Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Maryam Nasiri Aghdam"'
Autor:
Hossein Daghagh, Haniyeh Rahbar Kafshboran, Yousef Daneshmandpour, Maryam Nasiri Aghdam, Shahrzad Talebian, Jafar Nouri Nojadeh, Hamid Hamzeiy, Saskia Biskup, Ebrahim Sakhinia
Publikováno v:
BioImpacts, Vol 13, Iss 3, Pp 183-190 (2023)
Introduction: The CSF1R gene encodes the receptor for colony-stimulating factor-1, the macrophage, and monocyte-specific growth factor. Mutations in this gene cause hereditary diffuse leukoencephalopathy with spheroids (HDLS) with autosomal dominant
Externí odkaz:
https://doaj.org/article/8a36d94e52c446e09f23a4e3c3a7c0c0
Autor:
Hossein Daghagh, Haniyeh Rahbar Kafshboran, Yousef Daneshmandpour, Maryam Nasiri Aghdam, Shahrzad Talebian, Jafar Nouri Nojadeh, Hamid Hamzeiy, Saskia Biskup, Ebrahim Sakhinia
Publikováno v:
BioImpacts.
Introduction: The CSF1R gene encodes the receptor for colony-stimulating factor-1, the macrophage, and monocyte-specific growth factor. Mutations in this gene cause hereditary diffuse leukoencephalopathy with spheroids (HDLS) with autosomal dominant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7855c33d9e8156df70286270fda0d97
https://doi.org/10.34172/bi.2022.23528
https://doi.org/10.34172/bi.2022.23528
Autor:
Maryam Nasiri-Aghdam, Mariel Garcia-Chagollan, Ana Laura Pereira-Suarez, Adriana Aguilar-Lemarroy, Luis Felipe Jave-Suarez
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 9; Pages: 8347
Infection of epithelial cells with high-risk HPV (HR-HPV) types, followed by expression of virus oncogenic proteins (E5, E6, and E7), leads to genomic imbalance, suppression of tumor inhibitors, and induction of oncogenes. Low-risk HPV (LR-HPV) may s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b11b992791701bd58ec6f331e05e0d08
https://doi.org/10.3390/ijms24098347
https://doi.org/10.3390/ijms24098347
Autor:
Alireza Khabbazi, Hossein Daghagh, Maryam Nasiri Aghdam, Yousef Daneshmandpour, Haniyeh Rahbar Kafshboran, Ebrahim Sakhinia, Jafar Nouri Nojadeh, Hamid Hamzeiy, Mina Kazemzadeh
Publikováno v:
Immunology Letters. 221:27-32
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (APLAID) is an autosomal dominant autoinflammatory disease characterized by episodic skin, musculoskeletal, ophthalmic and gastrointestinal tract symptoms. Here we rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a73375332199f9b6ff335ede769e8cf6
https://doi.org/10.1016/j.imlet.2020.01.008
https://doi.org/10.1016/j.imlet.2020.01.008
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 11056, p 11056 (2021)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
Post-transcriptional modifications to coding and non-coding RNAs are unquestionably a pivotal way in which human mRNA and protein diversity can influence the different phases of a transcript’s life cycle. CELF (CUGBP Elav-like family) proteins are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2aed4394a93def34ecb4b1b343305dbd
https://doi.org/10.3390/ijms222011056
https://doi.org/10.3390/ijms222011056
Autor:
Bahram Memar, Mohammad Hasanzadeh Khayat, Maryam Nasiri Aghdam, Mohammad Reza Abbaszadegan, Azadeh Aarabi, Mohammad Mahdi Forghanifard, Ezzat Dadkhah
Publikováno v:
Environmental science and pollution research international. 27(25)
Esophageal cancer is the eighth most common cancer and the sixth most frequent cause of cancer mortality worldwide. Exposure to polycyclic aromatic hydrocarbons formed by incomplete combustion of organic matter is an important risk factor. Genetic po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6494215b070a4d05baa263f01444b9bc
https://pubmed.ncbi.nlm.nih.gov/32488710
https://pubmed.ncbi.nlm.nih.gov/32488710
Autor:
Alireza Tafazoli, Maryam Nasiri Aghdam, Mohammad Reza Abbaszadegan, Zohreh Mosavi, Mohammad Aslzare
Publikováno v:
Hormones. 15:65-72
Purpose: Multiple Endocrine Neoplasia type 2A (MEN 2A) is a complex autosomal dominant inherited syndrome characterized by medullary thyroid carcinoma (MTC), pheochromocytoma and primary parathyroid hyperplasia. In patients with only one or two clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c6429026ca6bbf73cba6b136e187ce9
https://doi.org/10.1007/bf03401404
https://doi.org/10.1007/bf03401404