Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Paniz Miar"'
WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family
Autor:
Mahnaz Norouzi, Mohammad Shafiei, Zeinab Abdollahi, Paniz Miar, Hamid Galehdari, Mohammad Hasan Emami, Mehrdad Zeinalian, Mohammad Amin Tabatabaiefar
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
BackgroundFamilial cancers comprise a considerable distribution of colorectal cancers (CRCs), of which only about 5% occurs through well-established hereditary syndromes. It has been demonstrated that deleterious variants at the newly identified canc
Externí odkaz:
https://doaj.org/article/93202274c1394737b50522c497d1b7df
Autor:
Paniz Miar, Mohammad Amin Tabatabaiefar, Zeinab Abdollahi, Mahnaz Noruzi, Mohammad Kazemi, Azar Naimi, Mohammad Hasan Emami, Shahrokh Izadi, Mehrdad Zeinalian
Publikováno v:
Advanced Biomedical Research, Vol 11, Iss 1, Pp 79-79 (2022)
Background: Microsatellite instability (MSI) in colorectal cancer (CRC) patients is considered as a diagnostic and prognostic marker. MSI is a consequence of mismatch repair deficiency which is evaluated using the different microsatellite markers on
Externí odkaz:
https://doaj.org/article/136700b332124311be54f43dd4d70d07
Autor:
Mohammad Amin Tabatabaiefar, Azar Naimi, Mehrdad Zeinalian, Paniz Miar, Mohammad Hasan Emami, Zeinab Abdollahi, Mahnaz Noruzi, Mohammad Kazemi
Publikováno v:
Laboratory medicine. 53(3)
Objective The most important tumor characteristic of Lynch syndrome (LS) is microsatellite instability (MSI). In the current study, BAT34c4 and BAT26 mononucleotide markers were evaluated as part of efforts to test a cost-effective panel for MSI test
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92c47c598e6a8076d905be30b1e883e7
https://pubmed.ncbi.nlm.nih.gov/34611695
https://pubmed.ncbi.nlm.nih.gov/34611695
Autor:
Mohammad Hussein Nilforoush, Mahsa Sepehrnejad, Sina Narrei, Hamidreza Abtahi, Mohammad Amin Tabatabaiefar, Paniz Miar, Samane Nasrniya
Publikováno v:
Laboratory medicine. 53(2)
Background Hearing loss (HL) is the most prevalent and genetically heterogeneous sensory disabilities in humans throughout the world. Methods In this study, we used whole-exome sequencing (WES) to determine the variant causing autosomal recessive non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19c8786917b79880bd525921ae79b9c2
https://pubmed.ncbi.nlm.nih.gov/34388253
https://pubmed.ncbi.nlm.nih.gov/34388253
Autor:
Mohammad Hassan Emami, Sina Narrei, Mehrdad Zeinalian, Morteza Hashemzadeh-Chaleshtori, Mohammad Amin Tabatabaiefar, Paniz Miar, Mohammad Reza Pourreza
Purpose Lynch syndrome is the most common hereditary cancer syndromes due to a germline mutation in one of the mismatch-repair (MMR) genes. It results in early-onset colorectal cancer (CRC) and other Lynch-associated cancers in an autosomal dominant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b635087b76b7d6404842ac62b5e4595f
https://doi.org/10.21203/rs.3.rs-158152/v1
https://doi.org/10.21203/rs.3.rs-158152/v1
Publikováno v:
Molecular neurobiology. 58(7)
The current pandemic of the new human coronavirus (CoV), i.e., severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has created an urgent global condition. The disease, termed coronavirus disease 2019 (COVID-19), is primarily known as a resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2285e3a02d2941c0e0abfeae25b5eabe
https://pubmed.ncbi.nlm.nih.gov/33765290
https://pubmed.ncbi.nlm.nih.gov/33765290
Autor:
Milad Saadatkish, Zeinab Abdollahi, Amirabbas Shiravi, Hossein Khanahmad, Paniz Miar, Mehrdad Zeinalian
Publikováno v:
International Journal for Vitamin and Nutrition Research
Abstract. The widespread COVID-19 pandemic has been, currently, converted to a catastrophic human health challenge. Vitamin D (VD) and its metabolites have been used as a palliative treatment for chronic inflammatory and infectious diseases from anci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb1ea1e19b6f046b6836e37add7abe38