Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Nuray Erin"'
Autor:
Nuray Erin, Arpad Szallasi
Publikováno v:
Biomolecules, Vol 13, Iss 6, p 983 (2023)
Both sensory neurons and immune cells, albeit at markedly different levels, express the vanilloid (capsaicin) receptor, Transient Receptor Potential, Vanilloid-1 (TRPV1). Activation of TRPV1 channels in sensory afferent nerve fibers induces local eff
Externí odkaz:
https://doaj.org/article/c9efcd5794ed451daf1ad5fae94e065c
Autor:
Hülya Eyigör, Mete Eyigör, Bekir Erol, Ömer Tarık Selçuk, Levent Renda, Mustafa Deniz Yılmaz, Üstün Osma, Cansu Demirkıran, Meral Gültekin, Nuray Erin
Publikováno v:
Brazilian Journal of Otorhinolaryngology, Vol 86, Iss 4, Pp 450-455 (2020)
Introduction: Mucosal contact headache is a referred pain that arises from contact between the nasal septum and the lateral nasal wall. Evidence supports the role of substance P in a contact headache such that release of substance P from sensory nerv
Externí odkaz:
https://doaj.org/article/fb2114f73c564203849a6630df9c6ada
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 24, p 15692 (2022)
Pterygium, a disease of the ocular surface, is characterized by the proliferation and invasion of fibrovascular tissue. Chronic inflammation contributes to pterygium occurrence. Sensory neuropeptides of TRPV1-positive nerve fibers are involved in inf
Externí odkaz:
https://doaj.org/article/c23aa270ca2f47e1965dafb9dcdc339c
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0189526 (2017)
Neprilysin (NEP, CD10) acts to limit excessive inflammation partly by hydrolyzing neuropeptides. Although deletion of NEP exacerbates intestinal inflammation in animal models, its role in ulcerative colitis (UC) is not well explored. Herein, we aimed
Externí odkaz:
https://doaj.org/article/2fae71dd80de46efbadeb6d99addc59c
Publikováno v:
Proceedings, Vol 2, Iss 25, p 1567 (2018)
Breast cancer treatments continue to be investigated with supported by new treatment methods. Melatonin is a hormone that can be effective in the treatment of breast cancer due to its anti-oxidant effect. Melatonin had previously shown to inhibit pro
Externí odkaz:
https://doaj.org/article/fd3d654cac474a3ab42d27159dd9bb6e
Autor:
Nuray Erin, Gary A. Clawson
Publikováno v:
BioTechniques, Vol 37, Iss 2, Pp 232-239 (2004)
Substance P (SP), a neuropeptide that is widely distributed both peripherally and centrally, mediates several pathophysiological processes. Among current assays for SP, enzyme-linked immunosorbent assay (ELISA) and radioimmunoassay (RIA) have been mo
Externí odkaz:
https://doaj.org/article/e2fae698d0634c50b40160d68f7331f2
Autor:
Cumhur İbrahim Başsorgun, Betül Ünal, Nuray Erin, Anıl Özlük, Özlem Ceren Uzun, Gülsüm Özlem Elpek
Publikováno v:
Gastroenterology Research and Practice, Vol 2014 (2014)
Introduction. In colorectal carcinoma, tumoral tissues infiltrate with various immune/inflammatory cells along their invasive margins and the increased S100A8/A9 expression in these immune cells infiltrating the tumor has recently been demonstrated.
Externí odkaz:
https://doaj.org/article/3ef51bb040ec40118da9b9862afae350
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e113597 (2014)
We have compared cure from local/metastatic tumor growth in BALB/c mice receiving EMT6 or the poorly immunogenic, highly metastatic 4THM, breast cancer cells following manipulation of immunosuppressive CD200:CD200R interactions or conventional chemot
Externí odkaz:
https://doaj.org/article/866073cb8b784ddf975f0592dfe653fc
Publikováno v:
World Journal of Clinical Cases
BACKGROUND Transient receptor potential vanilloid-1 (TRPV1), a nonselective cation channel, is activated by capsaicin, a pungent ingredient of hot pepper. Previous studies have suggested a link between obesity and capsaicin-associated pathways, and a
Publikováno v:
Cancer Immunology, Immunotherapy. 69:1639-1650
Substance P a neuro-immune mediator acts on Neurokinin-1 and -2 receptors (NK1R and NK2R). Inhibitors of NK1R are considered to be safe and effective approaches for cancer treatment since Aprepitant, a non-peptide antagonist of NK1R is widely used fo