CD40LG duplication-associated autoimmune disease is silenced by nonrandom X-chromosome inactivation - 06/06/18
Doi : 10.1016/j.jaci.2018.02.010
Carole Le Coz, PhD a, Melissa Trofa, BA a, Camille M. Syrett, BS b, Anna Martin, BS b, Harumi Jyonouchi, MD c, Soma Jyonouchi, MD a, d, Montserrat C. Anguera, PhD b, Neil Romberg, MD a, d 
a Division of Immunology and Allergy, The Children's Hospital of Philadelphia, Philadelphia, Pa
b Department of Biomedical Sciences, School of Veterinary Medicine, The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pa
c Pediatric Allergy/Immunology, Department of Pediatrics, Children's Hospital at Saint Peter's University Hospital, New Brunswick, NJ
d Department of Pediatrics, The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pa
| This work was supported by the National Institutes of Health-National Institute of Allergy and Infectious Diseases (grant no. K23 AI115001 to N.R., grant no. AI124084 to M.C.A, and grant no. T32-HD083185 to C.M.S.), the National Institutes of Health-Eunice Kennedy Shriver National Institute of Child Health and Human Development (grant no. HD085848 to M.C.A and grant no. T32-HD083185 to C.M.S.), the Jeffrey Modell Foundation (to N.R.), and the Howard Hughes Medical Institute/Burroughs Wellcome Fund (to A.M.). |
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| Disclosure of potential conflict of interest: The authors declare that they have no relevant conflicts of interest. |
© 2018
American Academy of Allergy, Asthma & Immunology. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 141 - N° 6
P. 2308 - juin 2018 Retour au numéro
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