Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Seyyed Mojtaba Mohaddes Ardebili"'
Autor:
Mahdiyeh Pashaei, Jamal Eivazi Ziaei, Alireza Nikanfar, Babak Emamalizadeh, Seyyed Mojtaba Mohaddes Ardebili
Publikováno v:
Biosciences, Biotechnology Research Asia. 15:671-677
Breast cancer is one of the main factors in the mortality of Iranian women. A large rearrangement genome is observed in most genes, especially in BRCA1 / BRCA2 genes lacking small mutations in breast cancer. Therefore, methods are needed to detect on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3d2107430ff40184d2147462cf78110
https://doi.org/10.13005/bbra/2675
https://doi.org/10.13005/bbra/2675
Autor:
Mahdiyeh Pashaei, Jamal Eivazi Ziaei, Alireza Nikanfar, Babak Emamalizadeh, Seyyed Mojtaba Mohaddes Ardebili
Publikováno v:
Journal of Research in Medical and Dental Science, Vol 6, Iss 2, Pp 501-505 (2018)
Background: Breast cancer is the most common cause of death among women in the world and in Iran. A number of risk factors for breast cancer development have been identified, among which the most important is positive family history. Alterations in d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c5d01c4bf1d75db1f83f69d6f353dc4
https://doi.org/10.13005/bbra/2651
https://doi.org/10.13005/bbra/2651
Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes
Autor:
Mohammad Keramatipour, Saeed Talebi, Seyede Zahra Sajedi, Golnaz-Ensieh Kazemi-sefat, Seyyed Mojtaba Mohaddes Ardebili, Masoumeh Razipour, Aria Setoodeh, Neda Mohajer, Jalal Gharesouran, Mona Entezam, Elaheh Alavinejad
Publikováno v:
Metabolic Brain Disease. 32:1685-1691
Phenylketonuria (PKU), one of the most common inborn errors of amino acid metabolism, is caused by mutations in the phenylalanine hydroxylase (PAH) gene (PAH). PKU has wide allelic heterogeneity, and over 600 different disease-causing mutations in PA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b402763adaaca7fb7a2b6220a12bb1b
https://doi.org/10.1007/s11011-017-0048-7
https://doi.org/10.1007/s11011-017-0048-7
Autor:
Leila Emrahi, Mehrnoush Toufan Tabrizi, Mehrdad Asghari Estiar, Jalal Gharehsouran, Seyyed Mojtaba Mohaddes Ardebili
Publikováno v:
Clinical laboratory. 62(5)
BACKGROUND Hypertrophic cardiomyopathy (HCM) is the leading cause of sudden cardiac death (SCD) in children and young adults and is the most frequent genetically determined cardiovascular disease following autosomal dominant pattern of inheritance. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::988c0dd949efa3bc7d551358f9e9622c
https://pubmed.ncbi.nlm.nih.gov/27348999
https://pubmed.ncbi.nlm.nih.gov/27348999
Autor:
Seyyed Mojtaba Mohaddes Ardebili, Najime Tarkesh-Esfahani, Sahar Ghohari-Lasaki, Morteza Ghojazadeh, Zahra Saadatian, Jalal Gharesouran
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 15(18)
Breast cancer is the most common cancer among women in the world. In Iran, the incidence of breast cancer is on the increase. We here studied the association of rs1219648 in FGFR2 and rs1042522 in TP53 and their interaction in development of early on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76881d414cd6589bc4be43d6a2c5a524
https://pubmed.ncbi.nlm.nih.gov/25292094
https://pubmed.ncbi.nlm.nih.gov/25292094