Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutations
Jennifer W. Leiding(Johns Hopkins University), Troy R. Torgerson(Allen Institute for Immunology), Kathleen E. Sullivan(University of Pennsylvania), Michael A. Pulsipher(Primary Children's Hospital), Andrew R. Gennery(Newcastle upon Tyne Hospitals NHS Foundation Trust), Juan Carlos Aldave Becerra(Hospital Nacional Cayetano Heredia), Akihiro Iguchi(Hokkaido University), Masao Kobayashi(Higashi Osaka City General Hospital), Satoshi Okada(Rockefeller University), Laura Martínez‐Martínez(Universitat Autònoma de Barcelona), Tomohiro Morio(Tokyo Institute of Psychiatry), Teppei Ohkawa(Tokyo Medical and Dental University), Caroline A. Lindemans(University Medical Center Utrecht), David Hagin(University of Washington), Annet van Royen‐Kerkhof(Wilhelmina Children's Hospital), Sebastian Fuchs(University of Miami), Hans D. Ochs(Infectious Disease Research Institute), Anna Shcherbina, Fikret Arpacı, Adi Ovadia(Tel Aviv University), Sara Şebnem Kılıç(Bursa Uludağ Üni̇versi̇tesi̇), Mary Slatter(First Pavlov State Medical University of St. Petersburg), Chaim M. Roifman(University of Toronto), Dmitry Balashov(Dmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology), Mario Abinun(North Tyneside General Hospital), Aleksandra Petrović(Seattle Children's Hospital), Kohsuke Imai(National Defense Medical College Hospital), Desa Lilić(Newcastle University), Vy H.D. Kim(Hospital for Sick Children), Mark Depner(University Medical Center Freiburg), Stephen L. Guthery(Primary Children's Hospital), Sharon Christie(University of Ulster), Nancy Bunin(University of Iowa), Lisa Devlin(University of Ulster), Oscar De La Calle-Martin(Hospital de Sant Pau)
Cited by 166
Related Papers
Tisagenlecleucel in Children and Young Adults with B-Cell Lymphoblastic Leukemia
|New England Journal of Medicine|2018|5.7k
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
|Nature Genetics|2001|3.4k
Chronic Granulomatous Disease: Report on a National Registry of 368 Patients
|Medicine|2000|1.7k
Activation-Induced Cytidine Deaminase (AID) Deficiency Causes the Autosomal Recessive Form of the Hyper-IgM Syndrome (HIGM2)
|Cell|2000|1.6k
Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways
|Nature Genetics|2009|1.4k