Karin Lindkvist

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Professor in Cell biology

Lund University

Sweden

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Professor Karin Lindkvist is a faculty member in Cell Biology at Lund University, Sweden. Her research focuses on the molecular mechanisms of immune response and protein structure, as evidenced by her recent publications on MHC class I in avian species, the activity of human aquaglyceroporins, and the regulation mechanisms of ion channels. She is actively engaged in exploring the intersection of cell biology and medicinal applications, particularly regarding inhibitors in cancer therapy.

Recent Grants

Grant: Close

Gut microbial molecules in diabetes

Open Date: 2023-01-01

Close Date: 2024-12-01

Grant: Close

Targeting chemo-induced metabolic reprogramming in acute myeloid leukemia

Open Date: 2021-01-01

Close Date: 2023-12-01

Grant: Close

Imidazolpropionat - en nyupptäckt länk mellan människans tarmmikrobiota och utveckling av insulinresistens i fettvävnad.

Open Date: 2021-01-01

Close Date: 2023-12-31

Grant: Close

Tillämpa strukturbaserad läkemedelsdesign för att blockera UrdA

Open Date: 2020-02-01

Close Date: 2021-07-31

Grant: Close

Metabol omprogrammering vid akut myeloisk leukemi.

Open Date: 2018-01-01

Close Date:

Positions (1)

Karin Lindkvist

University Name

Lund University

NaN years ago

Systemic Inflammatory Response Syndrome (SIRS) and AQP9 inhibition

No summary provided for this position.

NaN years ago

Karin Lindkvist

Research Interests

Explore related searches

Contact this professor

About

Recent Grants

Positions (1)

Systemic Inflammatory Response Syndrome (SIRS) and AQP9 inhibition

Articles (18)

The superantigen SEA binds to human γδ T cell receptor and activates γδ T cells with moderate MHC class II dependence.

MHC I of the Great Reed Warbler Promotes a Flat Peptide Binding Mode

Crystallization of Human Aquaglyceroporins for Neutron Diffraction Studies

Closed and open structures of the eukaryotic magnesium channel Mrs2 reveal the auto-ligand-gating regulation mechanism

SMS121, a new inhibitor of CD36, impairs fatty acid uptake and viability of acute myeloid leukemia

Molecular basis for human aquaporin inhibition

The structure and function of P5A-ATPases

The structure of songbird MHC class I reveals antigen binding that is flexible at the N-terminus and static at the C-terminus.

Cryo-EM structure supports a role of AQP7 as a junction protein.

The intracellular helical bundle of human glucose transporter GLUT4 is important for complex formation with ASPL

Principles to recover copper-conducting CTR proteins for the purpose of structural and functional studies.

Microfluidic-Derived Detection of Protein-Facilitated Copper Flux Across Lipid Membranes.

Structures of Atm1 provide insight into [2Fe-2S] cluster export from mitochondria

Analyses of the complex formation of staphylococcal enterotoxin A and the human gp130 cytokine receptor

Aquaglyceroporins and orthodox aquaporins in human adipocytes.

Activation of human γδ T cells and NK cells by Staphylococcal enterotoxins requires both monocytes and conventional T cells.

Structural characterization of the microbial enzyme urocanate reductase mediating imidazole propionate production

Targeting GLUT1 in acute myeloid leukemia to overcome cytarabine resistance.

Collaborators (15)

Ara Koh

Tiziano Tuccinardi

Kamil Górecki

Hannah Åbacka

Per Hägglund

kaituo wang

Mikael Akke

Peter Spégel

Eva Sverremark-Ekström

Kefeng Lu

Jonathan Bogan

Isabella Artner

Rashmi Prasad

Gabriele Meloni

Pontus Gourdon

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