Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Ladan Sadeghian"'
Autor:
Aliasgar Mohammadi, Marziyeh Hoseinzadeh, Sina Narrei, Mohammad Reza Pourreza, Yousof Mohammadi, Mahnaz Norouzi, Ladan Sadeghian, Mohammad Amin Tabatabaiefar
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-8 (2024)
Abstract Background Sensorineural hearing loss (SNHL) is a clinically and genetically heterogeneous group of disorders of the auditory system. SNHL can occur as a symptom in more than 400 syndromes, and mutations in more than 150 genes can lead to SN
Externí odkaz:
https://doaj.org/article/b98c4e75825f442c92fc2d8bd2454865
Autor:
Noushin Mohammadifard, Ladan Sadeghian, Razieh Hassannejad, Elham Khosravi, Mojgan Gharipour, Simin Karimi, Shidokht Hosseini, Mahtab Sepahifar, Ghazaleh Bahrami, Fahimeh Haghighatdoost, Nizal Sarrafzadegan
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-7 (2024)
Abstract The associations of vitamin D receptor (VDR)- single nucleotide polymorphisms (SNPs) with the symptoms of COVID-19 may vary between patients with different severities of COVID-19. Therefore, in the present study, we aim to compare VDR polymo
Externí odkaz:
https://doaj.org/article/d6abd57f4d2e414f82534c4107630b43
Autor:
Mojgan Gharipour, Minoo Dianatkhah, Noushin Mohammadifard, Elham Khosravi, Ladan Sadeghian, Zahra Jabarzare, Nizal Sarrafzadegan
Publikováno v:
ARYA Atherosclerosis, Vol 19, Iss 4, Pp 117-124 (2023)
Background: The Isfahan Twin Cohort (ITC) aims to provide a comprehensive understanding of the interplay between genetics and environment in the development of Non-Communicable Diseases (NCDs). As a type of specialized epidemiological investigation,
Externí odkaz:
https://doaj.org/article/4f875b1727114ab494ac00618e31dcb8
Autor:
Noushin Mohammadifard, Faezeh Moazeni, Fatemeh Azizian-Farsani, Mojgan Gharipour, Elham Khosravi, Ladan Sadeghian, Asieh Mansouri, Shahin Shirani, Nizal Sarrafzadegan
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract So far, few studies have examined the effect of salt taste receptors genetic variation on dietary intake in the Iranian population. We aimed to evaluate associations between single nucleotide polymorphisms (SNPs) in salt taste receptors’ g
Externí odkaz:
https://doaj.org/article/b830a1f3c0aa416ab9bcdb5b7e2da3e1
Autor:
Omid Zargari Samani, Lila Mahmoodnia, Maryam Izad, Hedayatollah Shirzad, Azam Jamshidian, Mahdi Ghatrehsamani, Soleiman Kheiri, Ladan Sadeghian, Amin Soltani, Akram Sarmadi
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 34, Iss 5, Pp 274-280 (2018)
Type 1 diabetes is a multi-factorial disease that can develop due to the combination of genetic and environmental factors. Viruses, particularly enteroviruses, are major environmental candidates in the pathogenesis of type 1 diabetes, even though the
Externí odkaz:
https://doaj.org/article/1d5681777c2a442682181819606370e3
Autor:
Mahsa Rahimi, Hossein Khanahmad, Mojgan Gharipour, Hamidreza Roohafza, Minoo Dianatkhah, Elham Khosravi, Ladan Sadeghian, Masoumeh Sadeghi
Publikováno v:
ARYA Atherosclerosis, Vol 17, Iss 1, p 2369 (2021)
BACKGROUND: Myocardial infarction (MI) is one of the leading causes of mortality globally. Although it is most prevalent in the elderly, it may occur in young adults (men ≤ 55 years or women ≤ 65 years) as premature MI (PMI). As awareness of gene
Externí odkaz:
https://doaj.org/article/3d73038a33ae43ba9beb4626bc9e2b34
Autor:
Golnaz Vaseghi, Zahra Malakoutikhah, Zahra Shafiee, Mojgan Gharipour, Laleh Shariati, Ladan Sadeghian, Elham Khosravi, Shaghayegh Haghjooy Javanmard, Ali Pourmoghaddas, Ismail Laher, Sonia Zarfeshani, Nizal Sarrafzadegan
Publikováno v:
Journal of Research in Medical Sciences, Vol 26, Iss 1, Pp 94-94 (2021)
Background: Familial hypercholesterolemia (FH) leads to elevated low-density lipoprotein cholesterol (LDL-C) levels in plasma. Mutations of its related gene; apolipoprotein B (APOB) is seen in about two percent of the patient with FH. Thyroid disease
Externí odkaz:
https://doaj.org/article/56c9b4764d844a3db005f30811b26d28
Autor:
Mina Mirian, Fatemeh Hajibabaie, Maryam Boshtam, Laleh Shariati, Azam Gheibi, Hossein Khanahmad, Ladan Sadeghian, Ilnaz Rahimmanesh, Shirin Kouhpayeh
Publikováno v:
Journal of Physiology and Biochemistry. 76:1-12
Atherosclerosis is considered as the most common cardiovascular disease and a leading cause of global mortality, which develops through consecutive steps. Various cellular and molecular biomarkers such as microRNAs are identified to be involved in at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::804d880ee0a34a4896f7d2561c121b0c
https://doi.org/10.1007/s13105-019-00710-7
https://doi.org/10.1007/s13105-019-00710-7
Autor:
Mojgan Gharipour, Shaghayegh Haghjooy Javanmard, Minoo Dianatkhah, Nizal Sarrafzadegan, Elham Khosravi, Zahra Jabarzare, Ladan Sadeghian, Marjan Mansourian, Mohammad Reza Sabri
Publikováno v:
Twin Research and Human Genetics. 22:579-582
Twin studies are one of the main tools for studying the interaction between genes and the environment in the development of complex diseases such as cancers, cardiovascular diseases and diabetes. The Isfahan Twin Registry (ITR) was launched in Isfaha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4306841197ba3cf833cc53f17ee46db1
https://doi.org/10.1017/thg.2019.119
https://doi.org/10.1017/thg.2019.119
Autor:
Mohammad Reza Pourreza, Hannane Mohammadi, Ladan Sadeghian, Samira Asgharzadeh, Mohammadreza Sehhati, Mohammad Amin Tabatabaiefar
Publikováno v:
Advanced Biomedical Research, Vol 7, Iss 1, Pp 141-141 (2018)
Background: Hearing loss (HL) is a highly prevalent heterogeneous deficiency of sensory-neural system with involvement of several dozen genes. Whole-exome sequencing (WES) is capable of discovering known and novel genes involved with HL. Materials an
Externí odkaz:
https://doaj.org/article/2d315402b9714eda880e30184f734faa