NFκB-regulation of c-FLIP promotes TNFα-mediated RAF inhibitor resistance in melanoma

od Shao, Yongping, Le, Kaitlyn, Cheng, Hanyin, Aplin, Andrew E.
Wydane w J Invest Dermatol (2015)

Phosphorylation of Human Jak3 at Tyrosines 904 and 939 Positively Regulates Its Activity

od Cheng, Hanyin, Ross, Jeremy A., Frost, Jeffrey A., Kirken, Robert A.
Wydane 2008

Protein Phosphatase 2A Regulates Interleukin-2 Receptor Complex Formation and JAK3/STAT5 Activation

od Ross, Jeremy A., Cheng, Hanyin, Nagy, Zsuzsanna S., Frost, Jeffrey A., Kirken, Robert A.
Wydane 2010

CARMA1 Regulation of Regulatory T Cell Development Involves Modulation of Interleukin-2 Receptor Signaling

od Lee, Andrew Joon, Wu, Xuefeng, Cheng, Hanyin, Zhou, Xiaofei, Cheng, Xuhong, Sun, Shao-Cong
Wydane 2010

Dual Targeting of CDK4/6 and cMET in Metastatic Uveal Melanoma

od Ohara, Masahiro, Saito, Kengo, Kageyama, Ken, Terai, Mizue, Cheng, Hanyin, Aplin, Andrew E., Sato, Takami
Wydane w Cancers (Basel) (2021)

Paracrine effect of NRG1 and HGF drives resistance to MEK inhibitors in metastatic uveal melanoma

od Cheng, Hanyin, Terai, Mizue, Kageyama, Ken, Ozaki, Shinji, McCue, Peter A., Sato, Takami, Aplin, Andrew E.
Wydane w Cancer Res (2015)

Co-targeting HGF-cMET signaling with MEK inhibitors in metastatic uveal melanoma

od Cheng, Hanyin, Chua, Vivian, Liao, Connie, Purwin, Timothy J., Terai, Mizue, Kageyama, Ken, Davies, Michael A., Sato, Takami, Aplin, Andrew E.
Wydane w Mol Cancer Ther (2017)

Establishment and Characterization of Orthotopic Mouse Models for Human Uveal Melanoma Hepatic Colonization

od Ozaki, Shinji, Vuyyuru, Raja, Kageyama, Ken, Terai, Mizue, Ohara, Masahiro, Cheng, Hanyin, Manser, Tim, Mastrangelo, Michael J., Aplin, Andrew E., Sato, Takami
Wydane w Am J Pathol (2016)

Circulating Plasma MiR-141 Is a Novel Biomarker for Metastatic Colon Cancer and Predicts Poor Prognosis

od Cheng, Hanyin, Zhang, Lina, Cogdell, David E., Zheng, Hong, Schetter, Aaron J., Nykter, Matti, Harris, Curtis C., Chen, Kexin, Hamilton, Stanley R., Zhang, Wei
Wydane 2011

Somatic Deletions of the PolyA Tract in the 3′ Untranslated Region of Epidermal Growth Factor Receptor Are Common in Microsatellite Instability–High Endometrial and Colorectal Carc...

od Ma, Deqin, Chen, Zhao, Nero, Christopher, Patel, Keyur P., Daoud, Emad M., Cheng, Hanyin, Djordjevic, Bojana, Broaddus, Russell R., Medeiros, L. Jeffrey, Rashid, Asif, Luthra, Rajyalakshmi
Wydane 2012

Integrated analyses identify a master microRNA regulatory network for the mesenchymal subtype in serous ovarian cancer

od Yang, Da, Sun, Yan, Hu, Limei, Zheng, Hong, Ji, Ping, Pecot, Chad V., Zhao, Yanrui, Reynolds, Sheila, Cheng, Hanyin, Rupaimoole, Rajesha, Cogdell, David, Nykter, Matti, Broaddus, Russell, Rodriguez-Aguayo, Cristian, Lopez-Berestein, Gabriel, Liu, Jinsong, Shmulevich, Ilya, Sood, Anil K., Chen, Kexin, Zhang, Wei
Wydane 2013

Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15

od Cheng, Hanyin, Gottlieb, Leah, Marchi, Elaine, Kleyner, Robert, Bhardwaj, Puja, Rope, Alan F, Rosenheck, Sarah, Moutton, Sébastien, Philippe, Christophe, Eyaid, Wafaa, Alkuraya, Fowzan S, Toribio, Janet, Mena, Rafael, Prada, Carlos E, Stessman, Holly, Bernier, Raphael, Wermuth, Marieke, Kauffmann, Birgit, Blaumeiser, Bettina, Kooy, R Frank, Baralle, Diana, Mancini, Grazia M S, Conway, Simon J, Xia, Fan, Chen, Zhao, Meng, Linyan, Mihajlovic, Ljubisa, Marmorstein, Ronen, Lyon, Gholson J
Wydane w Hum Mol Genet (2019)

Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15

od Cheng, Hanyin, Gottlieb, Leah, Marchi, Elaine, Kleyner, Robert, Bhardwaj, Puja, Rope, Alan F, Rosenheck, Sarah, Moutton, Sébastien, Philippe, Christophe, Eyaid, Wafaa, Alkuraya, Fowzan S, Toribio, Janet, Mena, Rafael, Prada, Carlos E, Stessman, Holly, Bernier, Raphael, Wermuth, Marieke, Kauffmann, Birgit, Blaumeiser, Bettina, Kooy, R Frank, Baralle, Diana, Mancini, Grazia M S, Conway, Simon J, Xia, Fan, Chen, Zhao, Meng, Linyan, Mihajlovic, Ljubisa, Marmorstein, Ronen, Lyon, Gholson J
Wydane w Hum Mol Genet (2020)

