Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mohammad Dehestani"'
Autor:
Mohammad Dehestani, Velina Kozareva, Cornelis Blauwendraat, Ernest Fraenkel, Thomas Gasser, Vikas Bansal
Publikováno v:
Molecular Brain, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Several prior studies have proposed the involvement of various brain regions and cell types in Parkinson’s disease (PD) pathology. Here, we performed snRNA-seq on the prefrontal cortex and anterior cingulate regions from a small cohort of
Externí odkaz:
https://doaj.org/article/eed45c239e5848d1b734879955c3654e
Autor:
Seyed Mostafa Shiryazdi, Mohammad Dehestani, Mohammad forat yazdi, Hamid Reza Soltani Gerdfaramarzi, Mansour Moghimi
Publikováno v:
Journal of Community Health Research, Vol 4, Iss 2, Pp 91-98 (2015)
Introduction: As a glycoprotein, Plasma Prostate-Specific Antigen (PSA) is mainly produced by prostate epithelial cells and is used as a major diagnostic tool for prostate cancer. A group of researchers relate the elevated number of estrogen receptor
Externí odkaz:
https://doaj.org/article/008f9c91f2e446a59d77edc29b8b40d9
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 30, Iss 191 (2012)
Background: Systemic hypertension is one of the major risk factors of heart failure and especially left ventricular dysfunction. Mild hypertension is mostly asymptomatic and can remain hidden for years. Moreover, it can lead to morphologic changes an
Externí odkaz:
https://doaj.org/article/fa3283ee4428421a9f832bf925496373
Several prior studies have proposed the involvement of various brain regions and cell types in Parkinson’s disease (PD) pathology. Here, we performed snRNA-seq on the prefrontal cortex and anterior cingulate regions from post-mortem control and PD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41813d79686ea268bb049b47e36b4830
https://doi.org/10.1101/2023.05.11.540329
https://doi.org/10.1101/2023.05.11.540329
Autor:
Hui Liu, Mohammad Dehestani, Mary B. Makarious, Sara Bandres-Ciga, Thomas Gasser, Jonggeol J. Kim
The SLC25A46 gene was recently reported to be associated with Parkinson’s disease (PD). Here, we comprehensively investigated the role of SLC25A46 variants in PD patients of European ancestry and assessed susceptibility using whole-genome sequencin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83118da59c1afd16e133e2793aa98aa0
https://doi.org/10.1101/2022.06.13.22276317
https://doi.org/10.1101/2022.06.13.22276317
Publikováno v:
Journal of Personalized Medicine, Vol 11, Iss 1030, p 1030 (2021)
Parkinson’s disease (PD) is the second most common neurodegenerative disorder characterized by the loss of dopaminergic neurons. The vast majority of PD patients develop the disease sporadically and it is assumed that the cause lies in polygenic an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::0585d96a721bb342baee3b66e3951371
https://www.mdpi.com/2075-4426/11/10/1030
https://www.mdpi.com/2075-4426/11/10/1030
Autor:
Mohammad Dehestani, Hui Liu, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Vikas Bansal, Thomas Gasser
Publikováno v:
Molecular and cellular neuroscience 121, 103751 (2022). doi:10.1016/j.mcn.2022.103751
Polygenic Risk Scores (PRS), which allow assessing an individuals' genetic risk for a complex disease, are calculated as the weighted number of genetic risk alleles in an individual's genome, with the risk alleles and their weights typically derived
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d34bece43feef53b2b31e51ded2626ec
https://doi.org/10.1016/j.mcn.2022.103751
https://doi.org/10.1016/j.mcn.2022.103751
Publikováno v:
Journal of Personalized Medicine 11(10), 1030-(2021). doi:10.3390/jpm11101030 special issue: "Omics Approaches and Personalized Medicine in Neurodegenerative Diseases"
Journal of Personalized Medicine
Journal of Personalized Medicine
Parkinson’s disease (PD) is the second most common neurodegenerative disorder characterized by the loss of dopaminergic neurons. The vast majority of PD patients develop the disease sporadically and it is assumed that the cause lies in polygenic an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d3f9f8e05555cc15a457d99f31300aef
https://pub.dzne.de/record/163360
https://pub.dzne.de/record/163360
Autor:
Mohammad Salehi, Mehdi Latif, Fatemeh Peighambari, Mohammad Dehestani, Seyed Vahid Ahmadi-Hanzaei
Publikováno v:
Internal Medicine and Medical Investigation, Vol 2, Iss 3, Pp 102-5 (2017)
Background: Overweight is currently considered as the main risk factor for various chronic disorders, especially cardiovascular diseases. Unexpected hypertension is the first reaction of heart to overburden imposed by obesity or overweight. The purpo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46315c3985ff56aee436392c09e51cdc
http://imminv.com/index.php/imminv/article/view/93
http://imminv.com/index.php/imminv/article/view/93