Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters











Database
Language
Publication year range
1.
HLA ; 102(1): 108-109, 2023 07.
Article in English | MEDLINE | ID: mdl-36908228

ABSTRACT

A novel HLA-DRB1*04 allele, officially designated HLA-DRB1*04:361, was identified by next-generation sequencing.


Subject(s)
High-Throughput Nucleotide Sequencing , Humans , HLA-DRB1 Chains/genetics , Alleles
2.
HLA ; 101(2): 170-171, 2023 02.
Article in English | MEDLINE | ID: mdl-36205591

ABSTRACT

A novel HLA-B*51 allele, officially designated HLA-B*51:371, was identified by next-generation sequencing.


Subject(s)
HLA-B Antigens , High-Throughput Nucleotide Sequencing , Humans , Base Sequence , Alleles , HLA-B Antigens/genetics
3.
Int J Mol Sci ; 23(10)2022 May 12.
Article in English | MEDLINE | ID: mdl-35628213

ABSTRACT

Adverse ventricular remodeling is the heart's response to damaging stimuli and is linked to heart failure and poor prognosis. Formyl-indolo [3,2-b] carbazole (FICZ) is an endogenous ligand for the aryl hydrocarbon receptor (AhR), through which it exerts pleiotropic effects including protection against inflammation, fibrosis, and oxidative stress. We evaluated the effect of AhR activation by FICZ on the adverse ventricular remodeling that occurs in the early phase of pressure overload in the murine heart induced by transverse aortic constriction (TAC). Cardiac structure and function were evaluated by cardiac magnetic resonance imaging (CMRI) before and 3 days after Sham or TAC surgery in mice treated with FICZ or with vehicle, and cardiac tissue was used for biochemical studies. CMRI analysis revealed that FICZ improved cardiac function and attenuated cardiac hypertrophy. These beneficial effects involved the inhibition of the hypertrophic calcineurin/NFAT pathway, transcriptional reduction in pro-fibrotic genes, and antioxidant effects mediated by the NRF2/NQO1 pathway. Overall, our findings provide new insight into the role of cardiac AhR signaling in the injured heart.


Subject(s)
Carbazoles , Heart Failure , Receptors, Aryl Hydrocarbon , Ventricular Remodeling , Animals , Carbazoles/pharmacology , Cardiomegaly/metabolism , Fibrosis , Heart Failure/drug therapy , Heart Failure/etiology , Heart Failure/metabolism , Ligands , Mice , Mice, Inbred C57BL , Myocytes, Cardiac/metabolism , Receptors, Aryl Hydrocarbon/genetics , Receptors, Aryl Hydrocarbon/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL