Detalhe da pesquisa
1.
Interdependency of NINJ2 gene expression and polymorphism with susceptibility and response to interferon beta in patients with multiple sclerosis.
Int J Neurosci
; : 1-6, 2022 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35912872
2.
Calcitonin-loaded octamaleimic acid-silsesquioxane nanoparticles in hydrogel scaffold support osteoinductivity in bone regeneration.
Pharm Dev Technol
; 26(2): 220-232, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33258707
3.
A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family.
BMC Med Genet
; 21(1): 127, 2020 06 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32517708
4.
Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss.
Mol Biol Rep
; 47(7): 5355-5364, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32623615
5.
Whole exome sequencing identified a novel LAMA2 frameshift variant causing merosin-deficient congenital muscular dystrophy in a patient with cardiomyopathy, and autism-like behavior.
Neuromuscul Disord
; 32(9): 776-784, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35989179
6.
Knockdown of SOX12 Expression Induced Apoptotic Factors is Associated with TWIST1 and CTNNB1 Expression in Human Acute Myeloid Leukemia Cells.
Int J Mol Cell Med
; 10(4): 249-258, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35875337
7.
Injectable gellan gum/lignocellulose nanofibrils hydrogels enriched with melatonin loaded forsterite nanoparticles for cartilage tissue engineering: Fabrication, characterization and cell culture studies.
Mater Sci Eng C Mater Biol Appl
; 115: 111114, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32600714
8.
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.
Adv Biomed Res
; 9: 25, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33072637
9.
Genetic Study of Hepatocyte Nuclear Factor 1 Alpha Variants in Development of Early-Onset Diabetes Type 2 and Maturity-Onset Diabetes of the Young 3 in Iran.
Adv Biomed Res
; 8: 55, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31673528
10.
Alteration in CD8+ T cell subsets in enterovirus-infected patients: An alarming factor for type 1 diabetes mellitus.
Kaohsiung J Med Sci
; 34(5): 274-280, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29699634