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Reproductive Biomedicine Online
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October 19, 2013
Preventing the transmission of mitochondrial DNA disorders: selecting the good guys or kicking out the bad guys
Hubert J M Smeets
Human Reproduction Update
|
May 16, 2015
Evolutionary defined role of the mitochondrial DNA in fertility, disease and ageing
Auke B C Otten, Hubert J M Smeets
Genomics
|
October 8, 2025
A bioinformatics pipeline for identifying homoplasmic and heteroplasmic mitochondrial DNA SNVs in single-cell RNA-Seq datasets
Zhiling Guan, Patrick Lindsey, Rick Kamps, et al.
Handbook of Clinical Neurology
|
February 22, 2023
Reproductive options in mitochondrial disease
Hubert J M Smeets, Suzanne C E H Sallevelt, Mary Herbert
Molecular Genetics and Metabolism
|
January 5, 2016
Leigh syndrome: Resolving the clinical and genetic heterogeneity paves the way for treatment options
Mike Gerards, Suzanne C E H Sallevelt, Hubert J M Smeets
Journal of Inherited Metabolic Disease
|
February 13, 2010
Biochemical abnormalities in a patient with thymidine phosphorylase deficiency with fatal outcome
Jaap A Bakker, Patrick Schlesser, Hubert J M Smeets, et al.
Human Reproduction (Oxford, England)
|
March 13, 2026
From disease prevention to fertility treatment: rethinking the use of mitochondrial donation for oocyte-related infertility in the light of safety and efficacy
Flor Pasturino, Guido M W R De Wert, Cathy Herbrand, et al.
BMC Genomics
|
September 16, 2015
Transcriptome analysis of complex I-deficient patients reveals distinct expression programs for subunits and assembly factors of the oxidative phosphorylation system
Robin van der Lee, Radek Szklarczyk, Jan Smeitink, et al.
International Journal of Molecular Sciences
|
May 11, 2024
Spinning Disk Confocal Microscopy for Optimized and Quantified Live Imaging of 3D Mitochondrial Network
Somaieh Ahmadian, Patrick J Lindsey, Hubert J M Smeets, et al.
Biochimica Et Biophysica Acta
|
October 20, 2009
Patients with Leber hereditary optic neuropathy fail to compensate impaired oxidative phosphorylation
Alex Korsten, Irenaeus F M de Coo, Liesbeth Spruijt, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 80) with videos related to
Sort By:
Page
of 8
Reproductive Biomedicine Online
|
October 19, 2013
Preventing the transmission of mitochondrial DNA disorders: selecting the good guys or kicking out the bad guys
Hubert J M Smeets
Human Reproduction Update
|
May 16, 2015
Evolutionary defined role of the mitochondrial DNA in fertility, disease and ageing
Auke B C Otten, Hubert J M Smeets
Genomics
|
October 8, 2025
A bioinformatics pipeline for identifying homoplasmic and heteroplasmic mitochondrial DNA SNVs in single-cell RNA-Seq datasets
Zhiling Guan, Patrick Lindsey, Rick Kamps, et al.
Handbook of Clinical Neurology
|
February 22, 2023
Reproductive options in mitochondrial disease
Hubert J M Smeets, Suzanne C E H Sallevelt, Mary Herbert
Molecular Genetics and Metabolism
|
January 5, 2016
Leigh syndrome: Resolving the clinical and genetic heterogeneity paves the way for treatment options
Mike Gerards, Suzanne C E H Sallevelt, Hubert J M Smeets
Journal of Inherited Metabolic Disease
|
February 13, 2010
Biochemical abnormalities in a patient with thymidine phosphorylase deficiency with fatal outcome
Jaap A Bakker, Patrick Schlesser, Hubert J M Smeets, et al.
Human Reproduction (Oxford, England)
|
March 13, 2026
From disease prevention to fertility treatment: rethinking the use of mitochondrial donation for oocyte-related infertility in the light of safety and efficacy
Flor Pasturino, Guido M W R De Wert, Cathy Herbrand, et al.
BMC Genomics
|
September 16, 2015
Transcriptome analysis of complex I-deficient patients reveals distinct expression programs for subunits and assembly factors of the oxidative phosphorylation system
Robin van der Lee, Radek Szklarczyk, Jan Smeitink, et al.
International Journal of Molecular Sciences
|
May 11, 2024
Spinning Disk Confocal Microscopy for Optimized and Quantified Live Imaging of 3D Mitochondrial Network
Somaieh Ahmadian, Patrick J Lindsey, Hubert J M Smeets, et al.
Biochimica Et Biophysica Acta
|
October 20, 2009
Patients with Leber hereditary optic neuropathy fail to compensate impaired oxidative phosphorylation
Alex Korsten, Irenaeus F M de Coo, Liesbeth Spruijt, et al.
Page
of 8