Kirsten Allan
Melbourne, VIC, Australia
Last Updated: 09/26/2026
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Found 8 publications
Breast cancer specialists' experiences and attitudes towards mainstream genetic testing for patients with breast cancer.
Journal: Hereditary cancer in clinical practice
Published: December 05, 2025
Functional Characterization of a Novel GPC3 Missense Variant in Simpson-Golabi-Behmel Syndrome.
Journal: American journal of medical genetics. Part A
Published: July 17, 2025
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders.
Journal: medRxiv : the preprint server for health sciences
Published: April 22, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.
Journal: Nature
Published: April 07, 2024
PTP61F Mediates Cell Competition and Mitigates Tumorigenesis.
Journal: International journal of molecular sciences
Published: October 29, 2021
Differential regulation of protein tyrosine kinase signalling by Dock and the PTP61F variants.
Journal: The FEBS journal
Published: August 19, 2016
A commonly used Drosophila model of Alzheimer's disease generates an aberrant species of amyloid-β with an additional N-terminal glutamine residue.
Journal: FEBS letters
Published: August 07, 2014
In Drosophila, RhoGEF2 cooperates with activated Ras in tumorigenesis through a pathway involving Rho1-Rok-Myosin-II and JNK signalling.
Journal: Disease models & mechanisms
Published: January 18, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026