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Search results (17)

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Developing a Blood Cell-Based Diagnostic Test for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Using Peripheral Blood Mononuclear Cells.

Xu J. et al, (2023), Adv Sci (Weinh), 10

Insights into pancreatic β cell energy metabolism using rodent β cell models

Morten KJ. et al, (2019), Wellcome Open Research, 2, 14 - 14

ssessing cellular energy dysfunction in CFS/ME using a commercially available laboratory test.

Tomas C. et al, (2019), Sci Rep, 9

Monitoring of Extracellular and Intracellular O2 on a Time-resolved Fluorescence Plate Reader

Morten K. et al, (2018), Quenched-phosphorescence Detection of Molecular Oxygen: Applications in Life Sciences

Validating the RedMIT/GFP-LC3 Mouse Model by Studying Mitophagy in Autosomal Dominant Optic Atrophy Due to the OPA1Q285STOP Mutation.

Diot A. et al, (2018), Front Cell Dev Biol, 6

CHAPTER 8. Monitoring of Extracellular and Intracellular O2 on a Time-resolved Fluorescence Plate Reader

Potter M. et al, (2018), 175 - 192

Insights into pancreatic β cell energy metabolism using rodent β cell models

Morten K. et al, (2017), Wellcome Open Research

Growth differentiation factor-11 causes neurotoxicity during oxygen and glucose deprivation in vitro

Sutherland BA. et al, (2017), JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 37, 273 - 274

Ophiobolin A, a sesterpenoid fungal phytotoxin, displays different mechanisms of cell death in mammalian cells depending upon the cancer cell origin.

Morrison R. et al, (2017), Int J Oncol, 50, 773 - 786

Insights into pancreatic β cell energy metabolism using rodent β cell models.

Morten KJ. et al, (2017), Wellcome Open Res, 2

Insights into pancreatic β cell energy metabolism using rodent β cell models.

Morten KJ. et al, (2017), Wellcome open research, 2, 14 - 14

Modulating mitochondrial quality control in disease transmission: towards enabling mitochondrial DNA disease carriers to have healthy children

Diot A. et al, (2016), MITOCHONDRION, 31, 110 - 110

Modulating mitochondrial quality in disease transmission: towards enabling mitochondrial DNA disease carriers to have healthy children.

Diot A. et al, (2016), Biochem Soc Trans, 44, 1091 - 1100

The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy.

Dombi E. et al, (2016), Neurology, 86, 1921 - 1923

novel quantitative assay of mitophagy: Combining high content fluorescence microscopy and mitochondrial DNA load to quantify mitophagy and identify novel pharmacological tools against pathogenic heteroplasmic mtDNA.

Diot A. et al, (2015), Pharmacol Res, 100, 24 - 35

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