Zobrazeno 1 - 10
of 182
pro vyhledávání: '"Mansoor Salehi"'
Autor:
Hengameh Mozaffarizadeh, Fariborz Mokarian, Mansoor Salehi, Seyyed Mohammad Reza Hakimian, Elham Moazam, Amirmohammad Amoozadehsamakoosh, Majid Hosseinzadeh, Mahdieh Behnam, Mohaddeseh Behjati, Alma Naseri, Marzieh Lotfi, Fatemeh Tohidi
Publikováno v:
Global Medical Genetics, Vol 11, Iss 01, Pp 069-075 (2024)
Background In addition to its multifaceted physiological functions, vitamin D is recognized for its protective role against cancer. To manifest its effects, vitamin D engages with the vitamin D receptor (VDR) gene responsible for its encoding. Invest
Externí odkaz:
https://doaj.org/article/e1a0b3433ca34d23a0a822c691c5df77
Autor:
Sara Saffar, Mojtaba Baktashian, Seyed Mohammad Hashemi, Hamideh Ghazizadeh, Zeynab Naserifr, Mohsen Moohebati, Hafezeh Davari, Maryam Saberi-Karimian, Roohollah Monsoori, Mahmoud Ebrahimi, Habibollah Esmaily, Mansoor Salehi, Gordon A. Ferns, Alireza Pasdar, Majid Ghayour-Mobarhan
Publikováno v:
Journal of Cardio-Thoracic Medicine, Vol 11, Iss 2, Pp 1159-1166 (2023)
Introduction : It has been shown that angioplasty and endovascular stent deployment, used after coronary revascularization, are associated with an inflammatory response. Inflammation has a key role in the complications of atherosclerotic plaque, coro
Externí odkaz:
https://doaj.org/article/c4ac9ff200ab47bb842c8794d280222b
Autor:
Negar Nouri, Valiollah Mehrzad, Zahra Khalaj, Erfan Zaker, Fateme Zare, Elham Abbasi, Maede Khosravi, Seyed Mehdi Kalantar, Mansoor Salehi
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 24, Iss 1, Pp 1-7 (2023)
Abstract Background Chronic myeloid leukemia (CML) is a multifactorial clonal myeloid neoplasm that mainly arises from the Philadelphia chromosome. Even though imatinib mesylate (IM) is considered the gold standard for first-line treatment, a number
Externí odkaz:
https://doaj.org/article/90e8ed56cebd4f17ae7c3ef3484ab566
Autor:
Mohammad Abdolvand, Zahra Mohammadi Chermahini, Sahar Bahaloo, Mohammad Hassan Emami, Alireza Fahim, Hojjatolah Rahimi, Elham Amjadi, Fatemeh Maghool, Fattah Rohani, Mina Dadkhah, Nooshin Farhadian, Nasimeh Vatandoust, Shirin Abdolvand, Maliheh Roozbahani Darehsari, Mohammad Chehelgerdi, Faeze Ahmadi Beni, Mahsa Khodadoostan, Simin Hemati, Mansoor Salehi
Publikováno v:
Journal of Research in Medical Sciences, Vol 29, Iss 1, Pp 10-10 (2024)
Background: Cancer development is aided by the role of long noncoding RNAs (lncRNAs) that act as competing endogenous RNAs (ceRNAs) absorbing microRNAs (miRNAs). We aimed to discover a novel regulatory axis in colorectal cancer (CRC) and potential bi
Externí odkaz:
https://doaj.org/article/f80c086baff1438fbd26f4a7c863d468
Autor:
Zahra Mohammadi Chermahini, Mansoor Salehi, Alaleh Gheissari, Faeze Ahmadi Beni, Farinaz Khosravian, Mohammad Kazemi
Publikováno v:
Advanced Biomedical Research, Vol 13, Iss 1, Pp 2-2 (2024)
Background: Nephropathic cystinosis (NC) is an uncommon autosomal recessive disease with abnormality in lysosomal storage that appearances in patients with mutations in the CTNS gene encoding a lysosomal transporter cystinosin. Disrupted function of
Externí odkaz:
https://doaj.org/article/11a926a92fd6422a8a4ecc229a058cbb
Autor:
Nasrin Hadi, Seyed Morteza Seifati, Behnaz Nateghi, Parisa Ravaghi, Farinaz Khosravian, Faezeh Namazi, Maryam Fotouhi Firouzabad, Vahid Shaygannejad, Mansoor Salehi
Publikováno v:
Cell Journal, Vol 24, Iss 7, Pp 403-409 (2022)
Objective: Multiple sclerosis (MS) is a complex multifactorial neuro-inflammatory disorder. This complexity arises from the evidence suggesting that MS is developed by interacting with environmental and genetic factors. This study aimed to evaluate t
Externí odkaz:
https://doaj.org/article/a1f99ab95ce64559b68ddf047b77836e
Publikováno v:
Journal of Epigenetics, Vol 3, Iss 1, Pp 1-6 (2022)
Background and Aim: Retinitis pigmentosa (RP) is the most common type of inherited progressive photoreceptor cells degeneration causing night blindness, progressive reduction of visual field, loss of retinal pigment epithelial function, and ultimatel
Externí odkaz:
https://doaj.org/article/85a9cb3d15e04ba6a914e5f06eda6a0f
Autor:
Hamidreza Mianesaz, Safoura Ghalamkari, Mansoor Salehi, Mahdiyeh Behnam, Majid Hosseinzadeh, Keivan Basiri, Majid Ghasemi, Maryam Sedghi, Behnaz Ansari
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Background Limb‐girdle muscular dystrophy (LGMD) is a non‐syndromic muscular dystrophy caused by variations in the genes involved in muscle structure, function and repair. The heterogeneity in the severity, progression, age of onset, and
Externí odkaz:
https://doaj.org/article/d474172c545b4bdaa3846f360e4c73ba
Autor:
Seyyed Reza Mousavi, Maryam Sadat Sajjadi, Farinaz Khosravian, Sara Feizbakhshan, Sharareh Salmanizadeh, Zahra Taherian Esfahani, Faeze Ahmadi Beni, Ameneh Arab, Mohammad Kazemi, Kiana Shahzamani, Ramin Sami, Majid Hosseinzadeh, Mansoor Salehi, Hajie Lotfi
Publikováno v:
BMC Research Notes, Vol 14, Iss 1, Pp 1-7 (2021)
Abstract Objective Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the novel coronavirus causing severe respiratory illness (COVID-19). This virus was initially identified in Wuhan city, a populated area of the Hubei province in China
Externí odkaz:
https://doaj.org/article/0acce0092dbf444286e3d45424c986f6
Autor:
Sajad Rafiee Komachali, Zakieh Siahpoosh, Sara Rafiee Komachali, Dor Mohammad Kordi Tamandani, Mansoor Salehi
Publikováno v:
European Journal of Biological Research, Vol 12, Iss 4 (2022)
Propionic acidemia (PROP) is an autosomal recessive inherited metabolic deficiency caused by multimeric mitochondrial enzyme propionyl‐coenzyme A (CoA) carboxylase (PCC). PCC enzyme contains a and b subunits, encoded by the PCCA and PCCB genes that
Externí odkaz:
https://doaj.org/article/55e0668c5d1043a6986d70bb1c0f9351