Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Marzieh, Rahbaran"'
Autor:
Marzieh Rahbaran, Maryam Hassani Doabsari, Simindokht Salavitabar, Neda Mokhberian, Ziba Morovvati, Saeid Morovvati
Publikováno v:
Cellular & Molecular Biology Letters, Vol 24, Iss 1, Pp 1-8 (2019)
Abstract Purpose Ectodermal dysplasias are characterized by developmental abnormalities in ectodermal structures. Hypohidrotic ectodermal dysplasias (HED) are the most common subtype. They are most commonly inherited via X-linked recessive routes. We
Externí odkaz:
https://doaj.org/article/41baa1c3fec74390b0eca820f9c5c84a
Autor:
Pantea Banihashemi, Mandana Hasanzad, Shahrzad Manavi Nameghi, Negar Sarhangi, Maryam Hassani Doabsari, Hamid Reza Aghaei Meybodi, Fatemeh Fazeli, Mehrnoush Ganji, Shekoufeh Nikfar, Marzieh Rahbaran
Publikováno v:
J Diabetes Metab Disord
BACKGROUND: Osteoporosis is often considered to be a disease of the elderly, which is characterized by two characteristics: low bone mineral density (BMD) and increased risk of fracture. MicroRNAs (miRNAs) have been reported to play a potential role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1f4c083969dced9dcec87e4b4f79719
https://doi.org/10.1007/s40200-021-00873-5
https://doi.org/10.1007/s40200-021-00873-5
Autor:
Mahdi Afshari, Davood Abbasi, Marzieh Rahbaran, Azadeh Malekizadeh, Mandana Hasanzad, Hamid Reza Aghaei Meybodi
Publikováno v:
Nucleosides, Nucleotides & Nucleic Acids. 40:530-541
Type 2 diabetes mellitus (T2DM) is a multifactorial polygenic disease. Potassium inwardly-rectifying channel, subfamily J, member 11 (KCNJ11) gene mutations can result in susceptibility of T2DM. Th...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::011308c54ac667d7bd235715fcdc06cc
https://doi.org/10.1080/15257770.2021.1905841
https://doi.org/10.1080/15257770.2021.1905841
Background: Prostate cancer (PC) is one of the most common cancers among men. Genetic predisposition is emerging as a risk factor for PC development. The Androgen receptor (AR) gene is associated with the development and prognosis of PC. Understandin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ce72b2ee0db6af0978e4f31f7227e36
https://doi.org/10.21203/rs.3.rs-1185476/v1
https://doi.org/10.21203/rs.3.rs-1185476/v1
Autor:
Neda Mokhberian, Ziba Morovvati, Simindokht Salavitabar, Marzieh Rahbaran, Maryam Hassani Doabsari, Saeid Morovvati
Publikováno v:
Cellular & Molecular Biology Letters, Vol 24, Iss 1, Pp 1-8 (2019)
Cellular & Molecular Biology Letters
Cellular & Molecular Biology Letters
Purpose Ectodermal dysplasias are characterized by developmental abnormalities in ectodermal structures. Hypohidrotic ectodermal dysplasias (HED) are the most common subtype. They are most commonly inherited via X-linked recessive routes. We report o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23157d9bb2c322881c968071a3be73d8
http://link.springer.com/article/10.1186/s11658-019-0174-9
http://link.springer.com/article/10.1186/s11658-019-0174-9
Autor:
Azadeh, Malekizadeh, Marzieh, Rahbaran, Mahdi, Afshari, Davood, Abbasi, Hamid Reza, Aghaei Meybodi, Mandana, Hasanzad
Publikováno v:
Nucleosides, nucleotidesnucleic acids. 40(5)
Type 2 diabetes mellitus (T2DM) is a multifactorial polygenic disease. Potassium inwardly-rectifying channel, subfamily J, member 11 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d0937cfa8ecdbb13c16c796ad1f49ee2
https://pubmed.ncbi.nlm.nih.gov/33853507
https://pubmed.ncbi.nlm.nih.gov/33853507
Autor:
Katayoun Heshmatzad, Farshad Sharifi, Maryam Hassani Doabsari, Marzieh Rahbaran, Hamid Reza Aghaei Meybodi, Seyed Hamid Jamaldini, Negar Sarhangi, Leila Hashemian, Mandana Hasanzad
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-18 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-18 (2020)
Type 2 diabetes mellitus (T2DM) is a complex disease caused by the interaction between genetic and environmental factors. A growing number of evidence suggests that the peroxisome proliferator-activated receptor gamma (PPARG) gene plays a major role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0bdd96f578ab8d044f518ecfc8c6495
https://doi.org/10.1038/s41598-020-69363-7
https://doi.org/10.1038/s41598-020-69363-7
Autor:
Anoosh Naghavi, Mandana Hasanzad, Negar Sarhangi, Hamid Reza Aghaei Meybodi, Shekoufeh Nikfar, Marzieh Rahbaran, Maryam Hassani Doabsari, Bagher Larijani
UNSTRUCTURED The objective of this systematic review is to determine the effect of genetic variants that associate with antidiabetic medications and their efficacy and toxicity in T2DM patients. The understanding may allow interventions for improving
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35baf04f0cc30562e44b9e804c7855e4
https://doi.org/10.2196/preprints.13605
https://doi.org/10.2196/preprints.13605
Autor:
Sarhangi, Negar1, Sharifi, Farshad2, Hashemian, Leila3, Hassani Doabsari, Maryam3, Heshmatzad, Katayoun3, Rahbaran, Marzieh3, Jamaldini, Seyed Hamid3, Aghaei Meybodi, Hamid Reza1,4, Hasanzad, Mandana1,3 mandanahasanzad@yahoo.com
Publikováno v:
Scientific Reports. 7/29/2020, Vol. 10 Issue 1, p1-18. 18p.
Autor:
Rahbaran, Marzieh, Hassani Doabsari, Maryam, Salavitabar, Simindokht, Mokhberian, Neda, Morovvati, Ziba, Morovvati, Saeid
Publikováno v:
Cellular & Molecular Biology Letters; 8/19/2019, Vol. 24 Issue 1, pN.PAG-N.PAG, 1p