Works by Mohammad Taghi Akbari

Results: 37

Chemical Composition of Essential Oils of Three Stachys Species Growing Wild in Iran: Stachys asterocalyx Rech. f., Stachys obtusicrena Boiss. and Stachys multicaulis Benth.

Published in:

Journal of Essential Oil Research, 2009, v. 21, n. 2, p. 101, doi. 10.1080/10412905.2009.9700123

By:

Jamzad, Mina;
Akbari, Mohammad Taghi;
Rustaiyan, Abdolhossein;
Masoudi, Shiva;
Azad, Leila

Publication type:

Article

Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 10, p. 639, doi. 10.1038/jhg.2010.96

By:

Mahdieh, Nejat;
Rabbani, Bahareh;
Wiley, Susan;
Akbari, Mohammad Taghi;
Zeinali, Sirous

Publication type:

Article

HLA-A*26 and Susceptibility of Iranian Patients with Non-Hodgkin Lymphoma.

Published in:

Iranian Journal of Immunology, 2014, v. 11, n. 4, p. 269

By:

Sayad, Arezou;
Akbari, Mohammad Taghi;
Mehdizadeh, Mahshid;
Taheri, Mohammad;
Hajifathali, Abbas

Publication type:

Article

Molecular Diagnosis of Duchenne/Becker Muscular Dystrophy: Analysis of Exons Deletion and Carrier Detection.

Published in:

Yakhteh Medical Journal, 2010, v. 12, n. 3, p. 421

By:

Akbari, Mohammad Taghi;
Karizi, Shohreh Zare;
Nafisi, Shahryar;
Zamani, Gholamreza

Publication type:

Article

Development and Application of Real-Time Quantitative Polymerase Chain Reaction Technique Using SYBR Green I in the Diagnosis of Down Syndrome.

Published in:

Yakhteh Medical Journal, 2010, v. 12, n. 2, p. 249

By:

Kamyab, Ahmad Reza;
Shahbazi, Shirin;
Dibajnia, Parvin;
Nosaeid, Mina Hayt;
Akbari, Mohammad Taghi;
Rafiee, Amir Reza;
Tamiz, Katayun Akhlagh;
Mahdian, Reza

Publication type:

Article

Molecular Analysis of HS-111 and 3`HS1 Variations in β-Thalassemia Intermedia Patients with High Levels of HbF.

Published in:

Yakhteh Medical Journal, 2010, v. 11, n. 4, p. 418

By:

Hamid, Mohammad;
Karimipoor, Morteza;
Zeinali, Sirous;
Akbari, Mohammad taghi;
Kokabi, Leila;
Mahjoubi, Frouzandeh

Publication type:

Article

Assessment of DAPK1 and CAVIN3 Gene Promoter Methylation in Breast invasive Ductal Carcinoma and Metastasis.

Published in:

Cell Journal (Yakhteh), 2021, v. 23, n. 4, p. 397, doi. 10.22074/cellj.2021.7251

By:

Ghalkhani, Esmat;
Akbari, Mohammad Taghi;
Izadi, Pantea;
Mahmoodzadeh, Habibollah;
Kamali, Fatemeh

Publication type:

Article

The Association of -475 and -631 Interleukin-2 Gene Polymorphism with Multiple Sclerosis in Iranian Patients.

Published in:

2013

By:

Sayad, Aida;
Allameh, Abdolamir;
Sayad, Arezou;
Noruzinia, Mehrdad;
Taghi Akbari, Mohammad;
Sarzaeem, Ali;
Akbari, Akbar;
Hoseini, Reza Haji

Publication type:

Case Study

Investigation The Role of Gender on The HLA-DRB1 and -DQB1 Association with Type 1 Diabetes Mellitus in Iranian Patient.

Published in:

2013

By:

Sayad, Arezou;
Taghi Akbari, Mohammad;
Pajouhi, Mohammad;
Mostafavi, Feridoon;
Kazemnejad, Anooshirvan;
Zamani, Mahdi

Publication type:

Case Study

Promoter Hypermethylation of Estrogen Receptor Alpha Gene Is Correlated to Estrogen Receptor Negativity in Iranian Patients with Sporadic Breast Cancer.

Published in:

Cell Journal (Yakhteh), 2012, v. 14, n. 2, p. 102

By:

Izadi, Pantea;
Noruzinia, Mehrdad;
Karimipoor, Morteza;
Karbassian, Mohammad Hamid;
Akbari, Mohammad Taghi

Publication type:

Article

The Frequency of DYT1 (GAG Deletion) Mutation in Primary Dystonia Patients from Iran.

Published in:

Cell Journal (Yakhteh), 2011, v. 13, n. 1, p. 55

By:

Hamid, Mohammad;
Akbari, Mohammad Taghi;
Shahidi, Gholam Ali;
Zand, Zahra

Publication type:

Article

Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency.

Published in:

Journal of Genetics, 2020, v. 99, n. 1, p. 1, doi. 10.1007/s12041-019-1171-5

By:

Salimy, Zeinab;
Akbari, Mohammad Taghi;
Khordadpoor Deilamani, Faravareh

Publication type:

Article

Development and diversity of a novel panel of short tandem repeat markers encompassing the SCN5A gene in Iranian population.

