Ryan Murchie

555 University Ave
Toronto, ON M5G1X8, Canada

Last Updated: 09/26/2026

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Found 13 publications

Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease.

Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease.

Journal: Scientific reports

Published: October 07, 2020

Loss of the Arp2/3 complex component ARPC1B causes platelet abnormalities and predisposes to inflammatory disease.

Loss of the Arp2/3 complex component ARPC1B causes platelet abnormalities and predisposes to inflammatory disease.

Journal: Nature communications

Published: November 09, 2016

Large B-Cell Lymphoma in an Adolescent Patient With Interleukin-10 Receptor Deficiency and History of Infantile Inflammatory Bowel Disease.

Large B-Cell Lymphoma in an Adolescent Patient With Interleukin-10 Receptor Deficiency and History of Infantile Inflammatory Bowel Disease.

Journal: Journal of pediatric gastroenterology and nutrition

Published: June 24, 2016

System-Wide Modulation of HECT E3 Ligases with Selective Ubiquitin Variant Probes.

System-Wide Modulation of HECT E3 Ligases with Selective Ubiquitin Variant Probes.

Journal: Molecular cell

Published: December 07, 2015

Variants in TRIM22 That Affect NOD2 Signaling Are Associated With Very-Early-Onset Inflammatory Bowel Disease.

Variants in TRIM22 That Affect NOD2 Signaling Are Associated With Very-Early-Onset Inflammatory Bowel Disease.

Journal: Gastroenterology

Published: September 25, 2015

Mutations in Plasmalemma Vesicle Associated Protein Result in Sieving Protein-Losing Enteropathy Characterized by Hypoproteinemia, Hypoalbuminemia, and Hypertriglyceridemia.

Mutations in Plasmalemma Vesicle Associated Protein Result in Sieving Protein-Losing Enteropathy Characterized by Hypoproteinemia, Hypoalbuminemia, and Hypertriglyceridemia.

Journal: Cellular and molecular gastroenterology and hepatology

Published: July 25, 2015

RNA Interference Screen to Identify Kinases That Suppress Rescue of ΔF508-CFTR.

RNA Interference Screen to Identify Kinases That Suppress Rescue of ΔF508-CFTR.

Journal: Molecular & cellular proteomics : MCP

Published: November 07, 2014

Tyrosine phosphorylation of NEDD4 activates its ubiquitin ligase activity.

Tyrosine phosphorylation of NEDD4 activates its ubiquitin ligase activity.

Journal: Science signaling

Published: October 09, 2014

Novel de novo mutations of the interleukin-10 receptor gene lead to infantile onset inflammatory bowel disease.

Novel de novo mutations of the interleukin-10 receptor gene lead to infantile onset inflammatory bowel disease.

Journal: Journal of Crohn's & colitis

Published: January 09, 2014

Protein tyrosine phosphatase σ targets apical junction complex proteins in the intestine and regulates epithelial permeability.

Protein tyrosine phosphatase σ targets apical junction complex proteins in the intestine and regulates epithelial permeability.

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

Published: January 04, 2014

Variants in nicotinamide adenine dinucleotide phosphate oxidase complex components determine susceptibility to very early onset inflammatory bowel disease.

Variants in nicotinamide adenine dinucleotide phosphate oxidase complex components determine susceptibility to very early onset inflammatory bowel disease.

Journal: Gastroenterology

Published: January 02, 2014

Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease.

Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease.

Journal: Gastroenterology

Published: October 02, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026