Search Results - "Rezaie, Tayebeh"

Therapeutic advantage of pro-electrophilic drugs to activate the Nrf2/ARE pathway in Alzheimer’s disease models by Lipton, Stuart A, Rezaie, Tayebeh, Nutter, Anthony, Lopez, Kevin M, Parker, James, Kosaka, Kunio, Satoh, Takumi, McKercher, Scott R, Masliah, Eliezer, Nakanishi, Nobuki

“…Alzheimer’s disease (AD) is characterized by synaptic and neuronal loss, which occurs at least partially through oxidative stress induced by oligomeric…”
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Protective effect of carnosic acid, a pro-electrophilic compound, in models of oxidative stress and light-induced retinal degeneration by Rezaie, Tayebeh, McKercher, Scott R, Kosaka, Kunio, Seki, Masaaki, Wheeler, Larry, Viswanath, Veena, Chun, Teresa, Joshi, Rabina, Valencia, Marcos, Sasaki, Shunsuke, Tozawa, Terumasa, Satoh, Takumi, Lipton, Stuart A

“…The herb rosemary has been reported to have antioxidant and anti-inflammatory activity. We have previously shown that carnosic acid (CA), present in rosemary…”
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Adult-Onset Primary Open-Angle Glaucoma Caused by Mutations in Optineurin by Rezaie, Tayebeh, Child, Anne, Hitchings, Roger, Brice, Glen, Miller, Lauri, Coca-Prados, Miguel, Héon, Elise, Krupin, Theodore, Ritch, Robert, Kreutzer, Donald, Crick, R. Pitts, Sarfarazi, Mansoor

“…Primary open-angle glaucoma (POAG) affects 33 million individuals worldwide and is a leading cause of blindness. In a study of 54 families with autosomal…”
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Dual neuroprotective pathways of a pro‐electrophilic compound via HSF‐1‐activated heat‐shock proteins and Nrf2‐activated phase 2 antioxidant response enzymes by Satoh, Takumi, Rezaie, Tayebeh, Seki, Masaaki, Sunico, Carmen R., Tabuchi, Takahito, Kitagawa, Tomomi, Yanagitai, Mika, Senzaki, Mutsumi, Kosegawa, Chihiro, Taira, Hideharu, McKercher, Scott R., Hoffman, Jennifer K., Roth, Gregory P., Lipton, Stuart A.

“…J. Neurochem. (2011) 119, 569–578. Activation of the Keap1/nuclear factor erythroid 2‐related factor 2 (Nrf2) pathway and consequent induction of phase 2…”
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Molecular cloning, genomic structure, and protein characterization of mouse optineurin by Rezaie, Tayebeh, Sarfarazi, Mansoor

“…We recently identified optineurin ( OPTN) as a novel gene for glaucoma and determined its mRNA and protein expression patterns in different human tissues…”
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Finding Genetic Contributions to Sporadic Disease: A Recessive Locus at 12q24 Commonly Contributes to Patent Ductus Arteriosus by Mani, Arya, Meraji, Seyed-Mahmoud, Houshyar, Roozbeh, Radhakrishnan, Jayaram, Mani, Alaleh, Ahangar, Mehrabeh, Rezaie, Tayebeh M., Taghavinejad, Mohammad-Ali, Broumand, Behrooz, Zhao, Hongyu, Nelson-Williams, Carol, Lifton, Richard P.

“…The causes of many sporadic diseases are unexplained; the contribution of recessive loci with reduced penetrance is one possibility that has been difficult to…”
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Molecular Cloning and Expression Profiling of Optineurin in the Rhesus Monkey by Rezaie, Tayebeh, Waitzman, David M, Seeman, Jennifer L, Kaufman, Paul L, Sarfarazi, Mansoor

“…It has been shown that mutations in the optineurin (OPTN) gene are involved in the etiology of adult-onset primary open-angle glaucoma (POAG). In view of close…”
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Ocular genetics in the genomics age by Walter, Michael A., Rezaie, Tayebeh, Hufnagel, Robert B., Arno, Gavin

“…Current genetic screening methods for inherited eye diseases are concentrated on the coding exons of known disease genes (gene panels, clinical exome). These…”
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eP369: Increased automation reduces turnaround time for submissions to ClinVar by Landrum, Melissa, Chitipiralla, Shanmuga, Brown, Garth, Chen, Chao, Gu, Baoshan, Hart, Jennifer, Hoffman, Douglas, Jang, Wonhee, Liu, Chunlei, Maddipatla, Zenith, Maglott, Donna, Maiti, Rama, Mitchell, Joseph, Rezaie, Tayebeh, Riley, George, Shao, David, Zhou, George, Lyoshin, Vitaly, Swallow, Chris, Kaur, Kuljeet, Russette, Andrew, Kattman, Brandi

