نتائج البحث - "Alessandra Mauri"

المساهمون: Institut de Recherche sur le Cancer et le Vieillissement (IRCAN), Université Nice Sophia Antipolis (1965 - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA), Biologie mitochondriale – Mitochondrial biology, Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Centre Commun de Microscopie Appliquée (CCMA), Université de Nice Sophia-Antipolis (UNSA), This work was made possible by grants to V.P.-F. from the ANR (Agence Nationale de la Recherche) ANR-16-CE16-0024-01 and from the FRM (Fondation pour la Recherche Médicale) FRM: MND202004011475., We acknowledge Thibault Léger and the Proteomics facility of the Institut Jacques Monod, University of Paris Cité for mass spectrometry analysis. We also thank Christelle Boscagli for technical help. We gratefully acknowledge the IRCAN’s Molecular and Cellular Core Imaging (PICMI) facility, supported financially by FEDER, Conseil régional Provence Alpes-Côte d’Azur, Conseil Départemental 06, Cancéropôle PACA, Gis Ibisa and Inserm, the IRCAN’s Animal core facility, supported by FEDER, Région Provence Alpes-Côte d’Azur, Conseil Départemental 06 and Inserm, the IRCAN’s Histology core facility, supported by Région Provence Alpes-Côte d’Azur, Cancéropôle PACA and Université Côte d’Azur and, the University’s CCMA Electron Microscopy facility supported by Université Côte d’Azur, Région Provence Alpes-Côte d’Azur, Conseil Départemental 06 and Gis Ibisa, ANR-16-CE16-0024,MicroGol,Implication des fonctions sécrétoires de l'appareil de Golgi dans le développement des microcéphalies postnatales avec déficit intellectuel(2016), Lemesle, Marie, Implication des fonctions sécrétoires de l'appareil de Golgi dans le développement des microcéphalies postnatales avec déficit intellectuel - - MicroGol2016 - ANR-16-CE16-0024 - AAPG2016 - VALID

المصدر: Brain-A Journal of Neurology
Brain-A Journal of Neurology, 2022, 145 (10), pp.3415-3430. ⟨10.1093/brain/awac197⟩

مصطلحات موضوعية: Motor Neurons, PHB = prohibitin, Amyotrophic Lateral Sclerosis, Membrane Proteins, PLA = proximity ligation assay, MICOS = mitochondrial contact site and cristae organizing system, MESH: Amyotrophic Lateral Sclerosis* / genetics Amyotrophic Lateral Sclerosis* / metabolism Animals Frontotemporal Dementia* / genetics Humans Membrane Proteins* / genetics Membrane Proteins* / metabolism Mice Mitochondria / metabolism Mitochondrial Proteins* / genetics Mitochondrial Proteins* / metabolism Motor Neurons / metabolism Prohibitins Transcription Factors / genetics, IMM = inner mitochondrial membrane, Mitochondria, Mitochondrial Proteins, Mice, ALS = amyotrophic lateral sclerosis, [SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie, Frontotemporal Dementia, Prohibitins, motor neuron disease, mitochondrion, Animals, Humans, FTD = frontotemporal dementia, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, Neurology (clinical), RC = respiratory chain, MN = motor neuron, Transcription Factors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43e4acee00dfd65b95c24c9f606e3ce2
https://pubmed.ncbi.nlm.nih.gov/35656794

5

SLP2/prohibitins aggregates and instability of the PHB complex are key elements in CHCHD10S59L-related disease

المؤلفون: Paquis-Flucklinger, Gaëlle Augé, Alessandra Mauri-Crouzet, Charlotte Cochaud, Ropert B, Sylvie Bannwarth, Françoise Lespinasse, Konstantina Fragaki, Sandra Lacas-Gervais, Emmanuelle Génin

مصطلحات موضوعية: MICOS complex, medicine.diagnostic_test, Chemistry, Apoptosis, Proteolysis, Mitophagy, medicine, PINK1, Mitochondrion, Prohibitin, Inner mitochondrial membrane, Cell biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::118873910de0ed24dcfcf1aaf065ecf9
https://doi.org/10.1101/2021.05.31.446377

6

A structured therapeutic education program for children and adolescents with type 1 diabetes: an analysis of the efficacy of the 'Pediatric Education for Diabetes' project

المؤلفون: Alessandra, Mauri, Susanna, Schmidt, Valentina, Sosero, Maria, Sambataro, Laura, Nollino, Francesco, Fabris, Anna, Corò, Antonella, Scantamburlo, Maria L, Marcon, Michela, Cazziola-Merlotto, Tania, Ciani, Michele, Tessarin, Agostino, Paccagnella

