Works by Mohammad Taghi Akbari
Results: 37
Association of Candidate Single Nucleotide Polymorphisms Related to Candidate Genes in Patients With Schizophrenia.
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- Basic & Clinical Neuroscience, 2020, v. 11, n. 5, p. 595, doi. 10.32598/bcn.9.10.470
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- Article
HLA-A*26 and Susceptibility of Iranian Patients with Non-Hodgkin Lymphoma.
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- Iranian Journal of Immunology, 2014, v. 11, n. 4, p. 269
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- Article
The Cretan type of nondeletional hereditary persistence of fetal hemoglobin in an Iranian family.
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- 2009
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- Publication type:
- Letter
Assessment of DAPK1 and CAVIN3 Gene Promoter Methylation in Breast invasive Ductal Carcinoma and Metastasis.
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- Cell Journal (Yakhteh), 2021, v. 23, n. 4, p. 397, doi. 10.22074/cellj.2021.7251
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- Article
The Association of -475 and -631 Interleukin-2 Gene Polymorphism with Multiple Sclerosis in Iranian Patients.
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- 2013
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- Publication type:
- Case Study
Investigation The Role of Gender on The HLA-DRB1 and -DQB1 Association with Type 1 Diabetes Mellitus in Iranian Patient.
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- 2013
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- Publication type:
- Case Study
Promoter Hypermethylation of Estrogen Receptor Alpha Gene Is Correlated to Estrogen Receptor Negativity in Iranian Patients with Sporadic Breast Cancer.
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- Cell Journal (Yakhteh), 2012, v. 14, n. 2, p. 102
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- Publication type:
- Article
The Frequency of DYT1 (GAG Deletion) Mutation in Primary Dystonia Patients from Iran.
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- Cell Journal (Yakhteh), 2011, v. 13, n. 1, p. 55
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- Article
Identification of a-globin Chain Variants: A Report from Iran.
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- 2012
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- Journal Article
Identification of a-globin Chain Variants: A Report from Iran.
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- Archives of Iranian Medicine (AIM), 2012, v. 15, n. 9, p. 564
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- Publication type:
- Article
Clinical Features, DYT1 Mutation Screening and Genotype-Phenotype Correlation in Patients with Dystonia from Iran.
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- Medical Principles & Practice, 2012, v. 21, n. 5, p. 462, doi. 10.1159/000336783
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- Article
A 13-bp deletion in the 3' untranslated region of the [beta]-globin gene causes [beta]-thalassemia major in compound heterozygosity with IVSII-1 mutation.
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- 2011
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- Publication type:
- Journal Article
A 13-bp Deletion in the 3′ Untranslated Region of the β-Globin Gene Causes β-Thalassemia Major in Compound Heterozygosity with IVSII-1 Mutation.
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- Medical Principles & Practice, 2011, v. 20, n. 5, p. 488, doi. 10.1159/000328425
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- Article
First report of preimplantation genetic diagnosis of mucopolysaccharidoses IVA and HLA typing for hematopoietic stem cell transplantation.
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- Bulletin of the National Research Centre, 2022, v. 46, n. 1, p. 1, doi. 10.1186/s42269-022-00972-0
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- Article
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
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- Journal of Human Genetics, 2010, v. 55, n. 10, p. 639, doi. 10.1038/jhg.2010.96
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- Article
Distribution of HLA Alleles and Genotypes in Patients with Chronic Inflammatory Demyelinating Polyneuropathy.
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- Journal of Molecular Neuroscience, 2022, v. 72, n. 3, p. 574, doi. 10.1007/s12031-021-01902-x
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- Article
Identification of a Mutation in SPG11 in an Iranian Patient with Spastic Paraplegia and Ears of the Lynx Sign.
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- Journal of Molecular Neuroscience, 2020, v. 70, n. 6, p. 959, doi. 10.1007/s12031-020-01501-2
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- Article
Evaluation and Comparison of Soluble Transferrin Receptor in Thalassemia Carriers and Iron Deficient Patients.
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- Hemoglobin, 2013, v. 37, n. 4, p. 387, doi. 10.3109/03630269.2013.780248
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- Article
Globin Chain Synthesis is a Useful Complementary Tool in the Differential Diagnosis of Thalassemias.
