يعرض 1 - 20 نتائج من 53 نتيجة بحث عن '"distrofia muscolare"', وقت الاستعلام: 0.54s تنقيح النتائج
  1. 1
    Book
    Abitare inclusivo per un’utenza specifica affetta da distrofia muscolare di Duchenne [Inclusive Living for Specific Users suffering from Duchenne Muscular Dystrophy]

    المؤلفون: M. Marchi, G. MIncolelli

    المساهمون: A. F. L. Baratta, C. Conti, V. Tatano, Marchi, M., Mincolelli, G.

    مصطلحات موضوعية: accesibilità, barriere architettoniche, distrofia muscolare, inclusività

    وصف الملف: STAMPA

    Relation: info:eu-repo/semantics/altIdentifier/isbn/978-88-32050-44-8; ispartofbook:Abitare inclusivo: il progetto per una vita autonoma e indipendente [Inclusive living: design for an autonomous and independent living]; volume:1; firstpage:256; lastpage:263; numberofpages:8; serie:CLUSTER ACCESSIBILITÀ AMBIENTALE; alleditors:A. F. L. Baratta, C. Conti, V. Tatano; http://hdl.handle.net/11392/2412307; https://www.anteferma.it/prodotto/abitare-inclusivo/

    الاتاحة: http://hdl.handle.net/11392/2412307
    https://www.anteferma.it/prodotto/abitare-inclusivo/

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  2. 2
    Duchenne's muscular dystrophy involves a defective transsulfuration pathway activity

    المؤلفون: Valentina Vellecco, Giuseppe Cirino, Elisabetta Panza, D. Paris, Fabio Arturo Iannotti, G. de Dominicis, Mariarosaria Bucci, Onorina L. Manzo, A. Boscaino, M. Smimmo, A. Di Lorenzo, N. Mitilini

    المساهمون: Panza, E., Vellecco, V., Iannotti, F. A., Paris, D., Manzo, O. L., Smimmo, M., Mitilini, N., Boscaino, A., de Dominicis, G., Bucci, M., Di Lorenzo, A., Cirino, G.

    المصدر: Redox Biology, Vol 45, Iss, Pp 102040-(2021)
    Redox Biology
    RedoxBiology 45 (2021). doi:10.1016/j.redox.2021.102040
    info:cnr-pdr/source/autori:Panza E.; Vellecco V.; Iannotti F.A.; Paris D.; Manzo O.L.; Smimmo M.; Mitilini N.; Boscaino A.; de Dominicis G.; Bucci M.; Di Lorenzo A.; Cirino G./titolo:Duchenne's muscular dystrophy involves a defective transsulfuration pathway activity/doi:10.1016%2Fj.redox.2021.102040/rivista:RedoxBiology/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume:45

    مصطلحات موضوعية: 0301 basic medicine, Taurine, Medicine (General), Duchenne muscular dystrophy, Clinical Biochemistry, Transsulfuration pathway, Biochemistry, Mice, chemistry.chemical_compound, 0302 clinical medicine, H2S donors, Sodium hydrosulfide (NaHS), Biology (General), biology, Chemistry, medicine.anatomical_structure, S donor, Dystrophin, Research Paper, musculoskeletal diseases, medicine.medical_specialty, Gastransmitters, QH301-705.5, 03 medical and health sciences, R5-920, Internal medicine, distrofia muscolare di Duchenne, medicine, Autophagy, Animals, Muscle, Skeletal, Inflammation, Methionine, Animal, Organic Chemistry, Cystathionine gamma-Lyase, Skeletal muscle, medicine.disease, Cystathionine beta synthase, Glutathione synthase, Mice, Inbred C57BL, Muscular Dystrophy, Duchenne, 030104 developmental biology, Endocrinology, Mice, Inbred mdx, biology.protein, 030217 neurology & neurosurgery

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae7632bb0ee4507440b44c46b734c6f5
    http://www.sciencedirect.com/science/article/pii/S2213231721001993

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  3. 3
    Studio del meccanismo molecolare che porta alla distrofia muscolare: il ruolo della sovraespressione della proteina legante l’RNA FRG1

    المؤلفون: Vallarola, Antonio

    مصطلحات موضوعية: distrofia muscolare, FSHD, metabolismo, risposta allo stress, infiammazione, Settore MED/03 - Genetica Medica, muscle immaturity, stress response, muscle dystrophy, metabolism

