M. Nooteboom

发表

Sustained accumulation of prelamin A and depletion of lamin A/C both cause oxidative stress and mitochondrial dysfunction but induce different cell fates

W. D. De Vos, A. Rajković, J. Broers, 2015, Nucleus.

Controlling T-Cell Activation with Synthetic Dendritic Cells Using the Multivalency Effect

C. Figdor, K. Blank, A. Rowan, 2017, ACS omega.

Controlling T-Cell Activation with Synthetic Dendritic Cells Using the Multivalency Effect

C. Figdor, K. Blank, A. Rowan, 2017, ACS omega.

Mitochondrial Biogenesis : Pharmacological approaches ” REGULATION AND QUANTIFICATION OF CELLULAR MITOCHONDRIAL MORPHOLOGY AND CONTENT

K. Tronstad, P. Willems, W. Koopman, 2013 .

Live-Cell Quantification of Mitochondrial Functional Parameters

P. Willems, W. Koopman, M. Nooteboom, 2012 .

Cellular and animal models for mitochondrial complex I deficiency: A focus on the NDUFS4 subunit

J. Smeitink, P. Willems, W. Koopman, 2013, IUBMB life.

Clonal Expansion of Early to Mid-Life Mitochondrial DNA Point Mutations Drives Mitochondrial Dysfunction during Human Ageing

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2014, PLoS genetics.

A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia.

Christian Gilissen, Johannes Zschocke, Radek Szklarczyk, 2013, Human molecular genetics.

Control of mitochondrial integrity in ageing and disease

H. Osiewacz, R. Szklarczyk, M. Nooteboom, 2014, Philosophical Transactions of the Royal Society B: Biological Sciences.

Mutations in mtDNA in relation to ageing and disease

H. Osiewacz, R. Szklarczyk, M. Nooteboom, 2014 .

Mitochondrial DNA mutations affect calcium handling in differentiated neurons

M. Whittington, D. Turnbull, A. Trevelyan, 2010, Brain : a journal of neurology.

Comparison of Mitochondrial Mutation Spectra in Ageing Human Colonic Epithelium and Disease: Absence of Evidence for Purifying Selection in Somatic Mitochondrial DNA Point Mutations

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2012, PLoS genetics.

BOLA1 is an aerobic protein that prevents mitochondrial morphology changes induced by glutathione depletion.

Jolein Gloerich, Radek Szklarczyk, M. Huynen, 2013, Antioxidants & redox signaling.

The role of mitochondrial OXPHOS dysfunction in the development of neurologic diseases

R. Rodenburg, J. Smeitink, P. Willems, 2013, Neurobiology of Disease.

Quantitative Glucose and ATP Sensing in Mammalian Cells

J. Smeitink, R. Brock, P. Willems, 2011, Pharmaceutical Research.

Age-associated mitochondrial DNA mutations lead to small but significant changes in cell proliferation and apoptosis in human colonic crypts

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2010, Aging cell.

Re: Mitochondria and Tumor Progression in Ulcerative Colitis

M. Nooteboom, Mathers Jc, C. Age-associated, 2014 .

A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia.

M. Huynen, J. Veltman, R. Rodenburg, 2013, Human molecular genetics.