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- Hemoglobin, 2007, v. 31, n. 3, p. 333, doi. 10.1080/03630260701462006
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- Article
Association study of the common polymorphisms in the folate-methionine pathway with retinoblastoma.
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- Ophthalmic Genetics, 2016, v. 37, n. 4, p. 384, doi. 10.3109/13816810.2015.1107596
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- Article
Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency.
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- Journal of Genetics, 2020, v. 99, n. 1, p. 1, doi. 10.1007/s12041-019-1171-5
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- Article
Development and diversity of a novel panel of short tandem repeat markers encompassing the SCN5A gene in Iranian population.
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- Journal of Genetics, 2018, v. 97, n. 1, p. 49, doi. 10.1007/s12041-018-0902-3
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- Article
A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients.
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- Journal of Genetics, 2009, v. 88, n. 3, p. 359, doi. 10.1007/s12041-009-0054-6
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- Article
Transcriptome mining of non‐BRCA1/A2 and BRCA1/A2 familial breast cancer.
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- Journal of Cellular Biochemistry, 2019, v. 120, n. 1, p. 575, doi. 10.1002/jcb.27413
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- Article
Chemical Composition of Essential Oils of Three Stachys Species Growing Wild in Iran: Stachys asterocalyx Rech. f., Stachys obtusicrena Boiss. and Stachys multicaulis Benth.
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- Journal of Essential Oil Research, 2009, v. 21, n. 2, p. 101, doi. 10.1080/10412905.2009.9700123
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- Article
Association of HLA alleles with autism.
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- Neuropsychiatric Disease & Treatment, 2018, v. 14, p. 3259, doi. 10.2147/NDT.S186673
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- Article
The Association of HLA Class 1 and Class 2 Antigens with Multiple Myeloma in Iranian Patients.
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- Turkish Journal of Hematology, 2014, v. 31, n. 4, p. 388, doi. 10.4274/tjh.2013.0098
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- Article
Identification of Nucleotide Changes of Two Known Causative Genes (BRCA2 and STK11) of Hereditary Breast Cancer in an Iranian Family using Exome Sequencing.
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- Modares Journal of Medical Sciences: Pathobiology, 2014, v. 17, n. 3, p. 81
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- Article
Detection of Rare Beta Globin Gene Mutation [+22 5UTR(G>A)] in an Infant, Despite Prenatal Screening.
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- Case Reports in Hematology, 2013, p. 1, doi. 10.1155/2013/906292
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- Publication type:
- Article
Molecular Analysis of HS-111 and 3`HS1 Variations in β-Thalassemia Intermedia Patients with High Levels of HbF.
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- Yakhteh Medical Journal, 2010, v. 11, n. 4, p. 418
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- Publication type:
- Article
The Association of HLA-Class I and Class II with Hodgkin's Lymphoma in Iranian Patients.
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- 2014
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- Publication type:
- Journal Article
The Association of HLA-Class I and Class II with Hodgkin's Lymphoma in Iranian Patients.
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- BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/231236
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- Article
Association of plasminogen activator inhibitor-1 (PAI-1) and angiotensin converting enzyme polymorphisms with recurrent pregnancy loss in Iranian women.
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- Iranian Journal of Reproductive Medicine, 2015, v. 13, n. 10, p. 625
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- Article
Assessing the Diagnostic Value of Plasma-Free DNA in Prostate Cancer Screening.
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- 2018
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- Publication type:
- journal article
Association between human leucocyte antigen alleles and risk of stroke in Iranian population.
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- International Journal of Immunogenetics, 2019, v. 46, n. 3, p. 179, doi. 10.1111/iji.12421
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- Article
Molecular Diagnosis of Duchenne/Becker Muscular Dystrophy: Analysis of Exons Deletion and Carrier Detection.
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- Yakhteh Medical Journal, 2010, v. 12, n. 3, p. 421
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- Publication type:
- Article
Development and Application of Real-Time Quantitative Polymerase Chain Reaction Technique Using SYBR Green I in the Diagnosis of Down Syndrome.
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- Yakhteh Medical Journal, 2010, v. 12, n. 2, p. 249
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- Publication type:
- Article