Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Shamsi Safari"'
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:
Pooria Hakimi, Shamsi Safari, Davood Zare-Abdollahi, Ali Khaligh, Alireza Moslem, Mahshid Meshkani, Mitra Eftekhariyazdi
Publikováno v:
The Journal of Gene Medicine. 22
Background Ellis-van Creveld syndrome (EvCS) is a rare autosomal recessive skeletal dysplasia that is characterized by short stature, short limbs, short ribs, polydactyly and structural heart defect. Despite locus heterogeneity, in the majority of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b74f4fedb3be66cda51aa5bca4913b8b
https://doi.org/10.1002/jgm.3175
https://doi.org/10.1002/jgm.3175
Autor:
Shamsi Safari, Hamid Reza Khorram Khorshid, Zahra Tahmasebi, Ata Bushehri, Mohammad Reza Safari, Mohsen Ghadami, Azadeh Dehghani, Davood Zare-Abdollahi
Publikováno v:
The Journal of Gene Medicine. 22
Bachground Leber congenital amaurosis (LCA) is a severe and congenital or early onset form of inherited retinitis pigmentosa (RP). To date, approximately 25 genes have been introduced in relation to LCA. In this regard, retinal pigment epithelium-spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31fdaa61c85d7e8ee6ac4e8b84fe7ed3
https://doi.org/10.1002/jgm.3154
https://doi.org/10.1002/jgm.3154
Autor:
Abolfazl Movafagh, Sahand Riazi-Isfahani, Shamsi Safari, Mahdi Tabarraee, L. Keyvan, Mojtaba Ghadiani, S. Gorji, Davood Zare-Abdollahi, L. Gachkar
Publikováno v:
International Journal of Laboratory Hematology. 38:125-132
Summary Introduction In acute myeloid leukemia (AML), it has been shown that AML-derived cells often remain sensitive to autophagy-inducing stimuli, leading to the idea that harnessing the autophagy can be pertinent to AML cytotoxic therapy. Despite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0a4d64f3ec76acd7e861a84217cf7b2
https://doi.org/10.1111/ijlh.12454
https://doi.org/10.1111/ijlh.12454
Autor:
Abolfazl Movafagh, Arezou Sayad, Hosein Darvish, Davood Zare-Abdollahi, Shamsi Safari, Azim Nejatizadeh, SeyedAbdol Reza Mortazavi-Tabatabaei, Mohammad Hassan Heidari
Publikováno v:
Nova Journal of Medical and Biological Sciences. :1-10
The World Health Organization classification of hematologic disorders takes into account specific chromosome aberrations and their molecular counterparts together with morphology, immune phenotype and clinical features; on this basis, distinct diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf637bcc794bc927dabd8802f4ec5427
https://doi.org/10.20286/nova-jmbs-030432
https://doi.org/10.20286/nova-jmbs-030432
Autor:
Abolfazl Movafagh, Nasser Salsabili, Pedram Azimzadeh, Walead Ebrahimizadeh, Siamak Salami, Milad Bastami, Reza Mirfakhraie, Shamsi Safari, Mirdavood Omrani, Davood Zare-Abdollahi
Publikováno v:
Europe PubMed Central
Summary Nuclear receptor subfamily 5 group A member 1 (NR5A1) encodes a nuclear receptor that regulates transcription of multiple genes involved in adrenal and gonadal development, steroidogenesis and the reproductive axis. Human mutations in NR5A1we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7858084e6bd429d7368ab734d0be828
https://doi.org/10.1111/and.12274
https://doi.org/10.1111/and.12274
Publikováno v:
Archives of Iranian medicine. 19(5)
In brief, we present a case of acute myeloid leukemia (AML) with 5, 17 and 18 monosomies as stemline clonal abnormality in his cytogenetic analysis. To the best of our knowledge, this is the first report of such a chromosomal abnormality as a clonal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b7b3e4a6de21420ee582b6ffac2c2d5b
https://pubmed.ncbi.nlm.nih.gov/27179172
https://pubmed.ncbi.nlm.nih.gov/27179172
Autor:
Davood, Zare-Abdollahi, Shamsi, Safari, Abolfazl, Movafagh, Sahand, Riazi-Isfahani, Mojtaba, Ghadyani, Feyzollah, Hashemi-Gorji, Hashemi-Gorji, Feyzollah, Mohammad Foad, Nasrollahi, Mir Davood, Omrani
Publikováno v:
Hematology (Amsterdam, Netherlands). 20(7)
Despite numerous studies in order to determine the allele frequency and clinical impact of DNA methyltransferase 3 A (DNMT3A) gene mutations in acute myeloid leukemia (AML), reports about the expression analysis of this gene are rare and between the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b76e96ca00b9ff390708bf1c7511621
https://pubmed.ncbi.nlm.nih.gov/29115182
https://pubmed.ncbi.nlm.nih.gov/29115182
Autor:
Mojtaba Ghadiani, Davood Zare-Abdollahi, Abolfazl Movafagh, Mir Davood Omrani, Shamsi Safari, Sahand Riazi-Isfahani
Publikováno v:
Medical oncology (Northwood, London, England). 31(1)
As a typical tumor suppressor gene, transcriptional silencing of ras-association domain family 1, isoform A (RASSF1A) is caused by biallelic methylation or the condition that one allele is methylated and then the other allele lost by allelic loss, as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a4d309c23a6e476b5251b7763ba5bb1
https://pubmed.ncbi.nlm.nih.gov/24248815
https://pubmed.ncbi.nlm.nih.gov/24248815