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BMC Cancer|December 6, 2018
Cancer survivors' needs during various treatment phases after multimodal treatment for colon cancer - is there a role for eHealth?C M den Bakker, F G Schaafsma, J A F Huirne, et al.
Analytical Biochemistry|May 21, 2009
Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography-mass spectrometry as a diagnostic test for Barth syndromeRiekelt H Houtkooper, Richard J Rodenburg, Charlotte Thiels, et al.
Biochemistry and Biophysics Reports|April 6, 2026
Sarco/endoplasmatic reticulum calcium ATPase activity in healthy muscle and Brody diseaseJ P Molenaar, M M Snoeck, S Treves, et al.
Human Mutation|April 23, 2009
Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiencySaskia J G Hoefs, Cindy E J Dieteren, Richard J Rodenburg, et al.
Nuklearmedizin. Nuclear Medicine|July 23, 2016
Treatment of painful bone metastases in prostate and breast cancer patients with the therapeutic radiopharmaceutical rhenium-188-HEDP. Clinical benefit in a real-world studyRogier Lange, Floor Overbeek, John M H de Klerk, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 30, 2024
Biallelic Variants of MRPS36 Cause a New Form of Leigh SyndromeSerena Galosi, Cecilia Mancini, Anna Commone, et al.
Stem Cell Research & Therapy|June 26, 2017
Modulation of oxidative phosphorylation and redox homeostasis in mitochondrial NDUFS4 deficiency via mesenchymal stem cellsMarlen Melcher, Katharina Danhauser, Annette Seibt, et al.
Nature Microbiology|December 20, 2016
Microbial stimulation of different Toll-like receptor signalling pathways induces diverse metabolic programmes in human monocytesEkta Lachmandas, Lily Boutens, Jacqueline M Ratter, et al.
Proteomics|May 17, 2012
Impaired ubiquitin-proteasome-mediated PGC-1α protein turnover and induced mitochondrial biogenesis secondary to complex-I deficiencyMurtada H Farhoud, Leo G Nijtmans, Ronald J A Wanders, et al.
Elife|March 7, 2023
Recessive pathogenic variants in <i>MCAT</i> cause combined oxidative phosphorylation deficiencyBryn D Webb, Sara M Nowinski, Ashley Solmonson, et al.
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