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Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors.

Autor: Giannelou A; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA.; Rheumatology Fellowship and Training Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland, USA., Wang H; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA., Zhou Q; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA., Park YH; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA., Abu-Asab MS; Section of Histopathology, National Eye Institute, Bethesda, Maryland, USA., Ylaya K; Experimental Pathology Laboratory, National Cancer Institute, Bethesda, Maryland, USA., Stone DL; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA., Sediva A; Department of Immunology Charles, University and University Hospital Motol, Prague, Czech Republic., Sleiman R; Dr. Sulaiman Al Habib Al Rayan Hospital, Riyadh, Saudi Arabia., Sramkova L; Department of Pediatric Hematology and Oncology, University Hospital Motol, Prague, Czech Republic., Bhatla D; SSM Health Cardinal Glennon Children's Hospital, Saint Louis University School of Medicine, St. Louis, Missouri, USA., Serti E; Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland, USA., Tsai WL; Translational Immunology Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland, USA., Yang D; Laboratory of Cardiovascular Regenerative Medicine, National Heart, Lung, and Blood Institute, Bethesda, Maryland, USA., Bishop K; Zebrafish Core, National Human Genome Research Institute, Bethesda, Maryland, USA., Carrington B; Zebrafish Core, National Human Genome Research Institute, Bethesda, Maryland, USA., Pei W; Zebrafish Core, National Human Genome Research Institute, Bethesda, Maryland, USA., Deuitch N; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA., Brooks S; Biodata Mining and Discovery Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland, USA., Edwan JH; Pediatric Translational Research Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland, USA., Joshi S; Department of Pathology, The Cleveland Clinic, Cleveland, Ohio, USA., Prader S; Department of Immunology, University Children's Hospital Zurich, Zurich, Switzerland., Kaiser D; Department of Pediatric Rheumatology, Children's Hospital, Lucerne, Switzerland., Owen WC; Children's Cancer and Blood Disorders Center, Children's Hospital of the King's Daughters, Norfolk, Virginia, USA., Sonbul AA; King Faisal Specialist Hospital &Research Center, Riyadh, Saudi Arabia., Zhang Y; Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, USA., Niemela JE; Department of Laboratory Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland, USA., Burgess SM; Zebrafish Core, National Human Genome Research Institute, Bethesda, Maryland, USA., Boehm M; Laboratory of Cardiovascular Regenerative Medicine, National Heart, Lung, and Blood Institute, Bethesda, Maryland, USA., Rehermann B; Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland, USA., Chae J; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA., Quezado MM; Laboratory of Pathology, National Cancer Institute, Bethesda, Maryland, USA., Ombrello AK; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA., Buckley RH; Departments of Pediatrics and Immunology, Duke University Medical Center, Durham, North Carolina, USA., Grom AA; Division of Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Remmers EF; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA., Pachlopnik JM; Department of Immunology, University Children's Hospital Zurich, Zurich, Switzerland., Su HC; Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, USA., Gutierrez-Cruz G; Laboratory of Muscle Stem Cells and Gene Regulation, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland, USA., Hewitt SM; Experimental Pathology Laboratory, National Cancer Institute, Bethesda, Maryland, USA., Sood R; Zebrafish Core, National Human Genome Research Institute, Bethesda, Maryland, USA., Risma K; Division of Allergy and Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Calvo KR; Department of Laboratory Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland, USA., Rosenzweig SD; Department of Laboratory Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland, USA., Gadina M; Translational Immunology Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland, USA., Hafner M; Division of Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Sun HW; Biodata Mining and Discovery Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland, USA., Kastner DL; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA., Aksentijevich I; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, Maryland, USA.

Publikováno v: Annals of the rheumatic diseases [Ann Rheum Dis] 2018 Apr; Vol. 77 (4), pp. 612-619. Date of Electronic Publication: 2018 Jan 22.

Identification of Interleukin-1β-Producing Monocytes That Are Susceptible to Pyronecrotic Cell Death in Patients With Neonatal-Onset Multisystem Inflammatory Disease.

Autor: Edwan JH; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Goldbach-Mansky R; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Colbert RA; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland.

Publikováno v: Arthritis & rheumatology (Hoboken, N.J.) [Arthritis Rheumatol] 2015 Dec; Vol. 67 (12), pp. 3286-97.

Flt3-L increases CD4+CD25+Foxp3+ICOS+ cells in the lungs of cockroach-sensitized and -challenged mice.

Autor: McGee HS; Department of Biomedical Sciences, Creighton University School of Medicine, Omaha, NE 68178, USA., Edwan JH, Agrawal DK

Publikováno v: American journal of respiratory cell and molecular biology [Am J Respir Cell Mol Biol] 2010 Mar; Vol. 42 (3), pp. 331-40. Date of Electronic Publication: 2009 May 15.