Evaluation and pilot testing of a multidisciplinary model of care to mainstream genomic testing for paediatric inborn errors of immunity

por Yanes, Tatiane, Sullivan, Anna, Barbaro, Pasquale, Brion, Kristian, Hollway, Georgina, Peake, Jane, McNaughton, Peter
Publicado 2023

Partially hydrolysed, prebiotic supplemented whey formula for the prevention of allergic manifestations in high risk infants: a multicentre double-blind randomised controlled trial

por Boyle, Robert, Brown, Nick, Chiang, Wen Chin, Chien, Chua Mei, Gold, Michael, Hourihane, Jonathan, Peake, Jane, Quinn, Patrick, Rao, Raj, Smith, Peter, Tang, Mimi, Ziegler, John, Warner, John
Publicado 2015

Retraction Note to: Partially hydrolysed, prebiotic supplemented whey formula for the prevention of allergic manifestations in high risk infants: a multicentre double-blind randomi...

por Boyle, Robert, Brown, Nick, Chiang, Wen Chin, Chien, Chua Mei, Gold, Michael, Hourihane, Jonathan, Peake, Jane, Quinn, Patrick, Rao, Raj, Smith, Peter, Tang, Mimi, Ziegler, John, Warner, John
Publicado 2020

Effects of an Amino Acid-Based Formula Supplemented with Two Human Milk Oligosaccharides on Growth, Tolerability, Safety, and Gut Microbiome in Infants with Cow’s Milk Protein Alle...

por Gold, Michael S., Quinn, Patrick J., Campbell, Dianne E., Peake, Jane, Smart, Joanne, Robinson, Marnie, O’Sullivan, Michael, Vogt, Josef Korbinian, Pedersen, Helle Krogh, Liu, Xiaoqiu, Pazirandeh-Micol, Elham, Heine, Ralf G.
Publicado 2022

Exome Sequencing Reveals Primary Immunodeficiencies in Children with Community-Acquired Pseudomonas aeruginosa Sepsis

por Asgari, Samira, McLaren, Paul J., Peake, Jane, Wong, Melanie, Wong, Richard, Bartha, Istvan, Francis, Joshua R., Abarca, Katia, Gelderman, Kyra A., Agyeman, Philipp, Aebi, Christoph, Berger, Christoph, Fellay, Jacques, Schlapbach, Luregn J.
Publicado 2016

Corrigendum: Exome Sequencing Reveals Primary Immunodeficiencies in Children with Community-Acquired Pseudomonas aeruginosa Sepsis

por Asgari, Samira, McLaren, Paul J., Peake, Jane, Wong, Melanie, Wong, Richard, Bartha, Istvan, Francis, Joshua R., Abarca, Katia, Gelderman, Kyra A., Agyeman, Philipp, Aebi, Christoph, Berger, Christoph, Fellay, Jacques, Schlapbach, Luregn J.
Publicado 2016

Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing

por Merico, Daniele, Roifman, Maian, Braunschweig, Ulrich, Yuen, Ryan K. C., Alexandrova, Roumiana, Bates, Andrea, Reid, Brenda, Nalpathamkalam, Thomas, Wang, Zhuozhi, Thiruvahindrapuram, Bhooma, Gray, Paul, Kakakios, Alyson, Peake, Jane, Hogarth, Stephanie, Manson, David, Buncic, Raymond, Pereira, Sergio L., Herbrick, Jo-Anne, Blencowe, Benjamin J., Roifman, Chaim M., Scherer, Stephen W.
Publicado 2015

STAT3 is a critical cell-intrinsic regulator of human unconventional T cell numbers and function

por Wilson, Robert P., Ives, Megan L., Rao, Geetha, Lau, Anthony, Payne, Kathryn, Kobayashi, Masao, Arkwright, Peter D., Peake, Jane, Wong, Melanie, Adelstein, Stephen, Smart, Joanne M., French, Martyn A., Fulcher, David A., Picard, Capucine, Bustamante, Jacinta, Boisson-Dupuis, Stephanie, Gray, Paul, Stepensky, Polina, Warnatz, Klaus, Freeman, Alexandra F., Rossjohn, Jamie, McCluskey, James, Holland, Steven M., Casanova, Jean-Laurent, Uzel, Gulbu, Ma, Cindy S., Tangye, Stuart G., Deenick, Elissa K.
Publicado 2015

B cell–intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans

por Avery, Danielle T., Deenick, Elissa K., Ma, Cindy S., Suryani, Santi, Simpson, Nicholas, Chew, Gary Y., Chan, Tyani D., Palendira, Umamainthan, Bustamante, Jacinta, Boisson-Dupuis, Stéphanie, Choo, Sharon, Bleasel, Karl E., Peake, Jane, King, Cecile, French, Martyn A., Engelhard, Dan, Al-Hajjar, Sami, Al-Muhsen, Saleh, Magdorf, Klaus, Roesler, Joachim, Arkwright, Peter D., Hissaria, Pravin, Riminton, D. Sean, Wong, Melanie, Brink, Robert, Fulcher, David A., Casanova, Jean-Laurent, Cook, Matthew C., Tangye, Stuart G.
Publicado 2010

