Zobrazeno 1 - 10
of 267
pro vyhledávání: '"Morteza Hashemzadeh"'
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 25, Iss 7, Pp 799-807 (2022)
Objective(s): The mechanisms underlying the beneficial effects of MSCs on hepatic I/R injury are still poorly described, especially the changes in hepatocyte gene expression. In this study, the effect of bone marrow-derived mesenchymal stem cells (BM
Externí odkaz:
https://doaj.org/article/e9c7c9888dcf4079b4f24c8d0e478825
Autor:
Ali Ahmadi, Majid Shirani, Arsalan Khaledifar, Morteza Hashemzadeh, Kamal Solati, Soleiman Kheiri, Mehraban Sadeghi, Abdollah Mohammadian-Hafshejani, Hadi Raeisi Shahraki, Alireza Asgharzadeh, Ali Zamen Salehifard, Masoumeh Mousavi, Elaheh Zarean, Reza Goujani, Seyed Saeed Hashemi Nazari, Hossein Poustchi, Pierre-Antoine Dugué
Publikováno v:
BMC Public Health, Vol 21, Iss 1, Pp 1-14 (2021)
Abstract Background Critical inter-provincial differences within Iran in the pattern of non-communicable diseases (NCDs) and difficulties inherent to identifying prevention methods to reduce mortality from NCDs have challenged the implementation of t
Externí odkaz:
https://doaj.org/article/8c363e01ebde472dbac24b10c1832b8b
Autor:
Somayeh Khatami, Masomeh Askari, Fatemeh Bahreini, Morteza Hashemzadeh-Chaleshtori, Saeed Hematian, Samira Asgharzade
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Abstract Background Clinical genetic diagnosis of non-syndromic hearing loss (NSHL) is quite challenging. With regard to its high heterogeneity as well as large size of some genes, it is also really difficult to detect causative mutations using tradi
Externí odkaz:
https://doaj.org/article/2c82a74a1b6e4c9198ce2666679245ff
Autor:
Ameneh Mehri-Ghahfarrokhi, Zahra Pourteymourfard-Tabrizi, Effat Farrokhi, Morteza Hashemzadeh Chaleshtori, Mohammad-Saeid Jami
Publikováno v:
Journal of Otology, Vol 14, Iss 4, Pp 121-127 (2019)
Auditory neuropathy is the particular form of deafness in humans which cannot be treated by replacement therapy. Human dental pulp stem cells (hDPSCs) are derived from an ectomesenchymal neural crest cell population. Therefore, they possess a promisi
Externí odkaz:
https://doaj.org/article/9338a30b2e7d43529075bb629c470c53
Publikováno v:
آب و فاضلاب, Vol 30, Iss 2, Pp 48-63 (2019)
In this research, hematite (α-Fe2O3) nanoparticles with novel surface- modified were synthesized using iron (III) chloride hexahydrate (FeCl3.6H2O) and oleic acid (C₁₈H₃₄O₂) as raw materials by hydrothermal method at 250°C. The structural
Externí odkaz:
https://doaj.org/article/d3b86f0f8feb4123a7358fc260f79bb4
Autor:
Arsalan Khaledifar, Morteza Hashemzadeh, Kamal Solati, Hosseion Poustchi, Valentina Bollati, Ali Ahmadi, Soleiman Kheiri, Keihan Ghatreh samani, Mehdi Banitalebi, Morteza Sedehi, Reza Malekzadeh
Publikováno v:
BMC Public Health, Vol 18, Iss 1, Pp 1-10 (2018)
Abstract Background Prospective cohort studies are considered ideal choices to study multiple outcomes and risk factors for Non-communicable diseases (NCDs). Our aim is to set-up the protocol and analyze risk factors, incidence rates, prevalence, tre
Externí odkaz:
https://doaj.org/article/2cf50eb0bc4f4c8e9c7179a2116cbf8d
Autor:
Mahtab Khosrofar, Mohammad Reza Pourreza, Samira Asgharzadeh, Parisa Tahmasebi, Elahe Ali Asgari, Reza Ghasemikhah, Nader Saki, Javad Mohammadi-asl, Morteza Hashemzadeh Chaleshtori, Mohammad Amin Tabatabaiefar
Publikováno v:
Majallah-i dānishgāh-i ̒ulūm-i pizishkī-i Arāk, Vol 20, Iss 3, Pp 31-38 (2017)
Abstract Background: Hearing loss (HL) is the most common congenital defect in humans. One or two in thousand newborn babies have prelingual hearing loss. Autosomal recessive non-syndromic hearing loss (ARNSHL) is the most common form of hereditary
Externí odkaz:
https://doaj.org/article/0b6436825bd847978cc57b11e4bf8bbf
Autor:
Mahbobeh KOOHIYAN, Somayeh REIISI, Fatemeh AZADEGAN-DEHKORDI, Mansoor SALEHI, Hamidreza ABTAHI, Morteza HASHEMZADEH-CHALESHTORI, Mohammad Reza NOORI-DALOII, Mohammad Amin TABATABAIEFAR
Publikováno v:
Iranian Journal of Public Health, Vol 48, Iss 9 (2019)
Background: Autosomal recessive non-syndromic hearing loss (ARNSHL), one of the global public health concerns, is marked by a high degree of genetic heterogeneity. The role of GJB2, as the most common cause of ARNSHL, is only
Externí odkaz:
https://doaj.org/article/9a816c0f7a2149e58a091c91566e75d1
Autor:
Somayeh Reiisi, Mohammad Amin Tabatabaiefar, Mohammad Hosein Sanati, Morteza Hashemzadeh Chaleshtori
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 19, Iss 7, Pp 772-778 (2016)
Objective(s): Non-syndromic sensorineural hearing loss (NSHL) is a common disorder affecting approximately 1 in 500 newborns. This type of hearing loss is extremely heterogeneous and includes over 100 loci. Mutations in the GJB2 gene have been implic
Externí odkaz:
https://doaj.org/article/ac64cd331f44480db0c7d94a0a1a9c8f
Autor:
Azam Pourahmadiyan, Mohammad Amin Tabatabaiefar, Somayeh Reiisi, Paria Alipour, Najmeh Fattahi, Morteza Hashemzadeh-Chaleshtori
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 34, Iss 374, Pp 214-220 (2016)
مقدمه: ناشنوایی حسی- عصبی، رایجترین ناهنجاری عصبی است که با میانگین 1 در 1000-500 نوزاد رخ میدهد. موارد غیر سندرمی، 70 درصد ناشنواییها را ش
Externí odkaz:
https://doaj.org/article/1b611da6347a4163a911526fb8086538