Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Erfan Heidari"'
Autor:
Ali Zare Dehnavi, Erfan Heidari, Maryam Rasulinezhad, Morteza Heidari, Mahmoud Reza Ashrafi, Mohammad Mahdi Hosseini, Fatemeh Sadeghzadeh, Mohammad-Sadegh Fallah, Noushin Rostampour, Amir Bahraini, Masoud Garshasbi, Ali Reza Tavasoli
Publikováno v:
Human Genomics, Vol 15, Iss 1, Pp 1-11 (2021)
Abstract Background Leukodystrophies are the main subgroup of inherited CNS white matter disorders which cause significant mortality and morbidity in early years of life. Diagnosis is mostly based on clinical context and neuroimaging findings; howeve
Externí odkaz:
https://doaj.org/article/11a6570647ec48b3b59482b202f47060
Autor:
Maryam Rasoulinezhad, Morteza Heidari, Masoud Garshasbi, Erfan Heidari, Ali Reza Tavasoli, Brenda Banwell, Neda Pak, Mahmoud Reza Ashrafi
Publikováno v:
Mitochondrion. 60:12-20
Complex III (CIII) is the third out of five mitochondrial respiratory chain complexes residing at the mitochondrial inner membrane. The assembly of 10 subunits encoded by nuclear DNA and one by mitochondrial DNA result in the functional CIII which tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cb9c07a943388e32187b2f733d1f8c6
https://doi.org/10.1016/j.mito.2021.07.001
https://doi.org/10.1016/j.mito.2021.07.001
Autor:
Ali Reza Tavasoli, Erfan Heidari, Stefano Romeo, Maryam Masoudi, Andrea Caddeo, Kiana Zarabadi, Masoud Garshasbi
Publikováno v:
Genomics. 112:4072-4077
The membrane bound O-acyltransferase domain-containing 7 (MBOAT7) gene codes for an enzyme involved in regulating arachidonic acid incorporation in lysophosphatidylinositol. Patients with homozygous nonsense mutations in MBOAT7 have intellectual disa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2207e07a4d79e847ca0eafd018e73f7
https://doi.org/10.1016/j.ygeno.2020.07.008
https://doi.org/10.1016/j.ygeno.2020.07.008
Autor:
Leila Mohammad Gholinia Sarpoli, Shohreh Zare-Karizi, Erfan Heidari, Akbar Hasanzadeh, Mehrdad Bayandori, Fereshteh Azedi, Michael R. Hamblin, Mahdi Karimi
Breast cancer is the second major cause of death worldwide among women. Co-delivery of anticancer drugs and nucleic acids targeting the apoptosis pathway could be a promising new approach. In the present study, we synthesized a novel nanostructure fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69bcdd4054b63ca532bb517a3d638ea6
Autor:
Maryam Rasulinezhad, Noushin Rostampour, Ali Zare Dehnavi, Morteza Heidari, Mahmoud Reza Ashrafi, Mohammad-Sadegh Fallah, Erfan Heidari, Mohammad Mahdi Hosseini, Ali Reza Tavasoli, Masoud Garshasbi, Fatemeh Sadeghzadeh, Amir Bahraini
Publikováno v:
Human Genomics, Vol 15, Iss 1, Pp 1-11 (2021)
Human Genomics
Human Genomics
Background Leukodystrophies are the main subgroup of inherited CNS white matter disorders which cause significant mortality and morbidity in early years of life. Diagnosis is mostly based on clinical context and neuroimaging findings; however, geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e5bb0cc3cf3a0654a40aee1d82e4222
https://doi.org/10.1186/s40246-021-00345-0
https://doi.org/10.1186/s40246-021-00345-0
Autor:
Morteza Heidari, Neda Pak, Masoud Garshasbi, Brenda Banwell, Erfan Heidari, Maryam Rasoulinezhad, Mahmoud Reza Ashrafi, Ali Reza Tavasoli
Background Complex III (CIII) is the third out of five mitochondrial respiratory chain complexes residing at the mitochondrial inner membrane. The assembly of 10 subunits encoded by nuclear DNA and one by mitochondrial DNA result in the functional CI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::127cee7df0ca221ba3e3338b6d866788
https://doi.org/10.21203/rs.3.rs-224767/v1
https://doi.org/10.21203/rs.3.rs-224767/v1
Autor:
Alexander N Harrison, Masoud Garshasbi, Ehsan Jafarinia, Ali Reza Tavasoli, Robert S. Molday, Navid Almadani, Erfan Heidari
Publikováno v:
Human mutationREFERENCES. 42(5)
ATP8A2 is a P4-ATPase that flips phosphatidylserine across membranes to generate and maintain transmembrane phospholipid asymmetry. Loss-of-function variants cause severe neurodegenerative and developmental disorders. We have identified three ATP8A2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6e57034a47ba88011869221d4cdb9fc
https://pubmed.ncbi.nlm.nih.gov/33565221
https://pubmed.ncbi.nlm.nih.gov/33565221
Publikováno v:
The Journal of Gene Medicine. 22
BACKGROUND The number of reported genes causing non-syndromic autosomal recessive intellectual disability (NS-ARID) is increasing. For example, mutations in the ST3GAL3 gene have been reported to be associated with NS-ARID. In the present study, we a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd6d67a778dddd70efda9e2456e8bd46
https://doi.org/10.1002/jgm.3253
https://doi.org/10.1002/jgm.3253
Publikováno v:
Annals of human geneticsREFERENCES. 84(4)
The human dopamine transporter (hDAT) participates in dopamine homeostasis by clearing dopamine from the extracellular space using secondary active transport. Dysregulation of hDAT has been reported to be associated with different neuropsychiatric di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ee26e6784ceffae98b2f3d90941e9c8
https://pubmed.ncbi.nlm.nih.gov/32077500
https://pubmed.ncbi.nlm.nih.gov/32077500
Autor:
Seyed Ataollah Sadat Shandiz, Sepideh Mohammadi, Erfan Heidari, Vahid Asgary, Hamidreza Jozaghkar, Reza Ahangari Cohan, Amir Mirzaie
Publikováno v:
Advanced Studies in Biology. 7:55-64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f637b528824e34cd3e135b143859325
https://doi.org/10.12988/asb.2015.41049
https://doi.org/10.12988/asb.2015.41049