Kamran Ghaedi
Kamran Ghaedi
Cercacor Laboratories
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Cited by
Cited by
Signaling pathways involved in colorectal cancer progression
Z Koveitypour, F Panahi, M Vakilian, M Peymani, F Seyed Forootan, ...
Cell & bioscience 9 (1), 97, 2019
Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane …
Y Matsuzono, N Kinoshita, S Tamura, N Shimozawa, M Hamasaki, ...
Proceedings of the National Academy of Sciences 96 (5), 2116-2121, 1999
Iron oxide nanoparticles may damage to the neural tissue through iron accumulation, oxidative stress, and protein aggregation
Z Yarjanli, K Ghaedi, A Esmaeili, S Rahgozar, A Zarrabi
BMC neuroscience 18, 1-12, 2017
The mammalian peroxin Pex5pL, the longer isoform of the mobile peroxisome targeting signal (PTS) type 1 transporter, translocates the Pex7p· PTS2 protein complex into …
H Otera, T Harano, M Honsho, K Ghaedi, S Mukai, A Tanaka, A Kawai, ...
Journal of Biological Chemistry 275 (28), 21703-21714, 2000
Electrospun aligned PLGA and PLGA/gelatin nanofibers embedded with silica nanoparticles for tissue engineering
M Mehrasa, MA Asadollahi, K Ghaedi, H Salehi, A Arpanaei
International journal of biological macromolecules 79, 687-695, 2015
The peroxin Pex14p: cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysis
N Shimizu, R Itoh, Y Hirono, H Otera, K Ghaedi, K Tateishi, S Tamura, ...
Journal of Biological Chemistry 274 (18), 12593-12604, 1999
Fndc5 knockdown significantly decreased neural differentiation rate of mouse embryonic stem cells
MS Hashemi, K Ghaedi, A Salamian, K Karbalaie, M Emadi-Baygi, ...
Neuroscience 231, 296-304, 2013
The peroxin Pex3p initiates membrane assembly in peroxisome biogenesis
K Ghaedi, S Tamura, K Okumoto, Y Matsuzono, Y Fujiki
Molecular biology of the cell 11 (6), 2085-2102, 2000
Diverse roles of fatty acid binding proteins (FABPs) in development and pathogenesis of cancers
M Amiri, S Yousefnia, FS Forootan, M Peymani, K Ghaedi, MHN Esfahani
Gene 676, 171-183, 2018
Huntington’s disease and mitochondria
M Jodeiri Farshbaf, K Ghaedi
Neurotoxicity research 32, 518-529, 2017
New insights into the cellular activities of Fndc5/Irisin and its signaling pathways
F Rabiee, L Lachinani, S Ghaedi, MH Nasr-Esfahani, TL Megraw, ...
Cell & Bioscience 10, 1-10, 2020
Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots
E ElInati, P Kuentz, C Redin, S Jaber, F Vanden Meerschaut, J Makarian, ...
Human molecular genetics 21 (16), 3695-3702, 2012
Does PGC1α/FNDC5/BDNF elicit the beneficial effects of exercise on neurodegenerative disorders?
M Jodeiri Farshbaf, K Ghaedi, TL Megraw, J Curtiss, ...
Neuromolecular medicine 18, 1-15, 2016
miR-326 and miR-26a, two potential markers for diagnosis of relapse and remission phases in patient with relapsing–remitting multiple sclerosis
MA Honardoost, A Kiani-Esfahani, K Ghaedi, M Etemadifar, M Salehi
Gene 544 (2), 128-133, 2014
The influence of peroxisome proliferator-activated receptor γ (PPARγ) ligands on cancer cell tumorigenicity
S Yousefnia, S Momenzadeh, FS Forootan, K Ghaedi, MHN Esfahani
Gene 649, 14-22, 2018
Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells
S Mukai, K Ghaedi, Y Fujiki
Journal of Biological Chemistry 277 (11), 9548-9561, 2002
Incorporation of mesoporous silica nanoparticles into random electrospun PLGA and PLGA/gelatin nanofibrous scaffolds enhances mechanical and cell proliferation properties
M Mehrasa, MA Asadollahi, B Nasri-Nasrabadi, K Ghaedi, H Salehi, ...
Materials Science and Engineering: C 66, 25-32, 2016
Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures
N Shimozawa, Y Suzuki, Z Zhang, A Imamura, K Ghaedi, Y Fujiki, ...
Human molecular genetics 9 (13), 1995-1999, 2000
Quantitative expression of phospholipase C zeta, as an index to assess fertilization potential of a semen sample
S Aghajanpour, K Ghaedi, A Salamian, MR Deemeh, M Tavalaee, ...
Human reproduction 26 (11), 2950-2956, 2011
PEX3 is the causal gene responsible for peroxisome membrane assembly–defective Zellweger syndrome of complementation group G
K Ghaedi, M Honsho, N Shimozawa, Y Suzuki, N Kondo, Y Fujiki
The American Journal of Human Genetics 67 (4), 976-981, 2000
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