Denny L. Cottle

Clayton, VIC, Australia

Last Updated: 09/26/2026

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Found 23 publications

PKD1 5'UTR variants are a rare cause of disease in ADPKD and suggest a new focus for therapeutic development.

PKD1 5'UTR variants are a rare cause of disease in ADPKD and suggest a new focus for therapeutic development.

Journal: European journal of human genetics : EJHG

Published: March 30, 2025

Disrupted glucocorticoid receptor cell signalling causes a ciliogenesis defect in the fetal mouse renal tubule.

Disrupted glucocorticoid receptor cell signalling causes a ciliogenesis defect in the fetal mouse renal tubule.

Journal: EMBO reports

Published: July 24, 2024

The activity of early-life gene regulatory elements is hijacked in aging through pervasive AP-1-linked chromatin opening.

The activity of early-life gene regulatory elements is hijacked in aging through pervasive AP-1-linked chromatin opening.

Journal: Cell metabolism

Published: August 21, 2023

Modulating inflammation with interleukin 37 treatment ameliorates murine Autosomal Dominant Polycystic Kidney Disease.

Modulating inflammation with interleukin 37 treatment ameliorates murine Autosomal Dominant Polycystic Kidney Disease.

Journal: Kidney international

Published: December 08, 2022

Deletion of Aurora kinase A prevents the development of polycystic kidney disease in mice.

Deletion of Aurora kinase A prevents the development of polycystic kidney disease in mice.

Journal: Nature communications

Published: January 30, 2022

BCL-XL exerts a protective role against anemia caused by radiation-induced kidney damage.

BCL-XL exerts a protective role against anemia caused by radiation-induced kidney damage.

Journal: The EMBO journal

Published: May 07, 2020

Topical Aminosalicylic Acid Improves Keratinocyte Differentiation in an Inducible Mouse Model of Harlequin Ichthyosis.

Topical Aminosalicylic Acid Improves Keratinocyte Differentiation in an Inducible Mouse Model of Harlequin Ichthyosis.

Journal: Cell reports. Medicine

Published: February 26, 2020

A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder.

A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder.

Journal: Development (Cambridge, England)

Published: February 17, 2020

CBE1 Is a Manchette- and Mitochondria-Associated Protein With a Potential Role in Somatic Cell Proliferation.

CBE1 Is a Manchette- and Mitochondria-Associated Protein With a Potential Role in Somatic Cell Proliferation.

Journal: Endocrinology

Published: June 24, 2019

ABCA12 regulates insulin secretion from β-cells.

ABCA12 regulates insulin secretion from β-cells.

Journal: EMBO reports

Published: June 18, 2019

AKT signaling promotes DNA damage accumulation and proliferation in polycystic kidney disease.

AKT signaling promotes DNA damage accumulation and proliferation in polycystic kidney disease.

Journal: Human molecular genetics

Published: April 07, 2019

Loss of GRHL3 leads to TARC/CCL17-mediated keratinocyte proliferation in the epidermis.

Loss of GRHL3 leads to TARC/CCL17-mediated keratinocyte proliferation in the epidermis.

Journal: Cell death & disease

Published: November 08, 2017

Showing 1-12 of 23

Last Updated: 09/26/2026