Zobrazeno 1 - 10
of 119
pro vyhledávání: '"FAM111B"'
Publikováno v:
International Journal of General Medicine, Vol Volume 16, Pp 1845-1865 (2023)
Hengmiao Wu, Chao Liang Department of General Surgery, the Affiliated Lihuili Hospital, Ningbo University, Ningbo, 315000, People’s Republic of ChinaCorrespondence: Chao Liang, Department of General Surgery, the Affiliated Lihuili Hospital, Ningbo
Externí odkaz:
https://doaj.org/article/855254c32a3b4b97a96d7321a0fb6a04
Autor:
Filippo M. Panfili, Andrea Pietrobattista, Davide Vecchio, Michaela V. Gonfiantini, Andrea Bartuli, Marina Macchiaiolo
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/ead20f10a52e4b09b3877d2fa2510611
Autor:
Maciej Kliszczak, Daniela Moralli, Julia D. Jankowska, Paulina Bryjka, Lamia Subha Meem, Tomas Goncalves, Svenja S. Hester, Roman Fischer, David Clynes, Catherine M. Green
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
Hereditary fibrosing poikiloderma (HFP) is a rare human dominant negative disorder caused by mutations in the FAM111B gene that encodes a nuclear trypsin-like serine protease. HFP patients present with symptoms including skin abnormalities, tendon co
Externí odkaz:
https://doaj.org/article/2b3ff36c5f3d4ac2a5aff013ae00c0a5
Publikováno v:
Translational Oncology, Vol 32, Iss , Pp 101659- (2023)
Backgrounds: Ovarian cancer (OC) is the second most common gynecological tumor with the highest mortality rate worldwide. High FAM111B expression has been reported as a predictor of poor prognosis in other cancers, but its correlation with OC has not
Externí odkaz:
https://doaj.org/article/257d6de81a074d1abcd2905a5e65780c
Autor:
Elise M. N. Ferré, Yunting Yu, Vasileios Oikonomou, Anna Hilfanova, Chyi-Chia R. Lee, Lindsey B. Rosen, Peter D. Burbelo, Sara E. Vazquez, Mark S. Anderson, Amisha Barocha, Theo Heller, Ariane Soldatos, Steven M. Holland, Magdalena A. Walkiewicz, Michail S. Lionakis
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionAutoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) and poikiloderma in association with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP) are rare inherited syndromes resulting from biallelic pathogenic
Externí odkaz:
https://doaj.org/article/692b04899b434bd4af0be2c0f51e1216
Publikováno v:
Cancer Treatment and Research Communications, Vol 34, Iss , Pp 100679- (2023)
Introduction: Mutations in the uncharacterised human FAM111B gene are associated with POIKTMP, a rare multi-organ fibrosing disease. Recent studies also reported the overexpression of FAM111B in specific cancers. Moreover, FAM111B mutation screening
Externí odkaz:
https://doaj.org/article/a013da94e415405788c9264fd887f95a
Akademický článek
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Autor:
Allison L. Welter, Yuichi J. Machida
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2022)
Proteolysis plays fundamental and regulatory roles in diverse cellular processes. The serine protease FAM111A (FAM111 trypsin-like peptidase A) emerged recently as a protease involved in two seemingly distinct processes: DNA replication and antiviral
Externí odkaz:
https://doaj.org/article/2e9d5a888b6f46fba73dccebdfc54075
Akademický článek
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Autor:
Yelena Dokic, BSA, Yasser Albahrani, MD, Thuy Phung, MD, PhD, Kalyani Patel, MD, Marietta de Guzman, MD, Paula Hertel, MD, Raegan Hunt, MD, PhD
Publikováno v:
JAAD Case Reports, Vol 6, Iss 12, Pp 1217-1220 (2020)
Externí odkaz:
https://doaj.org/article/bcb6561771ce4926ae371ebf10ec3317