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1دورية أكاديمية
المؤلفون: Izzo, Antonella, Mollo, Nunzia, Nitti, Maria, Paladino, Simona, Calì, Gaetano, Genesio, Rita, Bonfiglio, Ferdinando, Cicatiello, Rita, Barbato, Maria, Sarnataro, Viviana, Conti, AnnaAff1, Nitsch, Lucio
المصدر: Molecular Medicine. 24(1)
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2دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
3دورية أكاديمية
المؤلفون: Genesio, Rita, Maruotti, Giuseppe Maria, Saccone, Gabriele, Mormile, Angela, Conti, Anna, Cicatiello, Rita, Sarnataro, Viviana, Sirico, Angelo, Izzo, Antonella, Martinelli, Pasquale, Nitsch, Lucio
المصدر: Clinical Case Reports; Apr2018, Vol. 6 Issue 4, p592-595, 4p
مصطلحات موضوعية: DIAPHRAGMATIC hernia, DELETION mutation, PRENATAL diagnosis, CHROMATIN, DIAGNOSIS
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4دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
5دورية أكاديمية
المؤلفون: Mollo, Nunzia, Nitti, Maria, Zerillo, Lucrezia, Faicchia, Deriggio, Micillo, Teresa, Accarino, Rossella, Secondo, Agnese, Petrozziello, Tiziana, Calì, Gaetano, Cicatiello, Rita, Bonfiglio, Ferdinando, Sarnataro, Viviana, Genesio, Rita, Izzo, Antonella, Pinton, Paolo, Matarese, Giuseppe, Paladino, Simona, Conti, Anna, Nitsch, Lucio
المصدر: Frontiers in Genetics; 7/27/2020, Vol. 11, p1-1, 1p
مصطلحات موضوعية: DOWN syndrome, BIOENERGETICS, CELLS, ENERGY metabolism, OXIDATIVE stress
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6
المؤلفون: Gaetano Calì, Rita Genesio, Lucio Nitsch, Maria Barbato, Simona Paladino, Ferdinando Bonfiglio, Antonella Izzo, Maria Nitti, Nunzia Mollo, Rita Cicatiello, Viviana Sarnataro, Anna Conti
المساهمون: Izzo, Antonella, Mollo, Nunzia, Nitti, Maria, Paladino, Simona, Calì, Gaetano, Genesio, Rita, Bonfiglio, Ferdinando, Cicatiello, Rita, Barbato, Maria, Sarnataro, Viviana, Conti, Anna, Nitsch, Lucio
المصدر: Molecular Medicine, Vol 24, Iss 1, Pp 1-8 (2018)
Molecular medicine (Camb. Mass., Print) 24 (2018). doi:10.1186/s10020-018-0004-y
info:cnr-pdr/source/autori:Izzo, Antonella; Mollo, Nunzia; Nitti, Maria; Paladino, Simona; Cali, Gaetano; Genesio, Rita; Bonfiglio, Ferdinando; Cicatiello, Rita; Barbato, Maria; Sarnataro, Viviana; Conti, Anna; Nitsch, Lucio/titolo:Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targets/doi:10.1186%2Fs10020-018-0004-y/rivista:Molecular medicine (Camb. Mass., Print)/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:24
Molecular Medicineمصطلحات موضوعية: 0301 basic medicine, Down syndrome, Disease, Review, Biology, Pathogenesis, lcsh:Biochemistry, 03 medical and health sciences, 0302 clinical medicine, Genetic, Mitochondrial dynamic, Genetics, medicine, Animals, Humans, lcsh:QD415-436, Gene, Molecular Biology, Genetics (clinical), Down syndrome/trisomy of chromosome 21, Animal, lcsh:RM1-950, Down syndrome therapy, medicine.disease, Phenotype, Hypotonia, 3. Good health, Mitochondria, 030104 developmental biology, lcsh:Therapeutics. Pharmacology, Mitochondrial dynamics, Molecular Medicine, medicine.symptom, Down Syndrome, Chromosome 21, Trisomy, Chromosome 21 gene, Mitochondrial dysfunction, 030217 neurology & neurosurgery, Chromosome 21 genes, Human
