Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Solmaz Etemad"'
Autor:
Ahmad Salti, Solmaz Etemad, Marta Suarez Cubero, Eva Albertini, Beata Kovacs-Szalka, Max Holzknecht, Elia Cappuccio, Maria Cavinato, Frank Edenhofer, Pidder Jansen Dürr
Publikováno v:
Cells, Vol 10, Iss 8, p 2040 (2021)
Mitochondria play a key role in metabolic transitions involved in the reprogramming of somatic cells into induced pluripotent stem cells (iPSCs), but the underlying molecular mechanisms remain largely unexplored. To obtain new insight into the mechan
Externí odkaz:
https://doaj.org/article/82cf94bd3d604eb8bfae83ffb54d86d5
Publikováno v:
PLoS ONE, Vol 14, Iss 8, p e0220434 (2019)
Human fumarylacetoacetate hydrolase (FAH) domain containing protein 1 (FAHD1) is a mitochondrial oxalocatate decarboxylase, the first of its kind identified in eukaryotes. The physiological role of FAHD1 in other eukaryotes is still poorly understood
Externí odkaz:
https://doaj.org/article/18befc3000004e1f98397155a70bf540
Autor:
Michele Petit, Giorgia Baraldo, Alexander K. H. Weiss, Pidder Jansen-Dürr, Solmaz Etemad, André Schrattenholz
Publikováno v:
Mechanisms of Ageing and Development. 177:22-29
FAHD1, a member of the FAH superfamily of enzymes, was identified in a proteomic screen for mitochondrial proteins with differential expression in young versus senescent human endothelial cells. FAHD1 acts as oxaloacetate decarboxylase, and recent ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16d9e9b6aa873a9dabab27b12fa3d4d1
https://doi.org/10.1016/j.mad.2018.07.007
https://doi.org/10.1016/j.mad.2018.07.007
Publikováno v:
PLoS ONE
PLoS ONE, Vol 14, Iss 8, p e0220434 (2019)
PLoS ONE, Vol 14, Iss 8, p e0220434 (2019)
Human fumarylacetoacetate hydrolase (FAH) domain containing protein 1 (FAHD1) is a mitochondrial oxalocatate decarboxylase, the first of its kind identified in eukaryotes. The physiological role of FAHD1 in other eukaryotes is still poorly understood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f5500c8052b76bedd4ad39e2651d92f9
https://pubmed.ncbi.nlm.nih.gov/31412049
https://pubmed.ncbi.nlm.nih.gov/31412049
Autor:
Pidder Jansen-Dürr, Annabella Pittl, Alexander K. H. Weiss, Hubert Gstach, Klaus Scheffzek, Max Holzknecht, Theresia Dunzendorfer-Matt, Matthew W. Bowler, Elia Cappuccio, Klaus R. Liedl, Johannes R. Loeffler, Solmaz Etemad, Andreas Naschberger
Publikováno v:
Biochem J
Whereas enzymes in the fumarylacetoacetate hydrolase (FAH) superfamily catalyze several distinct chemical reactions, the structural basis for their multi-functionality remains elusive. As a well-studied example, human FAH domain-containing protein 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6951815dac59cfdd0f224fcf9bec41b0
https://pubmed.ncbi.nlm.nih.gov/30348641
https://pubmed.ncbi.nlm.nih.gov/30348641
Publikováno v:
Experimental gerontology. 92
In this study we report the identification of FAH domain containing protein 1 (FAHD1), a recently described member of the fumarylacetoacetate hydrolase (FAH) superfamily of metabolic enzymes, as a novel player in the regulation of cellular senescence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b965b5c405e3eab54196c8357361ba31
https://pubmed.ncbi.nlm.nih.gov/28286170
https://pubmed.ncbi.nlm.nih.gov/28286170
Autor:
Massoud Houshmand, Mostafa Moin, Mohammad Ali Bahar, Sadaf Kasraie, Solmaz Etemad Ahari, Akram Zamani
Publikováno v:
Archives of Medical Science : AMS
INTRODUCTION: Ataxia telangiectasia (AT) is a rare human neurodegenerative autosomal recessive multisystem disease. AT is the result of mutations in the AT-mutated (ATM) gene. ATM protein is required for radiation-induced apoptosis and acts before mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ded8d6ad3601cd6759a65feaa31deae
https://doi.org/10.5114/aoms.2011.23424
https://doi.org/10.5114/aoms.2011.23424
Autor:
Mohammad Bahar, Solmaz Etemad Ahari, Mostafa Moin, Sadaf Kasraie, Mohammad Mehdi Banoei, Massoud Houshmand, Parvin Shariati, Mehdi Shafa Shariat Panahi
Publikováno v:
Cellular and molecular neurobiology. 28(7)
Huntington disease (HD) is a genetically dominant condition caused by expanded CAG repeats which code for glutamine in the HD gene product, huntingtin. Huntingtin is expressed in almost all tissues, so abnormalities outside the brain can also be expe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e9b1850970eddda9527eae1d023981b
https://pubmed.ncbi.nlm.nih.gov/18386172
https://pubmed.ncbi.nlm.nih.gov/18386172
Autor:
Massoud Houshmand, Sadaf Kasraie, Mehdi Shafa Shariat Panahi, Solmaz Etemad Ahari, Mostafa Moin, Mohammad Ali Bahar
Publikováno v:
Cellular and molecular neurobiology. 27(6)
As with chromosomal DNA, the mitochondrial DNA (mtDNA) can contain mutations that are highly pathogenic . In fact, many diseases of the central nervous system are known to be caused by mutations in mtDNA. Dysfunction of the mitochondrial Respiratory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb4ae29f96585bbfc3a239ed0fdbad99
https://pubmed.ncbi.nlm.nih.gov/17619138
https://pubmed.ncbi.nlm.nih.gov/17619138
Autor:
Solmaz Etemad
Publikováno v:
Intrinsic Activity. 1:A2.10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2baa0cc8871e4ffbf0f10808d0de556
https://doi.org/10.25006/ia.1.s1-a2.10
https://doi.org/10.25006/ia.1.s1-a2.10