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1.
Significant heightened methylation levels of RUNX3 gene promoter in patients with systemic lupus erythematosus.
Lupus
; 33(6): 547-554, 2024 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-38511579
2.
Characterizing Homozygous Variants in Bardet-Biedl Syndrome-Associated Genes Within Iranian Families: Unveiling a Founder Variant in BBS2, c.471G>A.
Biochem Genet
; 2024 Feb 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-38407766
3.
Impact of miRNA-binding site polymorphisms in STAT3 gene on occurrence and clinical characteristics of systemic lupus erythematosus.
Lupus
; 31(3): 338-346, 2022 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-35073195
4.
Three functional variants in the NLRP3 gene are associated with susceptibility and clinical characteristics of systemic lupus erythematosus.
Lupus
; 30(8): 1273-1282, 2021 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-33951966
5.
Assessment of IL-10, IL-1ß and TNF-α gene polymorphisms in patients with peri-implantitis and healthy controls.
Mol Biol Rep
; 48(3): 2285-2290, 2021 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-33689092
6.
MiR-196: emerging of a new potential therapeutic target and biomarker in colorectal cancer.
Mol Biol Rep
; 47(12): 9913-9920, 2020 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-33130965
7.
Association of Fc gamma-receptor genes polymorphisms with chronic periodontitis and Peri-Implantitis.
J Cell Biochem
; 120(7): 12010-12017, 2019 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-30887566
8.
Curcumin ameliorates experimental autoimmune encephalomyelitis in a C57BL/6 mouse model.
Drug Dev Res
; 80(5): 629-636, 2019 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-31033006
9.
Discriminative features in White-Sutton syndrome: literature review and first report in Iran.
Psychiatr Genet
; 34(1): 8-14, 2024 Feb 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-38019139
10.
RARS1-related hypomyelinating leukodystrophy-9 (HLD-9) in two distinct Iranian families: Case report and literature review.
Mol Genet Genomic Med
; 12(4): e2435, 2024 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-38618971
11.
The Effect of Interferon Beta and Natalizumab on miR-20b Expression in Patients with Relapsing-Remitting Multiple Sclerosis is Potentially Mediated by Modulation of the Jak-STAT Signaling Pathway: A Case-control Study.
Iran J Immunol
; 21(2)2024 May 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-38761094
12.
Shikonin protects dopaminergic cell line PC12 against 6-hydroxydopamine-mediated neurotoxicity via both glutathione-dependent and independent pathways and by inhibiting apoptosis.
Neurochem Res
; 38(8): 1590-604, 2013 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-23636806
13.
Whole-exome sequencing revealed a novel homozygous missense variant in OSGEP gene: a case report of Galloway-Mowat syndrome in Iran.
CEN Case Rep
; 12(4): 374-377, 2023 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-36856752
14.
Association of MMP2 and MMP9 gene polymorphisms with nonsyndromic cleft lip/palate in an Iranian population.
J Dent Res Dent Clin Dent Prospects
; 17(3): 149-153, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-38023796
15.
Protective effects of Herbal Compound (IM253) on the inflammatory responses and oxidative stress in a mouse model of multiple sclerosis.
Mult Scler Relat Disord
; 67: 104076, 2022 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-35961059
16.
Identification of causative gene mutation in an Iranian family with coloboma and nephropathy using whole exome sequencing.
CEN Case Rep
; 11(4): 404-407, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-35179696
17.
Association of rs2013162 and rs2235375 Polymorphisms in IRF6 Gene with Susceptibility to Non-Syndromic Cleft Lip and Palate.
Avicenna J Med Biotechnol
; 14(2): 181-185, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35633982
18.
miRNA-binding site polymorphism in IL-15RA gene in rheumatoid arthritis and systemic lupus erythematosus: correlation with disease risk and clinical characteristics.
Clin Rheumatol
; 41(11): 3487-3494, 2022 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-35857215
19.
Whole Exome Sequencing Identified the Causative Mutation in a 4-Year-Old Female with Mulibrey Nanism: A Case Report.
Iran J Public Health
; 51(12): 2826-2830, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-36742244
20.
Association of a miRNA-binding site polymorphism in IL-16 gene with disease risk and clinical characteristics of rheumatoid arthritis and systemic lupus erythematosus.
Clin Rheumatol
; 41(7): 2189-2196, 2022 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-35332405