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المؤلفون: Anna Conti, Antonella Izzo, Gabriele Saccone, Angela Mormile, Rita Cicatiello, Pasquale Martinelli, Lucio Nitsch, Rita Genesio, Angelo Sirico, Viviana Sarnataro, Giuseppe Maria Maruotti
المساهمون: Genesio, Rita, Maruotti, Giuseppe Maria, Saccone, Gabriele, Mormile, Angela, Conti, Anna, Cicatiello, Rita, Sarnataro, Viviana, Sirico, Angelo, Izzo, Antonella, Martinelli, Pasquale, Nitsch, Lucio
المصدر: Clinical Case Reports
مصطلحات موضوعية: 0301 basic medicine, Pediatrics, medicine.medical_specialty, prenatal diagnosi, prenatal diagnosis, business.industry, Congenital diaphragmatic hernia, ultrasound fetal anomalies, Prenatal diagnosis, Case Report, General Medicine, Case Reports, medicine.disease, congenital diaphragmatic hernia, Diaphragm (structural system), 03 medical and health sciences, 030104 developmental biology, array‐CGH analysi, medicine, 16p11.2 deletion syndrome, business, array‐CGH analysis
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المؤلفون: Rita Cicatiello, Antonella Izzo, Teresa Micillo, Lucio Nitsch, Deriggio Faicchia, Paolo Pinton, Rita Genesio, Ferdinando Bonfiglio, Agnese Secondo, Nunzia Mollo, Rossella Accarino, Giuseppe Matarese, Gaetano Calì, Lucrezia Zerillo, Viviana Sarnataro, Simona Paladino, Anna Conti, Tiziana Petrozziello, Maria Nitti
المساهمون: Mollo, N., Nitti, M., Zerillo, L., Faicchia, D., Micillo, T., Accarino, R., Secondo, A., Petrozziello, T., Cali, G., Cicatiello, R., Bonfiglio, F., Sarnataro, Viviana, Genesio, R., Izzo, A., Pinton, P., Matarese, G., Paladino, S., Conti, A., Nitsch, L.
المصدر: Frontiers in Genetics, Vol 10 (2019)
Frontiers in Genetics
Frontiers in genetics 10 (2019): 1–11. doi:10.3389/fgene.2019.00606
info:cnr-pdr/source/autori:Nunzia Mollo, Maria Nitti, Lucrezia Zerillo, Deriggio Faicchia, Teresa Micillo, Rossella Accarino, Agnese Secondo, Tiziana Petrozziello, Gaetano Calì, Rita Cicatiello, Ferdinando Bonfiglio, Viviana Sarnataro, Rita Genesio, Antonella Izzo, Paolo Pinton, Giuseppe Matarese, Simona Paladino, Anna Conti and Lucio Nitsch/titolo:Pioglitazone Improves Mitochondrial Organization and Bioenergetics in Down Syndrome Cells/doi:10.3389%2Ffgene.2019.00606/rivista:Frontiers in genetics/anno:2019/pagina_da:1/pagina_a:11/intervallo_pagine:1–11/volume:10مصطلحات موضوعية: 0301 basic medicine, lcsh:QH426-470, Down syndrome/therapy, Energy metabolism, Mitochondrial dynamics, Mitochondrial dysfunction, Oxidative stress, Pioglitazone, Mitochondrion, Pharmacology, medicine.disease_cause, NO, 03 medical and health sciences, 0302 clinical medicine, Mitochondrial dynamic, energy metabolism, mitochondrial dysfunction, Genetics, medicine, MFN1, pioglitazone, oxidative stress, Genetics (clinical), Original Research, Chemistry, Neurodegeneration, medicine.disease, mitochondrial dynamics, Metformin, lcsh:Genetics, 030104 developmental biology, 030220 oncology & carcinogenesis, Oxidative stre, Molecular Medicine, Optic Atrophy 1, Down syndrome/therapy, PPARGC1A, Pioglitazone, Oxidative stress, medicine.drug
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12a4d4fd477685169cf75a3580c3b64d
https://pubmed.ncbi.nlm.nih.gov/32849775