Ella A. Martin
Sydney, NSW, Australia
Last Updated: 09/26/2026
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Found 11 publications
Comprehensive defect detection in mouse embryos and the heart by combining automated phenotyping with novel population averages and atlases.
Journal: Differentiation; research in biological diversity
Published: October 20, 2025
Identification of potential NAD-related biomarkers of recurrent miscarriage risk.
Journal: Human reproduction (Oxford, England)
Published: May 28, 2025
Atlas of multilineage stem cell differentiation reveals TMEM88 as a developmental regulator of blood pressure.
Journal: Nature communications
Published: March 06, 2024
Quantitative 3D analysis and visualization of cardiac fibrosis by microcomputed tomography.
Journal: STAR protocols
Published: January 10, 2022
Hif-1a suppresses ROS-induced proliferation of cardiac fibroblasts following myocardial infarction.
Journal: Cell stem cell
Published: January 09, 2021
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.
Journal: Human molecular genetics
Published: June 29, 2020
NAD deficiency due to environmental factors or gene-environment interactions causes congenital malformations and miscarriage in mice.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: February 05, 2020
Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants.
Journal: Human molecular genetics
Published: June 27, 2019
Gene-environment interaction impacts on heart development and embryo survival.
Journal: Development (Cambridge, England)
Published: October 24, 2018
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
Journal: The New England journal of medicine
Published: August 10, 2017
Showing 1-11 of 11
Last Updated: 09/26/2026