Department of Cell and Molecular Biology
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MYH9-related disease mutations cause abnormal red blood cell morphology through increased myosin-actin binding at the membrane.
American journal of hematology Jun, 2019 | Pubmed ID: 30916803
Age-related changes in eye lens biomechanics, morphology, refractive index and transparency.
Aging Dec, 2019 | Pubmed ID: 31844034
Megakaryocyte migration defects due to nonmuscle myosin IIA mutations underlie thrombocytopenia in MYH9-related disease.
Blood 05, 2020 | Pubmed ID: 32315395
The Tudor-domain protein TDRD7, mutated in congenital cataract, controls the heat shock protein HSPB1 (HSP27) and lens fiber cell morphology.
Human molecular genetics Jul, 2020 | Pubmed ID: 32420594
Non-uniform distribution of myosin-mediated forces governs red blood cell membrane curvature through tension modulation.
PLoS computational biology May, 2020 | Pubmed ID: 32453720
Tropomyosin 3.1 Association With Actin Stress Fibers is Required for Lens Epithelial to Mesenchymal Transition.
Investigative ophthalmology & visual science Jun, 2020 | Pubmed ID: 32492110
Tropomodulins.
Current biology : CB May, 2021 | Pubmed ID: 34033779
Nanoscale dynamics of actin filaments in the red blood cell membrane skeleton.
Molecular biology of the cell Mar, 2022 | Pubmed ID: 35020457
Erythroid differentiation in mouse erythroleukemia cells depends on Tmod3-mediated regulation of actin filament assembly into the erythroblast membrane skeleton.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 03, 2022 | Pubmed ID: 35195928
Proteomic and functional analyses of the periodic membrane skeleton in neurons.
Nature communications Jun, 2022 | Pubmed ID: 35680881
An interview with Velia M. Fowler, Department of Biological Sciences, University of Delaware, DE, USA.
Cytoskeleton (Hoboken, N.J.) Dec, 2022 | Pubmed ID: 36194087
Nonmuscle Myosin IIA Regulates the Precise Alignment of Hexagonal Eye Lens Epithelial Cells During Fiber Cell Formation and Differentiation.
Investigative ophthalmology & visual science Apr, 2023 | Pubmed ID: 37070941
Recessive TMOD1 mutation causes childhood cardiomyopathy.
Communications biology Jan, 2024 | Pubmed ID: 38168645
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