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Effects of vitamin A, C and E, or omega-3 fatty acid supplementation on the level of paraoxonase and arylesterase activity in streptozotocin-induced diabetic rats: an investigation of activities in plasma, and heart and liver homogenates.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Creation of an in vitro model of GM1 gangliosidosis by CRISPR/Cas9 knocking‐out the GLB1 gene in SH‐SY5Y human neuronal cell line.
- Published in:
- Cell Biochemistry & Function, 2024, v. 42, n. 6, p. 1, doi. 10.1002/cbf.4102
- By:
- Publication type:
- Article
Clinical Features of Okur-Chung Neurodevelopmental Syndrome: Case Report and Literature Review.
- Published in:
- Molecular Syndromology, 2022, v. 13, n. 5, p. 381, doi. 10.1159/000522353
- By:
- Publication type:
- Article
Efficacy of insulin targeted gene therapy for type 1 diabetes mellitus: A systematic review and meta-analysis of rodent studies.
- Published in:
- Iranian Journal of Basic Medical Sciences, 2020, v. 23, n. 4, p. 406, doi. 10.22038/ijbms.2020.39470.9359
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- Publication type:
- Article
Intronic OTOF mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorder.
- Published in:
- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01420-2
- By:
- Publication type:
- Article
Spastic paraplegia 51: phenotypic spectrum related to novel homozygous AP4E1 mutation.
- Published in:
- Journal of Genetics, 2022, v. 101, n. 2, p. 1, doi. 10.1007/s12041-022-01385-8
- By:
- Publication type:
- Article
MCM2 mutation causes autosomal dominant nonsyndromic hearing loss (DFNA70): novel variant in the second family.
- Published in:
- Journal of Genetics, 2022, v. 101, n. 1, p. 1, doi. 10.1007/s12041-022-01364-z
- By:
- Publication type:
- Article
Exome sequencing identified a de novo frameshift pathogenic variant of CTBP1 in an extremely rare case of HADDTS.
- Published in:
- Journal of Genetics, 2021, v. 100, n. 2, p. 1, doi. 10.1007/s12041-021-01315-0
- By:
- Publication type:
- Article
Genetic analysis of early onset familial coronary artery diseases.
- Published in:
- Archives of Medical Science - Atherosclerotic Diseases, 2019, v. 4, n. 1, p. e1, doi. 10.5114/amsad.2019.83149
- By:
- Publication type:
- Article
Novel insight into FCSK‐congenital disorder of glycosylation through a CRISPR‐generated cell model.
- Published in:
- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 5, p. 1, doi. 10.1002/mgg3.2445
- By:
- Publication type:
- Article
The effect of N-acetyl cysteine consumption on men with abnormal sperm parameters due to positive history of COVID-19 in the last three months.
- Published in:
- Archives of Italian Urology & Andrology / Archivio Italiano di Urologia Andrologia, 2021, v. 93, n. 4, p. 465, doi. 10.4081/aiua.2021.4.465
- By:
- Publication type:
- Article
Splicing defect in <italic>FKBP10</italic> gene causes autosomal recessive osteogenesis imperfecta disease: a case report.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Effects of N-acetylcysteine and metformin treatment on the stereopathological characteristics of uterus and ovary.
- Published in:
- European Journal of Translational Myology, 2022, v. 32, n. 2, p. 1, doi. 10.4081/ejtm.2022.10409
- By:
- Publication type:
- Article
Comparative analysis of mouse bone marrow and adipose tissue mesenchymal stem cells for critical limb ischemia cell therapy.
- Published in:
- Stem Cell Research & Therapy, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13287-020-02110-x
- By:
- Publication type:
- Article
A substitution mutation in LRP8 gene is significantly associated with susceptibility to familial myocardial infarction.
- Published in:
- ARYA Atherosclerosis, 2020, v. 16, n. 6, p. 301, doi. 10.22122/arya.v16i6.1797
- By:
- Publication type:
- Article
Alpha-Lipoic Acid Ameliorates Impaired Steroidogenesis in Human Granulosa Cells Induced by Advanced Glycation End-Products.
- Published in:
- Iranian Journal of Medical Sciences, 2024, v. 49, n. 8, p. 515, doi. 10.30476/IJMS.2023.99512.3168
- By:
- Publication type:
- Article
The Role of Circular RNAs in Male Infertility and Reproductive Cancers: A Narrative Review.
