يعرض 1 - 10 نتائج من 126 نتيجة بحث عن '"Tonlorenzi, R"', وقت الاستعلام: 0.78s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy

    المؤلفون: Galli, F., Bragg, L., Rossi, M., Proietti, D., Perani, L., Bagicaluppi, M., Tonlorenzi, R., Sibanda, T., Caffarini, M., Talapatra, A., Santoleri, S., Meregalli, M., Bano-Otalora, B., Bigot, A., Bozzoni, I., Bonini, C., Mouly, V., Torrente, Y., Cossu, G.

    مصطلحات موضوعية: Function and Dysfunction of the Nervous System

    وصف الملف: application/pdf

    العلاقة: http://edoc.mdc-berlin.de/24172/1/24172oa.pdfTest; http://edoc.mdc-berlin.de/24172/2/24172suppl.pdfTest; Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy. Galli, F. and Bragg, L. and Rossi, M. and Proietti, D. and Perani, L. and Bagicaluppi, M. and Tonlorenzi, R. and Sibanda, T. and Caffarini, M. and Talapatra, A. and Santoleri, S. and Meregalli, M. and Bano-Otalora, B. and Bigot, A. and Bozzoni, I. and Bonini, C. and Mouly, V. and Torrente, Y. and Cossu, G. EMBO Molecular Medicine 16 (4): 927-944. 15 April 2024

    الإتاحة: https://doi.org/10.1038/s44321-024-00031-3Test
    http://edoc.mdc-berlin.de/24172Test/
    https://edoc.mdc-berlin.de/24172Test/
    http://edoc.mdc-berlin.de/24172/1/24172oa.pdfTest
    http://edoc.mdc-berlin.de/24172/2/24172suppl.pdfTest

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  2. 2
    دورية أكاديمية
    Mesoangioblasts at 20: From the embryonic aorta to the patient bed

    المؤلفون: Cossu G., Tonlorenzi R., Brunelli S., Sampaolesi M., Messina G., Azzoni E., Benedetti S., Biressi S., Bonfanti C., Bragg L., Camps J., Cappellari O., Cassano M., Ciceri F., Coletta M., Covarello D., Crippa S., Cusella-De Angelis M. G., De Angelis L., Dellavalle A., Diaz-Manera J., Galli D., Galli F., Gargioli C., Gerli M. F. M., Giacomazzi G., Galvez B. G., Hoshiya H., Guttinger M., Innocenzi A., Minasi M. G., Perani L., Previtali S. C., Quattrocelli M., Ragazzi M., Roostalu U., Rossi G., Scardigli R., Sirabella D., Tedesco F. S., Torrente Y., Ugarte G.

    المساهمون: Cossu, G., Tonlorenzi, R., Brunelli, S., Sampaolesi, M., Messina, G., Azzoni, E., Benedetti, S., Biressi, S., Bonfanti, C., Bragg, L., Camps, J., Cappellari, O., Cassano, M., Ciceri, F., Coletta, M., Covarello, D., Crippa, S., Cusella-De Angelis, M. G., De Angelis, L., Dellavalle, A., Diaz-Manera, J., Galli, D., Galli, F., Gargioli, C., Gerli, M. F. M., Giacomazzi, G., Galvez, B. G., Hoshiya, H., Guttinger, M., Innocenzi, A., Minasi, M. G., Perani, L., Previtali, S. C., Quattrocelli, M., Ragazzi, M., Roostalu, U., Rossi, G., Scardigli, R., Sirabella, D., Tedesco, F. S., Torrente, Y., Ugarte, G.

