Výsledky vyhledávání - Tram N. Cao
- Zobrazuji výsledky 1 - 8 z 8
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Mutations in PI3K110δ cause impaired natural killer cell function partially rescued by rapamycin treatment Autor Raquel Ruiz‐García, Alexander Vargas‐Hernández, Iván K. Chinn, Laura S. Angelo, Tram N. Cao, Zeynep Coban‐Akdemir, Shalini N. Jhangiani, Qingchang Meng, Lisa R. Forbes, Donna M. Muzny, Luís M. Allende, M S Ehlayel, Richard A. Gibbs, James R. Lupski, Gülbû Uzel, Jordan S. Orange, Emily M. Mace
Vydáno 2018Artigo -
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Clinical, immunologic and genetic characteristics of 148 patients with NK cell deficiency Autor Manar Abdalgani, Evelyn R. Hernandez, Luis Alberto Pedroza, Iván K. Chinn, Lisa Forbes Satter, Nicholas L. Rider, Pinaki P. Banerjee, M. Cecilia Poli, Sanjana Mahaptra, Debra Canter, Tram N. Cao, Linda Shawver, Sara Nandiwada, James R. Lupski, Jennifer E. Posey, Rajasekhar Ramakrishnan, Emily M. Mace, Jordan S. Orange
Vydáno 2025Artigo -
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Biallelic mutations in IRF8 impair human NK cell maturation and function Autor Emily M. Mace, Venetia Bigley, Justin T. Gunesch, Iván K. Chinn, Laura S. Angelo, Matthew A. Care, Sheetal Maisuria, Michael D. Keller, Sumihito Togi, Levi B. Watkin, David F. LaRosa, Shalini N. Jhangiani, Donna M. Muzny, Asbjørg Stray‐Pedersen, Zeynep Coban‐Akdemir, Jansen B. Smith, Mayra Hernández-Sanabria, Duy Le, Graham D. Hogg, Tram N. Cao, Aharon G. Freud, Eva P. Szymanski, Sinisa Savic, Matthew Collin, Andrew J. Cant, Richard A. Gibbs, Steven M. Holland, Michael A. Caligiuri, Keiko Ozato, Silke Paust, Gina M. Doody, James R. Lupski, Jordan S. Orange
Vydáno 2016Artigo -
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Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis Autor Iván K. Chinn, Olive S. Eckstein, Erin C. Peckham‐Gregory, Baruch R. Goldberg, Lisa R. Forbes, Sarah K. Nicholas, Emily M. Mace, Tiphanie P. Vogel, Harshal Abhyankar, María I. Díaz, Helen E. Heslop, Robert A. Krance, Caridad Martinez, Trung C. Nguyen, Dalia Bashir, Jordana Goldman, Asbjørg Stray‐Pedersen, Luis Alberto Pedroza, M. Cecilia Poli, Juan Carlos Aldave Becerra, Sean McGhee, Waleed Al‐Herz, Aghiad Chamdin, Zeynep Coban‐Akdemir, Shalini N. Jhangiani, Donna M. Muzny, Tram N. Cao, Diana N. Hong, Richard A. Gibbs, James R. Lupski, Jordan S. Orange, Kenneth L. McClain, Carl E. Allen
Vydáno 2018Artigo -
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HEM1 deficiency disrupts mTORC2 and F-actin control in inherited immunodysregulatory disease Autor Sarah A. Cook, William A. Comrie, M. Cecilia Poli, Morgan Similuk, Andrew J. Oler, Aiman Faruqi, Douglas B. Kuhns, Sheng Yang, Alexander Vargas‐Hernández, Alexandre F. Carisey, Benjamin Fournier, David E. Anderson, Susan Price, Margery Smelkinson, Wadih Abou Chahla, Lisa R. Forbes, Emily M. Mace, Tram N. Cao, Zeynep Coban‐Akdemir, Shalini N. Jhangiani, Donna M. Muzny, Richard A. Gibbs, James R. Lupski, Jordan S. Orange, Geoff D.E. Cuvelier, Moza Al Hassani, Nawal Al Kaabi, Zain Al Yafei, Soma Jyonouchi, Nikita Raje, Jason W. Caldwell, Yanping Huang, Janis K. Burkhardt, Sylvain Latour, Baoyu Chen, Gehad ElGhazali, V. Koneti Rao, Iván K. Chinn, Michael J. Lenardo
Vydáno 2020Artigo -
