Zobrazeno 1 - 10
of 649
pro vyhledávání: '"Fut2"'
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-5 (2024)
Abstract Background Vitamin B12 deficiency is a recognised cause of neurological manifestations, including peripheral neuropathy, behavioural changes, and seizures. However, developmental and epileptic encephalopathy due to vitamin B12 deficiency is
Externí odkaz:
https://doaj.org/article/db797437587a4bea804680486e16e34c
Autor:
Dollwin Matharu, Alise J. Ponsero, Marton Lengyel, Agnes Meszaros-Matwiejuk, Kaija-Leena Kolho, Willem M. de Vos, Dora Molnar-Gabor, Anne Salonen
Publikováno v:
EBioMedicine, Vol 104, Iss , Pp 105182- (2024)
Summary: Background: Human milk oligosaccharides (HMOs), their determinants, infant gut microbiota and health are under extensive research; however, seldom jointly addressed. Leveraging data from the HELMi birth cohort, we investigated them collectiv
Externí odkaz:
https://doaj.org/article/7207f96d44c9485ea6746449e9ffb694
Publikováno v:
Эпидемиология и вакцинопрофилактика, Vol 22, Iss 6, Pp 148-154 (2024)
Relevance. Human Noroviruses (HuNoV) are highly contagious pathogens responsible of acute human norovirus infection. HuNoV is the cause of every fifth case of acute non-bacterial gastroenteritis, annually causing about 699 million cases of the diseas
Externí odkaz:
https://doaj.org/article/250725c4e48343e4a88ed371563b5417
Autor:
Jing Cai, Hao Wu, Chenxing Wang, Yujiao Chen, Dingli Zhang, Shiwei Guan, Beilei Fu, Yingli Jin, Cao Qian
Publikováno v:
BMC Immunology, Vol 24, Iss 1, Pp 1-12 (2023)
Abstract Inflammatory bowel disease (IBD) is a common immune-mediated condition with its molecular pathogenesis remaining to be fully elucidated. This study aimed to deepen our understanding of the role of FUT2 in human IBD, by studying a new surroga
Externí odkaz:
https://doaj.org/article/7dedb86b647f4170a8b7aff3cd46d977
Publikováno v:
Journal of Men's Health, Vol 19, Iss 11, Pp 116-119 (2023)
In this study, we aimed to determine and analyze the genetic differences of the FUT1 and FUT2 genes within an individual exhibiting the Para-Bombay phenotype. Standard serological tests were conducted to analyze the ABO phenotype. The amplification o
Externí odkaz:
https://doaj.org/article/a8dab3faedc94a63861cc4206ccb51f3
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss 4, Pp 449-455 (2023)
Introduction: The para-Bombay phenotype, or H-deficient secretor, results from different mutations of the FUT1, with or without the FUT2 mutation. Consequently, there is an absent or weak expression of the H antigen on red blood cells (RBCs). Routine
Externí odkaz:
https://doaj.org/article/5701d3f42a5443e5a6f12656d178efdc
Autor:
Kunio Kawanishi, Yuko Naito-Matsui, Livia Soares Zaramela, Nina M. van Sorge, Masaya Yamaguchi
Publikováno v:
Frontiers in Microbiology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/b3bb4f41dbac47418e5d28f06faba07e
Publikováno v:
Cell Communication and Signaling, Vol 21, Iss 1, Pp 1-14 (2023)
Abstract Background Fucosyltransferase 2(FUT2) and its induced α-1,2 fucosylation is associated with cancer metastasis. However, the role of FUT2 in colorectal cancer (CRC) metastasis remains unclear. Methods The expression levels and clinical analy
Externí odkaz:
https://doaj.org/article/58c74b3d3d784b19941f8906d7a81567
Autor:
Weijun Wang, Xuelian Tang, Caihan Duan, Shuxin Tian, Chaoqun Han, Wei Qian, Xin Jiang, Xiaohua Hou, Rong Lin
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-14 (2023)
Abstract Background Our previous study showed that fucosyltransferase 2 (Fut2) deficiency is closely related to colitis. Colitis increases the risk for the development of colorectal cancer (CRC). This study aimed to investigate the effect and underly
Externí odkaz:
https://doaj.org/article/6bf133c3469c40f4804bd75f773587b9
Autor:
Benjamin Lee, Md Abdul Kader, Masud Alam, Dorothy M. Dickson, Patrick Harvey, E. Ross Colgate, Mami Taniuchi, William A. Petri, Rashidul Haque, Beth D. Kirkpatrick
Publikováno v:
Pathogens, Vol 13, Iss 3, p 223 (2024)
The infant non-secretor histoblood group antigen phenotype is associated with reduced risk of symptomatic rotavirus diarrhea, one of the leading global causes of severe pediatric diarrheal disease and mortality. However, little is known regarding the
Externí odkaz:
https://doaj.org/article/708cedc9b64d4f72b1d1e47633f54e4a