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Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma by Aragon-Martin, Jose A, Ritch, Robert, Liebmann, Jeffrey, O'Brien, Colm, Blaaow, Karima, Mercieca, Franco, Spiteri, Anthony, Cobb, Caroline J, Damji, Karim F, Tarkkanen, Ahti, Rezaie, Tayebeh, Child, Anne H, Sarfarazi, Mansoor

“…To evaluate genetic susceptibility of lysyl oxidase-like 1 (LOXL1) gene polymorphisms to exfoliation syndrome (XFS) and exfoliation glaucoma (XFG) in a…”
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Clinical Features and Course of Patients with Glaucoma with the E50K Mutation in the Optineurin Gene by Aung, Tin, Rezaie, Tayebeh, Okada, Koji, Viswanathan, Ananth C, Child, Anne H, Brice, Glen, Bhattacharya, Shomi S, Lehmann, Ordan J, Sarfarazi, Mansoor, Hitchings, Roger A

“…To investigate the clinical features of subjects with glaucoma with the E50K mutation in the optineurin (OPTN) gene and to compare the onset, severity, and…”
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Embryonic expression of the optineurin (glaucoma) gene in different stages of mouse development by Rezaie, Tayebeh, Stoilov, Ivaylo, Sarfarazi, Mansoor

“…To analyze optineurin (Optn) gene expression in various embryonic stages of mouse development by whole mount in situ hybridization. FVB/NcrlBR mouse embryos…”
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Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2 by REZAIE, Tayebeh, GHOROGHCHIAN, Rose, CHILD, Anne, SARFARAZI, Mansoor, BELL, Rachel, BRICE, Glen, HASAN, Ali, BURNAND, Kevin, VERNON, Steve, MANSOUR, Sahar, MORTIMER, Peter, JEFFERY, Steve

“…Primary lymphoedema is a genetic disorder with numerous phenotypic subgroups. The most common form is the non-syndromic Meige disease, which is primarily of…”
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Building a Bridge Between Genetics and Outcomes Research: Application in Autism (The AutGO Study) by Talebizadeh, Zohreh, Shah, Ayten

“…Background Concerns over the need to improve translational aspects of genetics research studies and engaging community members in the research process have…”
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Optineurin in primary open angle glaucoma by Sarfarazi, Mansoor, Rezaie, Tayebeh

“…The authors' initial estimate indicated that mutations in Optineurin are responsible for a significant proportion of LPG/POAG families. Currently, there are up…”
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Expression of cytochrome P4501b1 (Cyp1b1) during early murine development by Stoilov, Ivaylo, Rezaie, Tayebeh, Jansson, Ingela, Schenkman, John B, Sarfarazi, Mansoor

“…To examine the embryonic expression of cytochrome P4501b1 (Cyp1b1) gene by whole mount in situ hybridization. FVB/NcrlBR mouse embryos staged at 9.5, 10.5, and…”
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Analysis of Rare Variants and Common Haplotypes in the Optineurin Gene in Swedish Glaucoma Cases by Jansson, Mattias, Wadelius, Claes, Rezaie, Tayebeh, Sarfarazi, Mansoor

“…Objective: Glaucoma, a leading cause of blindness in the world, is characterized by neuropathy of the retinal ganglion cells and the optic nerve. Recently,…”
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Genetic Screening of Leber Congenital Amaurosis in a Large Consanguineous Iranian Family by Rezaie, Tayebeh, Karimi-Nejad, Mohammad-Hassan, Meshkat, Mohammad-Reza, Sohbati, Saeed, Karimi-Nejad, Roxana, Najmabadi, Hossein, Sarfarazi, Mansoor

“…The molecular defect of one large consanguineous Iranian kindred with Leber Congenital Amaurosis (LCA) is presented. The phenotype mapped to 17p13.1 (LCA1) and…”
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Identification of a novel mutation in the paired domain of PAX3 in an Iranian family with Waardenburg syndrome Type I by Sotirova, Vihra N., Rezaie, Tayebeh, Khoshsorour, M.R., Sarfarazi, Mansoor

“…Waardenburg syndrome Type I (WS1) is an autosomal dominant disorder that has previously been associated with mutations in the PAX3 gene on the 2q35 region. In…”
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Identification of a novel mutation in the paired domain of PAX3 in an Iranian family with Waardenburg syndrome Type I by Sotirova, Vihra N., Rezaie, Tayebeh, Khoshsorour, M.R., Sarfarazi, Mansoor

“…Waardenburg syndrome Type I (WS1) is an autosomal dominant disorder that has previously been associated with mutations in the PAX3 gene on the 2q35 region. In…”
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