Items where Author is "Chaleshtori, M. H."

Article

(2020) Molecular genetic study in a cohort of Iranian families suspected to maturity-onset diabetes of the young, reveals a recurrent mutation and a high-risk variant in the CEL gene. Advanced Biomedical Research. ISSN 2277-9175

(2019) Genetic Study of Hepatocyte Nuclear Factor 1 Alpha Variants in Development of Early-Onset Diabetes Type 2 and Maturity-Onset Diabetes of the Young 3 in Iran. Adv Biomed Res. p. 55. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2019) Plasma Level Of miR-21 And miR-451 In Primary And Recurrent Breast Cancer Patients. Breast Cancer-Targets and Therapy. pp. 293-301. ISSN 1179-1314

(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) Investigation of the association between (CCTTT)n polymorphism in NOS2 gene and serum IgE level in patients with vernal keratoconjunctivitis in Chaharmahal va Bakhtiari Province. Gene Reports. pp. 165-170. ISSN 2452-0144

(2018) A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss. Otolaryngology-Head and Neck Surgery. pp. 1084-1092. ISSN 0194-5998

(2018) A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing. International Journal of Pediatric Otorhinolaryngology. pp. 8-11. ISSN 0165-5876

(2017) Inhibition of MicroRNA miR-222 with LNA Inhibitor Can Reduce Cell Proliferation in B Chronic Lymphoblastic Leukemia. Indian Journal of Hematology and Blood Transfusion. pp. 327-332. ISSN 0971-4502

(2017) Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran. Iranian Journal of Public Health. pp. 76-82. ISSN 2251-6085

(2017) A novel TECTA mutation causes ARNSHL. International Journal of Pediatric Otorhinolaryngology. pp. 88-93. ISSN 0165-5876

(2016) Mutation in Second Exon of Myo15a Gene Cause of Nonsyndromic Hearing Loss and Its Association in the Arab Population in Iran. Genetika-Belgrade. pp. 587-596. ISSN 0534-0012

(2016) Polymorphisms of p53 promoter and susceptibility to uterine leiomyoma. Clinical and Experimental Obstetrics & Gynecology. pp. 713-717. ISSN 0390-6663

(2016) 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. Iranian Journal of Basic Medical Sciences. pp. 772-778. ISSN 2008-3866

(2015) The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness. International Journal of Audiology. pp. 124-130. ISSN 1499-2027