Статті в журналах з теми "INTERFERONOPATIA"
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Souza, Victória Cabral de, Roberto de Barros Silva, and Caique Antunis. "INTERFERON-I COMO ALVO TERAPÊUTICO NO TRATAMENTO DO LÚPUS ERITEMATOSO SISTÊMICO: USO DOS ANTICORPOS MONOCLONAIS ANIFROLUMABE, RONTALIZUMABE E SIFALIMUMABE." Revista Ibero-Americana de Humanidades, Ciências e Educação 9, no. 1 (January 31, 2023): 717–31. http://dx.doi.org/10.51891/rease.v9i1.8303.
Повний текст джерелаTommasini, Alberto, Irene Bruno, Maria Elisa Morelli, and Loredana Lepore. "Le interferonopatie di tipo I." Medico e Bambino 40, no. 8 (September 23, 2021): 509–14. http://dx.doi.org/10.53126/meb40509.
Повний текст джерелаPayet, Cloé A., Axel You, Odessa-Maud Fayet, Nadine Dragin, Sonia Berrih-Aknin, and Rozen Le Panse. "Myasthenia Gravis: An Acquired Interferonopathy?" Cells 11, no. 7 (April 4, 2022): 1218. http://dx.doi.org/10.3390/cells11071218.
Повний текст джерелаBriggs, Tracy A., Anindita Paul, Gillian Rice, and Ariane L. Herrick. "RNASEH2B Related Adult-Onset Interferonopathy." Journal of Clinical Immunology 39, no. 6 (July 31, 2019): 620–22. http://dx.doi.org/10.1007/s10875-019-00673-w.
Повний текст джерелаRodero, Mathieu P., Marie-Louise Frémond, Gillian I. Rice, Bénédicte Neven, and Yanick J. Crow. "JAK inhibition in STING-associated interferonopathy." Annals of the Rheumatic Diseases 75, no. 12 (October 12, 2016): e75-e75. http://dx.doi.org/10.1136/annrheumdis-2016-210504.
Повний текст джерелаManoussakis, Menelaos N., Clio P. Mavragani, Adrianos Nezos, Evangelia Zampeli, Anastassios Germenis, and Haralampos M. Moutsopoulos. "Type I interferonopathy in a young adult." Rheumatology 56, no. 12 (August 14, 2017): 2241–43. http://dx.doi.org/10.1093/rheumatology/kex316.
Повний текст джерелаKrieger, Ben Zion, Theresa Calvelli, Anna Kadish, and Arye Rubinstein. "1042 INTERFERONOPATHY IN THE BARE LYMPHOCYTE SYNDROME." Pediatric Research 19, no. 4 (April 1985): 284A. http://dx.doi.org/10.1203/00006450-198504000-01072.
Повний текст джерелаPiotto, Daniela Gerent Petry, Kátia Tomie Kozu, and Sandro Félix Perazzio. "Quando suspeitar de doenças autoinflamatórias na infância?" Reumatologia Pediátrica, no. 2021 jan-mar;20(1) (March 31, 2021): 16–26. http://dx.doi.org/10.46833/reumatologiasp.2021.20.1.16-26.
Повний текст джерелаCrow, Yanick, Nandaki Keshavan, Jacques Patrick Barbet, Geanina Bercu, Vincent Bondet, Charlotte Boussard, Nathalie Dedieu, et al. "Cardiac valve involvement in ADAR-related type I interferonopathy." Journal of Medical Genetics 57, no. 7 (November 26, 2019): 475–78. http://dx.doi.org/10.1136/jmedgenet-2019-106457.
Повний текст джерелаKozlova, A. L., E. S. Romanenko, V. I. Burlakov, E. V. Deripapa, Sv P. Khomyakova, A. N. Remizov, G. V. Tereshenko, and A. Yu Shcherbina. "CLINICAL CASE OF TYPE I INTERFERONOPATHY: AICARDI–GOUTIERES SYNDROME." Pediatria. Journal named after G.N. Speransky 98, no. 3 (June 10, 2019): 257–65. http://dx.doi.org/10.24110/0031-403x-2019-98-3-257-265.
Повний текст джерелаManzano, Giovanna S., Jared K. Woods, and Anthony A. Amato. "Covid-19–Associated Myopathy Caused by Type I Interferonopathy." New England Journal of Medicine 383, no. 24 (December 10, 2020): 2389–90. http://dx.doi.org/10.1056/nejmc2031085.
