Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Shahram Torkamandi"'
Autor:
Mina Mohammadhosayni, Arezou Khosrojerdi, Keivan Lorian, Saeed Aslani, Danyal Imani, Bahman Razi, Farhad Babaie, Shahram Torkamandi
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-10 (2020)
Abstract Background Several studies have reported the association between polymorphisms in Matrix metalloproteinases (MMPs) gene family and risk of Multiple sclerosis (MS). However, the results have been inconsistent and inconclusive. To resolve this
Externí odkaz:
https://doaj.org/article/be24b8c155e747459261302ed69427ab
Autor:
Somaye Rezaei, Fariba Zarzanalivan, Pouya Pirouti, Mohammad Reza Amiri Nikpour, Abdolreza Javadi, Shahram Torkamandi
Publikováno v:
Journal of Research in Clinical Medicine, Vol 8, Iss 1, Pp 18-18 (2020)
Background: Isolated intracranial Rosai-Dorfman disease (RDD) is an extremely rare, idiopathic histo-proliferative disorder. RDD is associated with the proliferation of histiocytes and emperipolesis. Case Presentation: we report a case with isolated
Externí odkaz:
https://doaj.org/article/8fc46ef01c784f87a68531898001f938
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 17, Iss 11, Pp 912-916 (2014)
Objective(s): Epigenetic regulation of gene expression can be carried out through chromatin remodeling enzymes such as SWI/SNF. Brg1 also known as SMARCA4 is a catalytic subunit of SWI/SNF, which is necessary for MMPs expression. Matrix metalloprotei
Externí odkaz:
https://doaj.org/article/2be50634fd554449bb96799b73c8d037
Autor:
Amirhossein Sahebkar, Haleh Mikaeili, Shahram Torkamandi, Farhad Babaie, Melodi Omraninava, Armita Mahdavi Gorabi, Arezou Khosrojerdi, Saeed Aslani, Arsalan Yazdchi, Thozhukat Sathyapalan
Publikováno v:
Current Genomics. 23:163-174
Abstract: Psoriasis is an organ-specific autoimmune disease characterized by the aberrant proliferation and differentiation of keratinocytes, leading to skin lesions. Abnormal immune responses mediated by T cells and dendritic cells and increased pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f1c7d9f20453121ba6089eb094b7c1c
https://doi.org/10.2174/1389202923666220527111037
https://doi.org/10.2174/1389202923666220527111037
Autor:
Tahereh Ghorashi, Somaye Rezaei, Shahram Torkamandi, Hadi Bayat, Shima Bahrami, Mohsen Soosanabadi, Seyyed Mohamad Hoseini, Mohammad Dehani
Publikováno v:
Genes & Immunity. 22:322-326
Long noncoding RNA MEG3 and NLRC5 genes are both involved in the immune system and the regulation of NLRC5 by MEG3 is documented in rheumatoid arthritis. Therefore, we intended to evaluate the association between the expressions of MEG3 and NLRC5 in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d659dd8817240c84415c575e999d4c8c
https://doi.org/10.1038/s41435-021-00154-4
https://doi.org/10.1038/s41435-021-00154-4
Autor:
Jamshid Gholizadeh Navashenaq, Mehrdad Ebrazeh, Fatemeh Sadat Mohammadi, Fatemeh Ezzatifar, Farhad Babaie, Hamed Mohammadi, Arezoo Gowhari Shabgah, Maryam Hemmatzadeh, Farhad Jadidi-Niaragh, Saeed Aslani, Sevda Salimifard, Shahram Torkamandi
Publikováno v:
International Journal of Rheumatic Diseases. 24:567-581
Background: Genetic polymorphisms in the Endoplasmic reticulum aminopeptidase (ERAP) 2 gene has been attributed with the Ankylosing spondylitis (AS) etiopathogenesis. Here we assessed the association of ERAP2 gene single nucleotide polymorphisms (SNP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49c5e76d58b0796d2b19868a4ce66c27
https://doi.org/10.1111/1756-185x.14079
https://doi.org/10.1111/1756-185x.14079
Autor:
Shahram Torkamandi, Danyal Imani, Mina Mohammadhosayni, Bahman Razi, Keivan Lorian, Farhad Babaie, Saeed Aslani, Arezou Khosrojerdi
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-10 (2020)
BMC Neurology
BMC Neurology
Background Several studies have reported the association between polymorphisms in Matrix metalloproteinases (MMPs) gene family and risk of Multiple sclerosis (MS). However, the results have been inconsistent and inconclusive. To resolve this issue, h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06585973f9a31a2f65fd2bd4dde58137
http://link.springer.com/article/10.1186/s12883-020-01804-2
http://link.springer.com/article/10.1186/s12883-020-01804-2
Publikováno v:
Molecular Biology Reports. 47:4021-4027
Biotinidase deficiency is an autosomal recessive inherited inborn error of biotin metabolism. Biotin as a water-soluble vitamin is the prosthetic group of biotin-dependent carboxylase enzymes, and by enhancing their function plays a key role in amino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1864637fc6c5977ba92967012f205b2
https://doi.org/10.1007/s11033-020-05424-4
https://doi.org/10.1007/s11033-020-05424-4
Autor:
Shahram, Torkamandi, Shima, Bahrami, Tahereh, Ghorashi, Mohammad, Dehani, Hadi, Bayat, Seyyed Mohamad, Hoseini, Somaye, Rezaei, Mohsen, Soosanabadi
Publikováno v:
Genes and immunity. 22(7-8)
Long noncoding RNA MEG3 and NLRC5 genes are both involved in the immune system and the regulation of NLRC5 by MEG3 is documented in rheumatoid arthritis. Therefore, we intended to evaluate the association between the expressions of MEG3 and NLRC5 in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fafe89c2c4a2343fe6fe084dfde262a1
https://pubmed.ncbi.nlm.nih.gov/34782775
https://pubmed.ncbi.nlm.nih.gov/34782775
Autor:
Mir Davood Omrani, Hossein Darvish, Somaye Rezaei, Behnam Alipoor, Maryam Erfanian Omidvar, Shahram Torkamandi, Hamid Ghaedi
Publikováno v:
Journal of Neurology. 268:2065-2082
The hereditary spastic paraplegias (HSPs) are a heterogeneous group of inherited neurodegenerative disorders. Although, several genotype–phenotype studies have carried out on HSPs, the association between genotypes and clinical phenotypes remain in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::430a79adb6fb25016f087a79b6823b18
https://doi.org/10.1007/s00415-019-09633-1
https://doi.org/10.1007/s00415-019-09633-1