Items where Author is "Salehi, Mansoor"

Article

(2020) Association of Selenoprotein S Expression and its Variants with Metabolic Syndrome in Subjects with Cardiovascular Disease. Archives of Medical Research. pp. 535-541. ISSN 0188-4409

(2020) Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East. Human Genetics. pp. 1429-1441. ISSN 0340-6717

(2020) A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23. Audiology and Neuro-Otology. pp. 258-262. ISSN 1420-3030

(2020) Therapeutic plasma exchange may adjust IL-6 and TGF-beta signals in relapsed MS patients peripheral blood. Journal of Clinical Apheresis. pp. 72-78. ISSN 0733-2459

(2019) Association of high level of hs-CRP with in-stent restenosis: A case-control study. Cardiovascular Revascularization Medicine. pp. 583-587. ISSN 1553-8389

(2019) Clinical Trial: CYP2D6 Related Dose Escalation of Tamoxifen in Breast Cancer Patients With Iranian Ethnic Background Resulted in Increased Concentrations of Tamoxifen and Its Metabolites. Frontiers in Pharmacology. ISSN 1663-9812

(2019) A Comparison Between Full-COLD PCR/HRM and PCR Sequencing for Detection of Mutations in Exon 9 of PIK3CA in Breast Cancer Patients. APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY. ISSN 1559-0291 (Electronic) 0273-2289 (Linking)

(2019) Distribution of CYP2D6 polymorphism in the Middle Eastern region. Journal of Research in Medical Sciences. p. 6. ISSN 1735-1995

(2019) Engineered zinc-finger nuclease to generate site-directed modification in the KLF1 gene for fetal hemoglobin induction. JOURNAL OF CELLULAR BIOCHEMISTRY. ISSN 1097-4644 (Electronic) 0730-2312 (Linking)

(2019) Evaluation of GJB2 and GJB6 Mutations in Patients Afflicted with Non-syndromic Hearing Loss. International Journal of Pediatrics-Mashhad. pp. 9053-9060. ISSN 2345-5047

(2019) Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome. Iranian Journal of Child Neurology. pp. 25-34. ISSN 1735-4668

(2019) In Silico Analysis of Synaptonemal Complex Protein 1 (SYCP1) and Acrosin Binding Protein (ACRBP) Antigens to Design Novel Multiepitope Peptide Cancer Vaccine Against Breast Cancer. International Journal of Peptide Research and Therapeutics. pp. 1343-1359. ISSN 1573-3149

(2019) A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family. Audiology and Neuro-Otology. pp. 258-263. ISSN 1420-3030

(2019) Prevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran. International Journal of Pediatrics-Mashhad. pp. 9333-9339. ISSN 2345-5047

(2019) Production, purification, and in vivo evaluation of a novel multiepitope peptide vaccine consisted of immunodominant epitopes of SYCP1 and ACRBP antigens as a prophylactic melanoma vaccine. International Immunopharmacology. p. 8. ISSN 1567-5769

(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. pp. 1704-1713. ISSN 2251-6085

(2019) Whole Exome Sequencing Revealed a Novel GJB1 Pathogenic Variant and a Rare BSCL2 Mutation in Two Iranian Large Pedigrees with Multiple Affected Cases of Charcot-Marie-Tooth. International Journal of Molecular and Cellular Medicine. pp. 169-178. ISSN 2251-9637

(2018) Analysis of the expression of mir-34a, mir-199a, mir-30c and mir-19a in peripheral blood CD4+T lymphocytes of relapsing-remitting multiple sclerosis patients. Gene. pp. 109-117. ISSN 0378-1119

(2018) Association of high level of Hs-CRP with in-stent restenosis: A case-control study. Cardiovasc Revasc Med. ISSN 1878-0938 (Electronic) 1878-0938 (Linking)

(2018) Autism and Probable Prerequisites: Severe and Scheduled Prenatal Stresses at Spotlight. Iranian Journal of Public Health. pp. 1387-1395. ISSN 2251-6085

(2018) Estimating the Risk for Chromosomal Abnormalities and Heteromorphic Variants in Azoospermic and Severe Oligozoospermic Men. Crescent Journal of Medical and Biological Sciences. pp. 101-106. ISSN 2148-9696

(2018) Evaluation of the utility of peripheral blood vs bone marrow in karyotype and fluorescence in situ hybridization for myelodysplastic syndrome diagnosis. Journal of Clinical Laboratory Analysis. ISSN 0887-8013

(2018) GJA4/Connexin 37 Mutations Correlate with Secondary Lymphedema Following Surgery in Breast Cancer Patients. Biomedicines. ISSN 2227-9059

(2018) GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants. International Journal of Pediatric Otorhinolaryngology. pp. 121-126. ISSN 0165-5876

(2018) A homozygous NOP14 variant is likely to cause recurrent pregnancy loss. Journal of Human Genetics. pp. 425-430. ISSN 1434-5161

(2018) An insertion mutation in HOXC13 underlies pure hair and nail ectodermal dysplasia with lacrimal duct obstruction. British Journal of Dermatology. E265-E267. ISSN 0007-0963

(2018) A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features. Journal of Human Genetics. pp. 487-491. ISSN 1434-5161

(2017) Aberrant expression of PlncRNA-1 and TUG1: potential biomarkers for gastric cancer diagnosis and clinically monitoring cancer progression. Biomarkers in Medicine. pp. 1077-1090. ISSN 1752-0363

(2017) Application of Epstein-Barr Virus for Optimization of Immortalized B-lymphocyte Production as a Positive Control in Genetic Studies. Advanced biomedical research. p. 80. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2017) Association of AHSG with alopecia and mental retardation (APMR) syndrome. Human Genetics. pp. 287-296. ISSN 0340-6717

(2017) Evaluation of Energy Balance on Human Telomerase Reverse Transcriptase (hTERT) Alternative Splicing by Semi-quantitative RT-PCR in Human Umbilical Vein Endothelial Cells. Advanced biomedical research. p. 43. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2017) MeDIP Real-Time qPCR has the Potential for Noninvasive Prenatal Screening of Fetal Trisomy 21. International Journal of Molecular and Cellular Medicine. pp. 13-21. ISSN 2251-9637

(2017) Peroxiredons: Tryparedoxin peroxidase from Leishmania major. Current Regenerative Medicine. pp. 24-28. ISSN 24684244 (ISSN)

(2017) RORA and Autism in Isfahan Population: Is There An Epigenetic Relationship. Cell Journal. pp. 540-546. ISSN 2228-5806

(2017) Treatment Outcome of the Drug-resistant Zoonotic Cutaneous Leishmaniasis by Glucantime. Advanced biomedical research. p. 17. ISSN 2277-9175 (Print) 2277-9175 (Linking)