Pascal Reynier researcher
Reynier, Pascal, 1962-..
Reynier, Pascal
VIAF ID: 289156009850749580611 (Personal)
Permalink: http://viaf.org/viaf/289156009850749580611
Preferred Forms
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100 0 _ ‡a Pascal Reynier ‡c researcher
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100 1 _ ‡a Reynier, Pascal
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100 1 _ ‡a Reynier, Pascal, ‡d 1962-..
4xx's: Alternate Name Forms (1)
Works
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Approche métabolomique de la drépanocytose |
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Bioinformatics analysis of the mitochondrial proteome and the mutational spectrum of the Opa1 protein.. |
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Conditioning by G-protein coupled receptors : development of an in vitro cellular model. |
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Conditionnement par les récepteurs couplés aux protéines G : mise au point d'un modèle in vitro |
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Data science applied to precision medicine. |
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Dysfonctions mitochondriales et homéostasie bioénergétique des motoneurones dans un modèle de sclérose latérale amyotrophique |
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Étude de la variabilité du génome mitochondrial comme facteur de susceptibilité au cancer du sein |
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Etude épidémiologique, génétique et métabolomique des Troubles du Spectre Autistique au Liban |
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Étude métabolomique du dimorphisme sexuel cérébral chez la souris |
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Etude métabolomique d'un modèle in vitro de sclérose latérale amyotrophique exposé au stress oxydant |
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Génotoxicité de prophylaxies antirétrovirales administrées à des nourrissons nés de mères infectées par le Virus de l'Immunodéficience Humaine pour prévenir sa transmission par l'allaitement |
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Genotoxicity of antiretroviral prophylaxis given to infants born to mothers infected with the Human Immunodeficiency Virus to prevent its transmission through breastfeeding. |
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Homocysteine, adenosine and A2A receptors in relation with coronary artery disease. |
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Influence de la génétique mitochondriale en pathologie : apport des techniques de séquençage haut débit |
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The interactom of methionine synthase. |
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Interest of machine learning for the search for markers involved in cardiac remodelling and stroke heart syndrome. |
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Mitochondrial DNA alteration in male infertility. |
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The mitochondrial DNA content of cumulus granulosa cells is linked to embryo quality |
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Mitochondrial DNA deletions in muscular diseases. |
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Mitochondrial energetic function in a mice model of Acute Intermittent Porphyria (AIP). |
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Mitochondrie et reproduction |
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[Molecular characterization of corona radiata cells from patients with diminished ovarian reserve] |
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mtDNA controls expression of the Death Associated Protein 3. |
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mtDNA haplogroup J: a contributing factor of optic neuritis |
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[Multiorgan failure after sickle cell vaso occlusive attack: integrated clinical and biological emergency]. |
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Neuropathies optiques héréditaires : Etude des mécanismes physiopathologiques et recherche de molécules à visée thérapeutique |
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Neuropathies Périphériques Héréditaires : de la Génétique Moléculaire au modèle cellulaire de motoneurones dérivé d'hiPSC. |
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Neurotoxicity of pesticides: its relationship with neurodegenerative diseases |
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New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation |
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No evidence of thyrotropin receptor and G(s alpha) gene mutation in high iodine uptake thyroid carcinoma |
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Oligoasthenospermia associated with multiple mitochondrial DNA rearrangements |
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Oncocytic thyroid tumors : differential expression analysis. |
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OPA1 and dominant optic atrophy : physiopathological study by metabolomic and lipidomic approach.. |
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OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology |
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OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background |
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OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract |
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Ovarian ageing: the role of mitochondria in oocytes and follicles. |
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Oxidative stress contributes differentially to the pathophysiology of Charcot-Marie-Tooth disease type 2K |
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Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathy |
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Perspectives of drug-based neuroprotection targeting mitochondria. |
