Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tahereh Dadkhah"'
Autor:
Tahereh Dadkhah, Ehsan Assadollahi, Elham Ghadami, Mohsen Aghajanpour-Mir, Seyed Reza Hosseini, Fatemeh Amjadi-Moheb, Haleh Akhavan-Niaki, Alijan Ahmadi Ahangar
Publikováno v:
Molecular Biology Reports. 46:1033-1041
Clusterin (CLU) is the third most important associated risk gene in cognitive disorders. Regarding the controversy about the association of CLU rs11136000 with mild cognitive impairment (MCI), the aim of this study was to investigate a putative assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2770af6a05b1d14b2a1e00571c974cb0
https://doi.org/10.1007/s11033-018-4561-5
https://doi.org/10.1007/s11033-018-4561-5
Autor:
Behnam Safarpour Lima, Shaghayegh Taghavi, Monavvar Andarva, Mahmoud Shekari Khaniani, Parasto Shokraeian, Tannaz Safaralizadeh, Peyman Petramfar, Ali Kowsari, Minoo Atakhorrami, Abolfazl Movafagh, Gholam Ali Shahidi, Azadeh Ahmadifard, Tahereh Dadkhah, Mina Ohadi, Marzieh Motallebi, Babak Emamalizadeh, Hossein Darvish, Elham Alehabib, Neda Shahmohammadibeni, Ali Khaligh, Javad Jamshidi, Mohammad Javad Soltani Banavandi, Somayyeh Kazeminasab, Mehdi Khorrami, Ehteram Khademi, Akbar Biglarian, Abbas Tafakhori, Arash Mirabzadeh, Amir Ehtesham Shafiei Zarneh, Atena Fazeli
Publikováno v:
Molecular Neurobiology. 54:2234-2240
Neurological disorders include a wide variety of mostly multifactorial diseases related to the development, survival, and function of the neuron cells. Single-nucleotide polymorphisms (SNPs) have been extensively studied in neurological disorders, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2ea67477b0995804e8ecfd77416a757
https://doi.org/10.1007/s12035-016-9815-4
https://doi.org/10.1007/s12035-016-9815-4
Autor:
Mohsen, Aghajanpour-Mir, Fatemeh, Amjadi-Moheb, Tahereh, Dadkhah, Seyed Reza, Hosseini, Elham, Ghadami, Ehsan, Assadollahi, Haleh, Akhavan-Niaki, Alijan, Ahmadi Ahangar
Publikováno v:
Molecular biology reports. 46(1)
Clusterin (CLU) is the third most important associated risk gene in cognitive disorders. Regarding the controversy about the association of CLU rs11136000 with mild cognitive impairment (MCI), the aim of this study was to investigate a putative assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5726579e6a4c28b617b508b161243248
https://pubmed.ncbi.nlm.nih.gov/30560405
https://pubmed.ncbi.nlm.nih.gov/30560405
Publikováno v:
Journal of cellular physiology. 234(3)
Erythropoiesis is a multi-step process that involves the differentiation of hematopoietic stem cells into mature red blood cells (RBCs). This process is regulated by several signaling pathways, transcription factors and microRNAs (miRNAs). Many studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4230bac644a7dbbccaf8fd4f472e6f10
https://pubmed.ncbi.nlm.nih.gov/30192008
https://pubmed.ncbi.nlm.nih.gov/30192008
Autor:
Reza Tabaripour, Haleh Akhavan-Niaki, Mohammad Reza Esmaeili Dooki, Tahereh Dadkhah, Ali Mohammad Shirafkan, Elham Ghadami
Publikováno v:
International Biological and Biomedical Journal (2016)
Cystic fibrosis (CF) is the most common severe autosomal recessive disorder caused by a wide spectrum of mutations in the gene encoding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The frequencies, types and distributio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::095bdee589797db900e7c060ad86adcc
https://doaj.org/article/b7b7aea16b5e471ba0864059e50a3398
https://doaj.org/article/b7b7aea16b5e471ba0864059e50a3398
Autor:
Simin Rahimi-Aliabadi, Hamid Ghaedi, Hossein Darvish, Abbas Tafakhori, Parasto Shokraeian, Tahereh Dadkhah, Haleh Akhavan-Niaki, Mina Ohadi, Shaghyegh Taghavi, Javad Jamshidi
Publikováno v:
Journal of affective disorders. 208
Background Glutamate receptor 4, metabotropic (GRM4) expression is increased in the brain of patients with depression. The poorly conserved miR-1202 is downregulated in depression and is negatively correlated with GRM4. A variation located at the 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d9ec948f9240635a529c04f59cf5e6b
https://pubmed.ncbi.nlm.nih.gov/27792966
https://pubmed.ncbi.nlm.nih.gov/27792966
Autor:
Mahnoosh Rahimi, Mahnaz Shahmohammadibeni, Hossein Ali Shahmohammadibeni, Monavvar Andarva, Javad Jamshidi, Hajar Eftekhari, Haleh Akhavan-Niaki, Babak Emamalizadeh, Mahmoud Shekari Khaniani, Azadeh Ahmadifard, Ehteram Khademi, Shaghayegh Taghavi, Alireza Zare Bidoki, Hossein Darvish, Neda Shahmohammadibeni, Amir Ehtesham Shafiei Zarneh, Abbas Tafakhori, Atena Fazeli, Minoo Atakhorrami, Marzieh Motallebi, Tahereh Dadkhah, Elham Alehabib, Simin Rahimi-Aliabadi, Shokoufeh Abdollahi
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 37(5)
Parkinson's disease (PD) is the second most prevalent neurodegenerative disorder. Both genetic and environmental factors are involved in the etiology of the disease. Many studies have revealed the susceptibility genes and variations for PD which need
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::560834c8f76d74818e75ae469d17a41e
https://pubmed.ncbi.nlm.nih.gov/26732583
https://pubmed.ncbi.nlm.nih.gov/26732583