Výsledky vyhledávání - Luis Alberto Pedroza

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  1. 1
    The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17

    The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Kerat... Autor Vipul Kumar, Luis Alberto Pedroza, Emily M. Mace, Steven H. Seeholzer, George Cotsarelis, Antônio Condino‐Neto, Aimee Payne, Jordan S. Orange

    Vydáno 2011
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  2. 2
    Pro-inflammation Associated with a Gain-of-Function Mutation (R284S) in the Innate Immune Sensor STING

    Pro-inflammation Associated with a Gain-of-Function Mutation (R284S) in the Innate Immune Sensor STING Autor Hiroyasu Konno, Iván K. Chinn, Diana N. Hong, Jordan S. Orange, James R. Lupski, Alejandra Mendoza, Luis Alberto Pedroza, Glen N. Barber

    Vydáno 2018
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  3. 3
    Autoimmune regulator (AIRE) contributes to Dectin-1–induced TNF-α production and complexes with caspase recruitment domain–containing protein 9 (CARD9), spleen tyrosine kinase (Syk), and Dectin-1

    Autoimmune regulator (AIRE) contributes to Dectin-1–induced TNF-α production and complexes with caspase recruitment domain–containing protein 9 (CARD9), spleen tyrosine kinase (Syk... Autor Luis Alberto Pedroza, Vipul Kumar, Keri B. Sanborn, Emily M. Mace, Harri Niinikoski, Kari C. Nadeau, Dewton de Moraes Vasconcelos, Elena Pérez, Soma Jyonouchi, Harumi Jyonouchi, Pinaki P. Banerjee, Olli Ruuskanen, Antônio Condino‐Neto, Jordan S. Orange

    Vydáno 2011
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  4. 4
    High‐Performance Liquid Chromatography Under Partially Denaturing Conditions (dHPLC) is a Fast and Cost‐Effective Method for Screening Molecular Defects: Four Novel Mutations Found in X‐Linked Chronic Granulomatous Disease

    High‐Performance Liquid Chromatography Under Partially Denaturing Conditions (dHPLC) is a Fast and Cost‐Effective Method for Screening Molecular Defects: Four Novel Mutations Found... Autor Edgar Borges de Oliveira-Júnior, Carolina Prando, Juan Antonio López, Julián Camilo Arango Rincón, M. Buzolin, Jussara Rehder, Luis Alberto Pedroza, Josias Brito Frazão, Vera Maria Dantas, Pérsio Roxo Júnior, Anete Sevciovic Grumach, Beatriz Tavares Costa‐Carvalho, Jacinta Bustamante, Antônio Condino‐Neto

    Vydáno 2012
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  5. 5
    Clinical, immunologic and genetic characteristics of 148 patients with NK cell deficiency

    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 2025
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  6. 6
    The Role of AIRE in the Immunity Against Candida Albicans in a Model of Human Macrophages

    The Role of AIRE in the Immunity Against Candida Albicans in a Model of Human Macrophages Autor José Antônio Tavares de Albuquerque, Pinaki P. Banerjee, Ângela Castoldi, Royce Ma, Nuria Bengala Zurro, Leandro Hideki Ynoue, Christina Arslanian, Marina Uchoa Wall Barbosa-Carvalho, Joya Emilie de Menezes Correia-Deur, Fernanda Guimarães Weiler, Magnus R. Dias‐da‐Silva, Marise Lazaretti‐Castro, Luis Alberto Pedroza, Niels Olsen Saraiva Câmara, Emily M. Mace, Jordan S. Orange, Antônio Condino‐Neto

    Vydáno 2018
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  7. 7
    Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis

    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 2018
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  8. 8
    Individuals with <i>JAK1</i> variants are affected by syndromic features encompassing autoimmunity, atopy, colitis, and dermatitis

    Individuals with <i>JAK1</i> variants are affected by syndromic features encompassing autoimmunity, atopy, colitis, and dermatitis Autor Michael E. Horesh, Marta Martín-Fernández, Conor Gruber, Sofija Buta, Tom Le Voyer, Eve Puzenat, Harry Lesmana, Yiming Wu, Ashley Richardson, David Stein, Stephanie Hodeib, Mariam M. Youssef, Jacob A. Kurowski, Elizabeth Feuille, Luis Alberto Pedroza, Ramsay Fuleihan, Alexandria Haseley, Alain Hovnanian, Pierre Quartier, Jérémie Rosain, Georgina Davis, D.P. MULLAN, O’Jay Stewart, Roosheel S. Patel, Angelica E. Lee, R. Rubinstein, Leyla Ewald, Nikhil Maheshwari, Virginia Rahming, Iván K. Chinn, James R. Lupski, Jordan S. Orange, Vanessa Sancho‐Shimizu, Jean‐Laurent Casanova, Noura S. Abul‐Husn, Yuval Itan, Joshua D. Milner, Jacinta Bustamante, Dusan Bogunovic

    Vydáno 2024
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  9. 9
    Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders

    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 2016
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  10. 10
    Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

    Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations Autor Tiziana Lorenzini, Manfred Fliegauf, Nils Klammer, Natalie Frede, Michele Proietti, Alla Bulashevska, Nadezhda Camacho-Ordóñez, Markku Varjosalo, Matias Kinnunen, Esther de Vries, J.W.M. van der Meer, Rohan Ameratunga, Chaim M. Roifman, Yael Dinur Schejter, Robin Kobbe, Timo Hautala, Faranaz Atschekzei, Reinhold E. Schmidt, Claudia Schröder, Polina Stepensky, Bella Shadur, Luis Alberto Pedroza, Michiel van der Flier, Mónica Martínez‐Gallo, Luis Ignacio González‐Granado, Luís M. Allende, Anna Shcherbina, N. B. Kuzmenko, V.P. Zakharova, João Farela Neves, Peter Švec, Ute Fischer, Winnie Ip, Oliver Bartsch, Safa Barış, Christoph Klein, Raif S. Geha, Janet Chou, Mohammed F. Alosaimi, Lauren Weintraub, Kaan Boztuğ, Tatjana Hirschmugl, Maria Marluce dos Santos Vilela, Dirk Holzinger, Maximilian Seidl, Vassilios Lougaris, Alessandro Plebani, Laia Alsina, M. Piquer‐Gibert, Àngela Deyà‐Martínez, C Slade, Asghar Aghamohammadi, Hassan Abolhassani, Lennart Hammarström, Outi Kuismin, Merja Helminen, Hana Lango Allen, James E. Thaventhiran, Alexandra F. Freeman, Matthew Cook, Shahrzad Bakhtiar, Mette Christiansen, Charlotte Cunningham‐Rundles, Niraj Patel, William Rae, Tim Niehues, Nina Brauer, Jaana Syrjänen, Mikko Seppänen, Siobhán O. Burns, Paul Tuijnenburg, Taco W. Kuijpers, Klaus Warnatz, Bodo Grimbacher, Zoe Adhya, Hana Alachkar, Ariharan Anantharachagan, Richard Antrobus, Gururaj Arumugakani, Sofie Ashford, William J. Astle, Anthony Attwood, Chiara Bacchelli, Joana Batista, Helen Baxendale, Claire Bethune, Shahnaz Bibi, Marta Bleda, Barbara Boardman, Claire Booth, John R. Bradley, Gerome Breen, Matthew A. Brown, Michael J. Browning, Mary Brownlie, Matthew Buckland, Siobhán O. Burns, Oliver S. Burren, Keren Carss, John C. Chambers

    Vydáno 2020
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