Naive and memory human B cells have distinct requirements for STAT3 activation to differentiate into antibody-secreting plasma cells

por Deenick, Elissa K., Avery, Danielle T., Chan, Anna, Berglund, Lucinda J., Ives, Megan L., Moens, Leen, Stoddard, Jennifer L., Bustamante, Jacinta, Boisson-Dupuis, Stephanie, Tsumura, Miyuki, Kobayashi, Masao, Arkwright, Peter D., Averbuch, Diana, Engelhard, Dan, Roesler, Joachim, Peake, Jane, Wong, Melanie, Adelstein, Stephen, Choo, Sharon, Smart, Joanne M., French, Martyn A., Fulcher, David A., Cook, Matthew C., Picard, Capucine, Durandy, Anne, Klein, Christoph, Holland, Steven M., Uzel, Gulbu, Casanova, Jean-Laurent, Ma, Cindy S., Tangye, Stuart G.
Publicado 2013

Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance

por Asano, Takaki, Khourieh, Joëlle, Zhang, Peng, Rapaport, Franck, Spaan, András N., Li, Juan, Lei, Wei-Te, Pelham, Simon J., Hum, David, Chrabieh, Maya, Han, Ji Eun, Guérin, Antoine, Mackie, Joseph, Gupta, Sudhir, Saikia, Biman, Baghdadi, Jamila E.I., Fadil, Ilham, Bousfiha, Aziz, Habib, Tanwir, Marr, Nico, Ganeshanandan, Luckshman, Peake, Jane, Droney, Luke, Williams, Andrew, Celmeli, Fatih, Hatipoglu, Nevin, Ozcelik, Tayfun, Picard, Capucine, Abel, Laurent, Tangye, Stuart G., Boisson-Dupuis, Stéphanie, Zhang, Qian, Puel, Anne, Béziat, Vivien, Casanova, Jean-Laurent, Boisson, Bertrand
Publicado 2021

Human type I IFN deficiency does not impair B cell response to SARS-CoV-2 mRNA vaccination

por Sokal, Aurélien, Bastard, Paul, Chappert, Pascal, Barba-Spaeth, Giovanna, Fourati, Slim, Vanderberghe, Alexis, Lagouge-Roussey, Pauline, Meyts, Isabelle, Gervais, Adrian, Bouvier-Alias, Magali, Azzaoui, Imane, Fernández, Ignacio, de la Selle, Andréa, Zhang, Qian, Bizien, Lucy, Pellier, Isabelle, Linglart, Agnès, Rothenbuhler, Anya, Marcoux, Estelle, Anxionnat, Raphael, Cheikh, Nathalie, Léger, Juliane, Amador-Borrero, Blanca, Fouyssac, Fanny, Menut, Vanessa, Goffard, Jean-Christophe, Storey, Caroline, Demily, Caroline, Mallebranche, Coralie, Troya, Jesus, Pujol, Aurora, Zins, Marie, Tiberghien, Pierre, Gray, Paul E., McNaughton, Peter, Sullivan, Anna, Peake, Jane, Levy, Romain, Languille, Laetitia, Rodiguez-Gallego, Carlos, Boisson, Bertrand, Gallien, Sébastien, Neven, Bénédicte, Michel, Marc, Godeau, Bertrand, Abel, Laurent, Rey, Felix A., Weill, Jean-Claude, Reynaud, Claude-Agnès, Tangye, Stuart G., Casanova, Jean-Laurent, Mahévas, Matthieu
Publicado 2022

A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes

por Bastard, Paul, Hsiao, Kuang-Chih, Zhang, Qian, Choin, Jeremy, Best, Emma, Chen, Jie, Gervais, Adrian, Bizien, Lucy, Materna, Marie, Harmant, Christine, Roux, Maguelonne, Hawley, Nicola L., Weeks, Daniel E., McGarvey, Stephen T., Sandoval, Karla, Barberena-Jonas, Carmina, Quinto-Cortés, Consuelo D., Hagelberg, Erika, Mentzer, Alexander J., Robson, Kathryn, Coulibaly, Boubacar, Seeleuthner, Yoann, Bigio, Benedetta, Li, Zhi, Uzé, Gilles, Pellegrini, Sandra, Lorenzo, Lazaro, Sbihi, Zineb, Latour, Sylvain, Besnard, Marianne, Adam de Beaumais, Tiphaine, Jacqz Aigrain, Evelyne, Béziat, Vivien, Deka, Ranjan, Esera Tulifau, Litara, Viali, Satupa‘itea, Reupena, Muagututi‘a Sefuiva, Naseri, Take, McNaughton, Peter, Sarkozy, Vanessa, Peake, Jane, Blincoe, Annaliesse, Primhak, Sarah, Stables, Simon, Gibson, Kate, Woon, See-Tarn, Drake, Kylie Marie, Hill, Adrian V.S., Chan, Cheng-Yee, King, Richard, Ameratunga, Rohan, Teiti, Iotefa, Aubry, Maite, Cao-Lormeau, Van-Mai, Tangye, Stuart G., Zhang, Shen-Ying, Jouanguy, Emmanuelle, Gray, Paul, Abel, Laurent, Moreno-Estrada, Andrés, Minster, Ryan L., Quintana-Murci, Lluis, Wood, Andrew C., Casanova, Jean-Laurent
Publicado 2022