Julie Ruston

Toronto, ON M5G0A4, Canada

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 9 publications

Functional and molecular single-cell analyses implicate PRDM14 in the initiation of B cell leukemia in mice.

Functional and molecular single-cell analyses implicate PRDM14 in the initiation of B cell leukemia in mice.

Journal: Scientific reports

Published: December 30, 2024

A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects.

A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects.

Journal: Human molecular genetics

Published: January 24, 2023

Suppressor mutations in Mecp2-null mice implicate the DNA damage response in Rett syndrome pathology.

Suppressor mutations in Mecp2-null mice implicate the DNA damage response in Rett syndrome pathology.

Journal: Genome research

Published: October 18, 2019

Failure to identify modifiers of NEBULIN-related nemaline myopathy in two pre-clinical models of the disease.

Failure to identify modifiers of NEBULIN-related nemaline myopathy in two pre-clinical models of the disease.

Journal: Biology open

Published: September 19, 2019

Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes.

Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes.

Journal: Molecular autism

Published: December 09, 2016

Grb2 regulates the proliferation of hematopoietic stem and progenitors cells.

Grb2 regulates the proliferation of hematopoietic stem and progenitors cells.

Journal: Biochimica et biophysica acta. Molecular cell research

Published: October 27, 2016

Lnk adaptor suppresses radiation resistance and radiation-induced B-cell malignancies by inhibiting IL-11 signaling.

Lnk adaptor suppresses radiation resistance and radiation-induced B-cell malignancies by inhibiting IL-11 signaling.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: December 04, 2013

Podocyte-specific loss of Cdc42 leads to congenital nephropathy.

Podocyte-specific loss of Cdc42 leads to congenital nephropathy.

Journal: Journal of the American Society of Nephrology : JASN

Published: April 21, 2012

The adaptor protein Grb2 is not essential for the establishment of the glomerular filtration barrier.

The adaptor protein Grb2 is not essential for the establishment of the glomerular filtration barrier.

Journal: PloS one

Published: February 15, 2012

Showing 1-9 of 9

Last Updated: 09/26/2026