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Cells|July 26, 2024
Genetic Deficiencies of Hyaluronan DegradationStephen P Fink, Barbara Triggs-Raine
FEBS Letters|March 25, 2014
Diverse diseases from a ubiquitous process: the ribosomopathy paradoxJoy Armistead, Barbara Triggs-Raine
World Journal of Biological Chemistry|September 1, 2015
Biology of hyaluronan: Insights from genetic disorders of hyaluronan metabolismBarbara Triggs-Raine, Marvin R Natowicz
Histochemistry and Cell Biology|October 31, 2015
Hyaluronidase 2 (HYAL2) is expressed in endothelial cells, as well as some specialized epithelial cells, and is required for normal hyaluronan catabolismBiswajit Chowdhury, Richard Hemming, Sana Faiyaz, et al.
BBA Clinical|December 18, 2015
Mutation of EMG1 causing Bowen-Conradi syndrome results in reduced cell proliferation rates concomitant with G2/M arrest and 18S rRNA processing delayJoy Armistead, Richard Hemming, Nehal Patel, et al.
BMC Developmental Biology|September 23, 2010
EMG1 is essential for mouse pre-implantation embryo developmentXiaoli Wu, Sumit Sandhu, Nehal Patel, et al.
The American Journal of Clinical Nutrition|March 2, 2012
Serum lipids, plant sterols, and cholesterol kinetic responses to plant sterol supplementation in phytosterolemia heterozygotes and control individualsSemone B Myrie, David Mymin, Barbara Triggs-Raine, et al.
The Journal of Biological Chemistry|November 23, 2012
Murine hyaluronidase 2 deficiency results in extracellular hyaluronan accumulation and severe cardiopulmonary dysfunctionBiswajit Chowdhury, Richard Hemming, Sabine Hombach-Klonisch, et al.
The Journal of Biological Chemistry|March 28, 2012
Hyaluronidase 1 and β-hexosaminidase have redundant functions in hyaluronan and chondroitin sulfate degradationLara Gushulak, Richard Hemming, Dianna Martin, et al.
Diabetes Care|November 28, 2002
The prevalence of the HNF-1alpha G319S mutation in Canadian aboriginal youth with type 2 diabetesElizabeth A C Sellers, Barbara Triggs-Raine, Cheryl Rockman-Greenberg, et al.
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