ina, Lindner, Michael, Muscarella, Lucia A., la Torre, Annamaria, Field, John K., Jakopovic, Marko, Knezevic, Jelena, Castaños-Vélez, Esmeralda, Roz, Luca, Pastorino, Ugo, Brustugun, Odd-Terje, Lund-Iversen, Marius, Thunnissen, Erik, Köhler, Jens, Schuler, Martin, Botling, Johan, Sandelin, Martin, Sanchez-Cespedes, Montserrat, Salvesen, Helga B., Achter, Viktor, Lang, Ulrich, Bogus, Magdalena, Schneider, Peter M., Zander, Thomas, Ansén, Sascha, Hallek, Michael, Wolf, Jürgen, Vingron, Martin, Yatabe, Yasushi, Travis, William D., Nürnberg, Peter, Reinhardt, Christian, Perner, Sven, Heukamp, Lukas, Büttner, Reinhard, Haas, Stefan A., Brambilla, Elisabeth, Peifer, Martin, Sage, Julien, Thomas, Roman K.

    Published in Nature (London) (06-08-2015)
    “…We have sequenced the genomes of 110 small cell lung cancers (SCLC), one of the deadliest human cancers. In nearly all the tumours analysed we found bi-allelic…”
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    A Meta-analysis of Lung Cancer Gene Expression Identifies PTK7 as a Survival Gene in Lung Adenocarcinoma by RON CHEN, KHATRI, Purvesh, BUTTE, Atul J, SWEET-CORDERO, E. Alejandro, MAZUR, Pawel K, POLIN, Melanie, YANYAN ZHENG, VAKA, Dedeepya, HOANG, Chuong D, SHRAGER, Joseph, YUE XU, VICENT, Silvestre

    Published in Cancer research (Chicago, Ill.) (15-05-2014)
    “…Lung cancer remains the most common cause of cancer-related death worldwide and it continues to lack effective treatment. The increasingly large and diverse…”
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    Whole exome and whole genome sequencing with dried blood spot DNA without whole genome amplification by Bassaganyas, Laia, Freedman, George, Vaka, Dedeepya, Wan, Eunice, Lao, Richard, Chen, Flavia, Kvale, Mark, Currier, Robert J., Puck, Jennifer M., Kwok, Pui‐Yan

    Published in Human mutation (01-01-2018)
    “…Newborn screening (NBS) for rare conditions is performed in all 50 states in the USA. We have partnered with the California Department of Public Health Genetic…”
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