Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Ali HOSSEINI-BERESHNEH"'
Autor:
Sedigheh KHEIRANDISH, Nosratollah ESHGHYAR, Farzad YAZDANI, Pouyan AMINI SHAKIB, Ali HOSSEINI-BERESHNEH, Zahra NOURI, Ali KHEIRANDISH, Fatemeh KARAMI
Publikováno v:
Iranian Journal of Public Health, Vol 49, Iss 10 (2020)
Background: Oral squamous cell carcinoma (OSCC) is one of the most important types of oral malignancies. DKK gene family members as well as DKK2/4 have critical roles in regulation of Wnt signaling as one of the main determining pathway in oral carci
Externí odkaz:
https://doaj.org/article/fe47690e016f4e34adaf1344042aab04
Autor:
Gholamreza Zamani, Sareh Hosseinpour, Mahmoud Reza Ashrafi, Mahmoud Mohammadi, Reza Shervin Badv, Ali Reza Tavasoli, Masood Ghahvechi Akbari, Ali Hosseini Bereshneh, Reza Azizi Malamiri, Morteza Heidari
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-9 (2022)
Abstract Background Duchenne muscular dystrophy (DMD) is the most common muscular dystrophy in the pediatric population. The manifestations of this disease include progressive muscle weakness, gait dysfunction, and motor impairment, leading to a loss
Externí odkaz:
https://doaj.org/article/46d808fb5a5f461bb7a8856d26dabd27
Autor:
Shadi Javan, Alireza Andalib, Ali Hosseini Bereshneh, Mohammad Hassan Emami, Rasul Salehi, Fatemeh Karami
Publikováno v:
Acta Medica Iranica, Pp 147-151 (2019)
Hereditary non-polyposis colorectal cancer (HNPCC) is the most frequent autosomal dominant predisposition for development of colorectal cancer (CRC) caused by germline defects in mismatch repair (MMR) genes. Current study was aimed to find genetic va
Externí odkaz:
https://doaj.org/article/8fe741ba44ef42028d365666a405e87b
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-9 (2018)
Abstract Background The neuronal ceroid lipofuscinoses are a group of neurodegenerative, lysosomal storage disorders. They are inherited as an autosomal recessive pattern with the exception of adult neuronal ceroid lipofuscinosis, which can be inheri
Externí odkaz:
https://doaj.org/article/bb1c0ccd4d58473baed8ae78bc32864a
Autor:
Ali Hosseini Bereshneh, Danesh Soltani, Negar Veisi, Mohammad Khademi, Mohammad Hossein Modarressi
Publikováno v:
Tehran University Medical Journal, Vol 74, Iss 9, Pp 607-613 (2016)
Breast cancer that is caused by the accumulation of genetic and epigenetic alterations, is one of the main causes of death resulted from cancer. Various therapeutic approaches have been introduced for this cancer and the traditional diagnosis and tre
Externí odkaz:
https://doaj.org/article/fca2869c18e5487b8ecc6d9d784ca91f
Publikováno v:
Tehran University Medical Journal, Vol 74, Iss 2, Pp 77-83 (2016)
Stem cells are undifferentiated and multi pluripotent cells which can differentiate into a variety of mature cells and tissues such as nervous tissue, muscle tissue, epithelial tissue, skeletal tissue and etc. Stem cells from all different source hav
Externí odkaz:
https://doaj.org/article/0ddb6c64c6b6448494b647d9dc14ba3a
Publikováno v:
Acta Medica Iranica, Vol 55, Iss 3 (2017)
Pancreatic cancer (PC) is a progressive, fatal disease with a high degree of malignancy. More than 40000 peoplediefrom this cancer annually in the United States. As a multifactorial condition, PC has a complex nature, and there are several genes and
Externí odkaz:
https://doaj.org/article/4d386f2b32f64fd4a5d59607dd93c0eb
Autor:
Ali Reza Tavasoli, Sayna Bagheri, Mahmoud Mohammadi, Gholamreza Zamani, Masood Ghahvechi Akbari, Reza Azizi Malamiri, Reza Shervin Badv, Kamyar Moradi, Mahmoud Reza Ashrafi, Ali Hosseini Bereshneh, Morteza Heidari
Publikováno v:
Journal of Molecular Neuroscience. 70:1565-1573
Mutations in the dystrophin gene could cause Duchenne muscular dystrophy (DMD), which is the most common muscular disorder in pediatrics. Considering the growing evidence on appropriateness of gene therapies for DMD, precise genetic diagnosis seems e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d9934e9a10cab5d2260a6bc2e268e57
https://doi.org/10.1007/s12031-020-01594-9
https://doi.org/10.1007/s12031-020-01594-9
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-6 (2022)
BMC Pediatrics
BMC Pediatrics
Background Desbuquois dysplasia type 2 (DBQD2) is an infrequent dysplasia with a wide range of symptoms, including facial deformities, growth retardation and short long bones. It is an autosomal recessive disorder caused by mutations in the XYLT1 gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bced2f3fe9cd3072ec4d38f78c63198
https://doi.org/10.1186/s12887-022-03132-5
https://doi.org/10.1186/s12887-022-03132-5
Autor:
Mohamad Paktinat, Hamid Nemati, Soroor Inaloo, Pegah Katibeh, Kamran Hessami, Ali Hosseini Bereshneh, Mohammad Hassan Darabi, Marzieh Nejabat
Publikováno v:
International Journal of Pediatrics
International Journal of Pediatrics, Vol 2021 (2021)
International Journal of Pediatrics, Vol 2021 (2021)
Introduction. Acute necrotizing encephalopathy (ANE), a rare entity with unique clinical presentation, can be associated significant morbidity and mortality. The majority of ANE reported cases are sporadic. However, reports of extremely rare familial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::940694d9fd04a05839d27fb91f5e5c22
http://europepmc.org/articles/PMC7981175
http://europepmc.org/articles/PMC7981175