Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Mehdi Gharghabi"'
Autor:
Dongju Park, Mehdi Gharghabi, Colleen R. Reczek, Rebecca Plow, Charles Yungvirt, C. Marcelo Aldaz, Kay Huebner
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 7, p 3729 (2022)
Wwox-deficient human cells show elevated homologous recombination, leading to resistance to killing by double-strand break-inducing agents. Human Wwox binds to the Brca1 981-PPLF-984 Wwox-binding motif, likely blocking the pChk2 phosphorylation site
Externí odkaz:
https://doaj.org/article/cb7f36b8adc34394bccd8ce9ac2ad57e
Publikováno v:
Biomolecules, Vol 11, Iss 2, p 218 (2021)
Arrestins are a small family of four proteins in most vertebrates that bind hundreds of different G protein-coupled receptors (GPCRs). Arrestin binding to a GPCR has at least three functions: precluding further receptor coupling to G proteins, facili
Externí odkaz:
https://doaj.org/article/d0bce2dadd474cc686686acf1355f95e
Autor:
Pu, Zhang, Lindsey T, Brinton, Mehdi, Gharghabi, Steven, Sher, Katie, Williams, Matthew, Cannon, Janek S, Walker, Daniel, Canfield, Larry, Beaver, Casey B, Cempre, Hannah, Phillips, Xuyong, Chen, Pearlly, Yan, Amy, Lehman, Peggy, Scherle, Min, Wang, Kris, Vaddi, Robert, Baiocchi, Ruoning, Wang, Deepa, Sampath, Lapo, Alinari, James S, Blachly, Rosa, Lapalombella
Publikováno v:
Science advances. 8(37)
Using a genome-wide CRISPR screen, we identified
Autor:
Mehdi Ghasemi, Zohreh Abdolmaleki, Ramtin Gholizadeh, Mehdi Gharghabi, Ahmad Reza Dehpour, Taraneh Bahremand
Publikováno v:
Journal of Epilepsy Research
Background and Purpose: Licofelone is a dual 5-lipoxygenase/cyclooxygenase inhibitor, with well-documented anti-inflammatory and analgesic effects, which is used for treatment of osteoarthritis. Recent preclinical studies have also suggested neuropro
Autor:
Steven Sher, Pu Zhang, Lindsey Brinton, Mehdi Gharghabi, Katie Williams, Matthew Cannon, Janek S. Walker, Daniel Canfield, Larry Beaver, Casey B. Cempre, Hannah Phillips, Xuyong Chen, Pearlly S. Yan, Amy M. Lehman, Peggy Scherle, Min Wang, Kris Vaddi, Robert A. Baiocchi, Ruoning Wang, Deepa Sampath, Lapo Alinari, James S. Blachly, Rosa Lapalombella
Publikováno v:
Blood. 140:681-682
Publikováno v:
Trends Biochem Sci
Three classes of G-protein-coupled receptor (GPCR) partners - G proteins, GPCR kinases, and arrestins - preferentially bind active GPCRs. Our analysis suggests that the structures of GPCRs bound to these interaction partners available today do not re
Autor:
Ghorban Taghizadeh, Gelareh Vakilzadeh, Tina Khorshidahmad, Mehdi Gharghabi, Mehdi Sanati, Mehdi Aghsami, Mohammad Sharifzadeh, Shervin Gholizadeh, Hajar Mehdizadeh, Rojin Sharif
Publikováno v:
Behavioural Brain Research. 316:115-124
Oxidative stress and mitochondrial dysfunction play indispensable role in memory and learning impairment. Growing evidences have shed light on anti-oxidative role for melatonin in memory deficit. We have previously reported that inhibition of protein
Autor:
Ameneh, Eslamparast, Reza, Abbasgholizadeh, Seyed Nasser, Ostad, Mehdi, Gharghabi, Mohammad Hossein, Ghahremani
Publikováno v:
Iranian Journal of Pharmaceutical Research : IJPR
Fragile histidine triad (FHIT) serves a critical function as a tumor suppressor that inhibits p53 degradation by mouse double minute 2 (MDM2). The functional domains of FHIT involved in tumor inhibition was interpreted. In-silico screening data were
Publikováno v:
Biomolecules
Biomolecules, Vol 11, Iss 218, p 218 (2021)
Biomolecules, Vol 11, Iss 218, p 218 (2021)
Arrestins are a small family of four proteins in most vertebrates that bind hundreds of different G protein-coupled receptors (GPCRs). Arrestin binding to a GPCR has at least three functions: precluding further receptor coupling to G proteins, facili
Autor:
Mohammad Hossein Ghahremani, Seyed Nasser Ostad, Hamed Montazeri, Homa Mohseni kouchesfehani, Mehdi Gharghabi, Fereshteh Mir Mohammadrezaei
Publikováno v:
Cellular Signalling. 25:126-132
FHIT (Fragile Histidin Triad) is a tumor suppressor gene involved in regulating cell death during DNA damage conditions. The exact mechanism of DNA damage-induced FHIT signaling is not well understood. It is known that p38 kinase and CHK2 kinase are