Items where Author is "Mohammadi-Asl, J."

(2021) The antioxidant and anti-inflammatory effects of astaxanthin supplementation on the expression of miR-146a and miR-126 in patients with type 2 diabetes mellitus: A randomised, double-blind, placebo-controlled clinical trial. International Journal of Clinical Practice. ISSN 1368-5031

(2019) Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing. Audiology and Neuro-Otology. pp. 25-31. ISSN 1420-3030

(2019) A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Genomics. pp. 840-848. ISSN 0888-7543

(2019) A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family. Int J Audiol. pp. 1-7. ISSN 1708-8186 (Electronic) 1499-2027 (Linking)

(2018) Frequency of gjb2 mutations in families with autosomal recessive non-syndromic hearing loss in Khuzestan province. Genetika. pp. 837-846. ISSN 05340012 (ISSN)

(2018) A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Genomics. ISSN 1089-8646 (Electronic) 0888-7543 (Linking)

(2017) A novel pathogenic variant in an Iranian Ataxia telangiectasia family revealed by next-generation sequencing followed by in silico analysis. Journal of the Neurological Sciences. pp. 212-216. ISSN 0022-510X

(2016) Quantitation of CDH1 promoter methylation in formalin-fixed paraffin-embedded tissues of breast cancer patients using differential high resolution melting analysis. Advanced biomedical research. p. 91. ISSN 2277-9175 (Print) 2277-9175 (Linking)