In his work, Anatomy and Neuroscience is strongly intertwined with Optic nerve, which is a subfield of Optic neuropathy. Pascal Reynier connects Anatomy with Genetics in his research. His research links Mitochondrial disease with Genetics. His Neuroscience study frequently links to adjacent areas such as Optic nerve. Mitochondrial disease and mitochondrial fusion are inherently bound to his Mitochondrial DNA studies. Pascal Reynier performs integrative study on Gene and Mitochondrial biogenesis in his works. Pascal Reynier incorporates Mitochondrial biogenesis and Mitochondrial DNA in his studies. His work often combines Mitochondrion and mitochondrial fusion studies. Pascal Reynier integrates many fields in his works, including Mutation and Phenotype.
His Mitochondrial DNA study combines Mitochondrial disease and mitochondrial fusion studies. Pascal Reynier integrates several fields in his works, including mitochondrial fusion and Mitochondrial DNA. Borrowing concepts from Phenotype, he weaves in ideas under Gene. Genetics is closely attributed to Embryo in his work. He undertakes interdisciplinary study in the fields of Mitochondrion and Mitochondrial disease through his research. While working in this field, Pascal Reynier studies both Biochemistry and Enzyme. While working on this project, he studies both Enzyme and Biochemistry. In his research, he undertakes multidisciplinary study on Internal medicine and Endocrinology. While working in this field, he studies both Endocrinology and Internal medicine.
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Mitochondrial DNA content affects the fertilizability of human oocytes.
P Reynier;P May-Panloup;M F Chrétien;C J Morgan.
Molecular Human Reproduction (2001)
OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes
Patrizia Amati-Bonneau;Maria Lucia Valentino;Pascal Reynier;Maria Esther Gallardo.
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.
Gavin Hudson;Patrizia Amati-Bonneau;Emma L. Blakely;Joanna D. Stewart.
Resveratrol Induces a Mitochondrial Complex I-dependent Increase in NADH Oxidation Responsible for Sirtuin Activation in Liver Cells
Valérie Desquiret-Dumas;Valérie Desquiret-Dumas;Naïg Gueguen;Naïg Gueguen;Géraldine Leman;Géraldine Leman;Stéphanie Baron.
Journal of Biological Chemistry (2013)
Multi-system neurological disease is common in patients with OPA1 mutations
Patrick Yu-Wai-Man;Philip G. Griffiths;Philip G. Griffiths;G. Gorman;C.-M. Lourenco.
Low oocyte mitochondrial DNA content in ovarian insufficiency
P. May-Panloup;M.F. Chrétien;C. Jacques;C. Vasseur.
Human Reproduction (2005)
Mitochondrial dynamics and disease, OPA1.
Aurélien Olichon;Emmanuelle Guillou;Cécile Delettre;Thomas Landes.
Biochimica et Biophysica Acta (2006)
Ovarian ageing: the role of mitochondria in oocytes and follicles
Pascale May-Panloup;Lisa Boucret;Juan Manuel Chao de la Barca;Valérie Desquiret-Dumas.
Human Reproduction Update (2016)
Dominant optic atrophy
Guy Lenaers;Christian P Hamel;Cecile Delettre;Patrizia Amati-Bonneau;Patrizia Amati-Bonneau.
Orphanet Journal of Rare Diseases (2012)
Increased sperm mitochondrial DNA content in male infertility
May-Panloup P;Chrétien Mf;Savagner F;Vasseur C.
Human Reproduction (2003)
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