Items where Author is "Azadegan-Dehkordi, Fatemeh"

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Number of items: 13.

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Sanami, Samira and Azadegan-Dehkordi, Fatemeh and Rafieian-Kopaei, Mahmoud and Salehi, Majid and Ghasemi-Dehnoo, Maryam and Mahooti, Mehran and Alizadeh, Morteza and Bagheri, Nader (2021) Design of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches. SCIENTIFIC REPORTS, 11 (1).

Sanami, Samira and Alizadeh, Morteza and Nosrati, Masoud and Ashrafi Dehkordi, Korosh and Azadegan-Dehkordi, Fatemeh and Tahmasebian, Shahram and Nosrati, Hamed and Arjmand, Mohammad Hassan and Ghasemi-Dehnoo, Maryam and Rafiei, Ali and Bagheri, Nader (2021) Exploring SARS-COV-2 structural proteins to design a multi-epitope vaccine using immunoinformatics approach: An in silico study. Computers in Biology and Medicine, 133. ISSN 00104825

Abadi, Milad Shahini Shams and Ashrafi-Dehkordi, Korosh and Ahmadi, Reza and Rahimian, Ghorbanali and Mirzaei, Yousef and Fereidani, Rana and Shohan, Mojtaba and Azadegan-Dehkordi, Fatemeh (2021) Frequency of virulence-associated genotypes of Helicobacter pylori and their correlation with clinical outcome and histological parameters in infected patients. HELIYON, 7 (7).

Azadegan-Dehkordi, Fatemeh and Shirzad, Hedayatollah and Ahmadi, Reza and Bashash, Davood and Abdollahpour-Alitappeh, Meghdad and Luzza, Francesco and Larussa, Tiziana and Nahid-Samiei, Mahboobeh and Rahimian, Ghorbanali and Shafigh, Mohammad Hadi and Bagheri, Nader (2021) Increased Indoleamine 2, 3-Dioxygenase expression modulates Th1/Th17/Th22 and Treg pathway in humans with Helicobacter Pylori-Infected gastric mucosa. Human Immunology, 82 (1). pp. 46-53. ISSN 01988859

Koohiyan, Mahbobeh and Koohian, Farideh and Azadegan-Dehkordi, Fatemeh (2020) GJB2-related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations. Annals of Human Genetics, 84 (2). ISSN 00034800

Azadegan-Dehkordi, Fatemeh and Abbasi, Ardeshir and Talebi Bezmin Abadi, Amin and Minooie, Khaled and Aslani, Parya and Sadat Hosseini, Razieh and Zandi, Farid (2020) From genes polymorphisms to mucosal expression of cytokines: evaluating IL-23/IL-17 axis in adult patients with gastritis. African Health Sciences, 20 (3). pp. 1452-1462. ISSN 1680-6905

Koohiyan, Mahbobeh and Azadegan-Dehkordi, Fatemeh and Koohian, Farideh and Hashemzadeh-Chaleshtori, Morteza (2019) Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations. JOURNAL OF AUDIOLOGY AND OTOLOGY.

Koohiyan, Mahbobeh and Koohian, Farideh and Azadegan-Dehkordi, Fatemeh (2019) GJB2-related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations. ANNALS OF HUMAN GENETICS.

Koohiyan, Mahboobeh and Reiisi, Somayeh and Azadegan-Dehkordi, Fatemeh and Salehi, Mansour and Abtahi, Hamidreza and Hashemzadeh-Chaleshtori, Morteza and Noori-Daloii, Mohammad Reza and Tabatabaiefar, Mohammad Amin (2019) Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations. Iranian Journal of Public Health. ISSN 2251-6085

Koohiyan, Mahbobeh and Azadegan-Dehkordi, Fatemeh and Koohian, Farideh and Abolhasani, Marziye and Hashemzadeh-Chaleshtori, Morteza (2019) Genetics of hereditary hearing loss in east Iran population: A systematic review of GJB2 mutations. INTRACTABLE & RARE DISEASES RESEARCH.

Azadegan-Dehkordi, Fatemeh and Bahrami, Tayyebe and Shirzad, Maryam and Karbasi, Gelareh and Yazdanpanahi, Nasrin and Farrokhi, Effat and Koohiyan, Mahbobeh and Tabatabaiefar, Mohammad Amin and Hashemzadeh-Chaleshtori, Morteza (2019) Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran. Journal of Audiology & Otology. ISSN 2384-1621

Azadegan-Dehkordi, Fatemeh and Koohiyan, Mahbobeh and Shirzad, Maryam and Bahrami, Tayyeb and Yazdanpanahi, Nasrin and Tabatabaiefar, MohammadAmin and Pourpaknia, Reza and Farrokhi, Effat and Hashemzadeh-Chaleshtori, Morteza (2019) Mutation analysis of GJB2 and GJB6 genes and screening of nine common dfnb loci in iranian pedigrees with autosomal recessive nonsyndromic hearing loss. Indian Journal of Otology, 25 (2). p. 97. ISSN 0971-7749

Azadegan-Dehkordi, Fatemeh and Ahmadi, Reza and Koohiyan, Mahbobeh and Hashemzadeh-Chaleshtori, Morteza (2019) Update of spectrum c.35delG and c.-23+1G>A mutations on theGJB2gene in individuals with autosomal recessive nonsyndromic hearing loss. Annals of Human Genetics, 83 (1). pp. 1-10. ISSN 00034800

This list was generated on Sun Sep 26 01:19:23 2021 IRST.