Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Maliheh Alimardani"'
Autor:
Alireza Tafazoli, John Mikros, Faeze Khaghani, Maliheh Alimardani, Mahboobeh Rafigh, Mahboobeh Hemmati, Stavroula Siamoglou, Agnieszka Kitlas Golińska, Karol A. Kamiński, Magdalena Niemira, Wojciech Miltyk, George P. Patrinos
Publikováno v:
Human Genomics, Vol 17, Iss 1, Pp 1-14 (2023)
Abstract Background This pilot study aims to identify and functionally assess pharmacovariants in whole exome sequencing data. While detection of known variants has benefited from pharmacogenomic-dedicated bioinformatics tools before, in this paper w
Externí odkaz:
https://doaj.org/article/30b5f225f6ad48e983403cd9a312224c
Publikováno v:
Cancer Cell International, Vol 21, Iss 1, Pp 1-14 (2021)
Abstract Background Chemotherapy is one of the most common treatment options for breast cancer (BC) patients. However, about half of the BC patients are chemotherapeutic resistant. Doxorubicin (DOX) is considered as one of the first line drugs in the
Externí odkaz:
https://doaj.org/article/ac16e464f557470f9f44787d832fb671
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
Autor:
Amir Tajbakhsh, Maliheh Alimardani, Mahla Asghari, Soheila Abedini, Sohrab Saghafi Khadem, Abolfazl Nesaei Bajestani, Forough Alipoor, Maryam Alidoust, Amir Savardashtaki, Peyman Hashemian, Alireza Pasdar
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-10 (2021)
Abstract Background Genetic factors play an important role in susceptibility to methamphetamine dependency. In this line, protein that interact with C-kinase-1 (PICK1) and brain-derived neurotrophic factor (BDNF) genes are linked to methamphetamine d
Externí odkaz:
https://doaj.org/article/494c23ec26b944a49074bd89361602e5
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 16, Iss 6, Pp 784-789 (2013)
Objective(s): Recently we reported that the soybean 15-lipoxygenase (SLO) inhibitory activity of pyrimido[4,5-b][l,4]benzothiazines largely depends on the orientation of sulfur atom of thiazine core towards FeIII-OH in the active site pocket of the e
Externí odkaz:
https://doaj.org/article/ff843f6c054c4729925066c090d9ce85
Autor:
Toktam Dehghani, Esfehani, Reza Jafarzadeh, Maliheh Alimardani, Gholizadeh, Maryam, Hassibian, Sepideh, Sadr-Nabavi, Ariane, Abbaszadegan, Mohammad Reza, Saeid Eslami, Smart Phenotyping
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cde27eda1d30460d48fa6673df0b513f
Autor:
Sogand Chamanian, Mahnaz Ghorbani Farmad, Mohammad Reza Abbaszadegan, Maliheh Alimardani, Mohammad Mahdi Forghanifard
I. Background:Gastric cancer (GC) is ranked the third greatest cause of mortality globally and the second common cancer in Iran. To date, many pathways including HES family have been found to be linked to cellular proliferation, differentiation and c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::726c1f2a4558255d2803530847c66de2
https://doi.org/10.21203/rs.3.rs-857387/v1
https://doi.org/10.21203/rs.3.rs-857387/v1
Autor:
Mahsa Farjami, Alireza Esmaeilie, Arash Salmaninejad, Jamshid Motaee, Maliheh Alimardani, Alireza Pasdar
Publikováno v:
Ophthalmic Genetics. 40:393-402
Retinitis Pigmentosa (RP) is a major cause of heritable human blindness with a high genetic heterogeneity. It is characterized by the initial degeneration of rod photoreceptors followed by cone photoreceptors. RP is also a prominent reason of visual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5702a31ce8fcb7c987faaf0050596943
https://doi.org/10.1080/13816810.2019.1675178
https://doi.org/10.1080/13816810.2019.1675178
Autor:
Majid Mojarrad, Javad Chezgi, Maliheh Alimardani, Atieh Eslahi, Mashsa Farjami, Mahmoud Shekari Khaniani, Sima Mansoori Derakhshan, Mohsen Rajati Haghi, Seyed Mojtaba Hosseini
Publikováno v:
Fetal and Pediatric Pathology. 38:93-102
BACKGROUND Hearing loss (HL) is the most prevalent sensory disorder. The over 100 genes implicated in autosomal recessive nonsyndromic hearing loss (ARNSHL) makes it difficult to analyze and determine the accurate genetic causes of hearing loss. We s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10b312c9b6e0882c3220528a4ad6e58e
https://doi.org/10.1080/15513815.2018.1547336
https://doi.org/10.1080/15513815.2018.1547336
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