Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Farzaneh Mirzajani"'
Autor:
Farzaneh Mirzajani, Reza Mirfakhraei, Neda Naghib-Zadeh, Farah Nabati, Sasan Saki, Elham Talachian, Masoud Houshmand
Publikováno v:
Journal of Rehabilitation, Vol 6, Iss 1, Pp 19-22 (2005)
Objective: Galactosemia is an inborn error of galactose metabolism that is inherited in an autosomal recessive trait. Classical galactosemia is caused by deficient activity of the galactose-1-phosphate uridyltransferase (GALT) enzyme that can result
Externí odkaz:
https://doaj.org/article/a4e97d4a9f1e4b238919d9b2bf884525
Publikováno v:
Iranian Biomedical Journal
Background: Studies have revealed a strong association between mutations of CFTR gene and the congenital bilateral absence of the vas deferens (CBAVD), but the role of this gene in other types of male infertility is still unclear. The purpose of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2b6a47621cded8f270cef8a36591f2b
https://doi.org/10.29252/ibj.23.2.92
https://doi.org/10.29252/ibj.23.2.92
Autor:
Mehdi Shafa Shariat Panahi, Kurosh Gharagozli, Farzaneh Fesahat, Massoud Houshmand, Farzaneh Mirzajani
Publikováno v:
Cellular and Molecular Neurobiology. 27:329-334
1. Alzheimer’s disease (AD) is the most common form of dementia in the elderly in which interplay between genes and the environment is supposed to be involved. Mitochondrial DNA (mtDNA) has the only noncoding regions at the displacement loop (D-loo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::617dc12f48165f82b5a5806e55e1daff
https://doi.org/10.1007/s10571-006-9126-9
https://doi.org/10.1007/s10571-006-9126-9
Autor:
Jothilatha Krishnamoorthy, Polixenia Kesoglidou, Kamindla Rajesh, Antonis E. Koromilas, Andreas I. Papadakis, Farzaneh Mirzajani
Publikováno v:
Cell Cycle
The endoplasmic reticulum (ER)-resident protein kinase PERK is a major component of the unfolded protein response (UPR), which promotes the adaptation of cells to various forms of stress. PERK phosphorylates the α subunit of the translation initiati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f4c8dd6e941a3e3a932a7802df1ae8b
https://pubmed.ncbi.nlm.nih.gov/24401334
https://pubmed.ncbi.nlm.nih.gov/24401334
Autor:
Massoud Houshmand, Feyzollah Hashemi-Gorji, Nasser Salsabili, Farzaneh Mirzajani, Reza Mirfakhraie, Sayed-Mahdi Kalantar, Maryam Montazeri, Gholamreza Pourmand
Publikováno v:
Journal of andrology. 32(4)
Genetic factors including Y chromosome microdeletions and androgen receptor (AR) gene mutations are responsible for male infertility. In the present study, genetic analysis was performed in an infertile Iranian male with azoospermia. Multiplex polyme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::493981bde4f644c38dd8f661b2edf327
https://pubmed.ncbi.nlm.nih.gov/21127309
https://pubmed.ncbi.nlm.nih.gov/21127309
Autor:
Hassani Sm Sayed, Nasser Salsabili, H Fazli, G Modabber, Reza Mirfakhraie, S M Kalantar, Maryam Montazeri, Farzaneh Mirzajani
Publikováno v:
Reproductive BioMedicine Online. 16:s50-s51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3782c62649ab7201b204c420952ee51b
https://doi.org/10.1016/s1472-6483(10)61417-4
https://doi.org/10.1016/s1472-6483(10)61417-4