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Mitochondrion|September 9, 2015
The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human diseaseJoanna L Elson, Paul M Smith, Laura C Greaves, et al.
The Analyst|September 13, 2018
A new approach to find biomarkers in chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) by single-cell Raman micro-spectroscopyJiabao Xu, Michelle Potter, Cara Tomas, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
Characterization of mtDNA variation in a cohort of South African paediatric patients with mitochondrial diseaseElizna M van der Walt, Izelle Smuts, Robert W Taylor, et al.
The Analyst|June 8, 2019
Correction: A new approach to find biomarkers in chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) by single-cell Raman micro-spectroscopyJiabao Xu, Michelle Potter, Cara Tomas, et al.
ACS Nano|April 15, 2020
The Balance between Actomyosin Contractility and Microtubule Polymerization Regulates Hierarchical Protrusions That Govern Efficient Fibroblast-Collagen InteractionsDelaram Shakiba, Farid Alisafaei, Alireza Savadipour, et al.
Molecular Genetics & Genomic Medicine|September 17, 2020
Direct-to-consumer genetic testing for factor V Leiden and prothrombin 20210G>A: the consumer experienceSarah L Elson, Nicholas A Furlotte, Bethann S Hromatka, et al.
Biophysical Journal|September 27, 2012
Confidence intervals for concentration and brightness from fluorescence fluctuation measurementsKenneth M Pryse, Xi Rong, Jordan A Whisler, et al.
Lancet (London, England)|December 20, 2005
Mitochondrial DNA and survival after sepsis: a prospective studySimon V Baudouin, David Saunders, Watcharee Tiangyou, et al.
The Journal of Molecular Diagnostics : JMD|March 16, 2019
Panel-Based Nuclear and Mitochondrial Next-Generation Sequencing Outcomes of an Ethnically Diverse Pediatric Patient Cohort with Mitochondrial DiseaseMaryke Schoonen, Izelle Smuts, Roan Louw, et al.
Journal of Medical Genetics|June 7, 2007
Mitochondrial DNA haplogroups and type 2 diabetes: a study of 897 cases and 1010 controlsP F Chinnery, C Mowbray, S K Patel, et al.
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