Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Zahra Mortezaei"'
Autor:
Hamed Dabiri, Zahra Mortezaei
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Cardiovascular disease (CVD) is one of the main causes of death in the world. The increased level of blood cholesterol is significantly correlated to CVD incidents. Statins are a group of drugs that decrease the synthesis of cholesterol in t
Externí odkaz:
https://doaj.org/article/b158e073d5164b17bc8fd241d562c901
Publikováno v:
Informatics in Medicine Unlocked, Vol 39, Iss , Pp 101265- (2023)
One of the first important steps in elucidating the function of microRNAs (miRNAs) is expression profiling. Many methods including low-density qPCR arrays are increasingly used to profile the expression of miRNAs. Normalization techniques are necessa
Externí odkaz:
https://doaj.org/article/203df70155a4460eaea50e8c79ab5673
Publikováno v:
Heliyon, Vol 8, Iss 7, Pp e09910- (2022)
The first cases of the novel coronavirus, SARS-CoV-2, were detected in December 2019 in Wuhan, China. Nucleotide substitutions and mutations in the SARS-CoV-2 sequence can result in the evolution of the virus and its rapid spread across the world. Th
Externí odkaz:
https://doaj.org/article/903d7bdb6bd24ae989b1d49fea922dd0
Autor:
Zahra Mortezaei
Publikováno v:
Informatics in Medicine Unlocked, Vol 32, Iss , Pp 101054- (2022)
A tumor is a group of cells with abnormal cell growth. Sequencing technology can help recognize genetic mutations that cause cancer. Next-generation sequencing (NGS) can supply genetic data and determine the number of mutant genes in different cancer
Externí odkaz:
https://doaj.org/article/7f3be7f350a843e18db853fecb2cb4af
Autor:
Zahra Mortezaei, Mahmood Tavallaei
Publikováno v:
Informatics in Medicine Unlocked, Vol 24, Iss , Pp 100586- (2021)
A genome-wide association study (GWAS) is a standard population-based technique for identifying the heritable genetic basis of complex diseases by discovering correlations between trait variations and allele frequencies of genetic markers. This artic
Externí odkaz:
https://doaj.org/article/db659eda6533468cbfca9913e3df5076
Autor:
Zahra Mortezaei, Ali Khosravi
Publikováno v:
Informatics in Medicine Unlocked, Vol 24, Iss , Pp 100599- (2021)
Lung Squamous Cell Carcinoma (SQCC) is one of the deadliest non-small cell lung cancers that does not respond well to chemotherapy or radiation therapy. Targeted therapy can prevent SQCC progression by blocking messages sent to SQCC cells. Understand
Externí odkaz:
https://doaj.org/article/7ea6b1bb4d064ac0866b7be01fa553fe
Autor:
Zahra Mortezaei, Narges Hosseini
As one of the novel interesting fields of cardiology, cardio-oncology focuses on monitoring, detecting, and treating cardiovascular diseases caused due to chemotherapy or radiotherapy side effects. It has been observed that cardiovascular patients ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6f24231aa9854d3448738c18bc9d7d9
https://mts.intechopen.com/articles/show/title/cardio-oncology-and-the-covid-19-pandemic
https://mts.intechopen.com/articles/show/title/cardio-oncology-and-the-covid-19-pandemic
Autor:
Zahra Mortezaei, Mahmood Tavallaei
Publikováno v:
Heredity (Edinb)
In the past decade, the high throughput and low cost of sequencing/genotyping approaches have led to the accumulation of a large amount of data from genome-wide association studies (GWASs). The first aim of this review is to highlight how post-GWAS a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a484430728c2a1b1e14fbecd7c11c58
https://doi.org/10.1038/s41437-021-00479-w
https://doi.org/10.1038/s41437-021-00479-w
Publikováno v:
Journal of Cellular Biochemistry. 120:19172-19185
Non-small cell lung cancer (NSCLC) is the most common subtype of lung cancer among smokers, nonsmokers, women, and young individuals. Tobacco smoking and different stages of the NSCLC have important roles in cancer evolution and require different tre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::432d38fc526d2d25e62e308a04c63507
https://doi.org/10.1002/jcb.29246
https://doi.org/10.1002/jcb.29246
Publikováno v:
Journal of cellular biochemistry. 120(4)
Understanding the genetic causes of neurodegenerative disease (ND) can be useful for their prevention and treatment. Among the genetic variations responsible for ND, heritable germline variants have been discovered in genome-wide association studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2915ae09341c4aaafe4da4425402d0b
https://pubmed.ncbi.nlm.nih.gov/30302804
https://pubmed.ncbi.nlm.nih.gov/30302804