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Journal of Assisted Reproduction and Genetics|October 27, 2018
The mitochondrial DNA content of cumulus cells may help predict embryo implantationA Taugourdeau, V Desquiret-Dumas, J F Hamel, et al.
Functional & Integrative Genomics|January 17, 2002
Gene induction during differentiation of human monocytes into dendritic cells: an integrated study at the RNA and protein levelsC Angénieux, D Fricker, J M Strub, et al.
Mitochondrion|August 19, 2014
Mitochondrial macro-haplogroup JT may play a protective role in ovarian ageingP May-Panloup, V Desquiret, C Morinière, et al.
Human Reproduction (Oxford, England)|September 24, 2017
Deep sequencing shows that oocytes are not prone to accumulate mtDNA heteroplasmic mutations during ovarian ageingL Boucret, C Bris, V Seegers, et al.
Human Reproduction (Oxford, England)|October 18, 2017
Targeted metabolomics reveals reduced levels of polyunsaturated choline plasmalogens and a smaller dimethylarginine/arginine ratio in the follicular fluid of patients with a diminished ovarian reserveJ M Chao de la Barca, T Boueilh, G Simard, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 5, 2013
Key role of estrogens and endothelial estrogen receptor α in blood flow-mediated remodeling of resistance arteriesK Tarhouni, A L Guihot, M L Freidja, et al.
Molecular Genetics and Metabolism Reports|April 17, 2025
The recurrent p.Glu3Lys variant in EHHADH is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalitiesP Rollier, A Cospain, M Barth, et al.
Genetika|March 10, 2006
[Spectrum of pathogenic mtDNA mutations in Leber hereditary optic neuropathy families from Siberia]N V Volod'ko, M A L'vova, E B Starikovskaia, et al.
Mitochondrion|December 15, 2007
Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategyS Bannwarth, V Procaccio, C Rouzier, et al.
Journal of Inherited Metabolic Disease|May 31, 2012
Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 casesS Koene, R J Rodenburg, M S van der Knaap, et al.
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