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pro vyhledávání: '"Kara G Greenfield"'
Autor:
Kara G. Greenfield, Olivia S. Harlow, Lila T. Witt, Evelyn M. Dziekan, Christian R. Tamar, Josephine Meier, Jane E. Brumbaugh, Emily R. Levy, Kathryn A. Knoop
Publikováno v:
Gut Microbes, Vol 16, Iss 1 (2024)
Streptococcus agalactiae, also known as Group B Streptococcus (GBS), is a predominant pathogen of neonatal sepsis, commonly associated with early-onset neonatal sepsis. GBS has also been associated with cases of late-onset sepsis potentially originat
Externí odkaz:
https://doaj.org/article/504a9b7c79094db9905c4e02138ae454
Publikováno v:
iScience, Vol 27, Iss 5, Pp 109669- (2024)
Summary: Neonates born prematurely are vulnerable to life-threatening conditions such as bacterial sepsis. Streptococcus agalactiae (GBS) and Escherichia coli are frequent causative pathogens of neonatal sepsis, however, it remains unclear if these p
Externí odkaz:
https://doaj.org/article/5196691ac6784ef58ac9bb342972a7d3
Publikováno v:
ImmunoHorizons
Sepsis can result from a variety of pathogens, originating from a range of sources. A vast range of presenting symptoms is included in the catch-all term of “bacteremia,” making diagnosis and prognosis particularly troublesome. One underexplored
Publikováno v:
The Journal of Immunology. 208:59.08-59.08
The intestinal epithelial barrier is vital in preventing translocating bacteria and subsequent systemic infections. This protection is provided by host factors, by the intestinal microbiota, and, during early life, by breast milk. While the beneficia
Publikováno v:
The Journal of Immunology. 208:59.18-59.18
Neonatal sepsis remains a leading cause of death in preterm and low-birthweight infants and can be separated into two groups: early-onset sepsis (EOS) and late-onset sepsis (LOS). Previous studies have shown that LOS can result from translocation of
Publikováno v:
The Journal of Immunology. 208:59.09-59.09
Bloodstream infections, causing late-onset neonatal sepsis (LOS), have an incidence rate of 10% in very low birth weight ( Supported by grants from NIH (DK122187).
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 8, Iss Suppl 3 (2020)
Background Immune responses to cancer are highly variable and influenced by genetic and environmental factors.1 Syngeneic tumor models in mice with intact immune systems are required to study anti-tumor immune responses but are unable to adequately m