    مصطلحات موضوعية: mesoderm,muscle development,muscular dystrophy,myogenic stem cells,pericyte

    العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000917251400001; volume:13; journal:FRONTIERS IN GENETICS; https://hdl.handle.net/20.500.11768/138316Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85146379949; https://www.frontiersin.org/articles/10.3389/fgene.2022.1056114/fullTest

    الإتاحة: https://doi.org/20.500.11768/138316Test
    https://doi.org/10.3389/fgene.2022.1056114Test
    https://hdl.handle.net/20.500.11768/138316Test

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  3. 3
    دورية أكاديمية
    Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle

    المؤلفون: Boyer O., Butler-Browne G., Chinoy H., Cossu G., Galli F., Lilleker J. B., Magli A., Mouly V., Perlingeiro R. C. R., Previtali S. C., Sampaolesi M., Smeets H., Schoewel-Wolf V., Spuler S., Torrente Y., Van Tienen F., Aldearee H., Bisson A., Bragg L., Bridoux V., Duelen R., Farini A., Gazzero E., Giarratana N., Giverne C., Meggiolaro L., Negroni E., Porrello E., Tonlorenzi R., Villa C., Yedigaryan L., Zamboni A.

    المساهمون: O. Boyer, G. Butler-Browne, H. Chinoy, G. Cossu, F. Galli, J.B. Lilleker, A. Magli, V. Mouly, R.C.R. Perlingeiro, S.C. Previtali, M. Sampaolesi, H. Smeet, V. Schoewel-Wolf, S. Spuler, Y. Torrente, F. Van Tienen, H. Aldearee, A. Bisson, L. Bragg, V. Bridoux, R. Duelen, A. Farini, E. Gazzero, N. Giarratana, C. Giverne, L. Meggiolaro, E. Negroni, E. Porrello, R. Tonlorenzi, C. Villa, L. Yedigaryan, A. Zamboni

    مصطلحات موضوعية: cell transplantation, inflammatory myopathie, mitochondrial myopathie, muscle stem cell, muscular dystrophie, sphincter incontinence, volumetric muscle loss, Settore MED/26 - Neurologia

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34408774; info:eu-repo/semantics/altIdentifier/wos/WOS:000691311000001; volume:12; firstpage:1; lastpage:20; numberofpages:20; journal:FRONTIERS IN GENETICS; http://hdl.handle.net/2434/905483Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85113214574

    الإتاحة: https://doi.org/10.3389/fgene.2021.702547Test
    http://hdl.handle.net/2434/905483Test

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  4. 4
    دورية أكاديمية
    Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next-generation human artificial chromosomes for Duchenne muscular dystrophy

    المؤلفون: Benedetti, S, Uno, N, Hoshiya, H, Ragazzi, M, Ferrari, G, Kazuki, Y, Moyle, LA, Tonlorenzi, R, Lombardo, A, Chaouch, S, Mouly, V, Moore, M, Popplewell, L, Kazuki, K, Katoh, M, Naldini, L, Dickson, G, Messina, G, Oshimura, M, Cossu, G, Tedesco, FS

    المصدر: EMBO Molecular Medicine , 9 (12) pp. 1623-1764. (2017)

    مصطلحات موضوعية: DMD, gene therapy, human artificial chromosomes, human muscle stem/progenitor cells, immortalisation

    وصف الملف: text

    العلاقة: https://discovery.ucl.ac.uk/id/eprint/10040510/1/Tedesco_emmm.201607284.full.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10040510Test/

    الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10040510/1/Tedesco_emmm.201607284.full.pdfTest
    https://discovery.ucl.ac.uk/id/eprint/10040510Test/

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  5. 5
    دورية أكاديمية
    Alteration of the late endocytic pathway in Charcot–Marie–Tooth type 2B disease

    المؤلفون: Romano R., Rivellini C., De Luca M., Tonlorenzi R., Beli R., Manganelli F., Nolano M., Santoro L., Eskelinen E. -L., Previtali S. C., Bucci C.

    المساهمون: Romano, R., Rivellini, C., De Luca, M., Tonlorenzi, R., Beli, R., Manganelli, F., Nolano, M., Santoro, L., Eskelinen, E. -L., Previtali, S. C., Bucci, C.

