Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Afsaneh BAZGIR"'
Publikováno v:
Jorjani Biomedicine Journal, Vol 7, Iss 1, Pp 14-21 (2019)
Background: Disorders of sex development (DSD) are a medical condition that affects the normal process of sexual Various of the genes needed for gonad development have been identified by investigation of patients with disorders sex development (DSD).
Externí odkaz:
https://doaj.org/article/bdae8034979a402b87fffdb7e381f06e
Publikováno v:
Middle East Journal of Digestive Diseases, Vol 10, Iss 1, Pp 40-44 (2018)
BACKGROUND The association between X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln gene polymorphism and hepatocellular carcinoma (HCC) has been investigated in several populations. However, the findings are controversial. The aim of this
Externí odkaz:
https://doaj.org/article/6c9f2da9ca9b43cdbc5922d2699b610e
Publikováno v:
Iranian Journal of Public Health, Vol 48, Iss 11 (2019)
Autosomal recessive primary microcephaly (MCPH) is a rare genetic disorder, leading to the defect of neurogenic brain development. Individuals with MCPH reveal reduced head circumference and intellectual disability. Several MCPH loci have been identi
Externí odkaz:
https://doaj.org/article/7ef440e9ebf6467199f1c09096b46ef4
Autor:
Leila, Hajizadeh, Nader Mansour, Samaei, Afsaneh, Bazgir, Mehdi, Agha Gholizadeh, Ayoob, Khosravi
Publikováno v:
Middle East Journal of Digestive Diseases. 14:118-123
BACKGROUND: Hepatocellular carcinoma (HCC) is the fifth most common cancer in the world. The association of interleukin 28B (IL-28B) polymorphisms and HCC has been investigated in several populations. However, the findings are controversial. This stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c3b07646f2ed8c02692c0ae7b81bb5a
https://doi.org/10.34172/mejdd.2022.264
https://doi.org/10.34172/mejdd.2022.264
Publikováno v:
Iranian Journal of Public Health
Iranian Journal of Public Health, Vol 48, Iss 11 (2019)
Iranian Journal of Public Health, Vol 48, Iss 11 (2019)
Autosomal recessive primary microcephaly (MCPH) is a rare genetic disorder, leading to the defect of neurogenic brain development. Individuals with MCPH reveal reduced head circumference and intellectual disability. Several MCPH loci have been identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80b81f1c87d60eb85e40bfe45328d6bb
http://europepmc.org/articles/PMC6961191
http://europepmc.org/articles/PMC6961191
Autor:
Majid Shahbazi, Touraj Farazmandfar, Aref Salehi, Marzieh Attar, Afsaneh Bazgir, Reza Salehi Manzari
Publikováno v:
Meta Gene. 16:1-4
Background Coronary artery disease (CAD) is the leading cause of disability and mortality in the world. CAD includes a group of cardiovascular diseases such as angina, heart failure and myocardial infarction. Interleukin-18 (IL-18) is a pleiotropic p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72ff9ff3c16c8adc3f7c04424891c2b4
https://doi.org/10.1016/j.mgene.2018.01.001
https://doi.org/10.1016/j.mgene.2018.01.001
Publikováno v:
Middle East Journal of Digestive Diseases
Middle East Journal of Digestive Diseases, Vol 10, Iss 1, Pp 40-44 (2018)
Middle East Journal of Digestive Diseases, Vol 10, Iss 1, Pp 40-44 (2018)
BACKGROUND The association between X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln gene polymorphism and hepatocellular carcinoma (HCC) has been investigated in several populations. However, the findings are controversial. The aim of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf130918b4916c38c6483b20853a68b2
https://doi.org/10.15171/mejdd.2017.89
https://doi.org/10.15171/mejdd.2017.89