Violetta Steeples

Oxford, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 20 publications

Hypertrophic cardiomyopathy caused by filamin-C variants has restrictive and extracardiac features and a distinctive ECG.

Hypertrophic cardiomyopathy caused by filamin-C variants has restrictive and extracardiac features and a distinctive ECG.

Journal: Heart rhythm
Published: September 15, 2025

Assaying the myosin super-relaxed state across muscle types, cells and proteins for understanding muscle biology and use in drug discovery.

Assaying the myosin super-relaxed state across muscle types, cells and proteins for understanding muscle biology and use in drug discovery.

Journal: Nature protocols
Published: June 07, 2024

Comparing the effects of chemical Ca2+ dyes and R-GECO on contractility and Ca2+ transients in adult and human iPSC cardiomyocytes.

Comparing the effects of chemical Ca2+ dyes and R-GECO on contractility and Ca2+ transients in adult and human iPSC cardiomyocytes.

Journal: Journal of molecular and cellular cardiology
Published: November 25, 2022

Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in ACTN2.

Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in ACTN2.

Journal: Cells
Published: October 26, 2022

Activation of targetable inflammatory immune signaling is seen in myelodysplastic syndromes with SF3B1 mutations.

Activation of targetable inflammatory immune signaling is seen in myelodysplastic syndromes with SF3B1 mutations.

Journal: eLife
Published: February 24, 2022

CalTrack: High-Throughput Automated Calcium Transient Analysis in Cardiomyocytes.

CalTrack: High-Throughput Automated Calcium Transient Analysis in Cardiomyocytes.

Journal: Circulation research
Published: May 21, 2021

Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant.

Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant.

Journal: Basic research in cardiology
Published: October 06, 2020

U2AF1 mutations induce oncogenic IRAK4 isoforms and activate innate immune pathways in myeloid malignancies.

U2AF1 mutations induce oncogenic IRAK4 isoforms and activate innate immune pathways in myeloid malignancies.

Journal: Nature cell biology
Published: April 17, 2018

Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations.

Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations.

Journal: Blood
Published: April 06, 2018

Splicing factor mutations in the myelodysplastic syndromes: target genes and therapeutic approaches.

Splicing factor mutations in the myelodysplastic syndromes: target genes and therapeutic approaches.

Journal: Advances in biological regulation
Published: September 08, 2017

The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes.

The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes.

Journal: The Journal of clinical investigation
Published: September 02, 2017

Cell-specific proteome analyses of human bone marrow reveal molecular features of age-dependent functional decline.

Cell-specific proteome analyses of human bone marrow reveal molecular features of age-dependent functional decline.

Journal: Nature communications
Published: August 07, 2017
Showing 1-12 of 20

Last Updated: 09/26/2026