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A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function Autor Michael T. Lam, Simona Coppola, Oliver H.F. Krumbach, Giusi Prencipe, Antonella Insalaco, Cristina Cifaldi, Immacolata Brigida, Erika Zara, Serena Scala, Silvia Di Cesare, Simone Martinelli, Martina Di Rocco, Antonia Pascarella, Marcello Niceta, Francesca Pantaleoni, Andrea Ciolfi, Petra Netter, Alexandre F. Carisey, Michael Diehl, Mohammad Akbarzadeh, Francesca Conti, Pietro Merli, Anna Pastore, Stefano Levi Mortera, Serena Camerini, Luciapia Farina, Marcel Buchholzer, Luca Pannone, Tram N. Cao, Zeynep Coban‐Akdemir, Shalini N. Jhangiani, Donna M. Muzny, Richard A. Gibbs, Luca Basso‐Ricci, Maria Serena Chiriacò, Radovan Dvorský, Lorenza Putignani, Rita Carsetti, Petra Janning, Asbjørg Stray‐Pedersen, Hans Christian Erichsen, AnnaCarin Horne, Yenan T. Bryceson, Lamberto Torralba‐Raga, Kim Ramme, Vittorio Rosti, Claudia Bracaglia, Virginia Messia, Paolo Palma, Andrea Finocchi, Franco Locatelli, Iván K. Chinn, James R. Lupski, Emily M. Mace, Caterina Cancrini, Alessandro Aiuti, Mohammad Reza Ahmadian, Jordan S. Orange, Fabrizio De Benedetti, Marco Tartaglia
Vydáno 2019Artigo -
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Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders Autor Asbjørg Stray‐Pedersen, Hanne Sørmo Sorte, Pubudu Samarakoon, Tomasz Gambin, Iván K. Chinn, Zeynep H. Coban Akdemir, Hans Christian Erichsen, Lisa R. Forbes, Shen Gu, Bo Yuan, Shalini N. Jhangiani, Donna M. Muzny, Olaug K. Rødningen, Ying Sheng, Sarah K. Nicholas, Lenora M. Noroski, Filiz O. Seeborg, Carla M. Davis, Debra Canter, Emily M. Mace, Timothy J. Vece, Carl E. Allen, Harshal Abhyankar, Philip M. Boone, Christine R. Beck, Wojciech Wiszniewski, Børre Fevang, Pål Aukrust, Geir E. Tjønnfjord, Tobias Gedde‐Dahl, Henrik Hjorth‐Hansen, Ingunn Dybedal, Ingvild Nordøy, Silje F. Jørgensen, Tore G. Abrahamsen, Torstein Øverland, Anne Grete Bechensteen, Vegard Skogen, Liv Osnes, Mari Ann Kulseth, Trine Prescott, Cecilie F. Rustad, Ketil Heimdal, John W. Belmont, Nicholas L. Rider, Javier Chinen, Tram N. Cao, Eric A. Smith, María Soledad Caldirola, Liliana Bezrodnik, Saúl Oswaldo Lugo Reyes, Francisco Espinosa‐Rosales, Nina Denisse Guerrero-Cursaru, Luis Alberto Pedroza, M. Cecilia Poli, José Luis Franco, Claudia Milena Trujillo Vargas, Juan Carlos Aldave Becerra, Nicola Wright, Thomas B. Issekutz, Andrew C. Issekutz, Jordan K. Abbott, Jason W. Caldwell, Diana K. Bayer, Alice Chan, Alessandro Aiuti, Caterina Cancrini, Eva Holmberg, Christina West, Magnus Burstedt, Ender Karaca, Gözde Yeşil, Hasibe Artaç, Yavuz Bayram, Mehmed M. Atik, Mohammad K. Eldomery, Mohammad Ehlayel, Stephen Jolles, Berit Flatø, Alison A. Bertuch, I. Celine Hanson, Victor Wei Zhang, Lee-Jun Wong, Jianhong Hu, Magdalena Walkiewicz, Yaping Yang, Christine M. Eng, Eric Boerwinkle, Richard A. Gibbs, William T. Shearer, Robert Lyle, Jordan S. Orange, James R. Lupski
Vydáno 2016Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Immunology
Medicine
Immune system
Cell biology
Disease
Gene
Phenotype
Cell
Hemophagocytic lymphohistiocytosis
Internal medicine
Mutation
Pathology
Actin
Actin cytoskeleton
Alpha (finance)
Anthropology
Bone marrow
Breast cancer
Cancer
Cancer research
Chemistry
Construct validity
Copy-number variation
Cytopenia
Cytoskeleton
Cytotoxic T cell
Dermatology
Diversity (politics)