Výsledky vyhledávání - "Zahra Farbood"

A Two-Single-Nucleotide Polymorphism Haplotype in Promoter Region of CYP11B2 Gene Affects Plasma Aldosterone Concentration: A Matched Case-Control Study

Autor: Azim Nejatizadeh, Mahmood Khayatian, Fatemeh Kharaee, Tasnim Eghbal Eftekhaari, Elaheh Farahbakhsh, Shabnaz Koochakkhani, Zahra Farbood, Hossein Farshidi, Fatemeh Nabizadeh

Publikováno v: Electronic Physician. 12:7767-7775

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::065fe37991962b297e06751403130997
https://doi.org/10.19082/7767

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Endothelial nitric oxide synthase gene -922A>G, -786 T>C, 4b/4a, and 894 G>T variants and premature coronary artery disease: An association study with haplotype analysis

Autor: Amirsaeed Sabeti Aghabozorgi, Hossein Farshidi, Tasnim Eghbal Eftekhaari, Azim Nejatizadeh, Zahra Farbood, Amirhossein Bahreyni, Najmeh Ahangari

Publikováno v: Meta Gene. 19:111-116

Background Endothelium nitric oxide (eNO) deficiency may lead to premature coronary artery disease (pCAD). This defect could be due to the effect of some eNOS gene variants on its gene expression. The aim of the study The aim of this study is to inve

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f32c5cb41edd29431b0f46fc03157eb7
https://doi.org/10.1016/j.mgene.2018.11.008

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Endothelial Nitric Oxide Synthase Gene Polymorphisms (- 922A G, - 786 T C, Intron 4 b/a VNTR and 894 G T) and Essential Hypertension: An Association Study with Haplotypes Analysis

Autor: Mohammad Shekari, Amirhossein Bahreyni, Elahe Mansouri Babamansouri, Zahra Farbood, Leila Shams, Hossein Farshidi, Azim Nejatizadeh, Amirsaeed Sabeti Aghabozorgi

Publikováno v: Biochemical genetics. 58(4)

Endothelial Nitric Oxide Synthase (eNOS) is an indispensable regulator of blood pressure through producing Nitric Oxide (NO). There is some evidence to suggest that eNOS gene polymorphisms are associated with Essential Hypertension (EHT). In this stu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fa63f2d8574819fe7379d89e8225c09
https://pubmed.ncbi.nlm.nih.gov/32519277

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Two novel mutations in the MECP2 gene in patients with Rett syndrome

Autor: Marjan Masoudi, Zahra Farbood, Sanaz Mohammadi, Shayan Khalili Alashti, Majid Fardaei, Arezoo Jokar, Jafar Fallahi, Shiva Poorang, Fatemeh Dehghanian

Publikováno v: Gene. 732:144337

Rett syndrome (RTT) is an X-linked severe neurological disorder. Mutations in Methyl-CpG-Binding Protein2 (MECP2) gene are the main cause of RTT disease. In this study, we report the results of screening the MECP2 gene for mutations in 7 Iranian pati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0043b8c0c71e383757400577e9cbbd47
https://doi.org/10.1016/j.gene.2020.144337

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