Повний текст джерелаCrow, Yanick J., and Jean-Laurent Casanova. "STING-Associated Vasculopathy with Onset in Infancy — A New Interferonopathy." New England Journal of Medicine 371, no. 6 (August 7, 2014): 568–71. http://dx.doi.org/10.1056/nejme1407246.
Повний текст джерелаTüngler, Victoria, Nadja König, Claudia Günther, Kerstin Engel, Christoph Fiehn, Martin Smitka, Maja von der Hagen, Reinhard Berner, and Min Ae Lee-Kirsch. "Response to: ‘JAK inhibition in STING-associated interferonopathy’ by Crowet al." Annals of the Rheumatic Diseases 75, no. 12 (November 3, 2016): e76-e76. http://dx.doi.org/10.1136/annrheumdis-2016-210565.
Повний текст джерелаPicard, Cécile, Guillaume Thouvenin, Caroline Kannengiesser, Jean-Christophe Dubus, Nadia Jeremiah, Frédéric Rieux-Laucat, Bruno Crestani, et al. "Severe Pulmonary Fibrosis as the First Manifestation of Interferonopathy (TMEM173 Mutation)." Chest 150, no. 3 (September 2016): e65-e71. http://dx.doi.org/10.1016/j.chest.2016.02.682.
Повний текст джерелаGoldmann, Tobias, Nicolas Zeller, Jenni Raasch, Katrin Kierdorf, Kathrin Frenzel, Lars Ketscher, Anja Basters, et al. "USP 18 lack in microglia causes destructive interferonopathy of the mouse brain." EMBO Journal 34, no. 12 (April 20, 2015): 1612–29. http://dx.doi.org/10.15252/embj.201490791.
Повний текст джерелаRafat, Cédric, and Alice Doreille. "Could Plasmodium falciparum–related kidney disease stand as another example of interferonopathy?" Kidney International 102, no. 3 (September 2022): 669–70. http://dx.doi.org/10.1016/j.kint.2022.06.009.
Повний текст джерелаKozlova, А. L., М. Е. Leonteva, V. I. Burlakov, Z. А. Nesterenko, О. М. Laba, М. V. Pisareva, N. Yu Kan, et al. "Clinical case of type I interferonopathy: homozygous STAT2 gain-of-function mutation." Pediatric Hematology/Oncology and Immunopathology 20, no. 3 (October 8, 2021): 132–39. http://dx.doi.org/10.24287/1726-1708-2021-20-3-132-139.
Повний текст джерелаFrémond, M.-L., C. Gitiaux, D. Bonnet, T. Guiddir, Y. Crow, L. de Ponthual, and B. Bader-Meunier. "Mosaic tetrasomy 9p: a mendelian interferonopathy associated with pediatric-onset overlap myositis." Pediatric Rheumatology 13, Suppl 1 (2015): P140. http://dx.doi.org/10.1186/1546-0096-13-s1-p140.
Повний текст джерелаMeuwissen, Marije E. C., Rachel Schot, Sofija Buta, Grétel Oudesluijs, Sigrid Tinschert, Scott D. Speer, Zhi Li, et al. "Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome." Journal of Experimental Medicine 213, no. 7 (June 20, 2016): 1163–74. http://dx.doi.org/10.1084/jem.20151529.
Повний текст джерелаEmralino, Francine Lianne, Saya Satoh, Nobuhiro Sakai, Masamichi Takami, Fumihiko Takeuchi, Nan Yan, Frank Rutsch, Takashi Fujita, and Hiroki Kato. "Double-Stranded RNA Induces Mortality in an MDA5-Mediated Type I Interferonopathy Model." Journal of Immunology 209, no. 11 (December 1, 2022): 2093–103. http://dx.doi.org/10.4049/jimmunol.2200367.
Повний текст джерелаSifuentes-Dominguez, Luis, Petro Starokadomskyy, Jacob Welch, Bhaskar Gurram, Jason Y. Park, Prasad Koduru, and Ezra Burstein. "Mosaic Tetrasomy 9p Associated With Inflammatory Bowel Disease." Journal of Crohn's and Colitis 13, no. 11 (April 25, 2019): 1474–78. http://dx.doi.org/10.1093/ecco-jcc/jjz079.
