Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Leyla HaghNejad"'
Autor:
Abolfazl Movafagh, Mehrdad Hashemi, Mojtaba Ghadiani, Reza Mirfakhraei, Hossein Darvish, Davood Zare Abdollahi, Hamid Ghaedi, Shamsi Safari, Leyla HaghNejad, Sara Mosammami, Niloofar Safavi Naeini, Ramin Miri, Mostafa Rezaei Tavirani
Publikováno v:
Middle East Journal of Cancer, Vol 3, Iss 2 & 3, Pp 85-88 (2012)
Background: According to the literature, there are a number of chronic and acute myeloid leukemias with unique, complex chromosome translocations. This study aims to conduct a brief review of the incidence of complex chromosome translocations in myel
Externí odkaz:
https://doaj.org/article/c2738d232fa44559bf5711441e0f1e41
Autor:
Mohammad Heydarian Moghadam, Abolfazl Movafagh, MirDavood Omrani, Kiandokht Ghanati, Mehrdad Hashemi, Farhikhteh Poursafavi, Hossein Darvish, Davood Zare Abdolahi, Milad Gholami, Mohammad Reza Heidari Rostamy, Shamsi Safari, Leyla HaghNejad, Reyhaneh Darehgazani, Niloofar Safavi Naeini, Mehdi Ghandehari Motlagh, Davar Amani
Publikováno v:
Journal of Research in Medical Sciences, Vol 18, Iss 4, Pp 363-365 (2013)
Homogeneously staining regions (HSR) or double minute chromosomes (dmin) are autonomously replicating extra-chromosomal elements that are frequently associated with gene amplification in a variety of cancers. The diagnosis of leukemia patients was ba
Externí odkaz:
https://doaj.org/article/7fe9c45926c848468104437f0fcf398e
Autor:
Shahram Torkamandi, Shaghayegh Taghavi, Saeed Mohammadihosseinabad, Mohammad Reza Abbaszadegan, Neda Shahmohammadibeni, Shokoufeh Abdollahi, Marzieh Motallebi, Negar Pedram, Leyla HaghNejad, Masoumeh Amini Gavenaroudi, Ehsan Ahmadi, Abolfazl Movafagh, Hamid Ghaedi, Babak Emamalizadeh, Amir Ehtesham Shafiei Zarneh, Atena Fazeli, Gholam Ali Shahidi, Hossein Darvish, Javad Jamshidi, Alireza Zare Bidoki, Abbas Tafakhori
Publikováno v:
Journal of the Neurological Sciences. 355:72-74
DNA variations in the fibroblast growth factor 20 gene have been reported to be associated with Parkinson's disease (PD). The rs12720208, a functional SNP located in the 3'UTR region of the gene, was reported as a risk factor for PD. A number of stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60763c4a51a0fb9278bccfe9e686f52f
https://doi.org/10.1016/j.jns.2015.05.020
https://doi.org/10.1016/j.jns.2015.05.020
Autor:
Babak Emamalizadeh, Atefeh Talebi, Abolfazl Movafagh, Seyed Mohammad Hassan Paknejad, Negar Pedram, Leyla HaghNejad, Nilofar Safavi Naeini, Saghar Ghasemi Firouzabadi, Mir Davood Omrani, Eznollah Azargashb, Matin Kayyal, Gholam Ali Shahidi, Ali Khaligh, Javad Jamshidi, Hossein Ashrafian, Hamid Reza Heidari-Rostami, Hossein Darvish, Hamid Noorollahi-Moghaddam, Siamak Karkheiran, Mojdeh Akbari, Siamak Abdi
Publikováno v:
Neuroscience Letters. 551:75-78
Parkinson's disease (PD) is the second most common neurodegenerative disorder, after Alzheimer's disease. Genomic rearrangements are common mutations reported in PD patients. In this study, we investigated the prevalence of genomic rearrangements in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4e99002ccf80ceed1c9f73a24ddc6cf
https://doi.org/10.1016/j.neulet.2013.07.013
https://doi.org/10.1016/j.neulet.2013.07.013
Autor:
Movafagh, Abolfazl1 Movafagh_a@yahoo.com, Hashemi, Mehrdad2, Ghadiani, Mojtaba3, Mirfakhraei, Reza1, Darvish, Hossein1, Zare Abdollahi, Davood1, Ghaedi, Hamid1, Safari, Shamsi1, HaghNejad, Leyla1, Mosammami, Sara1, Safavi Naeini, Niloofar1, Miri, Ramin1, Rezaei Tavirani, Mostafa4
Publikováno v:
Middle East Journal of Cancer. Apr-Jul2012, Vol. 3 Issue 2/3, p85-88. 4p. 1 Diagram, 1 Graph.
Publikováno v:
Neurological Sciences. Jul2016, Vol. 37 Issue 7, p1119-1126. 8p. 1 Diagram, 4 Charts, 1 Graph.
Publikováno v:
Neurological Research; Apr2017, Vol. 39 Issue 4, p374-380, 7p