Zobrazeno 1 - 10
of 177
pro vyhledávání: '"Mahsa M AMOLI"'
Autor:
Hamidreza Mianesaz, Safoura Ghalamkari, Farzaneh Abbasi, Maryam Razzaghy‐Azar, Fatemeh Sayarifard, Rahim Vakili, Maryam Sedghi, Samaneh Noroozi Asl, Sousan Hosseini, Mahsa M Amoli, Hanieh Yaghootkar
Publikováno v:
Journal of Diabetes Investigation, Vol 15, Iss 10, Pp 1390-1402 (2024)
ABSTRACT Introduction Neonatal diabetes mellitus (NDM) is a rare non‐immunological monogenic disorder characterized by hyperglycemic conditions primarily occurring within the first 6 months of life. The majority of cases are attributed to pathogeni
Externí odkaz:
https://doaj.org/article/d5d59eee454645a18bc1d5fc7a3c602b
Autor:
Yasaman Ansari, Mojgan Asadi, Iman Salahshouri Far, Nahid Pashaie, Nafise Noroozi, Mahsa M Amoli
Publikováno v:
Advances in Human Biology, Vol 13, Iss 1, Pp 144-150 (2023)
Introduction: Obesity is primarily caused by the dysfunction of the energy homeostasis system. Numerous studies have reported an association between obesity and the rs17782313 variant near the melanocortin-4 receptor (MC4R) gene. In addition, the PKH
Externí odkaz:
https://doaj.org/article/64f76bddb5df4f38bb5c2764f2f3d7f7
Autor:
Golnaz Khakpour, Mehrdad Noruzinia, Pantea Izadi, Fatemeh Karami, Mohammad Ahmadvand, Ramin Heshmat, Mahsa M Amoli, Javad Tavakkoly-Bazzaz
Publikováno v:
Tumor Biology, Vol 39 (2017)
Critical roles of epigenomic alterations in the pathogenesis of breast cancer have recently seized great attentions toward finding epimarkers in either non-invasive or semi-non-invasive samples as well as peripheral blood. In this way, methylated DNA
Externí odkaz:
https://doaj.org/article/a77c3ebb644e4f849dea710aa8e906e7
Publikováno v:
Iranian Journal of Public Health, Vol 43, Iss Supple 1 (2015)
Obesity is currently considered as a serious global health problem which is influenced by environmental and genetic factors. Association of genetic variants with obesity is widely scrutinized in recent years. The aim of this study was to evaluate pre
Externí odkaz:
https://doaj.org/article/773358f1387843728c258f8b079479b8
Publikováno v:
Frontiers in Physiology, Vol 5 (2014)
Externí odkaz:
https://doaj.org/article/0ff356b05dcd4642b390d5065f1f54e9
Publikováno v:
J Diabetes Metab Disord
BACKGROUND: Obesity is a complicated phenomenon which is a combination of genetic, environmental, and psychological factors. Genetic factors of obesity play an important role in individual risk. It is well known that obese children have disturbed pub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a1d08141ef372d8c9e523172c9afd3b
https://doi.org/10.1007/s40200-022-01011-5
https://doi.org/10.1007/s40200-022-01011-5
Publikováno v:
J Diabetes Metab Disord
PURPOSE: Personal medicine is a new notion for individualizing treatment in the future. Studying pathogenic markers including genetic variants would be beneficial in better diagnosis and management of complex diseases such as diabetes and obesity. Ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d0876350c8930cfd0945fe141e66d5b
https://doi.org/10.1007/s40200-022-00978-5
https://doi.org/10.1007/s40200-022-00978-5
Publikováno v:
Journal of Medical Virology. 95
The genetic association of coronavirus disease 2019 (COVID-19) with its complications has not been fully understood. This study aimed to identify variants and haplotypes of candidate genes implicated in COVID-19 related traits by combining the litera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6946a028f5413f8d5b6e5cdc4c67e6d6
https://doi.org/10.1002/jmv.28355
https://doi.org/10.1002/jmv.28355
Autor:
Andreas Recke, Sarah Konitzer, Susanne Lemcke, Miriam Freitag, Nele Maxi Sommer, Mohammad Abdelhady, Mahsa M. Amoli, Sandrine Benoit, Farha El-Chennawy, Mohammad Eldarouti, Rüdiger Eming, Regine Gläser, Claudia Günther, Eva Hadaschik, Bernhard Homey, Wolfgang Lieb, Wiebke K. Peitsch, Claudia Pföhler, Reza M. Robati, Marjan Saeedi, Miklós Sárdy, Michael Sticherling, Soner Uzun, Margitta Worm, Detlef Zillikens, Saleh Ibrahim, Gestur Vidarsson, Enno Schmidt, the German AIBD Genetic Study Group, Alexander Kreuter, Christos C. Zouboulis, Georg Däschlein, Kerstin Steinbrink, Manfred Kunz, Nicolas Hunzelmann, Steven Goetze
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
IgG3 is the IgG subclass with the strongest effector functions among all four IgG subclasses and the highest degree of allelic variability among all constant immunoglobulin genes. Due to its genetic position, IgG3 is often the first isotype an antibo
Externí odkaz:
https://doaj.org/article/17fd9186200c4c10a069c5a63130ea05
Autor:
Maryam Razzaghy-Azar, Bagher Larijani, Ali Talea, Mitra Nourbakhsh, Mahsa M. Amoli, Mona Nourbakhsh
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-5 (2021)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background Permanent neonatal diabetes mellitus (PNDM) presents with dehydration and hyperglycemia, which usually occurs during the first 12 months of life. Activating mutations of beta-cell adenosine triphosphate-sensitive potassium [KATP] channel s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5b458ffc5620f6c6d34a788a349f8d9
https://doaj.org/article/c0f60f184bd1453d9cbb3af3ce3a5937
https://doaj.org/article/c0f60f184bd1453d9cbb3af3ce3a5937