Повний текст джерелаKomura, Kazuhiro, Yuki Ichimura, Naoko Okiyama, Kazuyoshi Watanabe, Hiroaki Muramoto, and Takashi Matsushita. "Interferon signature in cutaneous lesion of COVID toes." Journal of Immunology 206, no. 1_Supplement (May 1, 2021): 20.37. http://dx.doi.org/10.4049/jimmunol.206.supp.20.37.
Повний текст джерелаHauck, Fabian. "Angeborene autoinflammatorische Störungen der cGAS-STING- und OASRNase-L-vermittelten Nukleinsäure-Immunität." Translationale Immunologie 5, no. 3 (October 28, 2021): 160–65. http://dx.doi.org/10.47184/ti.2021.03.04.
Повний текст джерелаOkada, Yuri, Rumiko Izumi, Tatsuhiko Hosaka, Satoshi Watanabe, Tomomi Shijo, Naokazu Hatchome, Risa Konishi, et al. "Anti-NXP2 antibody-positive dermatomyositis developed after COVID-19 manifesting as type I interferonopathy." Rheumatology 61, no. 4 (November 30, 2021): e90-e92. http://dx.doi.org/10.1093/rheumatology/keab872.
Повний текст джерелаRuggeri, Paolo, and Gaetano Caramori. "Interferonopathy: a potential link between innate immunity and autoimmunity in the pathogenesis of COPD." American Journal of Physiology-Lung Cellular and Molecular Physiology 317, no. 6 (December 1, 2019): L888—L890. http://dx.doi.org/10.1152/ajplung.00439.2019.
Повний текст джерелаde Jesus, Adriana A., Anja Brehm, Rachel VanTries, Pascal Pillet, Anne-Sophie Parentelli, Gina A. Montealegre Sanchez, Zuoming Deng, Isabelle Koné Paut, Raphaela Goldbach-Mansky, and Elke Krüger. "Novel proteasome assembly chaperone mutations in PSMG2/PAC2 cause the autoinflammatory interferonopathy CANDLE/PRAAS4." Journal of Allergy and Clinical Immunology 143, no. 5 (May 2019): 1939–43. http://dx.doi.org/10.1016/j.jaci.2018.12.1012.
Повний текст джерелаOkada, Satoshi, Takaki Asano, Kunihiko Moriya, Stephanie Boisson-Dupuis, Masao Kobayashi, Jean-Laurent Casanova, and Anne Puel. "Human STAT1 Gain-of-Function Heterozygous Mutations: Chronic Mucocutaneous Candidiasis and Type I Interferonopathy." Journal of Clinical Immunology 40, no. 8 (August 27, 2020): 1065–81. http://dx.doi.org/10.1007/s10875-020-00847-x.
Повний текст джерелаde Carvalho, Luciana Martins, Gonza Ngoumou, Ji Woo Park, Nadja Ehmke, Nikolaus Deigendesch, Naoki Kitabayashi, Isabelle Melki, et al. "Musculoskeletal Disease in MDA5-Related Type I Interferonopathy: A Mendelian Mimic of Jaccoud's Arthropathy." Arthritis & Rheumatology 69, no. 10 (August 22, 2017): 2081–91. http://dx.doi.org/10.1002/art.40179.
Повний текст джерелаAl-Mayouf, Sulaiman M., Lujayn Akbar, Abdullatif AlEnazi, and Hamoud Al-Mousa. "Autosomal Recessive ISG15 Deficiency Underlies Type I Interferonopathy with Systemic Lupus Erythematosus and Inflammatory Myositis." Journal of Clinical Immunology 41, no. 6 (March 19, 2021): 1361–64. http://dx.doi.org/10.1007/s10875-021-01019-1.
Повний текст джерелаRood, Julia E., and Edward M. Behrens. "Inherited Autoinflammatory Syndromes." Annual Review of Pathology: Mechanisms of Disease 17, no. 1 (January 24, 2022): 227–49. http://dx.doi.org/10.1146/annurev-pathmechdis-030121-041528.
Повний текст джерелаKasher, Paul R., Emma M. Jenkinson, Valérie Briolat, David Gent, Catherine Morrissey, Leo A. H. Zeef, Gillian I. Rice, Jean-Pierre Levraud, and Yanick J. Crow. "Characterization of samhd1 Morphant Zebrafish Recapitulates Features of the Human Type I Interferonopathy Aicardi-Goutières Syndrome." Journal of Immunology 194, no. 6 (February 11, 2015): 2819–25. http://dx.doi.org/10.4049/jimmunol.1403157.
