Zobrazeno 1 - 10
of 335
pro vyhledávání: '"Mohammad Amin"'
Autor:
Zahra Nouri, Akram Sarmadi, Sina Narrei, Hamidreza Kianersi, Farzan Kianersi, Mohammad Amin Tabatabaiefar
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Background Autosomal recessive non-syndromic hearing loss (NSHL) and cone dystrophies (CODs) are highly genetically and phenotypically heterogeneous disorders. In this study, we applied the whole exome sequencing (WES) to find the cause of H
Externí odkaz:
https://doaj.org/article/0953796e171344b2b31b2ac8dbdb4ba3
Autor:
Atefeh Mir, Yongjun Song, Hane Lee, Hossein Khanahmad, Erfan Khorram, Jafar Nasiri, Mohammad Amin Tabatabaiefar
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-20 (2023)
Abstract Aim and Objective Intellectual disability (ID) is a heterogeneous condition affecting brain development, function, and/or structure. The X-linked mode of inheritance of ID (X-linked intellectual disability; XLID) has a prevalence of 1 out of
Externí odkaz:
https://doaj.org/article/f0e24bdf599b49d89ab47fdc8095f7fc
Autor:
Ahmad Daneshi, Masoud Garshasbi, Mohammad Farhadi, Khalil Ghasemi Falavarjani, Mohammad Vafaee-Shahi, Navid Almadani, MohammadSina Zabihi, Mohammad Amin Ghalavand, Masoumeh Falah
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-22 (2023)
Abstract Background Mutations in ABHD12 (OMIM: 613,599) are associated with polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract (PHARC) syndrome (OMIM: 612674), which is a rare autosomal recessive neurodegenerative disease. PHARC
Externí odkaz:
https://doaj.org/article/3d3039bb6e094fa08737ec43ea18b442
Autor:
Maryam Alidoust, Leila Hamzehzadeh, Asma Khorshid Shamshiri, Fahimeh Afzaljavan, Mohammad Amin Kerachian, Azar Fanipakdel, Seyed Amir Aledavood, Abolghasem Allahyari, Alireza Bari, Hooman Moosanen Mozaffari, Ladan Goshayeshi, Alireza Pasdar
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-9 (2022)
Abstract Purpose Colorectal cancer (CRC) is one of the common cancers with a high mortality rate worldwide. In Iran, there has been a trend of increased incidence of colorectal cancer in the last three decades that necessitates the early diagnosis. G
Externí odkaz:
https://doaj.org/article/1dbf287a066b4533a16076b63c7ee439
Autor:
Alireza Almasi Nokiani, Razieh Shahnazari, Mohammad Amin Abbasi, Farshad Ddivsalar, Marzieh Bayazidi, Azadeh Sadatnaseri
Publikováno v:
Caspian Journal of Internal Medicine, Vol 13, Iss Covid 19 Supplement 2, Pp 228-235 (2022)
Background: lung involvement in COVID-19 can be quantified by chest CT scan. We evaluated the triage and prognostication performance of seven proposed CT-severity score (CTSS) systems in two age groups of ≥65 and
Externí odkaz:
https://doaj.org/article/a2ab554859e447a6985c8a968434b99e
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-8 (2021)
Abstract Background The incidence of colorectal cancer (CRC) has increased during recent years in Iran and other developing countries. Clinical studies suggest that essential folate dietary intake and moderate deficiency of methylenetetrahydrofolate
Externí odkaz:
https://doaj.org/article/c78c0df8827c44eb88023e9299b013f3
Publikováno v:
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-16 (2020)
Abstract Background Colon adenocarcinoma (COAD) is one of the most common gastrointestinal cancers globally. Molecular aberrations of tumor suppressors and/or oncogenes are the main contributors to tumorigenesis. However, the exact underlying mechani
Externí odkaz:
https://doaj.org/article/a845c54b9bd346c7a0c0abe93fe0dc6c
Autor:
Akram Sarmadi, Samane Nasrniya, Maryam Soleimani Farsani, Sina Narrei, Zahra Nouri, Mahsa Sepehrnejad, Mohammad Hussein Nilforoush, Hamidreza Abtahi, Mohammad Amin Tabatabaiefar
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
Abstract Background Hearing loss (HL) is the most common sensorineural disorder with high phenotypic and genotypic heterogeneity, which negatively affects life quality. Autosomal recessive non-syndromic hearing loss (ARNSHL) constitutes a major share
Externí odkaz:
https://doaj.org/article/ce1312576bd5452a99c0ba2fb0d30240
Autor:
Maryam Sobhani, Mohammad Amin Tabatabaiefar, Soudeh Ghafouri-Fard, Asadollah Rajab, Asal Hojjat, Abdol-Mohammad Kajbafzadeh, Mohammad Reza Noori-Daloii
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background Mutations of the WFS1 gene are responsible for most cases of Wolfram syndrome (WS), a rare, recessively inherited neurodegenerative disorder characterized by juvenile-onset non-autoimmune diabetes mellitus and optic atrophy. Varia
Externí odkaz:
https://doaj.org/article/e01e790777cd4e7c96d523ef362d7652
Autor:
Samaneh Mollazadeh, Bibi Sedigheh Fazly Bazzaz, Vajiheh Neshati, Antoine A. F. de Vries, Hojjat Naderi-Meshkin, Majid Mojarad, Mahdi Mirahmadi, Zeinab Neshati, Mohammad Amin Kerachian
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-10 (2019)
Abstract Background Mesenchymal stem cells (MSCs) are attractive choices in regenerative medicine and can be genetically modified to obtain better results in therapeutics. Bone development and metabolism are controlled by various factors including mi
Externí odkaz:
https://doaj.org/article/0fe8757b83c94498954a53b04fdee079