Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mohsen Dibaj"'
Autor:
Zahra Rahmani, Mohammad Reza Fayyazi Bordbar, Mohsen Dibaj, Maliheh Alimardani, Meysam Moghbeli
Publikováno v:
Human Genomics, Vol 15, Iss 1, Pp 1-12 (2021)
Abstract Background Autism spectrum disorder (ASD) is a neurodevelopmental disease, characterized by impaired social communication, executive dysfunction, and abnormal perceptual processing. It is more frequent among males. All of these clinical mani
Externí odkaz:
https://doaj.org/article/a34d8a77bca14c9ba0337573dc00cf83
Publikováno v:
Metabolic Brain Disease. 37:2669-2675
Sandhoff disease is a rare neurodegenerative and autosomal recessive disorder, which is characterized by a defect in ganglioside metabolism. Also, it is caused by mutations in the HEXB gene for the β-subunit isoform 1 of β-N-acetyl hexosaminidase.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30a0869b91a9ada3a815bb99d764edf1
https://doi.org/10.1007/s11011-021-00669-9
https://doi.org/10.1007/s11011-021-00669-9
Autor:
Haidar Ranjbari, Masoud Dehghan Tezerjani, Fatemeh Sabaghi, Mohsen Dibaj, Abduladheem Turki Jalil, Mustafa M. Kadhim, Zinat Shams, Zeinab Karimi
Hepatoblastoma (HB) is a common pediatric hepatic tumor. Occurrence and progression of various malignancies are enhanced by abnormal competitive endogenous RNA (ceRNA) axes. Although, ceRNAs can be considered effective prognostic, diagnostic, and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dbdbf178e6edfb86729c6ee500113bf
https://doi.org/10.21203/rs.3.rs-1911511/v1
https://doi.org/10.21203/rs.3.rs-1911511/v1
Autor:
Mohsen Dibaj, Mohammad Reza Fayyazi Bordbar, Maliheh Alimardani, Meysam Moghbeli, Zahra Rahmani
Publikováno v:
Human Genomics
Human Genomics, Vol 15, Iss 1, Pp 1-12 (2021)
Human Genomics, Vol 15, Iss 1, Pp 1-12 (2021)
Background Autism spectrum disorder (ASD) is a neurodevelopmental disease, characterized by impaired social communication, executive dysfunction, and abnormal perceptual processing. It is more frequent among males. All of these clinical manifestation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d10f09be94c64255e55954d558f2303
http://europepmc.org/articles/PMC7953769
http://europepmc.org/articles/PMC7953769
Novel homozygous HEXB mutation identified in a consanguineous Iranian pedigree with Sandhoff disease
Background Sandhoff disease is a rare neurodegenerative and autosomal recessive disorder, characterized by a defect in ganglioside metabolism. It is caused by mutations in the HEXB gene for the β-subunit of β-N-acetyl hexosaminidase. Results In the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de4d528b3c1859cf2ba3a9072d87f0b1
https://doi.org/10.21203/rs.2.21720/v1
https://doi.org/10.21203/rs.2.21720/v1