
Morris F. Manolson
Hamilton, ON, Canada
Last Updated: 09/26/2026
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Found 29 publications
Systemic therapies for psoriatic disease and serious adverse events in older adults: A population-based cohort study.
Journal: The Journal of investigative dermatology
Published: September 02, 2025
Systemic Therapies for Psoriatic Disease and Serious Infections in Older Adults.
Journal: JAMA dermatology
Published: March 19, 2025
Evidence for Rab7b and Its Splice Isoforms Having Distinct Biological Functions from Rab7a.
Journal: International journal of molecular sciences
Published: December 31, 2024
The Human Mutation K237_V238del in a Putative Lipid Binding Motif within the V-ATPase a2 Isoform Suggests a Molecular Mechanism Underlying Cutis Laxa.
Journal: International journal of molecular sciences
Published: December 29, 2023
Top Ten Research Priorities for Psoriasis, Atopic Dermatitis and Hidradenitis Suppurativa: The SkIN Canada Priority Setting Initiative.
Journal: Journal of cutaneous medicine and surgery
Published: March 30, 2023
Characterization of a PIP Binding Site in the N-Terminal Domain of V-ATPase a4 and Its Role in Plasma Membrane Association.
Journal: International journal of molecular sciences
Published: January 30, 2023
Advances in understanding N-glycosylation structure, function, and regulation in health and disease.
Advances in understanding N-glycosylation structure, function, and regulation in health and disease.
Journal: European journal of cell biology
Published: August 06, 2021
Purification of active human vacuolar H+-ATPase in native lipid-containing nanodiscs.
Journal: The Journal of biological chemistry
Published: June 21, 2021
The V-ATPase a3 Subunit: Structure, Function and Therapeutic Potential of an Essential Biomolecule in Osteoclastic Bone Resorption.
Journal: International journal of molecular sciences
Published: June 01, 2021
Satisfaction and Awareness of Systemic Psoriasis Treatments: A National Survey Comparing Biologic and Nonbiologic Users.
Journal: Journal of cutaneous medicine and surgery
Published: February 26, 2019
Novel c.G630A TCIRG1 mutation causes aberrant splicing resulting in an unusually mild form of autosomal recessive osteopetrosis.
Journal: Journal of cellular biochemistry
Published: December 23, 2018
Last Updated: 09/26/2026