Zobrazeno 1 - 10
of 279
pro vyhledávání: '"Sadr Nabavi, A"'
Autor:
Mohammad Shariati, Alireza Davoudi, Reza Boostani, Farah Ashrafzadeh, Mehran Beiraghi Toosi, Nafiseh Todarbary, Javad Akhondian, Narges Hashemi, Ariane Sadr-Nabavi
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-9 (2024)
Abstract Background Spinal muscular atrophy (SMA) is a group of motor neuron diseases. In 95% of SMA patients, the telomeric copy of the SMN gene (SMN1) is homozygously deleted. Due to the autosomal recessive pattern of SMA inheritance, individuals w
Externí odkaz:
https://doaj.org/article/9726dff5249c4ddba995677341c249bf
Autor:
Mohammad Reza Seyedtaghia, Mohammad Soudyab, Mohammad Shariati, Reza Jafarzadeh Esfehani, Shabnam Vafadar, Neda Shalaei, Vahid Nouri, Michael Zech, Julianne Winkelmann, Ali shoeibi, Ariane Sadr-Nabavi
Publikováno v:
Heliyon, Vol 9, Iss 4, Pp e15393- (2023)
Parkinson's disease (PD), a neurodegenerative disease characterized by both motor neuron and non-motor neuron symptoms, is the most frequent neurodegenerative disease after Alzheimer's disease. Both genetic and environmental factors take part in dise
Externí odkaz:
https://doaj.org/article/31a4b48ae4a1462ea37dd4e5ecf297b4
Autor:
Radmanesh, Hoda, Liu, Di, Geffers, Robert, Shandiz, Fatemeh Homaei, Sadr-Nabavi, Ariane, Hillemanns, Peter, Park-Simon, Tjoung-Won, Dörk, Thilo
Publikováno v:
In European Journal of Medical Genetics March 2022 65(3)
Autor:
Peyvandi Karizbodagh, Mostafa, Sadr-Nabavi, Ariane, Hami, Javad, Mohammadipour, Abbas, Khoshdel-Sarkarizi, Hoda, Kheradmand, Hamed, Fallahnezhad, Somaye, Mahmoudi, Mahmoud, Haghir, Hossein
Publikováno v:
In Neuropeptides October 2021 89
Autor:
Ariane Sadr-Nabavi, Samaneh Bouromand-Noughabi, Naser Tayebi-Meybodi, Kimia Dadkhah, Nafiseh Amini, Alfons Meindl, Mohammad Reza Abbaszadegan
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 24, Iss 4, Pp 444-450 (2021)
Objective(s): Dermatopontin (DPT) is an extracellular matrix protein that plays roles in increasing the activity of transforming growth factor-β (TGF-β) and induction of cell quiescence. These roles suggest a tumor suppressor function for DPT. This
Externí odkaz:
https://doaj.org/article/81405cd711f240d391cb34346b11d30e
Autor:
Mohammad Reza Seyyed taghia, Reza Jafarzadeh Esfehani, Reza Boostani, Mohammad Shariati, Ariane Sadr Nabavi
Publikováno v:
Reviews in Clinical Medicine, Vol 8, Iss 1, Pp 35-40 (2021)
Facioscapulohumeral muscular dystrophy is one of the most common musculoskeletal diseases with a considerable burden. Most of the affected individuals experience muscle weakness as the common muscular symptom. Despite the underlying genetic mechanism
Externí odkaz:
https://doaj.org/article/b0b7d3ffcea44b93a4ff20fab5d46689
Autor:
Abdolreza Malek, Tina Zeraati, Ariane Sadr-Nabavi, Niloofar Vakili, Mohammad Reza Abbaszadegan
Publikováno v:
Case Reports in Rheumatology, Vol 2022 (2022)
Familial Mediterranean fever (FMF) typically presents with recurrent attacks of fever and serosal inflammation with peritoneum, pleura, and synovium. We usually do not expect pericardial involvement at the early stages. FMF is an autoinflammatory dis
Externí odkaz:
https://doaj.org/article/fbdb37d01ce54625bbfbe6ea8ab75f51
Publikováno v:
International Journal of Preventive Medicine, Vol 13, Iss 1, Pp 6-6 (2022)
Relative internet search volumes (RSV) is now being consider as a measurement of awareness for most of the trending topics. During the recent coronavirus disease (COVID-19) outbreak, many researchers used the RSVs to interpret the population response
Externí odkaz:
https://doaj.org/article/79b19f92938d409d9b23752c78b34884
Autor:
Mohammad, Soudyab, Mohammad, Shariati, Reza Jafarzadeh, Esfehani, Neda, Shalaei, Shabnam, Vafadar, Vahid, Nouri, Michael, Zech, Julianne, Winkelmann, Ali, Shoeibi, Ariane, Sadr-Nabavi
Publikováno v:
Journal of Molecular Neuroscience. 72:2486-2496
Parkinson's disease (PD) is a common progressive neurodegenerative disorder with motor and nonmotor symptoms. Recent studies demonstrate various susceptibility loci and candidate genes for familial forms of the disease. However, the genetic basis of
Autor:
Reihaneh Shafieian, Maryam Moghaddam Matin, Amin Rahpeyma, Alireza Fazel, Hamideh Salari Sedigh, Ariane Sadr-Nabavi, Halimeh Hassanzadeh, Alireza Ebrahimzadeh-Bideskan
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 20, Iss 10, Pp 1131-1140 (2017)
Objective(s): Autologous bone transplantation known as the “gold standard” to reconstruction of osseous defects has known disadvantages. This study was designed to explore the effects of hydroxy-apatite/tricalcium-phosphate (HA/TCP) and platelet-
Externí odkaz:
https://doaj.org/article/587056eee51c41168f1db125bca849c6