Mohammad Taghi Akbari
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View article: The Expression Levels of Circulating miR-129 and miR-203a in Association with Breast Cancer and Related Metastasis
The Expression Levels of Circulating miR-129 and miR-203a in Association with Breast Cancer and Related Metastasis Open
Background: A significant part of deaths related to breast cancer is the result of invasion to other organs. It is essential to discover new non-invasive biomarkers to improve anticipation of recurrence risk in breast cancer patients. In t…
View article: First report of preimplantation genetic diagnosis of mucopolysaccharidoses IVA and HLA typing for hematopoietic stem cell transplantation
First report of preimplantation genetic diagnosis of mucopolysaccharidoses IVA and HLA typing for hematopoietic stem cell transplantation Open
Background Mucopolysaccharidoses IVA is an autosomal recessive lysosomal storage disease resulting in skeletal and cartilage dysplasia. Hematopoietic stem cell transplantation is a good therapeutic option for MPS IV. Here we report the fir…
View article: Analysis Variants of the CFTR Gene in Iranian Cystic Fibrosis Patients
Analysis Variants of the CFTR Gene in Iranian Cystic Fibrosis Patients Open
Background: Cystic fibrosis (CF) is known as one of the most common autosomal recessive disorders, which is caused by mucosal glands. A deficiency in the Cystic fibrosis transmembrane conductance regulator gene (CFTR), which encodes a chlo…
View article: Spectrum of Mutations of Familial Mediterranean Fever Gene by Whole Sequencing Method in Iranian Patients
Spectrum of Mutations of Familial Mediterranean Fever Gene by Whole Sequencing Method in Iranian Patients Open
Background: Familial Mediterranean fever (FMF) is the most common type of periodic fever syndrome. The disease is most prevalent in the western Mediterranean population, but today it is widespread in the world due to the large ethnic migra…
View article: Preimplantation Genetic Diagnosis for Beta Thalassemia
Preimplantation Genetic Diagnosis for Beta Thalassemia Open
Background: Beta thalassemia is an autosomal recessive genetic disease with the symptoms of severe anaemia, ineffective erythropoiesis and bone deformities. Preimplantation genetic diagnosis is a noninvasive clinical tool for couples who a…
View article: A Splicing Variant in OCRL Gene Might Explain the Second Case of Lowe Syndrome in Iran
A Splicing Variant in OCRL Gene Might Explain the Second Case of Lowe Syndrome in Iran Open
: Lowe syndrome is a condition that primarily affects eyes, brain, and kidneys. This disorder follows X-linked recessive mode of inheritance and it occurs in males mainly. Mutations in OCRL (located at Xq25) gene can cause accumulation of …
View article: First Report of Preimplantation Genetic Diagnosis for Steroid-Resistant Nephrotic Syndrome
First Report of Preimplantation Genetic Diagnosis for Steroid-Resistant Nephrotic Syndrome Open
Background: Steroid-resistant nephrotic syndrome is a genetic disease with autosomal recessive inheritance pattern and symptoms such as proteinuria and hypoalbuminemia and rapid progress of kidney disease. Preimplantation genetic diagnosis…
View article: Study of the p.V617F and Exon 12 Mutations in JAK2 Gene Among Iranian Chronic Myeloproliferative Patients
Study of the p.V617F and Exon 12 Mutations in JAK2 Gene Among Iranian Chronic Myeloproliferative Patients Open
Study of the p.V617F and Exon 12 Mutations in JAK2 Gene Among Iranian Chronic Myeloproliferative Patients
View article: LncRNA SRA1 may play a role in the uterine leiomyoma tumor growth regarding the MED12 mutation pattern
LncRNA SRA1 may play a role in the uterine leiomyoma tumor growth regarding the MED12 mutation pattern Open
Mojdeh Akbari,1 Fakhrolmolouk Yassaee,2 Mona Aminbeidokhti,1 Atieh Abedin-Do,1,3 Reza Mirfakhraie1,41Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran; 2Department of Obstetric…
View article: Allele Frequency of 15 Autosomal Short Tandem Repeat Loci in Iranian Population with Comparison to Some Other Population
Allele Frequency of 15 Autosomal Short Tandem Repeat Loci in Iranian Population with Comparison to Some Other Population Open
Allele Frequency of 15 Autosomal Short Tandem Repeat Loci in Iranian Population with Comparison to Some Other Population
View article: Omega-3 fatty acid supplementation does not influence liver regeneration in rats after partial hepatectomy
Omega-3 fatty acid supplementation does not influence liver regeneration in rats after partial hepatectomy Open
Supplementation with omega-3 fatty acids showed no influence on the liver regeneration in rats undergoing 1/3 partial hepatectomy.
View article: Association of plasminogen activator inhibitor-1 and angiotensin converting enzyme polymorphisms with recurrent pregnancy loss in Iranian women.
Association of plasminogen activator inhibitor-1 and angiotensin converting enzyme polymorphisms with recurrent pregnancy loss in Iranian women. Open
Considering these results, because 4G/4G polymorphism for PAI-1 gene could be a thrombophilic variant leading to abortion, analysis of this mutation and other susceptibility factors are recommended in patients with RPL.