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3674::0468b7612a76a36bad49beb5d0c585f6
    https://hdl.handle.net/11380/1245415

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  4. 4
    Valutazione di un nuovo trattamento farmacologico per la distrofia muscolare di Duchenne nel modello murino D2-mdx ; Evaluation of a new pharmacological treatment for Duchenne muscular dystrophy in the D2-mdx mouse model

    المؤلفون: BRAZZALOTTO, ANNA

    المساهمون: VITIELLO, LIBERO

    مصطلحات موضوعية: Distrofia muscolare, D2-mdx, Fibrosi

    وصف الملف: application/pdf

    Relation: Dipartimento di Biologia - DiBio; BIOTECNOLOGIE Laurea di Primo Livello (D.M. 270/2004); 2023; https://hdl.handle.net/20.500.12608/68249

    الاتاحة: https://hdl.handle.net/20.500.12608/68249

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  5. 5
    Editing genico mediante CRISPR-Cas nel muscolo scheletrico ; Applications of CRISPR-Cas gene editing in skeletal muscle

    المؤلفون: FACCO, GIULIA

    المساهمون: CAGNIN, STEFANO

    مصطلحات موضوعية: CRISPR-Cas, muscolo scheletrico, distrofia muscolare

    وصف الملف: application/pdf

    Relation: Dipartimento di Biologia - DiBio; BIOTECNOLOGIE Laurea di Primo Livello (D.M. 270/2004); 2023; https://hdl.handle.net/20.500.12608/62732

    الاتاحة: https://hdl.handle.net/20.500.12608/62732

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  6. 6
    Sistemi di gene delivery lipidici per il silenziamento del fattore di trascrizione NFIX nella distrofia muscolare ; Lipid gene delivery systems for silencing of the transcription factor NFIX in muscular dystrophy

    المؤلفون: YZEIRAJ, KLEA

    المساهمون: PASUT, GIANFRANCO, GRIGOLETTO, ANTONELLA

    مصطلحات موضوعية: sistemi liposomiali, drug delivery, distrofia muscolare

    وصف الملف: application/pdf

    Relation: Dipartimento di Scienze del Farmaco - DSF; CHIMICA E TECNOLOGIA FARMACEUTICHE Laurea Magistrale (D.M. 270/2004); 2023; https://hdl.handle.net/20.500.12608/62647

    الاتاحة: https://hdl.handle.net/20.500.12608/62647

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  7. 7
    Dissertation/ Thesis
    Spatial RNA-mapping reveals the unique patterns of expression and localisation of dystrophin isoforms in the human adult normal brain to improve understanding of brain involvement in muscular dystrophy.

    المؤلفون: FALZARANO, Maria Sofia

    المساهمون: Falzarano, Maria Sofia, FERLINI, Alessandra, PINTON, Paolo

    مصطلحات موضوعية: isoforme distrofina, distrofia muscolare, cervello umano, localizzazione RNA, comorbidità SNC, Settore MED/03 - Genetica Medica

    Relation: https://hdl.handle.net/11392/2542913

    الاتاحة: https://hdl.handle.net/11392/2542913

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  8. 8
    Book
    Abitare inclusivo per un’utenza specifica affetta da distrofia muscolare di Duchenne [Inclusive Living for Specific Users suffering from Duchenne Muscular Dystrophy] ; Inclusive Living for Specific Users suffering from Duchenne Muscular Dystrophy

    المؤلفون: M. Marchi, G. MIncolelli

    المساهمون: A. F. L. Baratta, C. Conti, V. Tatano, Marchi, M., Mincolelli, G.

    مصطلحات موضوعية: accesibilità, barriere architettoniche, distrofia muscolare, inclusività, archi, demo

    Relation: http://hdl.handle.net/11392/2412307

    الاتاحة: http://hdl.handle.net/11392/2412307

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  9. 9
    Aspetti neuropsicologici della distrofia muscolare di Duchenne

    المؤلفون: Filippini, M, Lenzi, S, Pini, A, Briganti, E, Astrea, G, Pane, M, Battini, R

    مصطلحات موضوعية: Profilo neuropsicologico, Funzioni esecutive, Distrofia muscolare di Duchenne, Profilo neuropsicologico, Funzioni esecutive, Distrofia muscolare di Duchenne

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3728::a3717ad3c51acd46288515c7358cc4c3
    http://hdl.handle.net/11568/1035389

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  10. 10
    Abitare inclusivo per un’utenza specifica affetta da distrofia muscolare di Duchenne [Inclusive Living for Specific Users suffering from Duchenne Muscular Dystrophy]

    المؤلفون: Marchi, M., Mincolelli, G.

