Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Behnaz ANDASHTI"'
Publikováno v:
Clinical Case Reports, Vol 11, Iss 5, Pp n/a-n/a (2023)
Key Clinical Message In 1‐year‐old girl presenting with neurodegenerative mitochondrial disease (Leigh syndrome), mutation analysis was performed by whole exome sequencing. Pathogenic variants were then analyzed in parents and relatives by Sanger
Externí odkaz:
https://doaj.org/article/ae4d4bdac848420080dfe9643426ba03
Publikováno v:
Acta Medica Iranica, Vol 60, Iss 12 (2023)
Inosine 5-monophosphate dehydrogenase 1 (IMPDH1) is the rate-limiting enzyme in the de novo purine nucleotide biosynthesis. IMPDH1 catalyzes IMP-oxidation to XMP, which in continue is converted to guanine nucleotides. Like mammals, the mouse IMPDH1 (
Externí odkaz:
https://doaj.org/article/5ffcfc221cfe4d309849448b36196761
Autor:
Parvin JOOLA, Behnaz ANDASHTI, Seyed Ahmad HOSSEINI, Seyedeh Maryam MOLAEI ZADEH, Nosrat BAHRAMI
Publikováno v:
Iranian Journal of Public Health, Vol 49, Iss 12 (2020)
No Abstract
Externí odkaz:
https://doaj.org/article/517eab8cda3741af921b06daeb2149ec
Autor:
Mojtaba Oraki Kohshour, Manijeh Afra, Abdolhossein Shakurnia, Nepton Emad Mostofi, Behnaz Andashti
Publikováno v:
Women’s Health Bulletin, Vol 5, Iss 4, Pp 1-3 (2018)
Background: Cervical cancer ranked as the most common cancer of women in developing countries. Human Papillomaviruses (HPVs) belongs to the Papillomaviridea family, which is able to infect humans. Some HPV types are the causes of getting cervix cance
Externí odkaz:
https://doaj.org/article/fbfe7448c96141d0b519aae59e0488c4
Publikováno v:
Microsoft Academic Graph
Datacite
Molecular and Cellular Biochemistry
Datacite
Molecular and Cellular Biochemistry
Mutations in the retinal inosine monophosphate dehydrogenase1 (IMPDH1) gene is believed to be one cause of retinitis pigmentosa (RP). The main structural difference between the mutation-susceptible retinal isoforms with canonical one resides in the C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98a881ef834fa5daf56c6c2061779117
http://link.springer.com/article/10.1007/s11010-019-03675-9/fulltext.html
http://link.springer.com/article/10.1007/s11010-019-03675-9/fulltext.html
Publikováno v:
Cell biochemistry and biophysics. 79(2)
Defects in inosine monophosphate dehydrogenase-1 (IMPDH1) lead to insufficient biosyntheses of purine nucleotides. In eyes, these defects are believed to cause retinitis pigmentosa (RP). Major retinal isoforms of IMPDH1 are structurally distinct from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c41886992fc793bea240965930388875
https://pubmed.ncbi.nlm.nih.gov/33733369
https://pubmed.ncbi.nlm.nih.gov/33733369
Autor:
Behnaz Andashti, Nepton Emad Mostofi, Abdolhossein Shakurnia, Manijeh Afra, Mojtaba Oraki Kohshour
Publikováno v:
Women’s Health Bulletin, Vol 5, Iss 4, Pp 1-3 (2018)
Background: Cervical cancer ranked as the most common cancer of women in developing countries. Human Papillomaviruses (HPVs) belongs to the Papillomaviridea family, which is able to infect humans. Some HPV types are the causes of getting cervix cance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83bc8bd2317edb344dcfa2ebc4c3d6fd
https://doi.org/10.5812/whb.67230
https://doi.org/10.5812/whb.67230
Publikováno v:
Clinical Case Reports
Key Clinical Message Megalencephalic leukoencephalopathy (MLC) is a rare neurological disorder with an autosomal recessive pattern. Clinical diagnosis was based on macrocephaly, recurrent seizure, and magnetic resonance imaging (MRI). Here we report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3097cc7d17701266f53ae5148e988940
https://doi.org/10.1002/ccr3.168
https://doi.org/10.1002/ccr3.168
Autor:
Mojtaba Oraki, Kohshour, Hamid, Galehdari, Ali Mohammad, Foroughmand, Behnaz, Andashti, Mohammad Ali, Jalalifar, Ali, Bidmeshkipour
Publikováno v:
Hepatitis Monthly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6bf42610b611e7aaf05c9010e342ac3a
https://pubmed.ncbi.nlm.nih.gov/22312388
https://pubmed.ncbi.nlm.nih.gov/22312388
Publikováno v:
Iranian journal of immunology : IJI. 4(2)
Perforin gene (PRF1) mutations have been reported in 20-30% of patients with familial hemophagocytic lymphohistiocytosis (FHL), an immune disorder of infancy and early childhood. Cytotoxic T and natural killer (NK) cell activities are remarkably redu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f78cb7fb4cb75f32c0a60298494a6fb2
https://pubmed.ncbi.nlm.nih.gov/17652853
https://pubmed.ncbi.nlm.nih.gov/17652853