المصدر: Minerva Pediatrics. 73

مصطلحات موضوعية: Glycated Hemoglobin, Male, Patient Care Team, Adolescent, Blood Glucose Self-Monitoring, Self-Management, Type1 Diabetes-Therapeutic education-Adolescent, Self Care, Diabetes Mellitus, Type 1, Patient Education as Topic, Pediatrics, Perinatology and Child Health, Quality of Life, Humans, Female, Child, Child Nutritional Physiological Phenomena, Program Evaluation

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46517896a643eddf213f69deb403c8b8
https://doi.org/10.23736/s2724-5276.17.04634-5

7

Benessere percepito e pratiche mindfulness in pazienti ospedalieri

المؤلفون: Maddalena Tomas, Olga Riccato, Giulia Ongaro, Alessandra Mauri

المصدر: PSICOLOGIA DELLA SALUTE. :146-159

مصطلحات موضوعية: Health (social science), business.industry, Medicine, business, Applied Psychology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::cef9968048dc2101535d52ed2317e8a2
https://doi.org/10.3280/pds2018-001009

8

Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10S59L/+ mouse

المساهمون: CCMA - Centre Commun de Microscopie Appliquée, Université Nice Côte D'Azur

المصدر: Acta Neuropathologica
Acta Neuropathologica, Springer Verlag, 2019, 138 (1), pp.123-145. ⟨10.1007/s00401-019-01988-z⟩

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e531dfbddb5cd0ba97219486d7be7d83
https://hal.archives-ouvertes.fr/hal-03014387

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9

Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10

المصدر: Acta neuropathologica. 138(1)

مصطلحات موضوعية: DNA-Binding Proteins, Mitochondrial Proteins, Motor Neurons, Phenotype, Cell Death, Frontotemporal Dementia, Amyotrophic Lateral Sclerosis, Nerve Degeneration, Neuromuscular Junction, Animals, Mice, Transgenic, Mitochondria

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::de5c40166cc10019efb43e95243a0ce5
https://pubmed.ncbi.nlm.nih.gov/30874923

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10

Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases

المساهمون: CCMA - Centre Commun de Microscopie Appliquée, Université Nice Côte D'Azur, Research Programs Unit, Clinicum, Department of Neurosciences, Neurologian yksikkö, University of Helsinki, Research Programme for Molecular Neurology, Centre of Excellence in Stem Cell Metabolism, Medicum, Doctoral Programme Brain & Mind, Henna Tyynismaa / Principal Investigator, Department of Medical and Clinical Genetics, Doctoral Programme in Integrative Life Science, HUS Neurocenter

المصدر: Neurobiology of Disease
Neurobiology of Disease, Elsevier, 2018, 119, pp.159-171. ⟨10.1016/j.nbd.2018.07.027⟩
Neurobiology of Disease, Vol 119, Iss, Pp 159-171 (2018)

مصطلحات موضوعية: Male, 0301 basic medicine, Mitochondrial Diseases, TDP-43, [SDV]Life Sciences [q-bio], Mitochondrion, medicine.disease_cause, Severity of Illness Index, AMYOTROPHIC-LATERAL-SCLEROSIS, 3124 Neurology and psychiatry, 0302 clinical medicine, Mitochondrial myopathy, MOTOR-NEURON DISEASE, ComputingMilieux_MISCELLANEOUS, Mutation, MICOS complex, Neurodegeneration, NEURODEGENERATION, Middle Aged, Mitochondria, Cell biology, DNA-Binding Proteins, Neurology, Frontotemporal Dementia, Female, Adult, Mitochondrial DNA, Saccharomyces cerevisiae Proteins, Biology, PATIENT, Article, lcsh:RC321-571, Mitochondrial Proteins, 03 medical and health sciences, medicine, Humans, Allele, lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry, FRONTOTEMPORAL LOBAR DEGENERATION, HEXANUCLEOTIDE REPEAT, Amyotrophic Lateral Sclerosis, 3112 Neurosciences, Membrane Proteins, Spinal muscular atrophy, medicine.disease, ta3124, INDIVIDUALS, CHCHD10 MUTATIONS, HEK293 Cells, CHCHD10, 030104 developmental biology, SMAJ, CELLS, FTD-ALS, ALS, 030217 neurology & neurosurgery, HeLa Cells

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79452abee4df190a3c79f14893b26acd
https://hal.archives-ouvertes.fr/hal-03014491

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