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

A

(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

F

(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

H

(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.

J

(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

K

(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

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(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

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(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.

P

(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)

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(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

S

(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.