Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Pegah Ghandil"'
Publikováno v:
International Journal of Reproductive BioMedicine, Vol 22, Iss 2, Pp 127-138 (2024)
Abstract Background: Cytogenetics and association studies showed that folate gene polymorphisms can increase the risk of chromosomal nondisjunction and aneuploidies. The folate-metabolizing gene polymorphisms in Down syndrome mothers (DSM) have been
Externí odkaz:
https://doaj.org/article/5505900c8ce3485f9968a888f11bff67
Publikováno v:
BMC Psychiatry, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Antipsychotic drugs are the first line of treatment in schizophrenia; although antipsychotic responses indicate a wide interindividual variety in patients with schizophrenia. This study aimed to investigate the association between four polym
Externí odkaz:
https://doaj.org/article/717dab555d4e429695ab61e82b11958a
Publikováno v:
Archives of Medical Science, Vol 17, Iss 6, Pp 1722-1729 (2020)
Introduction Type 2 diabetes mellitus (T2DM) is known as one of the most common metabolic diseases and FTO polymorphism has been implicated in the susceptibility to this disease. Epigallocatechin-3-gallate (EGCG) has shown favorable effects on risk f
Externí odkaz:
https://doaj.org/article/a4b18910ddac4d2ca21764a6b12a6dc6
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 96, Iss 1, Pp 60-65 (2020)
Objective: Permanent hypoparathyroidism can be presented as part of genetic disorders such as Sanjad–Sakati syndrome (also known as hypoparathyroidism—intellectual disability‐dysmorphism), which is a rare autosomal recessive disorder. Our aim w
Externí odkaz:
https://doaj.org/article/2f3fa6b3819841979a2fe60ad262b4bf
Autor:
Karina S. Gobin, Mary Hintermeyer, Bertrand Boisson, Maya Chrabieh, Pegah Ghandil, Anne Puel, Capucine Picard, Jean-Laurent Casanova, John Routes, James Verbsky
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2018)
Externí odkaz:
https://doaj.org/article/2aae71bec1a7472aa4d5bc71054c8c0a
Autor:
Karina Gobin, Mary Hintermeyer, Bertrand Boisson, Maya Chrabieh, Pegah Ghandil, Anne Puel, Capucine Picard, Jean-Laurent Casanova, John Routes, James Verbsky
Publikováno v:
Frontiers in Pediatrics, Vol 5 (2017)
Primary immunodeficiencies are genetic defects of the innate or adaptive immune system, resulting in a propensity to infections. The innate immune system is the first line of defense against pathogens and is critical to recognize microbes and start t
Externí odkaz:
https://doaj.org/article/380d29f06ca44482ba701588ff9d7569
Autor:
Sevana Daneghian, Reza Amani, Seyed Ahmad Hosseini, Pegah Ghandil, Afshar Jafari, Amal Saki Malehi
Publikováno v:
Journal of Research in Medical Sciences, Vol 24, Iss 1, Pp 37-37 (2019)
Background: The aim of the present study was to evaluate the effect of natural antioxidant formula (blend of herbs: ginger root, cinnamon bark and raw almond fruit powder, rosemary leaf powder, and honey) on oxidative status, antioxidant enzyme activ
Externí odkaz:
https://doaj.org/article/f978b6ccd2ad473aa3e65e43b7096bb4
Publikováno v:
Immunology and Genetics Journal.
Both innate and adaptive arms of immune system play role in tumor development. Moreover, genetic and epigenetic alterations, widely demonstrated in cancer cells, result in disturbances in molecular pathways regulating cell growth, survival, and metas
Autor:
Malihe Mohamadian, Ata Ghadiri, Mandana Rastegar, Pegah Ghandil, Mohsen Naseri, Negin Pasamanesh
Publikováno v:
Journal of Molecular Neuroscience. 72:9-23
Muscular dystrophies encompass a wide and heterogeneous subset of hereditary myopathies that manifest by the structural or functional abnormalities in the skeletal muscle. Some pathogenic mutations induce a dysfunction or loss of proteins that are cr
Autor:
Zahra Roshanizadeh, Ahmadi Angali Kambiz, Heshmatollah Tavakol, Pegah Ghandil, Ata Ghadiri, Ali Khodadadi
Publikováno v:
Nucleosides, Nucleotides & Nucleic Acids. 40:914-925
Asthma is a heterogeneous chronic pulmonary disease that develops due to the interaction of genetic and environmental factors. This study aimed to investigate the polymorphisms of CTLA4(SNP-318C > T, SNP + 49A > G) and FCeRIα(SNP-344T > C) genes in