    مصطلحات موضوعية: PE8_11, accesibilità, Socio-culturale, barriere architettoniche, accesibilità, barriere architettoniche, distrofia muscolare, inclusività, distrofia muscolare, inclusività

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3709::ae3161782421175a4bb4dbe4c545cc6d
    http://hdl.handle.net/11392/2412307

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  11. 11
    Academic Journal
    Aspetti neuropsicologici della distrofia muscolare di Duchenne

    المؤلفون: Filippini M, Lenzi S, Pini A, Briganti E, Astrea G, Pane M, Battini R

    المساهمون: Filippini, M, Lenzi, S, Pini, A, Briganti, E, Astrea, G, Pane, M, Battini, R

    مصطلحات موضوعية: Distrofia muscolare di Duchenne, Profilo neuropsicologico, Funzioni esecutive

    وصف الملف: STAMPA

    Relation: volume:2019; issue:39; firstpage:65; lastpage:72; numberofpages:8; journal:GIORNALE DI NEUROPSICHIATRIA DELL'ETÀ EVOLUTIVA; http://hdl.handle.net/11568/1035389

    الاتاحة: http://hdl.handle.net/11568/1035389

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  12. 12
    Dissertation/ Thesis
    Mesoderm stem cells and inflammation: role in the Pathogenesis and potential therapy of selected Gynecological Deseases and primary Myopathies

    المؤلفون: CAFFARINI, MIRIAM

    المساهمون: Caffarini, Miriam, ORCIANI, Monia

    مصطلحات موضوعية: Cellule staminali mesenchimali (MSCs), Infiammazione, Leiomioma uterino, Neoplasia cervicale intraepiteliale (CIN), Distrofia muscolare di Duchenne (DMD), Mesenchymal stem cells (MSCs), Inflammation, Uterine leiomyoma, Cervical intraepithelial neoplasia (CIN), Duchenne muscular dystrophy (DMD), Settore BIO/17 - Istologia

    Relation: http://hdl.handle.net/11566/263543

    الاتاحة: http://hdl.handle.net/11566/263543

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  13. 13
    Studio di trattamenti farmacologici per la distrofia muscolare di Duchenne in animali modello ; Study of Pharmacological Tratments for Duchenne muscular Dystrophy in Anial Models

    المؤلفون: PRADELLA, MATTEO

    المساهمون: VITIELLO, LIBERO

    مصطلحات موضوعية: Distrofia Muscolare, Duchenne

    Relation: Dipartimento di Biologia - DiBio; BIOTECNOLOGIE Laurea di Primo Livello (D.M. 270/2004); 2022; https://hdl.handle.net/20.500.12608/51997

    الاتاحة: https://hdl.handle.net/20.500.12608/51997

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  14. 14
    Meccanismi di differenziamento delle cellule muscolari scheletriche e utilizzo delle SCs per la Distrofia Muscolare di Duchenne ; Mechanisms of skeletal muscle cell differentiation and use of SCs for Duchenne Muscular Dystrophy

    المؤلفون: DEL GIUDICE, VALENTINA

    المساهمون: MACCATROZZO, LISA

    مصطلحات موضوعية: Muscolo, Cellule satelliti, Distrofia muscolare, Miogenesi, MyoD

    وصف الملف: application/pdf

    Relation: Dipartimento di Biologia - DiBio; BIOTECNOLOGIE Laurea di Primo Livello (D.M. 270/2004); 2022; https://hdl.handle.net/20.500.12608/51972

    الاتاحة: https://hdl.handle.net/20.500.12608/51972

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  15. 15
    Ruolo della monoammino ossidasi B nei processi infiammatori in un modello murino di distrofia muscolare ; Role of monoamine oxidase B in inflammatory processes in a mouse model of muscular dystrophy

    المؤلفون: GORI, BIANCA

    المساهمون: CANTON, MARCELLA

    مصطلحات موضوعية: Monoammino ossidasi, Infiammazione, Distrofia muscolare

    وصف الملف: application/pdf

    Relation: Dipartimento di Biologia - DiBio; BIOLOGIA SANITARIA Laurea Magistrale (D.M. 270/2004); 2022; https://hdl.handle.net/20.500.12608/61216

