Profile of the Adelaide Centre for the Molecular Genetics of Development

Precise single base substitution in the shibire gene by CRISPR/Cas9-mediated homology directed repair in Bactrocera tryoni.

BMC genetics·2020

Maintenance of Cell Fate by the Polycomb Group Gene Sex Combs Extra Enables a Partial Epithelial Mesenchymal Transition in Drosophila.

G3 (Bethesda, Md.)·2020

Chromosomal instability causes sensitivity to protein folding stress and ATP depletion.

Biology open·2018

Frazzled can act through distinct molecular pathways in epithelial cells to regulate motility, apical constriction, and localisation of E-Cadherin.

PloS one·2018

Phosphoenolpyruvate Carboxykinase Maintains Glycolysis-driven Growth in Drosophila Tumors.

Scientific reports·2017

Autophagy regulates the survival of cells with chromosomal instability.

Oncotarget·2016

Spatiotemporal dynamics of lineage-specific epithelial maturation in the developing mouse stomach.

The International journal of developmental biology·2026

Dynein axonemal assembly factors (dnaaf) 5 and 9 are expressed in ciliated organs of zebrafish embryos.

The International journal of developmental biology·2026

A chloroquine sensitivity gradient induces tissue regeneration and maintenance phenotypes in planarians.

The International journal of developmental biology·2026

Sialylated glycoproteins and sialyltransferases involved in mesoderm-derived organ formation during embryogenesis.

The International journal of developmental biology·2026

The Hydra FGF family - dispersed across the genome and expressed locally.

The International journal of developmental biology·2026

Correction: Inhibition of COX2 impairs angiogenesis and causes vascular defects in developing zebrafish embryos.

The International journal of developmental biology·2025

Homozygous variants in ZSWIM6 cause severe syndromic short stature and developmental delay.

Hormone research in paediatrics·2026

Before hormones: early sex-specific mechanisms shaping nervous system development, function, and postnatal disease susceptibility.

Frontiers in behavioral neuroscience·2026

A Likely Diagnosis of Familial Partial Androgen Insensitivity Syndrome in Three 46, XY Siblings With Ambiguous Genitalia: A Case Series.

Clinical case reports·2026

The genome sequence of the Silver Colonel, Odontomyia argentata (Fabricius, 1794) (Diptera: Stratiomyidae).

Wellcome open research·2026

The genome sequence of a nematode, Thelazia callipaeda Railliet & Henry, 1910 (Rhabditida: Thelaziidae).

Wellcome open research·2026

Long-read sequencing resolves complex CYP21A2 variants and identifies 2+0 carriers in 21-hydroxylase deficiency.

The Journal of molecular diagnostics : JMD·2026

Related Experiment Videos

Profile of the Adelaide Centre for the Molecular Genetics of Development

Related Concept Videos

Precise single base substitution in the shibire gene by CRISPR/Cas9-mediated homology directed repair in Bactrocera tryoni.

Maintenance of Cell Fate by the Polycomb Group Gene Sex Combs Extra Enables a Partial Epithelial Mesenchymal Transition in Drosophila.

Chromosomal instability causes sensitivity to protein folding stress and ATP depletion.

Frazzled can act through distinct molecular pathways in epithelial cells to regulate motility, apical constriction, and localisation of E-Cadherin.

Phosphoenolpyruvate Carboxykinase Maintains Glycolysis-driven Growth in Drosophila Tumors.

Autophagy regulates the survival of cells with chromosomal instability.

Spatiotemporal dynamics of lineage-specific epithelial maturation in the developing mouse stomach.

Dynein axonemal assembly factors (dnaaf) 5 and 9 are expressed in ciliated organs of zebrafish embryos.

A chloroquine sensitivity gradient induces tissue regeneration and maintenance phenotypes in planarians.

Sialylated glycoproteins and sialyltransferases involved in mesoderm-derived organ formation during embryogenesis.

The Hydra FGF family - dispersed across the genome and expressed locally.

Correction: Inhibition of COX2 impairs angiogenesis and causes vascular defects in developing zebrafish embryos.

Homozygous variants in ZSWIM6 cause severe syndromic short stature and developmental delay.

Before hormones: early sex-specific mechanisms shaping nervous system development, function, and postnatal disease susceptibility.

A Likely Diagnosis of Familial Partial Androgen Insensitivity Syndrome in Three 46, XY Siblings With Ambiguous Genitalia: A Case Series.

The genome sequence of the Silver Colonel, Odontomyia argentata (Fabricius, 1794) (Diptera: Stratiomyidae).

The genome sequence of a nematode, Thelazia callipaeda Railliet & Henry, 1910 (Rhabditida: Thelaziidae).

Long-read sequencing resolves complex CYP21A2 variants and identifies 2+0 carriers in 21-hydroxylase deficiency.

Related Experiment Videos

Profile of the Adelaide Centre for the Molecular Genetics of Development

Related Concept Videos

Related Articles