Items where Author is "Kheirollahi, Majid"

(2020) The Clinical Effectiveness of Preimplantation Genetic Diagnosis for Chromosomal Translocation Carriers: A Meta-analysis. Global Medical Genetics. pp. 14-21. ISSN 2699-9404

(2020) The Effect of Parental Consanguinity on Clinical Course and Outcome of Children with Focal Segmental Glomerulosclerosis, a Report from Isfahan, Iran. Iranian Journal of Kidney Diseases. pp. 348-357. ISSN 1735-8582

(2020) Gene delivery by PeI-nanocomplex into breast and colorectal tumor cell lines, the impacts of N/P ratio, size and type of the cell. Fabad Journal of Pharmaceutical Sciences. pp. 19-27. ISSN 13004182 (ISSN)

(2020) Meta-Analysis on the Association of C-Reactive Protein Polymorphisms with Metabolic Syndrome. Global Medical Genetics. pp. 8-13. ISSN 2699-9404

(2020) New Variants in the CDH1 Gene in Iranian Families with Hereditary Diffuse Gastric Cancer. Middle East Journal of Cancer. pp. 493-501. ISSN 2008-6709

(2019) Clinical Feature and Genetics in Rett Syndrome: A Report on Iranian Patients. Iranian Journal of Child Neurology. pp. 37-51. ISSN 1735-4668

(2019) Correlations between the expression of hTERT and alpha and beta splice variants in human brain tumors. Advances in Clinical and Experimental Medicine. pp. 507-513. ISSN 1899-5276

(2019) MDA-7/interleukin 24 (IL-24) in tumor gene therapy: application of tumor penetrating/homing peptides for improvement of the effects. Expert Opinion on Biological Therapy. pp. 211-223. ISSN 1471-2598

(2019) The MTHFR C677T polymorphism influences the efficacy of folic acid supplementation on the nerve conduction studies in patients with diabetic polyneuropathy; A randomized, double blind, placebo-controlled study. Journal of Research in Medical Sciences. ISSN 1735-1995

(2019) Mn-doped ZnS quantum dots-chlorin e6 shows potential as a treatment for chondrosarcoma: an in vitro study. IET Nanobiotechnol. pp. 387-391. ISSN 1751-875X (Electronic) 1751-8741 (Linking)

(2019) A Novel Pathogenic Variant in NAGLU (N-Acetyl-Alpha-Glucosaminidase) gene Identified by Targeted Next-Generation Sequencing Followed by in Silico Analysis. Iranian Journal of Child Neurology. pp. 173-183. ISSN 1735-4668

(2019) Novel Variants and Copy Number Variation in CDH1 Gene in Iranian Patients with Sporadic Diffuse Gastric Cancer. Journal of Gastrointestinal Cancer. pp. 420-427. ISSN 1941-6628

(2019) Targeting MCF-7 Cell Line by Listeriolysin O Pore Forming Toxin Fusion with AHNP Targeted Peptide. Adv Biomed Res. p. 33. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2018) Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene. Iranian Journal of Pediatrics. ISSN 2008-2142

(2018) In silico analysis of SLC3A1 and SLC7A9 mutations in Iranian patients with Cystinuria. Molecular Biology Reports. pp. 1165-1173. ISSN 0301-4851

(2018) Meta-Analysis of the Association between GABA Receptor Polymorphisms and Autism Spectrum Disorder (ASD). Journal of Molecular Neuroscience. pp. 1-9. ISSN 0895-8696

(2018) Novel Variants and Copy Number Variation in CDH1 Gene in Iranian Patients with Sporadic Diffuse Gastric Cancer. J Gastrointest Cancer. ISSN 1941-6636 (Electronic)

(2018) TRPC6 Mutational Analysis in Iranian Children With Focal Segmental Glomerulosclerosis. Iranian Journal of Kidney Diseases. pp. 341-349. ISSN 1735-8582

(2018) Variants in human prostacyclin receptor gene in patients with migraine headache. Iranian Journal of Psychiatry. pp. 239-243. ISSN 17354587 (ISSN)

(2017) Assessment Effects of Resveratrol on Human Telomerase Reverse Transcriptase Messenger Ribonucleic Acid Transcript in Human Glioblastoma. Advanced biomedical research. p. 73. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2017) Comparative study on mutations in CDH1 gene in Iranian patients with hereditary diffuse gastric cancer (HDGC) and sporadic diffuse gastric cancer (SDGC). Journal of Isfahan Medical School. pp. 622-628. ISSN 10277595 (ISSN)

(2017) Comparison of the Frequency of Y-short Tandem Repeats Markers between Sadat and Non-Sadat Populations in Isfahan Province of Iran. Advanced biomedical research. p. 33. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2017) Evaluation of miR-362 Expression in Astrocytoma of Human Brain Tumors. Advanced biomedical research. p. 129. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2017) Identification of B and T cell epitope based peptide vaccine from IGF-1 receptor in breast cancer. Journal of Molecular Graphics & Modelling. pp. 316-321. ISSN 1093-3263

(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) Report of SLC3A1/rBAT gene mutations in Iranian cystinuria patients: A direct sequencing study. Journal of Research in Medical Sciences. ISSN 1735-1995

(2017) A Report of a Novel Mutation in Human Prostacyclin Receptor Gene in Patients Affected with Migraine. Iranian journal of psychiatry. pp. 219-222. ISSN 1735-4587 (Print) 1735-4587 (Linking)

(2017) Simple and Easy to Perform Preimplantation Genetic Diagnosis for beta-thalassemia Major Using Combination of Conventional and Fluorescent Polymerase Chain Reaction. Advanced biomedical research. p. 23. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2017) miR-145 and miR20a-5p Potentially Mediate Pleiotropic Effects of Interferon-Beta Through Mitogen-Activated Protein Kinase Signaling Pathway in Multiple Sclerosis Patients. Journal of Molecular Neuroscience. pp. 16-24. ISSN 0895-8696