Повний текст джерелаKong, Xiao-Fei, Lisa Worley, Darawan Rinchai, Vincent Bondet, Puthen Veettil Jithesh, Marie Goulet, Emilie Nonnotte, et al. "Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down Syndrome." Journal of Clinical Immunology 40, no. 6 (June 22, 2020): 807–19. http://dx.doi.org/10.1007/s10875-020-00803-9.
Повний текст джерелаDuncan, Christopher J. A., Benjamin J. Thompson, Rui Chen, Gillian I. Rice, Florian Gothe, Dan F. Young, Simon C. Lovell, et al. "Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2." Science Immunology 4, no. 42 (December 13, 2019): eaav7501. http://dx.doi.org/10.1126/sciimmunol.aav7501.
Повний текст джерелаBuers, Insa, Gillian I. Rice, Yanick J. Crow, and Frank Rutsch. "MDA5-Associated Neuroinflammation and the Singleton–Merten Syndrome: Two Faces of the Same Type I Interferonopathy Spectrum." Journal of Interferon & Cytokine Research 37, no. 5 (May 2017): 214–19. http://dx.doi.org/10.1089/jir.2017.0004.
Повний текст джерелаMeesilpavikkai, Kornvalee, Willem A. Dik, Benjamin Schrijver, Cornelia G. Helden‐Meeuwsen, Marjan A. Versnel, P. Martin Hagen, Emilia K. Bijlsma, Claudia A. L. Ruivenkamp, Margreet J. Oele, and Virgil A. S. H. Dalm. "Efficacy of Baricitinib in the Treatment of Chilblains Associated With Aicardi‐Goutières Syndrome, a Type I Interferonopathy." Arthritis & Rheumatology 71, no. 5 (March 6, 2019): 829–31. http://dx.doi.org/10.1002/art.40805.
Повний текст джерелаMills, Taylor, Bailee Kain, Erin Lucas, Matt Burchill, Beth Jiron Tamburini, Katherine King, and Eric Pietras. "3097 – AUTOIMMUNE INTERFERONOPATHY INDUCES A ‘TRAINED IMMUNITY’ PROGRAM IN HSC THAT PRIMES MACROPHAGES FOR INCREASED PATHOGEN KILLING AND INFLAMMATORY ACTIVITY." Experimental Hematology 100 (August 2021): S89. http://dx.doi.org/10.1016/j.exphem.2021.12.314.
Повний текст джерелаCazzato, Salvatore, Alessia Omenetti, Claudia Ravaglia, and Venerino Poletti. "Lung involvement in monogenic interferonopathies." European Respiratory Review 29, no. 158 (December 15, 2020): 200001. http://dx.doi.org/10.1183/16000617.0001-2020.
Повний текст джерелаKataoka, Shinsuke, Nozomu Kawashima, Yusuke Okuno, Hideki Muramatsu, Shunsuke Miwata, Kotaro Narita, Motoharu Hamada, et al. "Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor." Journal of Allergy and Clinical Immunology 148, no. 2 (August 2021): 639–44. http://dx.doi.org/10.1016/j.jaci.2021.03.010.
Повний текст джерелаPoeschla, Eric M., and Laura Bankers. "Development of interferon-stimulated gene expression from embryogenesis through adulthood, with and without constitutive MDA5 pathway activation." Journal of Immunology 204, no. 1_Supplement (May 1, 2020): 68.15. http://dx.doi.org/10.4049/jimmunol.204.supp.68.15.
Повний текст джерелаBryant, Andrew J., Ann Pham, Himanshu Gogoi, Carly R. Mitchell, Faye Pais, and Lei Jin. "The Third Man: DNA sensing as espionage in pulmonary vascular health and disease." Pulmonary Circulation 11, no. 1 (January 2021): 204589402199657. http://dx.doi.org/10.1177/2045894021996574.
Повний текст джерелаAdang, Laura, Francesco Gavazzi, Micaela De Simone, Elisa Fazzi, Jessica Galli, Jamie Koh, Julia Kramer-Golinkoff, et al. "Developmental Outcomes of Aicardi Goutières Syndrome." Journal of Child Neurology 35, no. 1 (September 27, 2019): 7–16. http://dx.doi.org/10.1177/0883073819870944.
