Jessica Peel
Close
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Journal Articles

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity

Iris Fagniez, Miyuki Tsumura, Antoine Guérin, Hassan Abolhassani, Samin Sharafian, Mehrnaz Mesdaghi, Toyoki Nishimura, Harsha Prasada Lashkari, Sadashiva Rao, Stephanie Richards, Ji Eun Han, Ottavia M. Delmonte, Camille Kergaravat, Janet G. Markle, Masato Ogishi, Jing Han, Jessica Peel, Joseph Vellutini, Yi Feng, Camille Soudée, Mélanie Migaud, Boaz Palterer, Katherine J.L. Jackson, Shiho Nishimura, Sonoko Sakata, Keishiro Kinoshita, Ayako Yamamoto, Hiroshi Moritake, Mohammed Alzahrani, Francisco Vallejos, Theresa Cole, Joanne M. Smart, Sharon Choo, Zahra Chavoshzadeh, Shahnaz Armin, Antoine Toubert, Peng Zhang, Jérémie Rosain, Luigi D. Notarangelo, Qiang Pan-Hammarström, Stuart G. Tangye, Jean-Laurent Casanova, Cindy S. Ma, Anne Puel, Jacinta Bustamante, Satoshi Okada, Stephanie Boisson-Dupuis, Rui Yang
Journal: Journal of Experimental Medicine
J Exp Med (2026) 223 (10): e20252038.
https://doi.org/10.1084/jem.20252038
Published: 04 September 2026
View article titled, Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity
Open the PDF for Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity in another window
Includes: Supplementary data
Journal Articles

Familial pulmonary alveolar proteinosis and type I interferonopathy by mutation of STAT2 (TIMS2)

In Special Collection:
Journal-Based CME Activities with Journal of Experimental Medicine (JEM)
Conor Gruber, Meredith Ramba, Bineeta Debnath, Lorenzo Cuollo, Anna-Lena Neehus, Angelica Lee, Sofija Buta, Marta Martin-Fernandez, Jérémie Rosain, Laureline Berteloot, Philippe Drabent, Tom Le Voyer, Camille Soudée, Jessica Peel, Yoann Seeleuthner, Anne Puel, Shen-Ying Zhang, Michael J. Ciancanelli, Carlos A. Arango-Franco, Mélanie Migaud, Marie-Louise Frémond, Florence Renaldo, Odile Boespflug-Tanguy, Imen Dorboz, Beatrice Dubern, Tristan Fonteneau, Nima Parvaneh, Rasol Molatefi, Mohammad Shahrooei, Darragh Duffy, Vincent Bondet, Gillian I. Rice, Yanick J. Crow, Thierry Jo Molina, Nathalie Boddaert, Jean-Laurent Casanova, Veronique Houdouin, Isabelle Melki, Alice Hadchouel, Jacinta Bustamante, Dusan Bogunovic
Journal: Journal of Experimental Medicine
J Exp Med (2026) 223 (8): e20251331.
https://doi.org/10.1084/jem.20251331
Published: 16 July 2026
View article titled, Familial pulmonary alveolar proteinosis and type I interferonopathy by mutation of STAT2 (TIMS2)
Open the PDF for Familial pulmonary alveolar proteinosis and type I interferonopathy by mutation of STAT2 (TIMS2) in another window
Includes: Supplementary data

Advertisement

This Feature Is Available To Subscribers Only

or Create an Account

Close subscription notice
Close access options