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Monique Stoffels

Showing results (11-20 of 19) with videos related to

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Plos One|April 15, 2011
Inflammasome-independent modulation of cytokine response by autophagy in human cellsTania O Crişan, Theo S Plantinga, Frank L van de Veerdonk, et al.
Arthritis Research & Therapy|July 23, 2015
The role of interleukin-1 beta in the pathophysiology of Schnitzler's syndromeHeleen D de Koning, Joost Schalkwijk, Monique Stoffels, et al.
Ophthalmology|October 3, 2013
Mutations in the mevalonate kinase (MVK) gene cause nonsyndromic retinitis pigmentosaAnna M Siemiatkowska, L Ingeborgh van den Born, P Martin van Hagen, et al.
Annals of the Rheumatic Diseases|March 19, 2013
MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory diseaseMonique Stoffels, Agata Szperl, Anna Simon, et al.
Journal of Leukocyte Biology|May 3, 2011
The dectin-1/inflammasome pathway is responsible for the induction of protective T-helper 17 responses that discriminate between yeasts and hyphae of Candida albicansShih-Chin Cheng, Frank L van de Veerdonk, Megan Lenardon, et al.
BMC Immunology|November 20, 2014
The discriminative capacity of soluble Toll-like receptor (sTLR)2 and sTLR4 in inflammatory diseasesJaap Ten Oever, Matthijs Kox, Frank L van de Veerdonk, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|October 6, 2020
Sequence-Based Screening of Patients With Idiopathic Polyarteritis Nodosa, Granulomatosis With Polyangiitis, and Microscopic Polyangiitis for Deleterious Genetic Variants in ADA2Oskar Schnappauf, Natalia Sampaio Moura, Ivona Aksentijevich, et al.
Nature Genetics|December 8, 2015
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory diseaseQing Zhou, Hongying Wang, Daniella M Schwartz, et al.
Nature|December 13, 2019
Mutations that prevent caspase cleavage of RIPK1 cause autoinflammatory diseaseNajoua Lalaoui, Steven E Boyden, Hirotsugu Oda, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Plos One|April 15, 2011
Inflammasome-independent modulation of cytokine response by autophagy in human cellsTania O Crişan, Theo S Plantinga, Frank L van de Veerdonk, et al.
Arthritis Research & Therapy|July 23, 2015
The role of interleukin-1 beta in the pathophysiology of Schnitzler's syndromeHeleen D de Koning, Joost Schalkwijk, Monique Stoffels, et al.
Ophthalmology|October 3, 2013
Mutations in the mevalonate kinase (MVK) gene cause nonsyndromic retinitis pigmentosaAnna M Siemiatkowska, L Ingeborgh van den Born, P Martin van Hagen, et al.
Annals of the Rheumatic Diseases|March 19, 2013
MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory diseaseMonique Stoffels, Agata Szperl, Anna Simon, et al.
Journal of Leukocyte Biology|May 3, 2011
The dectin-1/inflammasome pathway is responsible for the induction of protective T-helper 17 responses that discriminate between yeasts and hyphae of Candida albicansShih-Chin Cheng, Frank L van de Veerdonk, Megan Lenardon, et al.
BMC Immunology|November 20, 2014
The discriminative capacity of soluble Toll-like receptor (sTLR)2 and sTLR4 in inflammatory diseasesJaap Ten Oever, Matthijs Kox, Frank L van de Veerdonk, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|October 6, 2020
Sequence-Based Screening of Patients With Idiopathic Polyarteritis Nodosa, Granulomatosis With Polyangiitis, and Microscopic Polyangiitis for Deleterious Genetic Variants in ADA2Oskar Schnappauf, Natalia Sampaio Moura, Ivona Aksentijevich, et al.
Nature Genetics|December 8, 2015
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory diseaseQing Zhou, Hongying Wang, Daniella M Schwartz, et al.
Nature|December 13, 2019
Mutations that prevent caspase cleavage of RIPK1 cause autoinflammatory diseaseNajoua Lalaoui, Steven E Boyden, Hirotsugu Oda, et al.
Pageof 2