Published in:

Journal of Genetics, 2018, v. 97, n. 1, p. 49, doi. 10.1007/s12041-018-0902-3

By:

Zafari, Zahra;
Amirian, Azam;
Nejad, Faezeh Rahimi;
Akbari, Vahid;
Akbari, Mohammad Taghi;
Zeinali, Sirus

Publication type:

Article

A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients.

Published in:

Journal of Genetics, 2009, v. 88, n. 3, p. 359, doi. 10.1007/s12041-009-0054-6

By:

HAMID, MOHAMMAD;
KARIMIPOOR, MORTEZA;
CHALESHTORI, MORTEZA HASHEMZADEH;
AKBARI., MOHAMMAD TAGHI

Publication type:

Article

Association between human leucocyte antigen alleles and risk of stroke in Iranian population.

Published in:

International Journal of Immunogenetics, 2019, v. 46, n. 3, p. 179, doi. 10.1111/iji.12421

By:

Sayad, Arezou;
Akbari, Mohammad Taghi;
Inoko, Hidetoshi;
Khazaei, Mojtaba;
Mehdizadeh, Bijan;
Taheri, Mohammad;
Ghafouri‐Fard, Soudeh

Publication type:

Article

First report of preimplantation genetic diagnosis of mucopolysaccharidoses IVA and HLA typing for hematopoietic stem cell transplantation.

Published in:

Bulletin of the National Research Centre, 2022, v. 46, n. 1, p. 1, doi. 10.1186/s42269-022-00972-0

By:

Khordadpoor Deilamani, Faravareh;
Akbari, Mohammad Taghi

Publication type:

Article

Association study of the common polymorphisms in the folate-methionine pathway with retinoblastoma.

Published in:

Ophthalmic Genetics, 2016, v. 37, n. 4, p. 384, doi. 10.3109/13816810.2015.1107596

By:

Soleimani, Elaheh;
Saliminejad, Kioomars;
Akbari, Mohammad Taghi;
Kamali, Koorosh;
Ahani, Ali

Publication type:

Article

Association of HLA alleles with autism.

Published in:

Neuropsychiatric Disease & Treatment, 2018, v. 14, p. 3259, doi. 10.2147/NDT.S186673

By:

Sayad, Arezou;
Akbari, Mohammad Taghi;
Noroozi, Rezvan;
Omrani, Mir Davood;
Inoko, Hidetoshi;
Taheri, Mohammad;
Ghafouri-Fard, Soudeh

Publication type:

Article

Transcriptome mining of non‐BRCA1/A2 and BRCA1/A2 familial breast cancer.

Published in:

Journal of Cellular Biochemistry, 2019, v. 120, n. 1, p. 575, doi. 10.1002/jcb.27413

By:

Akbari, Vahid;
Kallhor, Marzieh;
Akbari, Mohammad Taghi

Publication type:

Article

Identification of Nucleotide Changes of Two Known Causative Genes (BRCA2 and STK11) of Hereditary Breast Cancer in an Iranian Family using Exome Sequencing.

Published in:

Modares Journal of Medical Sciences: Pathobiology, 2014, v. 17, n. 3, p. 81

By:

Ataei-Kachouei, Mojgan;
Nadaf, Javad;
Akbari, Mohammad Taghi;
Atri, Morteza;
Majewski, Jacek;
Riazalhosseini, Yasser;
Garshasbi, Masoud

Publication type:

Article

Evaluation and Comparison of Soluble Transferrin Receptor in Thalassemia Carriers and Iron Deficient Patients.

Published in:

Hemoglobin, 2013, v. 37, n. 4, p. 387, doi. 10.3109/03630269.2013.780248

By:

Khatami, Shohreh;
Dehnabeh, Soghra Rouhi;
Mostafavi, Ehsan;
Kamalzadeh, Neda;
Yaghmaei, Paricheher;
Saeedi, Parinaz;
Shariat, Farangis;
Bagheriyan, Hamideh;
Zeinali, Sirous;
Akbari, Mohammad Taghi

Publication type:

Article

Globin Chain Synthesis is a Useful Complementary Tool in the Differential Diagnosis of Thalassemias.

Published in:

Hemoglobin, 2007, v. 31, n. 3, p. 333, doi. 10.1080/03630260701462006

By:

Khatami, Shohreh;
Dehboneh, Soghra Rouhi;
Sadeghi, Sedigheh;
Mirzazadeh, Roghieh;
Saeedi, Parinaz;
Bayat, Parastoo;
Najmabadi, Hossein;
Zeinali, Sirous;
Akbari, Mohammad Taghi;
Ardjmand, Mohammad;
Amirkhani, Aref

Publication type:

Article

Assessing the Diagnostic Value of Plasma-Free DNA in Prostate Cancer Screening.

