Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Seyed Mohammad Bagher Hashemi-Soteh"'
Publikováno v:
Journal of Pediatrics Review, Vol 9, Iss 2, Pp 83-96 (2021)
Context: Phenylketonuria (PKU) is the most frequent inborn error of metabolism, in which newborns cannot metabolize phenylalanine to tyrosine. Increased phenylalanine in untreated patients with PKU can cause serious intellectual disability; its onero
Externí odkaz:
https://doaj.org/article/01ced2817cfc45febc2ba0633e27678e
Publikováno v:
Iranian Journal of Reproductive Medicine, Vol 14, Iss 5, Pp 323-328 (2016)
Background: Spontaneous abortion is considered as the most complex problem during pregnancy. Thrombophilia is resumed as a cause of recurrent pregnancy loss (RPL). Glycoprotein IIIa (GPIIIa) gene is involved in thrombosis and abortion. Angiotensin co
Externí odkaz:
https://doaj.org/article/765a8f903d45473dbb7a546672e48d81
Autor:
Adeleh Rafati, Pooria Gill, Mehdi Shabani, Maryam Peyrovei, Seyed Mohammad Bagher Hashemi-Soteh, Mohammad-Reza Shiran
Publikováno v:
Research in Molecular Medicine, Vol 3, Iss 2, Pp 17-21 (2015)
Background: Genetic polymorphisms of cytochrome p450 in humans are the main cause of differences in the metabolism. The allele and genotype frequencies of CYP2C19 and CYP2C9 have been studied in some Iranian populations. The aim of present study was
Externí odkaz:
https://doaj.org/article/ab24e122cd654eaa87f1ea042140bc28
Publikováno v:
Journal of Mazandaran University of Medical Sciences, Vol 30, Iss 183, Pp 73-83 (2020)
Background and purpose: Generational health analysis on the acquisition, application, and transfer of intergenerational values is an important issue from the perspective of religion and genetics. Healthy generation means generational solidarity and l
Externí odkaz:
https://doaj.org/article/7071b096ef8945ce846046ba4de3cc17
Publikováno v:
Journal of Pediatrics Review, Vol 9, Iss 2, Pp 83-96 (2021)
Context: Phenylketonuria (PKU) is the most frequent inborn error of metabolism, in which newborns cannot metabolize phenylalanine to tyrosine. Increased phenylalanine in untreated patients with PKU can cause serious intellectual disability; its onero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bef615d31184ee88c6abc4f904657c64
https://doi.org/10.32598/jpr.9.2.826.2
https://doi.org/10.32598/jpr.9.2.826.2
Autor:
Seyed Mohammad Bagher Hashemi-Soteh, Hossein Karami, Touraj Farazmandfar, Ahmad Tamadoni, Seyed Saeid Mousavi
Publikováno v:
Journal of Clinical Laboratory Analysis
Background It is estimated about 7% of the world population is carriers of hemoglobin diseases. Alpha‐thalassemia is one of the most common hereditary hemoglobin disorders in the world. This study investigated alpha‐globin mutations in potential
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d833584333547eb788d3cb36761fbc99
https://doi.org/10.1002/jcla.23018
https://doi.org/10.1002/jcla.23018
Autor:
Fatemeh Sarzare, Fatemeh Merat, Mohammad Reza Shiran, Seyed Mohammad Bagher Hashemi-Soteh, Ebrahim Salehifar
Publikováno v:
Genetic Testing and Molecular Biomarkers. 15:821-825
Although the frequencies of CYP2D6 nonfunctional alleles have been extensively studied in most populations worldwide, limited information is available for those of the Iranian population. The present study aimed to determine the frequency of three CY
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb77d363fac5fd081d4ddaaf36b7a743
https://doi.org/10.1089/gtmb.2011.0033
https://doi.org/10.1089/gtmb.2011.0033
Autor:
Seyed Mohammad Bagher Hashemi-Soteh, Mohammad Reza Shiran, Ali-Reza Gholizadeh, Naghi Shahabi-Majd
Publikováno v:
Genetic testing and molecular biomarkers. 16(7)
Cytochrome P450 2C9 (CYP2C9) is a polymorphic enzyme responsible for the metabolism of different drugs, some with low therapeutic index. The frequency of functionally important mutations and alleles of the gene coding for CYP2C9 shows wide ethnic var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c4915a4924cbedc9abf206d54434255
https://pubmed.ncbi.nlm.nih.gov/22288731
https://pubmed.ncbi.nlm.nih.gov/22288731
Autor:
Mohammad Reza, Shiran, Fatemeh, Sarzare, Fatemeh, Merat, Ebrahim, Salehifar, Ali Akbar, Moghadamnia, Seyed Mohammad Bagher, Hashemi Soteh
Publikováno v:
Caspian journal of internal medicine. 2(2)
CYP2D6 is polymorphically expressed enzyme that show marked interindividual and interethnic variation. Phenotyping of CYP2D6 provides valuable information about real-time activity of this important drug-metabolizing enzymes through the use of specifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::137700d9ba87c5e60221a4a10f1546a7
https://pubmed.ncbi.nlm.nih.gov/24024018
https://pubmed.ncbi.nlm.nih.gov/24024018
Publikováno v:
Scopus-Elsevier
Iranian Journal of Reproductive Medicine, Vol 14, Iss 5, Pp 323-328 (2016)
International Journal of Reproductive Biomedicine
ResearcherID
Iranian Journal of Reproductive Medicine, Vol 14, Iss 5, Pp 323-328 (2016)
International Journal of Reproductive Biomedicine
ResearcherID
Background: Spontaneous abortion is considered as the most complex problem during pregnancy. Thrombophilia is resumed as a cause of recurrent pregnancy loss (RPL). Glycoprotein IIIa (GPIIIa) gene is involved in thrombosis and abortion. Angiotensin co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04b2cb1f378727eb1b2b8f7784301ee1
http://www.scopus.com/inward/record.url?eid=2-s2.0-84975709065&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84975709065&partnerID=MN8TOARS
