Zobrazeno 1 - 10
of 240
pro vyhledávání: '"Hamid GALEHDARI"'
Autor:
Rezvan Zabihi, Mina Zamani, Majid Aminzadeh, Niloofar Chamanrou, Fatemeh Zahra Kiani, Tahere Seifi, Jawaher Zeighami, Tahere Yadegari, Alireza Sedaghat, Alihossein Saberi, Mohammad Hamid, Gholamreza Shariati, Hamid Galehdari
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Introduction: Mucopolysaccharidoses are a group of lysosomal storage disorders that include seven types that are classified based on the enzymes that are disrupted. Malfunction of these enzymes leads to the accumulation of glycosaminoglycans (GAGs) i
Externí odkaz:
https://doaj.org/article/10be7dec0c684c42be05458add309a27
Autor:
Fatemeh Yaghoobizadeh, Mohammad Roayaei Ardakani, Mohammad Mehdi Ranjbar, Mohammad Khosravi, Hamid Galehdari
Publikováno v:
Advanced Pharmaceutical Bulletin, Vol 13, Iss 3, Pp 563-572 (2023)
Purpose: Among all known human coronaviruses, some viruses (e.g., SARS-CoV-2) cause severe pneumonia or even death. With the regard to its spread and the importance of its rapid identification/treatment, and because pAbs are relatively cheap, able to
Externí odkaz:
https://doaj.org/article/e4120284e9aa4887a4bb39319d7c619a
Autor:
Mogge Hajiesmaeil, Francesco Ravasini, Flavia Risi, Giorgia Magnarini, Anna Olivieri, Eugenia D’Atanasio, Hamid Galehdari, Beniamino Trombetta, Fulvio Cruciani
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract The ampliconic region of the human Y chromosome consists of large duplicated sequences that can undergo non-allelic homologous recombination (NAHR), resulting in structural rearrangements that may cause infertility, especially when they occu
Externí odkaz:
https://doaj.org/article/31ba1a4b2dfc47e1b2d7d81d30e8f8fe
Autor:
Rauan Kaiyrzhanov, Maha S. Zaki, Tracy Lau, Sambuddha Sen, Reza Azizimalamiri, Mina Zamani, Gözde Yeşil Sayin, Taru Hilander, Stephanie Efthymiou, Viorica Chelban, Ruth Brown, Kyle Thompson, Maria Irene Scarano, Jaya Ganesh, Kairgali Koneev, Ismail Musab Gülaçar, Richard Person, Dinara Sadykova, Yerdan Maidyrov, Tahereh Seifi, Aizhan Zadagali, Geneviève Bernard, Katrina Allis, Houda Zghal Elloumi, Amanda Lindy, Ehsan Taghiabadi, Sumit Verma, Rachel Logan, Brian Kirmse, Renkui Bai, Shaimaa M. Khalaf, Mohamed S. Abdel‐Hamid, Alireza Sedaghat, Gholamreza Shariati, Mahmoud Issa, Jawaher Zeighami, Hasnaa M. Elbendary, Garry Brown, Robert W. Taylor, Hamid Galehdari, Joseph J. Gleeson, Christopher J. Carroll, James A. Cowan, Andres Moreno‐De‐Luca, Henry Houlden, Reza Maroofian
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 9, Iss 12, Pp 2025-2035 (2022)
Abstract Bi‐allelic variants in Iron–Sulfur Cluster Scaffold (NFU1) have previously been associated with multiple mitochondrial dysfunctions syndrome 1 (MMDS1) characterized by early‐onset rapidly fatal leukoencephalopathy. We report 19 affecte
Externí odkaz:
https://doaj.org/article/711cfaa4bbdd40c88cf90df5e876adc6
Publikováno v:
Journal of Current Oncology and Medical Sciences, Vol 2, Iss 3, Pp 249-256 (2022)
Introduction: The risk factors for the metallothionein (MT) polymorphism in concentrations of heavy metals, especially mercury, in the blood are subject to several confounding factors, including differences in the ethnicity of the population analyzed
Externí odkaz:
https://doaj.org/article/5e831b307ced45bbba368abcf003167f
Autor:
Amir Jalali, Masoud Mahdavinia, Hamid Galehdari, Masoumeh Baradaran, Davood Valdi-Biranvand, Maryam Naderi Soorki
Publikováno v:
Pharmaceutical and Biomedical Research, Vol 8, Iss 3, Pp 199-204 (2022)
Background: The venom peptides from the scorpion fauna of Iran have been poorly characterized so far. Objectives: In this study, we identified a cDNA encoding of an anionic cysteine-free antimicrobial peptide from the Iranian yellow scorpion odontobu
Externí odkaz:
https://doaj.org/article/1cbee8b88d3048e4975d767a1db69943
Publikováno v:
International Journal of Reproductive BioMedicine, Vol 18, Iss 7, Pp 561-568 (2022)
Abstract Background: Preimplantation genetic diagnosis (PGD) has been used as an option for couples with the possibility of having a baby with a genetic disorder. The common method for performing this test involves isolating 1 cell from day 3 or a fe
Externí odkaz:
https://doaj.org/article/a523fdc0e21e4d7da53ba1a2c3250f95
Publikováno v:
Basic and Clinical Neuroscience, Vol 13, Iss 3, Pp 315-324 (2022)
Introduction: Sialic acid is pivotal in various critical physiological events at molecular and cellular levels and pathological processes. Changes in sialic acid concentration are observed in many pathological processes; for example, some available d
Externí odkaz:
https://doaj.org/article/545c52d64f7843529b7dc6f7b6369137
Autor:
Mohammad Hamid, Bijan keikhaei, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Gholamreza Shariati, Marziye Mohammadi-Anaei
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-7 (2022)
Abstract We studied the alpha-globin gene genotypes, hematologic values, and transfusion-dependence of patients with Hb H disease. Molecular characterization of alpha-thalassemia was performed. We identified 120 patients with Hb H disease. Of these p
Externí odkaz:
https://doaj.org/article/705c41e1ec984ca0873e9ba140e7c232
Autor:
Atefe Papi, Mina Zamani, Gholamreza Shariati, Alireza Sedaghat, Tahere Seifi, Samira Negahdari, Sahar Sadat Sedighzadeh, Jawaher Zeighami, Alihossein Saberi, Mohammad Hamid, Hamid Galehdari
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Background Congenital disorder of glycosylation (CDG) and Glycogen storage diseases (GSDs) are inborn metabolic disorders caused by defects in some metabolic pathways. These disorders are a heterogeneous group of diseases caused by impaired
Externí odkaz:
https://doaj.org/article/e7160f880c5e4592936d54159ff4662d