Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Neda Fatahi"'
Autor:
Amaneh Hadadan, Seyed Reza Mirjalili, Razieh Sadat Tabatabaei, Reza Bahrami, Bahare Meibodi, Hossein Neamatzadeh, Atiyeh Javaheri, Mojgan Karimi-Zarchi, Hajar Abbasi, Neda Fatahi-Meibodi
Publikováno v:
Fetal and pediatric pathology. 41(2)
Background: MTHFR gene may be a key epigenetic regulation-related factor crucial during embryogenesis. We performed a meta-analysis to determine the association of fetal MTHFR C677T polymorphism with neural tube defects (NTDs).Methods: A comprehensiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f89ba09b17cf7a5265a826d40bbb956
https://pubmed.ncbi.nlm.nih.gov/32536242
https://pubmed.ncbi.nlm.nih.gov/32536242
Autor:
Morteza Taheri, Hossein Ghalaenovi, Neda Fatahi, Jalil Koohpayehzadeh, Alireza Azimi, Mahmoud Khodadost, Hessam Rahatlou, Arash Fattahi, Sadra Rohani
Publikováno v:
Brain Injury. 32:1050-1055
Introduction: Amantadine, as a dopamine receptor agonist, may stimulate and help the recovery of the nervous system after traumatic brain injury (TBI).Methods: We performed this study as a double-blind, randomized, controlled clinical trial with targ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c74ccdcf3a5bf96b62075e9c5728ac9
https://doi.org/10.1080/02699052.2018.1476733
https://doi.org/10.1080/02699052.2018.1476733
Autor:
Neda Fatahi, Tahereh Esmaeilnia Shirvani, Nikoo Niknafs, Nasrin Ghasemi-Fakhr, Javad Tavakkoly-Bazzaz, Fatemeh Nayeri, Amir Kamal Hardani, Elaheh Amini, Roya Taheritafti, Hosein Dalili, Mamak Shariat, Majid Kalani, Ali Rashidi-Nezhad, Ramin Rashidi-Nezhad, Mohsen Ghadami
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 31:2965-2970
Respiratory distress syndrome (RDS) is a severe pulmonary disease predominantly affects preterm newborns. Polymorphisms of surfactant-protein genes have been mostly evaluated as the candidate contributors in genetics of RDS. However the results are d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4af005c0b6dd4632837b8ff8df249b7b
https://doi.org/10.1080/14767058.2017.1359829
https://doi.org/10.1080/14767058.2017.1359829
Autor:
Javad Tavakkoly-Bazzaz, Majid Kalani, Fatemeh Nayeri, Nikoo Niknafs, Roya Taheritafti, Neda Fatahi, Tahereh Esmaeilnia Shirvani, Mohsen Ghadami, Elaheh Amini, Mamak Shariat, Amir Kamal Hardani, Ali Rashidi-Nezhad, Nasrin Ghasemi-Fakhr, Hosein Dalili
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 30:2585-2589
Respiratory distress syndrome (RDS) is a severe pulmonary disease that mainly affects preterm neonates. Surfactant-protein genes' polymorphisms have been mostly evaluated as the candidate contributors in genetics of RDS. However, the results are dive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5608faea4d1215fafb44ce1bd53dea08
https://doi.org/10.1080/14767058.2016.1256994
https://doi.org/10.1080/14767058.2016.1256994
Publikováno v:
Journal of Cancer Research and Therapeutics. 16:884
Objective Paraoxonase 1 (PON1) plays a defensive role against oxidative stress by destroying oxidized lipids. Q192R single nucleotide polymorphism of PON1 gene alters the enzyme's activity. Several investigations reported a link between Q192R and an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ed93999ea29231178daf03c5c0b841a
https://doi.org/10.4103/jcrt.jcrt_923_16
https://doi.org/10.4103/jcrt.jcrt_923_16
Publikováno v:
Medicine
Hematological parameters are appraised routinely to determine overall human health and to diagnose and monitor certain diseases. In GWASs, more than 30 loci carrying common deoxyribonucleic acid (DNA) polymorphisms have been identified related to hem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98436b96685620352a5af87810aa746a
http://europepmc.org/articles/PMC4674197
http://europepmc.org/articles/PMC4674197
Publikováno v:
American journal of cancer research. 5(8)
Uterine leiomyomas are steroid-hormone dependent tumors of myometrial smooth muscle cells that affect numerous women throughout the world. Based on previous studies, we evaluated the mutations of MED12 gene which encodes a co-activator protein involv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::96c9015719b077c49fde0b7761c5dcd1
https://pubmed.ncbi.nlm.nih.gov/26396919
https://pubmed.ncbi.nlm.nih.gov/26396919