    الاتاحة: https://hdl.handle.net/20.500.12608/61216

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  16. 16
    Book
    DESIGN FOR DUCHENNE. Linee guida per il progetto di costruzione o ristrutturazione di abitazioni per famiglie Duchenne

    المؤلفون: MARCHI, Michele

    المساهمون: Marchi, Michele

    مصطلحات موضوعية: distrofia muscolare, accessibilità, barriere architettoniche, design for all, normativa

    وصف الملف: STAMPA

    Relation: info:eu-repo/semantics/altIdentifier/isbn/9788891729378; firstpage:1; lastpage:248; numberofpages:248; http://hdl.handle.net/11392/2364598; https://www.francoangeli.it/Ricerca/Scheda_Libro.aspx?ID=23352&Tipo=Libro&strRicercaTesto=23352&lingua=it&titolo=design+for+duchenne.+linee+guida+per+il+progetto+di+costruzione+o+ristrutturazione+di+abitazioni+per+famiglie+duchenne.+distrofia+muscolare,+accessibilita',+barriere+architettoniche

    الاتاحة: http://hdl.handle.net/11392/2364598
    https://www.francoangeli.it/Ricerca/Scheda_Libro.aspx?ID=23352&Tipo=Libro&strRicercaTesto=23352&lingua=it&titolo=design+for+duchenne.+linee+guida+per+il+progetto+di+costruzione+o+ristrutturazione+di+abitazioni+per+famiglie+duchenne.+distrofia+muscolare,+accessibilita',+barriere+architettoniche

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  17. 17
    Conference
    Le distrofie muscolari

    المؤلفون: R. Maggi, A. Berardinelli

    المساهمون: P. Chicarella, C. Carra, R. Maggi, A. Berardinelli

    مصطلحات موضوعية: distrofia muscolare, Settore BIO/09 - Fisiologia, Settore MED/39 - Neuropsichiatria Infantile

    Relation: ispartofbook:Gabriele, storia vera di un ragazzo speciale; firstpage:85; lastpage:98; numberofpages:14; alleditors:C. Carra; http://hdl.handle.net/2434/236309

    الاتاحة: http://hdl.handle.net/2434/236309

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  18. 18
    Mantenimento a lungo termine dell'espressione della distrofina e della resistenza ai danni del muscolo scheletrico in topi DMD modificati mediante editing del gene. ; Long-term maintenance of dystrophin expression and resistance to injury of skeletal muscle in gene edited DMD mice

    المؤلفون: VALENTE, GIULIA

    المساهمون: LAVEDER, PAOLO

    مصطلحات موضوعية: Distrofia muscolare, Crispr-Cas9, Gene editing

    وصف الملف: application/pdf

    Relation: Dipartimento di Biologia - DiBio; BIOTECNOLOGIE Laurea di Primo Livello (D.M. 270/2004); 2021; http://hdl.handle.net/20.500.12608/34835

    الاتاحة: https://hdl.handle.net/20.500.12608/34835

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  19. 19
    Distrofia Muscolare: Espressione, purificazione e caratterizzazione della regione extracellulare del delta Sarcoglicano ; Muscolar Dystrophy: Expression, purification, and characterization of the extracellular region of delta Sarcoglycan

    المؤلفون: BUSSOLAN, NICOLÒ

    المساهمون: ACQUASALIENTE, LAURA, SANDONA', DORIANNA

    مصطلحات موضوعية: Sarcoglicano, Distrofia Muscolare, Biochimica

    وصف الملف: application/pdf

    Relation: Dipartimento di Scienze del Farmaco - DSF; CHIMICA E TECNOLOGIA FARMACEUTICHE; 2021; http://hdl.handle.net/20.500.12608/35906

    الاتاحة: https://hdl.handle.net/20.500.12608/35906

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  20. 20
    La proteina BET come nuovo bersaglio terapeutico nella distrofia muscolare di Duchenne ; BET protein as a new therapeutic target in Duchenne muscular dystrophy

    المؤلفون: BALDAN, ILENIA

    المساهمون: CANTON, MARCELLA

    مصطلحات موضوعية: Distrofia muscolare, DMD, distrofina, stress ossidativo, proteine BET

    وصف الملف: application/pdf

    Relation: Dipartimento di Scienze del Farmaco - DSF; FARMACIA Laurea Magistrale (D.M. 270/2004); 2021; http://hdl.handle.net/20.500.12608/10069

    الاتاحة: https://hdl.handle.net/20.500.12608/10069

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