Daniel L Kastner

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Daniel L



Publications in SciGraph latest 50 shown

  • 2017-11 Corrigendum: The monogenic autoinflammatory diseases define new pathways in human innate immunity and inflammation in NATURE IMMUNOLOGY
  • 2017-08 The monogenic autoinflammatory diseases define new pathways in human innate immunity and inflammation in NATURE IMMUNOLOGY
  • 2017-08 A guiding map for inflammation in NATURE IMMUNOLOGY
  • 2017-03 Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behcet's disease susceptibility in NATURE GENETICS
  • 2016-12 Evaluation of KIR3DL1/KIR3DS1 polymorphism in Behçet’s disease in GENES & IMMUNITY
  • 2016-12 Hypophosphatasia and the risk of atypical femur fractures: a case–control study in BMC MUSCULOSKELETAL DISORDERS
  • 2016-08 Pyrin inflammasome activation and RhoA signaling in the autoinflammatory diseases FMF and HIDS in NATURE IMMUNOLOGY
  • 2016-08 Control of the innate immune response by the mevalonate pathway in NATURE IMMUNOLOGY
  • 2016-01 Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease in NATURE GENETICS
  • 2015-12 Activation of the pyrin inflammasome through the RhoA signaling pathway in FMF and HIDS in PEDIATRIC RHEUMATOLOGY
  • 2015-12 Description of a case of daily fever, developmental abnormalities, and a heterozygous M694I MEFV mutation in PEDIATRIC RHEUMATOLOGY
  • 2015-12 Identification of ERAP1 protein allotypes in the Turkish population and evaluation of their contributions to Behçet's disease risk in PEDIATRIC RHEUMATOLOGY
  • 2015-12 Identification of pyrin targets by CHiP-Seq in PEDIATRIC RHEUMATOLOGY
  • 2015-12 Cofilin-1 is an essential redox sensor for NLRP3 inflammasome activation in PEDIATRIC RHEUMATOLOGY
  • 2015-12 Update on CECR1 molecular diagnostics: new mutations in the deficiency of ADA2 (DADA2) and the North American polyarteritis nodosa (PAN) cohort in PEDIATRIC RHEUMATOLOGY
  • 2015-12 Use of TNF inhibitors in the treatment of PAPA syndrome in PEDIATRIC RHEUMATOLOGY
  • 2015-12 HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis in PEDIATRIC RHEUMATOLOGY
  • 2015-12 Immune dysregulation in patients with TRNT1 deficiency in PEDIATRIC RHEUMATOLOGY
  • 2015-12 A dominantly-inherited Behcet-like disorder caused by haploinsufficiency of the TNFAIP3/A20 protein in PEDIATRIC RHEUMATOLOGY
  • 2015-12 Clinical follow-up on a cohort of patients with deficiency of adenosine deaminase 2 (DADA2) in PEDIATRIC RHEUMATOLOGY
  • 2015-12 The deficiency of adenosine deaminase type 2-results of therapeutic intervention in PEDIATRIC RHEUMATOLOGY
  • 2015-12 CECR1 p.Gly47Arg mutations are not increased in frequency in Turkish Behçet's disease patients compared with healthy controls in PEDIATRIC RHEUMATOLOGY
  • 2015-10 Reply to Stoimenis et al in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-05 Identification of possible pathogenic pathways in Behçet’s disease using genome-wide association study data from two different populations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-03 A small-molecule inhibitor of the NLRP3 inflammasome for the treatment of inflammatory diseases in NATURE MEDICINE
  • 2014-09 TRNT1 missense mutations define an autoinflammatory disease characterized by recurrent fever, severe anemia, and b-cell immunodeficiency in PEDIATRIC RHEUMATOLOGY
  • 2013-11 OR7-001 – By chip pyrin binds the IRF2 promoter in PEDIATRIC RHEUMATOLOGY
  • 2013-11 P02-003 - HIDS in a consanguineous family form Saudi Arabia? in PEDIATRIC RHEUMATOLOGY
  • 2013-11 OR10-001 - Altered mitochondrial ROS and metabolism in TRAPS in PEDIATRIC RHEUMATOLOGY
  • 2013-11 PW03-017 – Combination TNF and IL-1 blockade in PAPA syndrome in PEDIATRIC RHEUMATOLOGY
  • 2013-11 PW02-002 - Single MVK mutation and recurrent fevers in PEDIATRIC RHEUMATOLOGY
  • 2013-11 PW03-014 - TLR4 and MEFV variants are Behçet's risk factors in PEDIATRIC RHEUMATOLOGY
  • 2013-11 OR9-001 - Exome sequencing in monogenic Behçet-like disease in PEDIATRIC RHEUMATOLOGY
  • 2013-11 OR13-001 Loss-of-function mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause recurrent fevers and early onset strokes in PEDIATRIC RHEUMATOLOGY
  • 2013-11 PW02-001 - Exome sequencing for autoinflammatory disorders in PEDIATRIC RHEUMATOLOGY
  • 2013-11 PW03-013 - Behçet's disease: genotype-phenotype correlations in PEDIATRIC RHEUMATOLOGY
  • 2013-11 P02-023 - NLRP3 mosaicism as a cause of late-onset CAPS in PEDIATRIC RHEUMATOLOGY
  • 2013-11 OR11-003 - The NLRP3 inflammasome is regulated by CaSR in PEDIATRIC RHEUMATOLOGY
  • 2013-11 PW01-038 – Genomewide association study of Still’s disease in PEDIATRIC RHEUMATOLOGY
  • 2013-11 PW03-011 – New Behçet's loci and gene-gene interactions in PEDIATRIC RHEUMATOLOGY
  • 2013-11 PW03-010 - MHC complexity in Behçet's disease in PEDIATRIC RHEUMATOLOGY
  • 2013-11 PW02-003 - Efficacy of anakinra in etanercept-resistant TRAPS in PEDIATRIC RHEUMATOLOGY
  • 2013-02 Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1 in NATURE GENETICS
  • 2012-12 HOIL and water: the two faces of HOIL-1 deficiency in NATURE IMMUNOLOGY
  • 2012-12 The calcium-sensing receptor regulates the NLRP3 inflammasome through Ca2+ and cAMP in NATURE
  • 2012-08 Lighting the fires within: the cell biology of autoinflammatory diseases in NATURE REVIEWS IMMUNOLOGY
  • 2012-07 Systemic juvenile idiopathic arthritis is associated with HLA-DRB1 in Europeans and Americans of European descent in PEDIATRIC RHEUMATOLOGY
  • 2012-07 PFAPA: a single phenotype with genetic heterogeneity in PEDIATRIC RHEUMATOLOGY
  • 2011-12 Rilonacept (IL-1 TRAP) for treatment of colchicine resistant familial mediterranean fever (FMF): a randomized, multicenter double-blinded, alternating treatment trial in PEDIATRIC RHEUMATOLOGY
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