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Clinical Chemistry
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January 2, 2010
High-throughput assay to measure oxygen consumption in digitonin-permeabilized cells of patients with mitochondrial disorders
An I Jonckheere, Merei Huigsloot, Antoon J M Janssen, et al.
Mitochondrion
|
July 9, 2017
Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasia
Gudrun Schottmann, Sylvie Picker-Minh, Jana Marie Schwarz, et al.
JIMD Reports
|
July 14, 2021
Human d-lactate dehydrogenase deficiency by <i>LDHD</i> mutation in a patient with neurological manifestations and mitochondrial complex IV deficiency
Anna Ka-Yee Kwong, Sheila Suet-Na Wong, Richard J T Rodenburg, et al.
Environmental Toxicology and Pharmacology
|
July 26, 2011
Androgenic activity in surface water samples detected using the AR-LUX assay: indications for mixture effects
Barry M G Blankvoort, Richard J T Rodenburg, Albertinka J Murk, et al.
Journal of Proteome Research
|
December 13, 2005
In search of secreted protein biomarkers for the anti-inflammatory effect of beta2-adrenergic receptor agonists: application of DIGE technology in combination with multivariate and univariate data analysis tools
Kitty C M Verhoeckx, Marco Gaspari, Sabina Bijlsma, et al.
European Journal of Pain (London, England)
|
January 26, 2011
Mitochondrial dysfunction in muscle tissue of complex regional pain syndrome type I patients
Edward C T Tan, Antoon J M Janssen, Peggy Roestenberg, et al.
JIMD Reports
|
February 23, 2013
Inheritance of the m.3243A>G mutation
Paul de Laat, Saskia Koene, Lambert P W J Vd Heuvel, 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 Disease
Maryke Schoonen, Izelle Smuts, Roan Louw, et al.
International Immunopharmacology
|
September 8, 2004
Characterization of anti-inflammatory compounds using transcriptomics, proteomics, and metabolomics in combination with multivariate data analysis
Kitty C M Verhoeckx, Sabina Bijlsma, Sonja Jespersen, et al.
Journal of Inherited Metabolic Disease
|
March 10, 2012
Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutation
Paul de Laat, Saskia Koene, Lambert P W J van den Heuvel, et al.
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of 7
Search research articles
Search
Showing results (11-20 of 61) with videos related to
Sort By:
Page
of 7
Clinical Chemistry
|
January 2, 2010
High-throughput assay to measure oxygen consumption in digitonin-permeabilized cells of patients with mitochondrial disorders
An I Jonckheere, Merei Huigsloot, Antoon J M Janssen, et al.
Mitochondrion
|
July 9, 2017
Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasia
Gudrun Schottmann, Sylvie Picker-Minh, Jana Marie Schwarz, et al.
JIMD Reports
|
July 14, 2021
Human d-lactate dehydrogenase deficiency by <i>LDHD</i> mutation in a patient with neurological manifestations and mitochondrial complex IV deficiency
Anna Ka-Yee Kwong, Sheila Suet-Na Wong, Richard J T Rodenburg, et al.
Environmental Toxicology and Pharmacology
|
July 26, 2011
Androgenic activity in surface water samples detected using the AR-LUX assay: indications for mixture effects
Barry M G Blankvoort, Richard J T Rodenburg, Albertinka J Murk, et al.
Journal of Proteome Research
|
December 13, 2005
In search of secreted protein biomarkers for the anti-inflammatory effect of beta2-adrenergic receptor agonists: application of DIGE technology in combination with multivariate and univariate data analysis tools
Kitty C M Verhoeckx, Marco Gaspari, Sabina Bijlsma, et al.
European Journal of Pain (London, England)
|
January 26, 2011
Mitochondrial dysfunction in muscle tissue of complex regional pain syndrome type I patients
Edward C T Tan, Antoon J M Janssen, Peggy Roestenberg, et al.
JIMD Reports
|
February 23, 2013
Inheritance of the m.3243A>G mutation
Paul de Laat, Saskia Koene, Lambert P W J Vd Heuvel, 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 Disease
Maryke Schoonen, Izelle Smuts, Roan Louw, et al.
International Immunopharmacology
|
September 8, 2004
Characterization of anti-inflammatory compounds using transcriptomics, proteomics, and metabolomics in combination with multivariate data analysis
Kitty C M Verhoeckx, Sabina Bijlsma, Sonja Jespersen, et al.
Journal of Inherited Metabolic Disease
|
March 10, 2012
Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutation
Paul de Laat, Saskia Koene, Lambert P W J van den Heuvel, et al.
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of 7