Reanalysis of Clinical Exome Sequencing Data

od Liu, Pengfei, Meng, Linyan, Normand, Elizabeth A., Xia, Fan, Song, Xiaofei, Ghazi, Andrew, Rosenfeld, Jill, Magoulas, Pilar L., Braxton, Alicia, Ward, Patricia, Dai, Hongzheng, Yuan, Bo, Bi, Weimin, Xiao, Rui, Wang, Xia, Chiang, Theodore, Vetrini, Francesco, He, Weimin, Cheng, Hanyin, Dong, Jie, Gijavanekar, Charul, Benke, Paul J., Bernstein, Jonathan A., Eble, Tanya, Eroglu, Yasemen, Erwin, Deanna, Escobar, Luis, Gibson, James B., Gripp, Karen W., Kleppe, Soledad, Koenig, Mary Kay, Lewis, Andrea M., Natowicz, Marvin, Mancias, Pedro, Minor, LaKeesha, Scaglia, Fernando, Schaaf, Christian P., Streff, Haley, Vernon, Hilary, Uhles, Crescenda L, Zackai, Elaine H., Wu, Nan, Sutton, V. Reid, Beaudet, Arthur L., Muzny, Donna, Gibbs, Richard A., Posey, Jennifer E., Lalani, Seema, Shaw, Chad, Eng, Christine M., Lupski, James R., Yang, Yaping
Wydane w N Engl J Med (2019)

Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity

od Cheng, Hanyin, Capponi, Simona, Wakeling, Emma, Marchi, Elaine, Li, Quan, Zhao, Mengge, Weng, Chunhua, Piatek, Stefan G., Ahlfors, Helena, Kleyner, Robert, Rope, Alan, Lumaka, Aimé, Lukusa, Prosper, Devriendt, Koenraad, Vermeesch, Joris, Posey, Jennifer E., Palmer, Elizabeth E., Murray, Lucinda, Leon, Eyby, Diaz, Jullianne, Worgan, Lisa, Mallawaarachchi, Amali, Vogt, Julie, de Munnik, Sonja A., Dreyer, Lauren, Baynam, Gareth, Ewans, Lisa, Stark, Zornitza, Lunke, Sebastian, Gonçalves, Ana R., Soares, Gabriela, Oliveira, Jorge, Fassi, Emily, Willing, Marcia, Waugh, Jeff L., Faivre, Laurence, Riviere, Jean-Baptiste, Moutton, Sebastien, Mohammed, Shehla, Payne, Katelyn, Walsh, Laurence, Begtrup, Amber, Sacoto, Maria J. Guillen, Douglas, Ganka, Alexander, Nora, Buckley, Michael F., Mark, Paul R., Adès, Lesley C., Sandaradura, Sarah A., Lupski, James R., Roscioli, Tony, Agrawal, Pankaj B., Kline, Antonie D., Wang, Kai, Timmers, H. T. Marc, Lyon, Gholson J.
Wydane w Hum Mutat (2019)

Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies

od Cheng, Hanyin, Dharmadhikari, Avinash V., Varland, Sylvia, Ma, Ning, Domingo, Deepti, Kleyner, Robert, Rope, Alan F., Yoon, Margaret, Stray-Pedersen, Asbjørg, Posey, Jennifer E., Crews, Sarah R., Eldomery, Mohammad K., Akdemir, Zeynep Coban, Lewis, Andrea M., Sutton, Vernon R., Rosenfeld, Jill A., Conboy, Erin, Agre, Katherine, Xia, Fan, Walkiewicz, Magdalena, Longoni, Mauro, High, Frances A., van Slegtenhorst, Marjon A., Mancini, Grazia M.S., Finnila, Candice R., van Haeringen, Arie, den Hollander, Nicolette, Ruivenkamp, Claudia, Naidu, Sakkubai, Mahida, Sonal, Palmer, Elizabeth E., Murray, Lucinda, Lim, Derek, Jayakar, Parul, Parker, Michael J., Giusto, Stefania, Stracuzzi, Emanuela, Romano, Corrado, Beighley, Jennifer S., Bernier, Raphael A., Küry, Sébastien, Nizon, Mathilde, Corbett, Mark A., Shaw, Marie, Gardner, Alison, Barnett, Christopher, Armstrong, Ruth, Kassahn, Karin S., Van Dijck, Anke, Vandeweyer, Geert, Kleefstra, Tjitske, Schieving, Jolanda, Jongmans, Marjolijn J., de Vries, Bert B.A., Pfundt, Rolph, Kerr, Bronwyn, Rojas, Samantha K., Boycott, Kym M., Person, Richard, Willaert, Rebecca, Eichler, Evan E., Kooy, R. Frank, Yang, Yaping, Wu, Joseph C., Lupski, James R., Arnesen, Thomas, Cooper, Gregory M., Chung, Wendy K., Gecz, Jozef, Stessman, Holly A.F., Meng, Linyan, Lyon, Gholson J.
Wydane w Am J Hum Genet (2018)