Zobrazeno 1 - 10
of 251
pro vyhledávání: '"GTF2I"'
Publikováno v:
Annals of Medicine, Vol 55, Iss 2 (2023)
AbstractBackground Metaplastic thymoma (MT) is a very uncommon thymoma type, with biphasic differentiation as one of its histological characteristics. This histological pattern, however, can also be mistaken for type A thymoma and the A component in
Externí odkaz:
https://doaj.org/article/68f3d2f71f6d43d99038a08105e80015
Autor:
Eleonora Pardini, Federico Cucchiara, Sara Palumbo, Giulia Tarrini, Alessia Di Vita, Fabio Coppedè, Vanessa Nicolì, Melania Guida, Michelangelo Maestri, Roberta Ricciardi, Vittorio Aprile, Marcello C. Ambrogi, Serena Barachini, Marco Lucchi, Iacopo Petrini
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundThymic epithelial tumors are rare malignant neoplasms that are frequently associated with paraneoplastic syndromes, especially myasthenia gravis. GTF2I is an oncogene mutated in a subgroup of thymomas that is reputed to drive their growth.
Externí odkaz:
https://doaj.org/article/1317aeb6d08d463381873c513bc9a53d
Publikováno v:
BMC Genomics, Vol 23, Iss 1, Pp 1-13 (2022)
Abstract Background General transcription factor IIi (GTF2I) mutations are very common in thymic epithelial tumors (TETs) and are related to a more favorable prognosis in TET patients. However, limited research has been conducted on the role of GTF2I
Externí odkaz:
https://doaj.org/article/cf84f42e4eb247ba98a33e52a233c5b5
Autor:
Serena Barachini, Eleonora Pardini, Irene Sofia Burzi, Gisella Sardo Infirri, Marina Montali, Iacopo Petrini
Publikováno v:
Cancers, Vol 16, Iss 1, p 166 (2023)
Thymic epithelial tumors, comprising thymic carcinomas and thymomas, are rare neoplasms. They differ in histology, prognosis, and association with autoimmune diseases such as myasthenia gravis. Thymomas, but not thymic carcinomas, often harbor GTF2I
Externí odkaz:
https://doaj.org/article/c75c15ae62104d0aaa581ec06fa1757f
Autor:
Amit Singh, Mary Kaileh, Supriyo De, Krystyna Mazan-Mamczarz, Dashzeveg Bayarsaihan, Ranjan Sen, Ananda L. Roy
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
The ubiquitously expressed transcription factor TFII-I is a multifunctional protein with pleiotropic roles in gene regulation. TFII-I associated polymorphisms are implicated in Sjögren’s syndrome and Lupus in humans and, germline deletion of the G
Externí odkaz:
https://doaj.org/article/e12b30c6e59b4bb0a08d25cb577b1e47
Autor:
Omer Ophir, Gilad Levy, Ela Bar, Omri Kimchi Feldhorn, May Rokach, Galit Elad Sfadia, Boaz Barak
Publikováno v:
Biomedicines, Vol 11, Iss 8, p 2273 (2023)
Williams syndrome (WS) is a neurodevelopmental disorder characterized by distinctive cognitive and personality profiles which also impacts various physiological systems. The syndrome arises from the deletion of about 25 genes located on chromosome 7q
Externí odkaz:
https://doaj.org/article/7598d15b0fcd4806b1dfb7db76302c1f
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
PeerJ, Vol 10, p e13735 (2022)
Background Nonalcoholic fatty liver disease (NAFLD) is the most common liver disease worldwide that endangers human health. Transcription factors (TFs) have gradually become hot spots for drug development in NAFLD for their impacts on metabolism. How
Externí odkaz:
https://doaj.org/article/0893220ac8df4fdcbdcd722fdb6bfe96
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.