Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Nurit Hadad"'
Autor:
Yafa Fetfet Malada Edelstein, Yulia Solomonov, Nurit Hadad, Leenor Alfahel, Adrian Israelson, Rachel Levy
Publikováno v:
Journal of Neuroinflammation, Vol 18, Iss 1, Pp 1-18 (2021)
Abstract Background Amyotrophic lateral sclerosis (ALS) is a fatal multifactorial neurodegenerative disease characterized by the selective death of motor neurons. Cytosolic phospholipase A2 alpha (cPLA2α) upregulation and activation in the spinal co
Externí odkaz:
https://doaj.org/article/a92dd4b6023c46f99cde3f6de6d2c91d
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0248183 (2021)
Collagen is the major structural protein in the extracellular matrix of skin produced by fibroblasts. UV exposure results in infiltration of neutrophils within the epidermis and dermis, inducing collagen damage and contributing to the process of phot
Externí odkaz:
https://doaj.org/article/2261c79894cc4cb1ae4682b7e875622a
Publikováno v:
Journal of Lipid Research, Vol 49, Iss 9, Pp 1894-1903 (2008)
Chronic inflammation of adipose tissue in obesity is by now an established phenomenon, but the initiating event(s) of the inflammatory cascade are still unknown. We hypothesized that neutrophil infiltration into adipose tissue may precede macrophage
Externí odkaz:
https://doaj.org/article/ab6dfc7da1e8456192fa751774a49af4
Publikováno v:
Molecular Biology Reports. 49:3511-3518
Autor:
Odeya David, Eyal Kristal, Galina Ling, Arnon Broides, Nurit Hadad, George Shubinsky, Amit Nahum
Background: Hypoparathyroidism, retardation, and dysmorphism (HRD) syndrome is a disease composed of hypoparathyroidism, growth retardation, developmental delay and typical dysmorphic features, caused by Tubulin-specific chaperone E gene mutation. Ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d802a43404665b580ce74b74dd174ae
https://doi.org/10.21203/rs.3.rs-1792160/v1
https://doi.org/10.21203/rs.3.rs-1792160/v1
Autor:
Odeya David, Eyal Kristal, Galina Ling, Arnon Broides, Nurit Hadad, George Shubinsky, Amit Nahum
Publikováno v:
Journal of clinical immunology.
Hypoparathyroidism-retardation-dysmorphism (HRD) syndrome is a disease composed of hypoparathyroidism, growth retardation, severe developmental delay, and typical dysmorphic features caused by the tubulin-specific chaperone E gene variant. Many patie
Autor:
Eduard Ling, Arnon Broides, Galina Ling, Amos J. Simon, Amit Nahum, Nurit Hadad, George Shubinsky, Atar Lev, Raz Somech
Publikováno v:
Immunologic Research. 69:100-106
Biallelic mutations in the zeta-associated protein 70 (ZAP70) gene cause combined immunodeficiency (CID). Neonatal screening for severe CID in Israel is implemented since 2015. We report on clinical, flow cytometry, and genetic data of an unusual ZAP
Background: Previous studies have demonstrated that Cytosolic phospholipase A2a (cPLA2a) is absolutely required for NOX2 NADPH oxidase activation in human and mouse phagocytes. Moreover, upon stimulation, cPLA2a translocates to the plasma membranes o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9f55d21f9025bbcf9ca6ac477f2dc7d
https://doi.org/10.21203/rs.3.rs-1039201/v1
https://doi.org/10.21203/rs.3.rs-1039201/v1
Publikováno v:
Molecular biology reports. 49(5)
Previous studies have demonstrated that cytosolic phospholipase AA significant binding of mouse GST-p47