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PGC-1-related coactivator and targets are upregulated in thyroid oncocytoma. |
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Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesions. |
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Pro-oxidant effect of ALA is implicated in mitochondrial dysfunction of HepG2 cells. |
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Un profil métabolomique dans les larmes montrant l’implication de la spermine dans l’orbitopathie de Basedow |
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Recurrent Isolated Neonatal Hemolytic Anemia: Think About Glutathione Synthetase Deficiency. |
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Régulation de la fonction mitochondriale par le rapport NADH/NAD+ : le rôle clef du complexe I |
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Relative frequencies of inherited retinal dystrophies and optic neuropathies in Southern France: assessment of 21-year data management. |
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Remote ischemic conditioning : roles of hypoxia-inducible factor-1α and apolipoprotein A1. |
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Reply: The expanding neurological phenotype of DNM1L-related disorders |
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Resveratrol Directly Binds to Mitochondrial Complex I and Increases Oxidative Stress in Brain Mitochondria of Aged Mice |
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Resveratrol induces a mitochondrial complex I-dependent increase in NADH oxidation responsible for sirtuin activation in liver cells |
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Retinal Neuronal Loss in Visually Asymptomatic Patients With Myoclonic Epilepsy With Ragged-Red Fibers |
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Reversible optic neuropathy with OPA1 exon 5b mutation |
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Risk factors, genetics and metabolomocis of autism spectrum disorders in Lebanon. |
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Rôle des sphingolipides et des MAM dans l'activité des protéines pro-apoptotiques Bax et Bak |
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Role of OPA1 in striated muscle cell function and architecture and in response to stress. |
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Role of sphingolipids and MAM in the control of Bax and Bak proapoptotic activity. |
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La science des données au service de la médecine de précision |
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SGLT-2 inhibitors and the risk of infections: a systematic review and meta-analysis of randomized controlled trials. |
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Sickle Cell Disease: Metabolomic Profiles of Vaso-Occlusive Crisis in Plasma and Erythrocytes |
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Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT |
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Spinal motor neurons from Indiuced Pluripotent Stem Cells (iPSc) : cellular models of genetic peripheral neuropathies. |
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Sporadic optic atrophy due to synonymous codon change altering mRNA splicing of OPA1 |
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Standardized mitochondrial analysis gives new insights into mitochondrial dynamics and OPA1 function. |
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Study of mitochondrial alterations in optic neuropathies associated with OPA1 gene mutations. |
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Study of mitochondrial function in placental insufficiency |
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Study of the metabolic alterations induced by glutamate in an in vitro model of amyotrophic lateral sclerosis (ALS) using a metabolomic approach. |
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Study of therapeutic effects of curcumin on in vitro and in vivo models of peripheral neuropathies. |
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Thanatobiochemistry: its contribution to the diagnosis of hypothermia fatalities |
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Thanatobiochemistry: post mortem study of the vitreous humor for the diagnosis of diabetic ketoacidosis death |
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The timing of onset of hypertensive disorders in pregnancy and the risk of incident hypertension and cardiovascular disease |
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Transfer into a mesothelioma cell line of tumor suppressor gene p16 by cholesterol-based cationic lipids. |
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Tumeurs oncocytaires thyroïdiennes : étude des mécanismes responsables de la prolifération mitochondriale par analyse transcriptomique |
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Type I hyperlipidaemia caused by lipoprotein lipase deficiency in a nurseling: the role of the clinical laboratory in processing biological samples and contributing to the diagnosis and therapeutic follow-up of patients |
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Updated review of postmortem biochemical exploration of hypothermia with a presentation of standard strategy of sampling and analyses |
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Variabilité glycémique : exploration in vitro des fonctions cellulaires et mitochondriales sur la lignée de cardiomyocyte HL-1 |
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Variation d'hydrophobicité et structure secondaire des protéines transmembranaires |
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Warburg-like effect is a hallmark of complex I assembly defects |
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Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip. |
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Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies |
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