Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Parvaneh, Keshavarz"'
Publikováno v:
Journal of BioScience and Biotechnology, Vol 10, Iss 2, Pp 75-80 (2021)
Gastric cancer is one of the most common malignancies worldwide and it is the fourth leading cause of cancer-related death. Staphylococcus aureus enterotoxin A (SEA) is one of the toxins affecting the expression of apoptotic-related genes. The aim of
Externí odkaz:
https://doaj.org/article/f110a01ba95b4bd9b583ad96e8129b92
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 5, Iss 4, Pp 168-174 (2019)
Background: Addiction is a polygenic disorder caused by genetic and environmental factors. The opioid material can act as an epigenetic element, like DNA methylation. Objectives: The present study aimed to examine the effect of epigenetic drugs such
Externí odkaz:
https://doaj.org/article/ed99dcecb4ea48eba24b3c21724a0d8a
Publikováno v:
Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, Vol 27, Iss 6, Pp 1677-1685 (2019)
Introduction: Breast cancer is one of the most prevalent malignancies among women. Patients whose suffering from this condition, as a result of the use of conventional therapies often have a poor response to treatment and the relapse among them is fr
Externí odkaz:
https://doaj.org/article/26d78fb50a664bcf88161bb115031040
Autor:
Aghil Esmaeili-Bandboni, Arash Davoudi, Forozan Milani, Sara Afzali, Alireza Sharafshah, Fereshteh Fallahabadi, Parvaneh Keshavarz
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 5, Iss 1, Pp 41-47 (2019)
Background: The common causes of 18p deletion syndrome are spontaneous errors in the chromosomal structure in the early stages of human embryonic development. Clinical Presentation and Intervention: In this study, a 29-year-old girl was introduced wi
Externí odkaz:
https://doaj.org/article/37933adebf8e42f9894317bcadfb8542
Publikováno v:
Biochemical Genetics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b25fbc7824067f658ddcc0fb3a62b8d
https://doi.org/10.1007/s10528-023-10402-z
https://doi.org/10.1007/s10528-023-10402-z
Publikováno v:
Nucleosides, Nucleotides & Nucleic Acids. 41:841-850
The association between methylation of MAOA gene promoter and alcohol and nicotine dependence has been demonstrated in women but not in men yet. Antisocial personality disorder (ASPD) and substance use disorders (SUD) are two types of disorders that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77494303f7f800227750498c6c8357ad
https://doi.org/10.1080/15257770.2022.2085291
https://doi.org/10.1080/15257770.2022.2085291
Autor:
Ehsan Kazemnejad-Leili, Sajjad Rezaei, Mozaffar Hosseini-Nejad, Babak Bakhshayesh-Eghbali, Alia Saberi, Parvaneh Keshavarz
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 2, Iss 4, Pp 18-28 (2016)
Background: The National Institutes of Health Stroke Scale (NIHSS) can objectively quantify the severity of stroke. However no information is available about psychometric properties and it’s applicability in the Iranian population. Objectives: The
Externí odkaz:
https://doaj.org/article/b014cc6efd0645e6be280e56ab756a9c
Publikováno v:
Journal of autism and developmental disorders.
Autism spectrum disorders (ASDs) are described as generalized developmental disorders, with an average age of onset of 36 months. Genetic and environmental factors may contribute to this multifactorial disorder. The present study aimed to investigate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dec6177c04797df24f0ee21dbb4ea4d
https://pubmed.ncbi.nlm.nih.gov/36399225
https://pubmed.ncbi.nlm.nih.gov/36399225
Publikováno v:
Journal of Molecular Neuroscience. 71:1301-1305
Twins studies indicate that many individual factors are associated with genetic polymorphisms in tobacco use, dependence vulnerability, and the ability to quit smoking. Opioid receptor delta-type 1 (OPRD1) is one of the most important genes in the op
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b709ea25a0c15f8a4415d8f9d4cd9374
https://doi.org/10.1007/s12031-020-01757-8
https://doi.org/10.1007/s12031-020-01757-8
Autor:
Shohre Zare Karizi, Gholamreza Javadi, Nadia Mirzaei Gisomi, Parvaneh Keshavarz, Mohammad Miryounesi
Publikováno v:
Transfusion Clinique et Biologique. 27:243-252
Objective Invasive biopsy during the pregnancy is associated with an abortion risk of approximately 1% for the fetus. Free fetal DNA in maternal plasma is an excellent source of genetic material for prenatal molecular diagnoses. This study was conduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38e60900a1a6656b88d1f9d34fdb5aa6
https://doi.org/10.1016/j.tracli.2020.05.003
https://doi.org/10.1016/j.tracli.2020.05.003