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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
July 31, 2020
A case for measuring both cellular and cell-free mitochondrial DNA as a disease biomarker in human blood
Hannah S Rosa, Saima Ajaz, Luigi Gnudi, et al.
Cells
|
October 11, 2019
A Diet Induced Maladaptive Increase in Hepatic Mitochondrial DNA Precedes OXPHOS Defects and May Contribute to Non-Alcoholic Fatty Liver Disease
Afshan N Malik, Inês C M Simões, Hannah S Rosa, et al.
Scientific Reports
|
August 8, 2019
Regional mitochondrial DNA and cell-type changes in post-mortem brains of non-diabetic Alzheimer's disease are not present in diabetic Alzheimer's disease
Elisabeth B Thubron, Hannah S Rosa, Angela Hodges, et al.
International Journal of Molecular Sciences
|
December 15, 2019
The Detection and Partial Localisation of Heteroplasmic Mutations in the Mitochondrial Genome of Patients with Diabetic Retinopathy
Afshan N Malik, Hannah S Rosa, Eliane S de Menezes, et al.
Neuromuscular Disorders : NMD
|
September 27, 2016
Dysferlin mutations and mitochondrial dysfunction
Amy E Vincent, Hannah S Rosa, Charlotte L Alston, et al.
Nucleic Acids Research
|
June 1, 2019
Understanding mitochondrial DNA maintenance disorders at the single muscle fibre level
Diana Lehmann, Helen A L Tuppen, Georgia E Campbell, et al.
Annals of Neurology
|
December 29, 2017
Pathological mechanisms underlying single large-scale mitochondrial DNA deletions
Mariana C Rocha, Hannah S Rosa, John P Grady, et al.
Annals of Neurology
|
July 18, 2018
Subcellular origin of mitochondrial DNA deletions in human skeletal muscle
Amy E Vincent, Hannah S Rosa, Kamil Pabis, et al.
The EMBO Journal
|
February 24, 2023
Stress-dependent macromolecular crowding in the mitochondrial matrix
Elianne P Bulthuis, Cindy E J Dieteren, Jesper Bergmans, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
July 31, 2020
A case for measuring both cellular and cell-free mitochondrial DNA as a disease biomarker in human blood
Hannah S Rosa, Saima Ajaz, Luigi Gnudi, et al.
Cells
|
October 11, 2019
A Diet Induced Maladaptive Increase in Hepatic Mitochondrial DNA Precedes OXPHOS Defects and May Contribute to Non-Alcoholic Fatty Liver Disease
Afshan N Malik, Inês C M Simões, Hannah S Rosa, et al.
Scientific Reports
|
August 8, 2019
Regional mitochondrial DNA and cell-type changes in post-mortem brains of non-diabetic Alzheimer's disease are not present in diabetic Alzheimer's disease
Elisabeth B Thubron, Hannah S Rosa, Angela Hodges, et al.
International Journal of Molecular Sciences
|
December 15, 2019
The Detection and Partial Localisation of Heteroplasmic Mutations in the Mitochondrial Genome of Patients with Diabetic Retinopathy
Afshan N Malik, Hannah S Rosa, Eliane S de Menezes, et al.
Neuromuscular Disorders : NMD
|
September 27, 2016
Dysferlin mutations and mitochondrial dysfunction
Amy E Vincent, Hannah S Rosa, Charlotte L Alston, et al.
Nucleic Acids Research
|
June 1, 2019
Understanding mitochondrial DNA maintenance disorders at the single muscle fibre level
Diana Lehmann, Helen A L Tuppen, Georgia E Campbell, et al.
Annals of Neurology
|
December 29, 2017
Pathological mechanisms underlying single large-scale mitochondrial DNA deletions
Mariana C Rocha, Hannah S Rosa, John P Grady, et al.
Annals of Neurology
|
July 18, 2018
Subcellular origin of mitochondrial DNA deletions in human skeletal muscle
Amy E Vincent, Hannah S Rosa, Kamil Pabis, et al.
The EMBO Journal
|
February 24, 2023
Stress-dependent macromolecular crowding in the mitochondrial matrix
Elianne P Bulthuis, Cindy E J Dieteren, Jesper Bergmans, et al.
Page
of 1