Zobrazeno 1 - 10
of 43
pro vyhledávání: '"ifih1 gene"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Background Interferon-induced helicase C domain-containing protein 1 (IFIH1) is one of the main pattern recognition receptors that sense viral RNA and activate host cells to mount an effective antiviral immunity. Methods A case–control stu
Externí odkaz:
https://doaj.org/article/8b202d78fc464e0ebc590bde5d8b30da
Akademický článek
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Autor:
Mojca Železnik, Aneta Soltirovska Šalamon, Maruša Debeljak, Aleš Goropevšek, Nataša Šuštar, Damjana Ključevšek, Alojz Ihan, Tadej Avčin
Publikováno v:
Frontiers in Immunology, Vol 13 (2023)
Aicardi–Goutières syndrome (AGS) is a genetically determined early-onset progressive encephalopathy caused by mutations leading to overexpression of type I interferon (IFN) and resulting in various clinical phenotypes. A gain-of-function (GOF) mut
Externí odkaz:
https://doaj.org/article/0d893e5433364629b656927ea39fc09d
Autor:
Marta Rydzewska, Aleksandra Góralczyk, Joanna Gościk, Natalia Wawrusiewicz-Kurylonek, Anna Bossowska, Adam Krętowski, Artur Bossowski
Publikováno v:
Autoimmunity, Vol 51, Iss 4, Pp 183-190 (2018)
Background: Autoimmune thyroid diseases are multifactorial diseases with a genetic susceptibility and environmental factors. A potential role of the protein tyrosine phosphatase non-receptor type 22 (PTPN22) gene, the interferon-induced helicase doma
Externí odkaz:
https://doaj.org/article/e325521aecbc45c0a75c6420ea7c1a21
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
A Kozsar, Romana R. Gerner, Christina Watschinger, N Przysiecki, Alexander R. Moschen, S Macheiner
Publikováno v:
Zeitschrift für Gastroenterologie.
Autor:
Kadir Mutlu Hayran, Duru Onan, Ahu Yorulmaz, Fatih Süheyl Ezgü, Seray Cakmak Kulcu, Başak Yalçin, Refika Ferda Artüz
Publikováno v:
Turkish Journal of Medical Sciences
Volume: 49, Issue: 1 206-211
Volume: 49, Issue: 1 206-211
Background and Aim: Interferon-induced helicase (IFIH1) is a gene locus that has been recently defined as a candidate for susceptibility to generalized vitiligo (GV). The objectives of this study were to assess the association of IFIH1 gene, rs211148
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics
Frontiers in Genetics
The IFIH1 gene encodes melanoma differentiation-associated gene 5 (MDA5) and has been associated with Aicardi-Goutières syndrome (AGS), Singleton-Merten syndrome (SMS), and other autoimmune diseases. The mechanisms responsible for how a functional c
Autor:
Nicolás Guillermo Pineda Trujillo, Diana M. Cornejo-Sánchez, Claudia Janeth Echavarría Sierra, Gloria Sanclemente, Evelyn Vanesa Erazo Luna
Publikováno v:
Medwave, Vol 21, Iss 11, Pp e002099-e002099 (2021)
Psoriasis is a chronic inflammatory dermatosis, a with variable clinical presentation and whose multifactorial etiology carries an essential genetic component. Multiple genetic variations associated with psoriasis have been described around the world
Autor:
Timothy J. Thauland, Stanley F. Nelson, Manish J. Butte, Hane Lee, Rebecca Signer, Christin Deal
Viral respiratory infections are the most common childhood infection worldwide. However, even common pathogens can have significant consequences in the context of patients with primary immunodeficiency diseases. More than half or viral infections ann
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6519feadcb808de1e495cba552a6bb4b
https://doi.org/10.1101/2020.07.01.20105379
https://doi.org/10.1101/2020.07.01.20105379