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MicroRNAs: effective elements in ear-related diseases and hearing loss.
- Published in:
- European Archives of Oto-Rhino-Laryngology, 2017, v. 274, n. 6, p. 2373, doi. 10.1007/s00405-017-4470-6
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- Article
MIR96 Has Good Potential to Differentiate Human Bone Marrow-Derived Mesenchymal Stem Cells into Photoreceptor-Like Cells.
- Published in:
- Experimental & Clinical Transplantation, 2024, v. 22, n. 2, p. 148, doi. 10.6002/ect.2023.0300
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- Publication type:
- Article
MicroRNA-183 Family in Inner Ear: Hair Cell Development and Deafness.
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- Journal of Audiology & Otology, 2016, v. 20, n. 3, p. 131, doi. 10.7874/jao.2016.20.3.131
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- Article
Basal cell carcinoma: From molecule to therapy.
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- Dermatology & Cosmetic, 2013, v. 4, n. 4, p. 226
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- Publication type:
- Article
Evaluation of response to hepatitis B vaccine in Iranian 6-18-year-old students.
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- Journal of Research in Medical Sciences, 2017, v. 22, p. 1, doi. 10.4103/jrms.JRMS_204_17
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- Publication type:
- Article
Tumor microsatellite instability and clinicopathologic features in Iranian colorectal cancer patients at risk for Lynch syndrome.
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- Journal of Research in Medical Sciences, 2015, v. 20, n. 2, p. 154
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- 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
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- Publication type:
- Article
Variation of DAT1 VNTR Alleles and Genotypes Among Old Ethnic Groups in Mesopotamia to the Oxus Region.
- Published in:
- Human Biology, 2008, v. 80, n. 1, p. 73, doi. 10.3378/1534-6617(2008)80[73:VODVAA]2.0.CO;2
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- Publication type:
- Article
Investigation on the deletion and duplication of PMP22 gene in patients with Charcot-Marie-Tooth using Real-time PCR in Chaharmahal and Bakhtiari and Isfahan Provinces.
- Published in:
- Journal of Shahrekord University of Medical Sciences, 2019, v. 21, n. 6, p. 254, doi. 10.34172/jsums.2019.44
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- Publication type:
- Article
Genetic linkage analysis of DFNB22 in families with autosomal recessive non-syndromic hearing loss in Khuzestan province.
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- Journal of Shahrekord University of Medical Sciences, 2019, v. 21, n. 5, p. 200, doi. 10.34172/jsums.2019.35
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- Publication type:
- Article
Diversity and relationship between Iranian ethnic groups: Human dopamine transporter gene ( DAT1) VNTR genotyping.
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- American Journal of Human Biology, 2007, v. 19, n. 6, p. 821, doi. 10.1002/ajhb.20647
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- Publication type:
- Article
Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01168-x
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- Publication type:
- Article
A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran.
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- Indian Journal of Medical Research, 2015, v. 142, n. 1, p. 46, doi. 10.4103/0971-5916.162096
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- Article
A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23.
- Published in:
- 2020
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- Publication type:
- journal article
A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family.
- Published in:
- 2019
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- Publication type:
- journal article
Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing.
- Published in:
- 2019
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- Publication type:
- journal article
شناسایی عامل موثربرناشنوایی مادرزادی با استفاده از داده کاوی
- Published in:
- Iranian Journal of Medical Informatics, 2016, v. 5, n. 3, p. 1
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- Publication type:
- Article
Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent.
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- Cell Journal (Yakhteh), 2014, v. 16, n. 2, p. 225
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- Publication type:
- Article
Detection of two pathogenesis previously unreported myosin xva pathogenic variants in two large Iranian pedigrees with autosomal recessive nonsyndromic hearing loss.
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- Indian Journal of Otology, 2021, v. 27, n. 1, p. 14, doi. 10.4103/indianjotol.INDIANJOTOL_73_19
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- Publication type:
- Article
Mutation analysis of GJB2 and GJB6 genes and screening of nine common dfnb loci in iranian pedigrees with autosomal recessive nonsyndromic hearing loss.
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- Indian Journal of Otology, 2019, v. 25, n. 2, p. 97, doi. 10.4103/indianjotol.INDIANJOTOL_113_18
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- Publication type:
- Article
Study of VSX1 Mutations in Patients with Keratoconus in Southwest Iran Using PCR-Single-Strand Conformation Polymorphism/Heteroduplex Analysis and Sequencing Method.
- Published in:
- Acta Cytologica, 2013, v. 57, n. 6, p. 646, doi. 10.1159/000353297
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- Publication type:
- Article
Silencing of α‐N‐acetylgalactosaminidase in the gastric cancer cells amplified cell death and attenuated migration, while the multidrug resistance remained unchanged.
- Published in:
- Cell Biology International, 2022, v. 46, n. 2, p. 255, doi. 10.1002/cbin.11727
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- Publication type:
- Article
In silico and in vitro effects of the I30T mutation on myelin protein zero instability in the cell membrane.
- Published in:
- Cell Biology International, 2020, v. 44, n. 2, p. 671, doi. 10.1002/cbin.11268
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- Publication type:
- Article
Molecular Mechanisms behind Free Radical Scavengers Function against Oxidative Stress.
- Published in:
- Antioxidants, 2017, v. 6, n. 3, p. 51, doi. 10.3390/antiox6030051
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- Article
Familial Colorectal Cancer Type X in Central Iran: A New Clinicopathologic Description.
