Items where Division is "Research Institute for Primordial Prevention of Non-communicable Disease > Pediatric Inherited Diseases Research Center" and Year is 2020

(2020) Upregulation ofMTOR,RPS6KB1, andEIF4EBP1in the whole blood samples of Iranian patients with multiple sclerosis compared to healthy controls. Metabolic Brain Disease. pp. 1309-1316. ISSN 0885-7490

(2020) Sensitivity, Specificity, and Accuracy of Color Doppler Ultrasonography for Diagnosis of Retinal Detachment. Journal of Ophthalmic & Vision Research. pp. 166-171. ISSN 2008-2010

(2020) Association between the microbiota and women's cancers - Cause or consequences? Biomedicine & Pharmacotherapy. ISSN 0753-3322

(2020) Combination of Intravitreal Bevacizumab and Topical Dorzolamide versus Intravitreal Bevacizumab Alone for Diabetic Macular Edema: A Randomized Contralateral Clinical Trial. Biomed Research International. ISSN 2314-6133

(2020) Intravitreal injections of bevacizumab plus methotrexate versus bevacizumab alone for the treatment of diabetic macular edema: A randomized, sham-controlled trial. Journal of Current Ophthalmology. pp. 164-169. ISSN 2452-2325

(2020) Therapeutic inhibition of microRNA-21 (miR-21) using locked-nucleic acid (LNA)-anti-miR and its effects on the biological behaviors of melanoma cancer cells in preclinical studies. Cancer Cell International.

(2020) Rapid noninvasive detection of bladder cancer using survivin antibody-conjugated gold nanoparticles (GNPs) based on localized surface plasmon resonance (LSPR). Cancer Immunology Immunotherapy. pp. 1833-1840. ISSN 0340-7004

(2020) Human placental extract attenuates neurological symptoms in the experimental autoimmune encephalomyelitis model of multiple sclerosis-a putative approach in MS disease? Autoimmunity Highlights. ISSN 2038-0305

(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

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

(2020) A pathogenic variant in the transforming growth factor beta I ( TGFBI ) in four Iranian extended families segregating granular corneal dystrophy type II: A literature review. Iranian Journal of Basic Medical Sciences. pp. 1020-1027. ISSN 2008-3866

(2020) Construction of a sensitive and specific lead biosensor using a genetically engineered bacterial system with a luciferase gene reporter controlled bypbrandcadApromoters. Biomedical Engineering Online.

(2020) C1QTNF4gene p.His198Gln mutation is correlated with early-onset systemic lupus erythematosus in Iranian patients. International Journal of Rheumatic Diseases. pp. 1594-1598. ISSN 1756-1841

(2020) Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome family. Acta Diabetol. pp. 81-87. ISSN 1432-5233 (Electronic) 0940-5429 (Linking)

(2020) Efficacy of insulin targeted gene therapy for type 1 diabetes mellitus: A systematic review and meta-analysis of rodent studies. Iranian Journal of Basic Medical Sciences. pp. 406-415. ISSN 2008-3866

(2020) The challenging nature of primary T lymphocytes for transfection: Effect of protamine sulfate on the transfection efficiency of chemical transfection reagents. Research in Pharmaceutical Sciences. pp. 437-446. ISSN 1735-5362

(2020) Gut Microbiota and Host Gene Mutations in Colorectal Cancer Patients and Controls of Iranian and Finnish Origin. Anticancer Research. pp. 1325-1334. ISSN 0250-7005

(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

(2020) A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Bmc Medical Genetics.

(2020) Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss. Molecular Biology Reports. pp. 5355-5364. ISSN 0301-4851

(2020) Genetic polymorphisms of Y-chromosome short tandem repeats (Y-STRs) in a male population from Golestan province, Iran. Molecular Biology Research Communications. pp. 11-16. ISSN 2322-181X

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

(2020) Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report. Bmc Medical Genetics.