- Published in:
- Iranian Journal of Medical Sciences, 2023, v. 48, n. 6, p. 527, doi. 10.30476/IJMS.2022.95302.2661
- By:
- Publication type:
- Article
Novel insight into the ectodermal dysplasia 11A: Splicing variant of the EDARADD gene in a family with clinical variability and literature review.
- Published in:
- Journal of Dermatology, 2023, v. 50, n. 10, p. 1357, doi. 10.1111/1346-8138.16849
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- Publication type:
- Article
Novel mutation in the MED23 gene for intellectual disability: A case report and literature review.
- Published in:
- Clinical Case Reports, 2019, v. 7, n. 2, p. 331, doi. 10.1002/ccr3.1942
- By:
- Publication type:
- Article
A novel nonsense variant in the ATL3 gene is associated with disturbed pain sensitivity, numbness of distal limbs and muscle weakness.
- Published in:
- Annals of Human Genetics, 2023, v. 87, n. 4, p. 147, doi. 10.1111/ahg.12501
- By:
- Publication type:
- Article
Clinical features of patients with Yin Yang 1 deficiency causing Gabriele‐de Vries syndrome: A new case and review of the literature.
- Published in:
- Annals of Human Genetics, 2022, v. 86, n. 1, p. 52, doi. 10.1111/ahg.12448
- By:
- Publication type:
- Article
Comparative study of mouse adipose- and bone marrow mesenchymal stem cells in diabetic model with critical limb ischemia.
- Published in:
- Cell & Tissue Banking, 2022, v. 23, n. 4, p. 923, doi. 10.1007/s10561-022-10007-7
- By:
- Publication type:
- Article
The effects of melatonin and metformin on histological characteristics of the ovary and uterus in letrozole-induced polycystic ovarian syndrome mice: A stereological study.
- Published in:
- International Journal of Reproductive Biomedicine, 2022, v. 20, n. 11, p. 973, doi. 10.18502/ijrm.v20i11.12365
- By:
- Publication type:
- Article
Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Two novel Warburg micro syndrome 1 cases caused by pathogenic variants in RAB3GAP1.
- Published in:
- Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00171-9
- By:
- Publication type:
- Article
A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report.
- Published in:
- Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00164-8
- By:
- Publication type:
- Article
Severe phenotype of an Iranian patient with methemoglobinemia type II due to a novel mutation in the CYB5R3 gene.
- Published in:
- Iranian Journal of Pediatric Hematology & Oncology, 2021, v. 11, n. 4, p. 280
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- Publication type:
- Article
Creating cell and animal models of human disease by genome editing using CRISPR/Cas9.
- Published in:
- Journal of Gene Medicine, 2019, v. 21, n. 4, p. N.PAG, doi. 10.1002/jgm.3082
- By:
- Publication type:
- Article
EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature review.
- Published in:
- Human Genome Variation, 2023, v. 10, n. 1, p. 1, doi. 10.1038/s41439-023-00229-w
- By:
- Publication type:
- Article
Pyridoxamine protects human granulosa cells against advanced glycation end-products-induced steroidogenesis disturbances.
- Published in:
- Molecular Biology Reports, 2023, v. 50, n. 10, p. 8537, doi. 10.1007/s11033-023-08723-8
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- Publication type:
- Article
A New Mutation in WT1 Gene Associated with Wilms Tumor with Reduced Penetrance in an Iranian Family.
- Published in:
- International Journal of Cancer Management, 2017, v. 10, n. 8, p. 1, doi. 10.5812/ijcm.7500
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- Publication type:
- Article
Two Novel Mutations in LAMC2 Gene in Iranian Families Affected by Junctional Epidermolysis Bullosa.
- Published in:
- Reports of Biochemistry & Molecular Biology, 2022, v. 10, n. 4, p. 597, doi. 10.52547/rbmb.10.4.597
- By:
- Publication type:
- Article
A Candidate Gene Association Study of Bone Mineral Density in an Iranian Population.
- Published in:
- Frontiers in Endocrinology, 2016, v. 7, p. 1, doi. 10.3389/fendo.2016.00141
- By:
- Publication type:
- Article
Evaluation of the Effect of Ascorbic Acid Administration on Gene Expression Level of IL-6 and TNF-α Cytokines in Deceased Donors.
- Published in:
- Iranian Journal of Allergy, Asthma & Immunology, 2015, v. 14, n. 2, p. 149
- By:
- Publication type:
- Article