David K. Wood

University of Minnesota

United States

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Articles (11)

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2023

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2022

Year:

2022

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2022

Sickle cell blood flow and hemoglobin oxygen saturation can be simultaneously measured using a microfluidic device. This combined measurement platform provides a tool to evaluate the potential clinical benefit of anti-sickling therapies.

Year:

2022

Year:

2022

Year:

2022

Collaborators (6)

Carolyn Kingsley

University of Minnesota

UNITED STATES

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Philip Pearce

University College London

UNITED KINGDOM

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Umut A. Gurkan

Professor

Case Western Reserve University Case School of Engineering

UNITED STATES

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Yuan-Nan Young

Professor

New Jersey Institute of Technology

UNITED STATES

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Joan Beckman

University of Minnesota

UNITED STATES

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Rodolfo Brandao

Imperial College London

UNITED KINGDOM

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David K. Wood

Research Interests

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Contact this professor

Articles (11)

Hydrodynamic interactions between rough surfaces

Next generation microfluidics: fulfilling the promise of lab-on-a-chip technologies

JAK-STAT inhibition reduces endothelial prothrombotic activation and leukocyte–endothelial proadhesive interactions

High-throughput quantification of red blood cell deformability and oxygen saturation to probe mechanisms of sickle cell disease

Robust microtubule dynamics facilitate low-tension kinetochore detachment in metaphase

The effect of rigid cells on blood viscosity: linking rheology and sickle cell anemia

Fluorescence Lifetime Measurement of Prefibrillar Sickle Hemoglobin Oligomers as a Platform for Drug Discovery in Sickle Cell Disease

Microfluidic Methods to Advance Mechanistic Understanding and Translational Research in Sickle Cell Disease

Simultaneous quantification of blood rheology and oxygen saturation to evaluate affinity-modifying therapies in sickle cell disease

Feature tracking microfluidic analysis reveals differential roles of viscosity and friction in sickle cell blood

Simultaneous quantification of blood rheology and oxygen saturation to evaluate affinity-modifying therapies in sickle cell disease

Collaborators (6)

Carolyn Kingsley

Philip Pearce

Umut A. Gurkan

Yuan-Nan Young

Joan Beckman

Rodolfo Brandao

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