Výsledky vyhledávání

Akademický článek

T cells specific to multiple Bet v 1 peptides are highly cross-reactive toward the corresponding peptides from the homologous group of tree pollens

Autor: Gitte Lund, Lars Harder Christensen, Jacob Ihlemann, Peter Sejer Andersen, Erik Wambre, Peter Adler Würtzen, Shashank Gupta

Publikováno v: Frontiers in Immunology, Vol 14 (2023)

BackgroundAllergens from Fagales trees frequently cause spring allergy in Europe, North America, and some parts of Asia. The definition of the birch homologous group, which includes birch (Bet v), oak (Que a), alder (Aln g), hazel (Cor a), hornbeam (

Externí odkaz: https://doaj.org/article/69abf5ffe9404fc09b4f385da6c4a960

Zobrazit plný text záznamu

Akademický článek

Distinct trajectories distinguish antigen-specific T cells in peanut-allergic individuals undergoing oral immunotherapy

Autor: Kim, Edwin H., Nadeau, Kari C., Nowak-Wegrzyn, Anna, Wood, Robert A., Sampson, Hugh A., Scurlock, Amy M., Chinthrajah, Sharon, Wang, Julie, Pesek, Robert D., Sindher, Sayantani B., Kulis, Mike, Johnson, Jacqueline, Spain, Katharine, Babineau, Denise C., Chin, Hyunsook, Laurienzo-Panza, Joy, Rachel Yan, Larson, David, Tielin Qin, Whitehouse, Don, Sever, Michelle L., Sanda, Srinath, Plaut, Marshall, Wheatley, Lisa M., Wesley Burks, A., Marchesini, Gina, Gilroy, Kavitha, Posso, Sylvia, Skiba, Sabrina, Nguyen, Thien-Son, Wojno, Adam, Nguyen, Tuan, Gersuk, Vivian, Nguyen, Quynh-Anh, Garber, Jessica, O’Brien, Kimberly, Larson, Brandon, Cousens-Jacobs, C., Hu, Alex, Calise, Justine, DeBerg, Hannah, Garabatos, Nahir, Khosa, Sugandhika, Bajzik, Veronique, Calderon, Lorena Botero, Aldridge, Kelly, Rosasco, Mario, Ferslew, Brian C., Zhu, Tong, Smulders, Ronald, Laidlaw, Tanya M., Qin, Tielin, Chichili, Gurunadh R., Adelman, Daniel C., Farrington, Mary, Robinson, David, Jeong, David, Jones, Stacie M., Kwok, William W., Baloh, Carolyn, Nepom, Gerald T., Wambre, Erik

Publikováno v: In The Journal of Allergy and Clinical Immunology July 2023 152(1):155-166

Zobrazit plný text záznamu

Akademický článek

Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)

Autor: Elodie Fiot, Bertille Alauze, Bruno Donadille, Dinane Samara-Boustani, Muriel Houang, Gianpaolo De Filippo, Anne Bachelot, Clemence Delcour, Constance Beyler, Emilie Bois, Emmanuelle Bourrat, Emmanuel Bui Quoc, Nathalie Bourcigaux, Catherine Chaussain, Ariel Cohen, Martine Cohen-Solal, Sabrina Da Costa, Claire Dossier, Stephane Ederhy, Monique Elmaleh, Laurence Iserin, Hélène Lengliné, Armelle Poujol-Robert, Dominique Roulot, Jerome Viala, Frederique Albarel, Elise Bismuth, Valérie Bernard, Claire Bouvattier, Aude Brac, Patricia Bretones, Nathalie Chabbert-Buffet, Philippe Chanson, Regis Coutant, Marguerite de Warren, Béatrice Demaret, Lise Duranteau, Florence Eustache, Lydie Gautheret, Georges Gelwane, Claire Gourbesville, Mickaël Grynberg, Karinne Gueniche, Carina Jorgensen, Veronique Kerlan, Charlotte Lebrun, Christine Lefevre, Françoise Lorenzini, Sylvie Manouvrier, Catherine Pienkowski, Rachel Reynaud, Yves Reznik, Jean-Pierre Siffroi, Anne-Claude Tabet, Maithé Tauber, Vanessa Vautier, Igor Tauveron, Sebastien Wambre, Delphine Zenaty, Irène Netchine, Michel Polak, Philippe Touraine, Jean-Claude Carel, Sophie Christin-Maitre, Juliane Léger

Publikováno v: Orphanet Journal of Rare Diseases, Vol 17, Iss S1, Pp 1-39 (2022)

Abstract Turner syndrome (TS; ORPHA 881) is a rare condition in which all or part of one X chromosome is absent from some or all cells. It affects approximately one in every 1/2500 liveborn girls. The most frequently observed karyotypes are 45,X (40�

Externí odkaz: https://doaj.org/article/47d7e0d1bd19414b82a3ff48728cebb1

Zobrazit plný text záznamu

Plný text ve formátu HTML