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- International Journal of Hematology-Oncology & Stem Cell Research, 2017, v. 11, n. 3, p. 241
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- Publication type:
- Article
Plasma Level Of miR-21 And miR-451 In Primary And Recurrent Breast Cancer Patients.
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- Breast Cancer: Targets & Therapy, 2019, v. 11, p. 293, doi. 10.2147/BCTT.S224333
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- Publication type:
- Article
Immunohistochemical Analysis of Mismatch Repair Proteins in Iranian Colorectal Cancer Patients at Risk for Lynch Syndrome.
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- Iranian Journal of Cancer Prevention, 2015, v. 8, n. 1, p. 11
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- Publication type:
- Article
Mesenchymal stem cells versus their conditioned medium in the treatment of ischemia/reperfusion injury: Evaluation of efficacy and hepatic specific gene expression in mice.
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- Iranian Journal of Basic Medical Sciences, 2022, v. 25, n. 7, p. 799, doi. 10.22038/IJBMS.2022.62642.13860
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- Publication type:
- Article
Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family.
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- Iranian Journal of Basic Medical Sciences, 2016, v. 19, n. 7, p. 772
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- Publication type:
- Article
In Vitro Differentiation of Human Bone Marrow Mesenchymal Stem Cells to Hair Cells Using Growth Factors.
- Published in:
- International Tinnitus Journal, 2017, v. 21, n. 2, p. 179, doi. 10.5935/0946-5448.20170030
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- Publication type:
- Article
Comparison of Three Types of Mesenchymal Stem Cells (Bone Marrow, Adipose Tissue, and Umbilical Cord-Derived) as Potential Sources for Inner Ear Regeneration.
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- International Tinnitus Journal, 2017, v. 21, n. 2, p. 122, doi. 10.5935/0946-5448.20170023
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- Publication type:
- Article
Ginkgo biloba in the treatment of tinnitus: An updated literature review.
- Published in:
- International Tinnitus Journal, 2017, v. 21, n. 1, p. 58, doi. 10.5935/0946-5448.20170011
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- Publication type:
- Article
A Review of Medicinal Plants for the Treatment of Earache and Tinnitus in Iran.
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- International Tinnitus Journal, 2017, v. 21, n. 1, p. 44, doi. 10.5935/0946-5448.20170009
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- Publication type:
- Article
Effect of Oxidized Low Density Lipoprotein on the Expression of Runx2 and SPARC Genes in Vascular Smooth Muscle Cells.
- Published in:
- Iranian Biomedical Journal, 2015, v. 19, n. 3, p. 160
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- Article
Comparison of human dermal fibroblasts (HDFs) growth rate in culture media supplemented with or without basic fibroblast growth factor (bFGF).
- Published in:
- 2015
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- Publication type:
- journal article
FREQUENCY OF GJB2 MUTATIONS IN FAMILIES WITH AUTOSOMAL RECESSIVE NON-SYNDROMIC HEARING LOSS IN KHUZESTAN PROVINCE.
- Published in:
- Genetika (0534-0012), 2018, v. 50, n. 3, p. 837, doi. 10.2298/GENSR1803837T
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- Publication type:
- Article
GENOTYPING OF Trichomonas vaginalis ISOLATES FROM WOMEN IN SHAHREKORD CITY (SOUTHWESTERN IRAN).
- Published in:
- Genetika (0534-0012), 2017, v. 49, n. 3, p. 1059, doi. 10.2298/GENSR1703059K
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- Publication type:
- Article
THE LACK OF CORRELATION BETWEEN TP53 MUTATIONS AND GASTRIC CANCER: A REPORT FROM A PROVINCE OF IRAN.
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- Genetika (0534-0012), 2017, v. 49, n. 1, p. 235, doi. 10.2298/GENSR1701235S
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- Publication type:
- Article
DEGRADATION OF PHENANTHRENE AND PYRENE USING GENETICALLY ENGINEERED DIOXYGENASE PRODUCING Pseudomonas putida IN SOIL.
- Published in:
- Genetika (0534-0012), 2016, v. 48, n. 3, p. 837, doi. 10.2298/GENSR1603837M
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- Publication type:
- Article
Association of Hypoxia-inducible factor α subunits with TSGA10 transcripts in HeLa, MCF7 and MDA-MB231-cell lines.
- Published in:
- Basic & Clinical Cancer Research, 2017, v. 9, n. 3, p. 23
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- Publication type:
- Article
Correlation Between Mucosal IL-6 mRNA Expression Level and Virulence Factors of Helicobacter pylori in Iranian Adult Patients With Chronic Gastritis.
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- Jundishapur Journal of Microbiology, 2015, v. 8, n. 8, p. 1, doi. 10.5812/jjm.21701
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- Publication type:
- Article
A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 8, p. 2021, doi. 10.1002/ajmg.a.34096
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- Publication type:
- Article
BRAF gene mutation in Iranian familial colorectal cancer patients at risk for Lynch syndrome.
- Published in:
- Iranian Journal of Gastroenterology & Hepatology (GOVARESH), 2017, v. 22, n. 3, p. 26
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- Publication type:
- Article
Oxidized Low-Density Lipoprotein and Upregulated Expression of Osteonectin and Bone Sialoprotein in Vascular Smooth Muscle Cells.
- Published in:
- Laboratory Medicine, 2014, v. 45, n. 4, p. 297, doi. 10.1309/LMUJWVQFW6CJMSOQ
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- Publication type:
- Article
A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Update of spectrum c.35delG and c.‐23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss.
- Published in:
- Annals of Human Genetics, 2019, v. 83, n. 1, p. 1, doi. 10.1111/ahg.12284
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- Publication type:
- Article