Published in:

2018

By:

Seyedolmohadessin, Seyedeh Maryam;
Akbari, Mohammad Taghi;
Nourmohammadi, Zahra;
Basiri, Abbas;
Pourmand, Gholamreza

Publication type:

journal article

Distribution of HLA Alleles and Genotypes in Patients with Chronic Inflammatory Demyelinating Polyneuropathy.

Published in:

Journal of Molecular Neuroscience, 2022, v. 72, n. 3, p. 574, doi. 10.1007/s12031-021-01902-x

By:

Ghafouri-Fard, Soudeh;
Akbari, Mohammad Taghi;
Houlden, Henry;
Mazdeh, Mehrdokht;
Nazer, Naghme;
Rezaei, Omidvar;
Taheri, Mohammad;
Sayad, Arezou

Publication type:

Article

Identification of a Mutation in SPG11 in an Iranian Patient with Spastic Paraplegia and Ears of the Lynx Sign.

Published in:

Journal of Molecular Neuroscience, 2020, v. 70, n. 6, p. 959, doi. 10.1007/s12031-020-01501-2

By:

Sayad, Arezou;
Akbari, Mohammad Taghi;
Hesami, Omid;
Ghafouri-Fard, Soudeh;
Taheri, Mohammad

Publication type:

Article

Clinical Features, DYT1 Mutation Screening and Genotype-Phenotype Correlation in Patients with Dystonia from Iran.

Published in:

Medical Principles & Practice, 2012, v. 21, n. 5, p. 462, doi. 10.1159/000336783

By:

Akbari, Mohammad Taghi;
Zand, Zahra;
Shahidi, Gholam Ali;
Hamid, Mohammad

Publication type:

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.

Published in:

2011

By:

Hamid, Mohammad;
Akbari, Mohammad Taghi

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.

Published in:

Medical Principles & Practice, 2011, v. 20, n. 5, p. 488, doi. 10.1159/000328425

By:

Hamid, Mohammad;
Akbari, Mohammad Taghi

Publication type:

Article

The Association of HLA-Class I and Class II with Hodgkin's Lymphoma in Iranian Patients.

Published in:

2014

By:

Sayad, Arezou;
Akbari, Mohammad Taghi;
Mehdizadeh, Mahshid;
Movafagh, Abolfazl;
Hajifathali, Abbas

Publication type:

Journal Article

The Association of HLA-Class I and Class II with Hodgkin's Lymphoma in Iranian Patients.

Published in:

BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/231236

By:

Sayad, Arezou;
Taghi Akbari, Mohammad;
Mehdizadeh, Mahshid;
Movafagh, Abolfazl;
Hajifathali, Abbas

Publication type:

Article

Detection of Rare Beta Globin Gene Mutation [+22 5UTR(G>A)] in an Infant, Despite Prenatal Screening.

Published in:

Case Reports in Hematology, 2013, p. 1, doi. 10.1155/2013/906292

By:

Mahdavi, Mohammad Reza;
Karami, Hosein;
Akbari, Mohammad Taghi;
Jalali, Hosein;
Roshan, Payam

Publication type:

Article

Association of Candidate Single Nucleotide Polymorphisms Related to Candidate Genes in Patients With Schizophrenia.

Published in:

Basic & Clinical Neuroscience, 2020, v. 11, n. 5, p. 595, doi. 10.32598/bcn.9.10.470

By:

Karimian, Seyedeh Sara;
Akbari, Mohammad Taghi;
Sadr, Seyed Saeed;
Javadi, Gholamreza

Publication type:

Article

Identification of a-globin Chain Variants: A Report from Iran.

Published in:

2012

By:

Akbari, Mohammad Taghi;
Hamid, Mohammad

Publication type:

Journal Article

Identification of a-globin Chain Variants: A Report from Iran.

Published in:

Archives of Iranian Medicine (AIM), 2012, v. 15, n. 9, p. 564

By:

Akbari, Mohammad Taghi;
Hamid, Mohammad

Publication type:

Article

Association of plasminogen activator inhibitor-1 (PAI-1) and angiotensin converting enzyme polymorphisms with recurrent pregnancy loss in Iranian women.

Published in:

Iranian Journal of Reproductive Medicine, 2015, v. 13, n. 10, p. 625

By:

Shakarami, Fatemeh;
Mohammad Taghi Akbari;
Shohreh Zare Karizi

Publication type:

Article

The Cretan type of nondeletional hereditary persistence of fetal hemoglobin in an Iranian family.

Published in:

2009

By:

Hamid, Mohammad;
Mahjoubi, Frouzandeh;
Akbari, Mohammad Taghi;
Zeinali, Sirous;
Karimipoor, Morteza

Publication type:

Letter

The Association of HLA Class 1 and Class 2 Antigens with Multiple Myeloma in Iranian Patients.

Published in:

Turkish Journal of Hematology, 2014, v. 31, n. 4, p. 388, doi. 10.4274/tjh.2013.0098

By:

Sayad, Arezou;
Akbari, Mohammad Taghi;
Mehdizadeh, Mahshid;
Roshandel, Elham;
Abedinpour, Soheila;
Hajifathali, Abbas

Publication type:

Article