Повний текст джерелаSandling, Johanna K., Pascal Pucholt, Lina Hultin Rosenberg, Fabiana H. G. Farias, Sergey V. Kozyrev, Maija-Leena Eloranta, Andrei Alexsson, et al. "Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing." Annals of the Rheumatic Diseases 80, no. 1 (October 9, 2020): 109–17. http://dx.doi.org/10.1136/annrheumdis-2020-218636.
Повний текст джерелаTesser, Alessandra, Giulia Maria Piperno, Alessia Pin, Elisa Piscianz, Valentina Boz, Federica Benvenuti, and Alberto Tommasini. "Priming of the cGAS-STING-TBK1 Pathway Enhances LPS-Induced Release of Type I Interferons." Cells 10, no. 4 (April 1, 2021): 785. http://dx.doi.org/10.3390/cells10040785.
Повний текст джерелаDaou, Salima, Manisha Talukdar, Jinle Tang, Beihua Dong, Shuvojit Banerjee, Yize Li, Nicole M. Duffy, et al. "A phenolic small molecule inhibitor of RNase L prevents cell death from ADAR1 deficiency." Proceedings of the National Academy of Sciences 117, no. 40 (September 21, 2020): 24802–12. http://dx.doi.org/10.1073/pnas.2006883117.
Повний текст джерелаWang, Qingde, Xinfeng Guo, Yi Sheng, Tony Wang, Richard Steinman, and Timothy R. Billiar. "An AGS associated mutation causes cellular RNA editing deficiency in mouse brain which lead to IFN pathway activation, mimicking the interferonopathy of patient brains." Journal of Immunology 206, no. 1_Supplement (May 1, 2021): 15.07. http://dx.doi.org/10.4049/jimmunol.206.supp.15.07.
Повний текст джерелаSu, Yu-Jih, Hung-Yu Lin, Shao-Wen Weng, Cheng-Hsien Lu, Ching-Yi Lin, Wen-Chan Chiu, and Pei-Wen Wang. "Metformin Represses Interferonopathy Through Suppression of Melanoma Differentiation-Associated Protein 5 and Mitochondrial Antiviral Signaling Protein Activation: Comment on the Article by Wang et al." Arthritis & Rheumatology 68, no. 12 (November 28, 2016): 3042–43. http://dx.doi.org/10.1002/art.39935.
Повний текст джерелаDavid, Clémence, and Marie-Louise Frémond. "Lung Inflammation in STING-Associated Vasculopathy with Onset in Infancy (SAVI)." Cells 11, no. 3 (January 18, 2022): 318. http://dx.doi.org/10.3390/cells11030318.
Повний текст джерелаYoshikawa, T., K. Azuma, T. Furukawa, M. Tamura, T. Hashimoto, M. Morimoto, N. Azuma, and K. Matsui. "AB0311 INCREASED LEVELS OF SERUM WISTERIA FLORIBUNDA AGGLUTININPOSITIVE MAC-2 BINDING PROTEIN IN RHEUMATIC DISEASES INCLUDING SLE." Annals of the Rheumatic Diseases 80, Suppl 1 (May 19, 2021): 1181.1–1181. http://dx.doi.org/10.1136/annrheumdis-2021-eular.1494.
Повний текст джерелаStathopoulou, C., D. Konstantopoulos, S. Papanikolaou, G. Vatsellas, G. Panagopoulos, P. Sidiropoulos та G. Bertsias. "POS0404 IFNα-MEDIATED METABOLIC REPROGRAMMING IN HUMAN SLE MONOCYTES INVOLVES PERTURBATIONS IN GLYCOLYTIC AND LIPID METABOLISM TO REGULATE PROINFLAMMATORY MARKERS AND CYTOKINES". Annals of the Rheumatic Diseases 81, Suppl 1 (23 травня 2022): 458.1–458. http://dx.doi.org/10.1136/annrheumdis-2022-eular.2035.
Повний текст джерелаPennisi, Alessandra, Agnès Rötig, Charles-Joris Roux, Raphaël Lévy, Marco Henneke, Jutta Gärtner, Pelin Teke Kisa, et al. "Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?" Journal of Medical Genetics, November 16, 2020, jmedgenet—2020–107367. http://dx.doi.org/10.1136/jmedgenet-2020-107367.
Повний текст джерела