Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Bita Faam"'
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 17, Iss 8, Pp 577-582 (2014)
Objective(s):Obesity considered being a low-grade inflammatory disease. The objective of this study was to examine the association between inflammatory markers (IM) including C-reactive protein (hs-CRP), Interleukin-6 (IL-6), and homocystein (Hcy) an
Externí odkaz:
https://doaj.org/article/4248b2da82b5454ab1e23fa430efae0a
Autor:
Fereidoun Azizi, Hajeih B Shahbazian, Ata Ghadiri, Mohammad Ali Ghaffari, S. Ahmad Fanaei, Layasadat Khorsandi, Mahmoud Hashemi Tabar, Mehdi Totonchi, Atieh Amouzegar, Bita Faam
Publikováno v:
Cytogenetic and Genome Research. 161:227-235
Inactivation of tumor suppressor genes, such as RAP1GAP, by hypermethylation of their regulatory region can give rise to thyroid tumors. The aim of this study was to investigate the expression of the RAP1GAP gene and the DNA methylation patterns of i
Autor:
Hengameh Abdi, Safoora Gharibzadeh, Maryam Tohidi, Bita Faam, Ladan Mehran, Atieh Amouzegar, Fereidoun Azizi
Publikováno v:
Endocrine Research. 46:37-43
Introduction: To determine age and sex-specific thyrotropin (TSH) and free thyroxine (FT4) reference ranges according to body mass index (BMI) categories. Methods: With regards to the National Academy of Clinical Biochemistry (NACB) criteria, a total
Autor:
Bita, Faam, Mohammad A, Ghaffari, Layasadat, Khorsandi, Ata A, Ghadiri, Mehdi, Totonchi, Atieh, Amouzegar, S Ahmad, Fanaei, Fereidoun, Azizi, Hajeih B, Shahbazian, Mahmoud, Hashemi Tabar
Publikováno v:
Cytogenetic and genome research. 161(5)
Inactivation of tumor suppressor genes, such as RAP1GAP, by hypermethylation of their regulatory region can give rise to thyroid tumors. The aim of this study was to investigate the expression of the RAP1GAP gene and the DNA methylation patterns of i
Autor:
Bita Faam, Ata. A Ghadiri, Mohammad Ali Ghaffari, Mehdi Totonchi, Atieh Amouzegar, Fereidoun Azizi, Hajiehbibi Shahbazian, Mahmoud Hashemitabar, Seyed Ahmad Fanaei, Layasadat Khorsandi
Publikováno v:
Archives of Iranian medicine. 25(3)
Background: Medullary thyroid cancer (MTC) is a rare type of neuroendocrine tumor. This study aimed to investigate the gene and protein expression of RAP1GAP and DNA methylation patterns of its CpG74a , CpG74b , and CpG24 in an Iranian population wit
Publikováno v:
International Journal of Endocrinology and Metabolism
Background: Oxidative stress is commonly accrued in thyroid tissue during hormone synthesis. Objectives: We aimed to examine oxidative stress in patients with thyroid cancer, benign thyroid nodules, and healthy individuals. Methods: In this study, 13
Autor:
Mehdi Hedayati, Maryam Zarkesh, Sara Sheikholeslami, Marjan Zarif Yeganeh, Maryam S. Daneshpour, Fereidoun Azizi, Bita Faam
Publikováno v:
International Journal of Endocrinology and Metabolism
Context The Tehran Lipid and Glucose Study (TLGS) is a community-based study to reveal the frequency of non-communicable diseases (NCDs) in Tehran's population. This research consists of two main parts, a cross-sectional study on the prevalence of ca
Publikováno v:
Biomedical Reports. 3:3-8
Thyroid carcinoma is the most common endocrine malignancy of the endocrine organs, and its incidence rate has steadily increased over the last decade. Over 95% of thyroid carcinoma is derived from follicular cells that have a spectrum of differentiat
Autor:
Farhad Hosseinpanah, Bita Faam, Kamran Guity, Nima Hosseinzadeh, Maryam S. Daneshpour, Maryam Zarkesh, Amir Abbas Momenan, Mohammad-Sadegh Fallah, Fereidoun Azizi
Publikováno v:
Genetics Research. 94:331-337
SummaryGrowing evidence suggests that metabolic syndrome (MetS) has both genetic and environmental bases. We estimated the heritability of the MetS and its components in the families from the Tehran Lipid and Glucose Study (TLGS). We investigated 904
Publikováno v:
Genetic Testing and Molecular Biomarkers. 16:234-238
Aims: The CD36 gene encodes for a membrane receptor that facilitates fatty-acid uptake and utilization. Genetic variants of the CD36 gene have been associated with metabolic syndrome (MetS). We aimed to evaluate the association between the rs10499859