Irene Hiniesto-Inigo
Overview
Explore the profile of Irene Hiniesto-Inigo including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
3
Citations
6
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Hiniesto-Inigo I, Sridhar A, Louradour J, Cruz A, de la Cruz A, Lundholm S, et al.
Br J Pharmacol
. 2025 Mar;
PMID: 40083204
Background And Purpose: Congenital long QT syndrome (LQTS) involves genetic mutations affecting ion channels, leading to a prolonged QT interval and increased risk of potentially lethal ventricular arrhythmias. Mutations in...
2.
Hiniesto-Inigo I, Linhart V, Kusay A, Liin S
Channels (Austin)
. 2024 Oct;
18(1):2420651.
PMID: 39462453
The endogenous endocannabinoid-like compound N-arachidonoyl-L-serine (ARA-S) facilitates activation of the human Kv7.1/KCNE1 channel and shortens a prolonged action potential duration and QT interval in guinea pig hearts. Hence, ARA-S is...
3.
de la Cruz A, Wu X, Rainer Q, Hiniesto-Inigo I, Perez M, Edler I, et al.
Int J Mol Sci
. 2023 Aug;
24(15).
PMID: 37569465
Long QT syndrome (LQTS) can lead to ventricular arrhythmia and sudden cardiac death. The most common congenital cause of LQTS is mutations in the channel subunits generating the cardiac potassium...
4.
Hiniesto-Inigo I, Castro-Gonzalez L, Corradi V, Skarsfeldt M, Yazdi S, Lundholm S, et al.
EBioMedicine
. 2023 Feb;
89:104459.
PMID: 36796231
Background: Genotype-positive patients who suffer from the cardiac channelopathy Long QT Syndrome (LQTS) may display a spectrum of clinical phenotypes, with often unknown causes. Therefore, there is a need to...