Found: 16
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A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23.
- Published in:
- 2020
- By:
- 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
- By:
- Publication type:
- journal article
Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome family.
- Published in:
- Acta Diabetologica, 2020, v. 57, n. 1, p. 81, doi. 10.1007/s00592-019-01381-y
- By:
- Publication type:
- Article
Investigation of mRNA Expression Levels of TGIFLX and OCT1 Homeobox Genes in Colorectal Cancer.
- Published in:
- Acta Medica Iranica, 2018, v. 56, n. 10, p. 653
- By:
- Publication type:
- Article
Differential Expression of Human Homeodomain TGIFLX in Brain Tumor Cell Lines.
- Published in:
- Acta Medica Iranica, 2013, v. 51, n. 12, p. 834
- By:
- Publication type:
- Article
Correction to: Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report.
- Published in:
- 2020
- By:
- Publication type:
- Correction Notice
Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-0950-4
- By:
- Publication type:
- Article
Association of P1635 and P1655 polymorphisms in dysbindin ( DTNBP1) gene with schizophrenia.
- Published in:
- Acta Neuropsychiatrica, 2012, v. 24, n. 3, p. 155, doi. 10.1111/j.1601-5215.2011.00598.x
- By:
- Publication type:
- Article
Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome.
- Published in:
- Endocrine (1355008X), 2019, v. 66, n. 2, p. 185, doi. 10.1007/s12020-019-02004-w
- By:
- Publication type:
- Article
TGF-β Codon 25 Polymorphism and the Risk of Graft-Versus-Host Disease after Allogenic Hematopoietic Stem Cell Transplantation.
- Published in:
- Iranian Journal of Allergy, Asthma & Immunology, 2010, v. 9, n. 1, p. 1
- By:
- Publication type:
- Article
Induced pluripotent stem cells in research and therapy of diseases: review article.
- Published in:
- Tehran University Medical Journal, 2014, v. 72, n. 7, p. 423
- By:
- Publication type:
- Article
Upregulation of MTOR, RPS6KB1, and EIF4EBP1 in the whole blood samples of Iranian patients with multiple sclerosis compared to healthy controls.
- Published in:
- Metabolic Brain Disease, 2020, v. 35, n. 8, p. 1309, doi. 10.1007/s11011-020-00590-7
- By:
- Publication type:
- Article
Use of siRNA in knocking down of dopamine receptors, a possible therapeutic option in neuropsychiatric disorders.
- Published in:
- Molecular Biology Reports, 2012, v. 39, n. 2, p. 2003, doi. 10.1007/s11033-011-0947-3
- By:
- Publication type:
- Article
Molecular genetics and gene therapy in esophageal cancer: a review article.
- Published in:
- Tehran University Medical Journal, 2011, v. 69, n. 6, p. 331
- By:
- Publication type:
- Article
Applications of comparative genomic hybridization in cancer and genetic disorders: a review article.
- Published in:
- Tehran University Medical Journal, 2010, v. 68, n. 1, p. 1
- By:
- Publication type:
- Article
Genetic variants of susceptible genes to schizophrenia and their role on disease progress.
- Published in:
- Medical Sciences Journal of Islamic Azad University Tehran Medical Branch, 2014, v. 24, n. 2, p. 61
- By:
- Publication type:
- Article