Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mahmoud, Ghanei"'
Autor:
Faezeh Tolue Ghasaban, Mahmoud Ghanei, Reihaneh Alsadat Mahmoudian, Negin Taghehchian, Mohammad Reza Abbaszadegan, Meysam Moghbeli
Publikováno v:
Heliyon, Vol 10, Iss 9, Pp e30599- (2024)
Pancreatic cancer (PC), as one of the main endocrine and digestive systems malignancies has the highest cancer related mortality in the world. Lack of the evident clinical symptoms and appropriate diagnostic markers in the early stages of tumor progr
Externí odkaz:
https://doaj.org/article/b8e0db72032948da8e142b7b53a2ab5b
Autor:
Mahmoud Ghanei, Arash Poursjeikhani, Azadeh Aarabi, Negin Taghehchian, Mohammad Reza Abbaszadegan
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 25, Iss 6, Pp 704-714 (2022)
Objective(s): Due to diagnosis of gastric cancer in advanced stages as well as its poor prognosis, finding biomarkers is essential. In this study, using the TCGA RNAseq data of gastric cancer patients, we evaluated the diagnostic value of lncRNAs tha
Externí odkaz:
https://doaj.org/article/f987a533a8fd463b8f6eff5010949f24
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 12, Pp n/a-n/a (2022)
Abstract Background Hyperphenylalaninemia (HPA) is the most common inborn error of amino acid metabolism worldwide. At least 2% of HPA cases are caused by a deficiency in tetrahydrobiopterin (BH4) metabolism. Genes such as QDPR and PTS are essential
Externí odkaz:
https://doaj.org/article/c9e36746086646a2a1e5e104eb263cff
Autor:
Mahmoud Ghanei, Mohammad R. Abbaszadegan, Mohammad M. Forghanifard, Azadeh Aarabi, Hamidreza Arab
Publikováno v:
Clinical and Experimental Dental Research, Vol 7, Iss 4, Pp 568-573 (2021)
Abstract Objectives In this study, we analyzed the whole exomes of CTSC gene in a family with history of PLS. Materials and methods Genomic DNA was extracted from peripheral blood and genotype analysis was performed. The mutated protein sequence was
Externí odkaz:
https://doaj.org/article/3d34c828a6bd4d09855c802102cd00d6
Publikováno v:
Neurology Asia. 27:955-962
Spinal muscular atrophy (SMA)(OMIM#:253300) is an autosomal recessive disorder, resulting in symmetrical progressive weakness of skeletal and respiratory muscles and atrophy. The corresponding gene for the disease is the survival motor neuron 1 (SMN1
Publikováno v:
Human Heredity.
Background: Hyperphenylalaninemia (HPA) is an autosomal recessive disorder that results from a deficiency in the phenylalanine hydroxylase enzyme (PAH) or from a flaw in the genes that are responsible for the biosynthesis or regeneration of the cofac
Autor:
Mahmoud, Ghanei, Arash, Poursheikhani, Azadeh, Aarabi, Negin, Taghechian, Mohammad Reza, Abbaszadegan
Publikováno v:
Iranian journal of basic medical sciences. 25(6)
Due to diagnosis of gastric cancer in advanced stages as well as its poor prognosis, finding biomarkers is essential. In this study, using the TCGA RNAseq data of gastric cancer patients, we evaluated the diagnostic value of lncRNAs that had differen
Autor:
Mahmoud Ghanei, Arash Poursheikhani, Azadeh Aarabi, Negin Taghehchian, Mohammad Reza Abbaszadegan
BACKGROUND: Due to the diagnosis of gastric cancer in advance stages as well as its poor prognosis, finding biomarkers is essential.OBJECTIVE: In this study, using the TCGA RNAseq data of gastric cancer patients, we evaluated the diagnostic value of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f97379ea2cb244643405b9d753b861f3
https://doi.org/10.21203/rs.3.rs-712731/v1
https://doi.org/10.21203/rs.3.rs-712731/v1
Autor:
Mahmoud Ghanei, Alireza Pasdar, Sadegh Dehghani, Malihe Hasanzadeh, Arash Salmaninejad, Meysam Yousefi, Sara Rajaie, Rahim Nosrati
Publikováno v:
Cellular oncology (Dordrecht). 43(4)
Ovarian cancer is the most lethal gynecologic cancer and the fifth leading cause of cancer-related mortality in women worldwide. Despite various attempts to improve the diagnosis and therapy of ovarian cancer patients, the survival rate for these pat