Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Parham Nejati"'
Autor:
Parham Nejati, Saba Naseri, Maryam Eini, Reza Alibakhshi, Sousan Mahmoudi, Lida Haghnazari, Nazanin Jalilian
Publikováno v:
Journal of Mazandaran University of Medical Sciences, Vol 33, Iss 219, Pp 16-26 (2023)
Background and purpose: Hypertension is a global health challenge due to its high prevalence and increased risk of cardiovascular disease. It is a multifactorial disease in which both genetic and environmental factors are involved. So far, a number o
Externí odkaz:
https://doaj.org/article/f7de717c883b498dafdc72c3666ff1d1
Publikováno v:
Journal of Human Reproductive Sciences, Vol 13, Iss 3, Pp 216-220 (2020)
Objectives: Recurrent pregnancy loss (RPL) is a serious complication of pregnancies, affecting almost 2%–5% of couples. Among numerous underlying causes, chromosomal anomalies in one of the partners are regarded as important issues, with varying fr
Externí odkaz:
https://doaj.org/article/20fa5f66b02e488e9758509ef33e4abd
Publikováno v:
Iranian Journal of Immunology, Vol 14, Iss 3, Pp 231-239 (2017)
Background: Multiple sclerosis (MS), as a multifactorial autoimmune disease with complex genetic basis, causes demyelination in the central nervous system via cytokine responses to myelin antigens. Myelin basic protein (MBP) is the main protein compo
Externí odkaz:
https://doaj.org/article/4d2d276f6f02408e9cd41a378ab13632
Publikováno v:
Hemoglobin. 44:139-142
We describe a novel compound heterozygous genotype which consists of two point mutations named Hb Adana (HBA1: c.179G>A) and codon 127 (HBA2: c.382A>T) in a Kurdish family with two girls affected with severe α-thalassemia (α-thal). Both patients (t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26ad1668ba4c770af8eefa0a71a07607
https://doi.org/10.1080/03630269.2020.1766485
https://doi.org/10.1080/03630269.2020.1766485
Publikováno v:
Biomedical Research and Therapy. 6:3088-3092
Gastrointestinal (GI) metastasis is very rare in patients with breast cancer (BC). This study reports a case with colon carcinoma metastasis originated from breast cancer in Western Iran. A 37-yearold female was diagnosed with infiltrating ductal car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9ee5ed31afa6bb74577b45d0d487a6e
https://doi.org/10.15419/bmrat.v6i3.532
https://doi.org/10.15419/bmrat.v6i3.532
Publikováno v:
Meta Gene. 18:122-126
Background umor necrosis factor-alpha (TNF-α) is a pro-inflammatory cytokine that may play an important role in inflammatory diseases like coronary artery disease (CAD). As a result of controversy on the impact of polymorphisms in the promoter regio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be21f27786a37f1111e7ac6f7c0f9c49
https://doi.org/10.1016/j.mgene.2018.08.009
https://doi.org/10.1016/j.mgene.2018.08.009
Publikováno v:
Hemoglobin. 44(2)
We describe a novel compound heterozygous genotype which consists of two point mutations named Hb Adana (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5c8e710baecf3ae95966bf9fbf43c26d
https://pubmed.ncbi.nlm.nih.gov/32498570
https://pubmed.ncbi.nlm.nih.gov/32498570
Publikováno v:
Journal of Human Reproductive Sciences
Journal of Human Reproductive Sciences, Vol 13, Iss 3, Pp 216-220 (2020)
Journal of Human Reproductive Sciences, Vol 13, Iss 3, Pp 216-220 (2020)
Objectives: Recurrent pregnancy loss (RPL) is a serious complication of pregnancies, affecting almost 2%–5% of couples. Among numerous underlying causes, chromosomal anomalies in one of the partners are regarded as important issues, with varying fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e11f904d639fc1f9094db4c07e69faa7
https://pubmed.ncbi.nlm.nih.gov/33311908
https://pubmed.ncbi.nlm.nih.gov/33311908
Publikováno v:
Hemoglobin. 43(1)
β-Thalassemia (β-thal) is the most frequently observed hereditary blood disorder that results from genetic defects causing deficient synthesis of hemoglobin (Hb) polypeptide chains. Detecting thalassemia mutations are necessary for prenatal diagnos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c1b92a6a6a9a674cf385de677f97eb6
https://pubmed.ncbi.nlm.nih.gov/31146650
https://pubmed.ncbi.nlm.nih.gov/31146650