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Langping He

Showing results (41-50 of 76) with videos related to

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Life Science Alliance|January 8, 2025
COA5 has an essential role in the early stage of mitochondrial complex IV assemblyJia Xin Tang, Alfredo Cabrera-Orefice, Jana Meisterknecht, et al.
Annals of Neurology|December 29, 2017
Pathological mechanisms underlying single large-scale mitochondrial DNA deletionsMariana C Rocha, Hannah S Rosa, John P Grady, et al.
Neuromuscular Disorders : NMD|March 29, 2025
Late-onset multiple-acyl-CoA-dehydrogenase deficiency-like condition: a case series from the West of ScotlandTaylor Watson-Fargie, Autumn Coomber, Rachel Edwards, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|January 15, 2016
Impaired mitochondrial biogenesis is a common feature to myocardial hypertrophy and end-stage ischemic heart failureAnnalinda Pisano, Bruna Cerbelli, Elena Perli, et al.
Neurogenetics|October 28, 2017
Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunitsRuth I C Glasgow, Kyle Thompson, Inês A Barbosa, et al.
EMBO Molecular Medicine|September 24, 2020
Bi-allelic pathogenic variants in NDUFC2 cause early-onset Leigh syndrome and stalled biogenesis of complex IAhmad Alahmad, Alessia Nasca, Juliana Heidler, et al.
Clinical Science (London, England : 1979)|January 29, 2015
Novel MTND1 mutations cause isolated exercise intolerance, complex I deficiency and increased assembly factor expressionGrainne S Gorman, Emma L Blakely, Hue-Tran Hornig-Do, et al.
American Journal of Human Genetics|May 3, 2016
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain DeficienciesMetodi D Metodiev, Kyle Thompson, Charlotte L Alston, et al.
EMBO Molecular Medicine|February 29, 2020
Metabolic effects of bezafibrate in mitochondrial diseaseHannah Steele, Aurora Gomez-Duran, Angela Pyle, et al.
Scientific Reports|March 27, 2019
Novel compound mutations in the mitochondrial translation elongation factor (TSFM) gene cause severe cardiomyopathy with myocardial fibro-adipose replacementElena Perli, Annalinda Pisano, Ruth I C Glasgow, et al.
Pageof 8

Showing results (41-50 of 76) with videos related to

Sort By:
Pageof 8
Life Science Alliance|January 8, 2025
COA5 has an essential role in the early stage of mitochondrial complex IV assemblyJia Xin Tang, Alfredo Cabrera-Orefice, Jana Meisterknecht, et al.
Annals of Neurology|December 29, 2017
Pathological mechanisms underlying single large-scale mitochondrial DNA deletionsMariana C Rocha, Hannah S Rosa, John P Grady, et al.
Neuromuscular Disorders : NMD|March 29, 2025
Late-onset multiple-acyl-CoA-dehydrogenase deficiency-like condition: a case series from the West of ScotlandTaylor Watson-Fargie, Autumn Coomber, Rachel Edwards, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|January 15, 2016
Impaired mitochondrial biogenesis is a common feature to myocardial hypertrophy and end-stage ischemic heart failureAnnalinda Pisano, Bruna Cerbelli, Elena Perli, et al.
Neurogenetics|October 28, 2017
Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunitsRuth I C Glasgow, Kyle Thompson, Inês A Barbosa, et al.
EMBO Molecular Medicine|September 24, 2020
Bi-allelic pathogenic variants in NDUFC2 cause early-onset Leigh syndrome and stalled biogenesis of complex IAhmad Alahmad, Alessia Nasca, Juliana Heidler, et al.
Clinical Science (London, England : 1979)|January 29, 2015
Novel MTND1 mutations cause isolated exercise intolerance, complex I deficiency and increased assembly factor expressionGrainne S Gorman, Emma L Blakely, Hue-Tran Hornig-Do, et al.
American Journal of Human Genetics|May 3, 2016
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain DeficienciesMetodi D Metodiev, Kyle Thompson, Charlotte L Alston, et al.
EMBO Molecular Medicine|February 29, 2020
Metabolic effects of bezafibrate in mitochondrial diseaseHannah Steele, Aurora Gomez-Duran, Angela Pyle, et al.
Scientific Reports|March 27, 2019
Novel compound mutations in the mitochondrial translation elongation factor (TSFM) gene cause severe cardiomyopathy with myocardial fibro-adipose replacementElena Perli, Annalinda Pisano, Ruth I C Glasgow, et al.
Pageof 8