    مصطلحات موضوعية: EGFR, Endocytosi, Lysosome, Migration, RAB7A, RAC1

    وصف الملف: STAMPA

    العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000534393400001; volume:78; firstpage:351; lastpage:372; numberofpages:22; journal:CELLULAR AND MOLECULAR LIFE SCIENCES; http://hdl.handle.net/11587/447142Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85083090714

    الإتاحة: https://doi.org/10.1007/s00018-020-03510-1Test
    http://hdl.handle.net/11587/447142Test

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  6. 6
    دورية أكاديمية
    Necdin enhances muscle reconstitution of dystrophic muscle by vessel-associated progenitors, by promoting cell survival and myogenic differentiation

    المؤلفون: Pessina, P, Conti, V, Tonlorenzi, R, Touvier, T, Meneveri, R, Cossu, G, Brunelli, S

    المصدر: Cell Death & Differentiation ; volume 19, issue 5, page 827-838 ; ISSN 1350-9047 1476-5403

    مصطلحات موضوعية: Cell Biology, Molecular Biology

    الإتاحة: https://doi.org/10.1038/cdd.2011.160Test
    http://www.nature.com/articles/cdd2011160.pdfTest
    http://www.nature.com/articles/cdd2011160Test

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  7. 7
    دورية أكاديمية
    Partial dysferlin reconstitution by adult murine mesoangioblasts is sufficient for full functional recovery in a murine model of dysferlinopathy

    المؤلفون: Díaz-Manera, J, Touvier, T, Dellavalle, A, Tonlorenzi, R, Tedesco, F S, Messina, G, Meregalli, M, Navarro, C, Perani, L, Bonfanti, C, Illa, I, Torrente, Y, Cossu, G

    المصدر: Cell Death & Disease ; volume 1, issue 8, page e61-e61 ; ISSN 2041-4889

    مصطلحات موضوعية: Cancer Research, Cell Biology, Cellular and Molecular Neuroscience, Immunology

    الإتاحة: https://doi.org/10.1038/cddis.2010.35Test
    http://www.nature.com/articles/cddis201035.pdfTest
    http://www.nature.com/articles/cddis201035Test
    https://www.nature.com/articles/cddis201035.pdfTest

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  8. 8
    دورية أكاديمية
    Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR)

    المؤلفون: Meloni, I, Vitelli, F, Pucci, L, Lowry, R B, Tonlorenzi, R, Rossi, E, Ventura, M, Rizzoni, G, Kashtan, C E, Pober, B, Renieri, A

    مصطلحات موضوعية: Letters to JMG

    وصف الملف: text/html

    العلاقة: http://jmg.bmj.com/cgi/content/short/39/5/359Test; http://dx.doi.org/10.1136/jmg.39.5.359Test

    الإتاحة: https://doi.org/10.1136/jmg.39.5.359Test
    http://jmg.bmj.com/cgi/content/short/39/5/359Test

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  9. 9
    دورية أكاديمية
    Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressor

    المؤلفون: Meroni G., Reymond A., Alcalay M., Borsani G., Tanigami A., Tonlorenzi R., Lo Nigro C., Messali S., Zollo M., Ledbetter D. H., Brent R., Ballabio A., Carrozzo R.

    المساهمون: G. Meroni, A. Reymond, M. Alcalay, G. Borsani, A. Tanigami, R. Tonlorenzi, C. Lo Nigro, S. Messali, M. Zollo, D.H. Ledbetter, R. Brent, A. Ballabio, R. Carrozzo

    مصطلحات موضوعية: bHLHZip protein, Max-interacting protein, Myc, sin3, transcriptional repressor, Settore MED/03 - Genetica Medica

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/9184233; info:eu-repo/semantics/altIdentifier/wos/WOS:A1997XC30700032; volume:16; issue:10; firstpage:2892; lastpage:2906; numberofpages:15; journal:EMBO JOURNAL; http://hdl.handle.net/2434/810436Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0030981453

    الإتاحة: https://doi.org/10.1093/emboj/16.10.2892Test
    http://hdl.handle.net/2434/810436Test

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  10. 10
    دورية أكاديمية
    Jab1 in the pathogenesis of Merosin deficient congenital muscular dystrophy (MDC1A)

    المؤلفون: Velardo, D., Porrello, E., Tonlorenzi, R., Lorenzetti, I., Pardi, R., Goldhamer, D., Previtali, S.

    المصدر: Neuromuscular Disorders ; volume 27, page S108 ; ISSN 0960-8966

    مصطلحات موضوعية: Genetics (clinical), Neurology (clinical), Neurology, Pediatrics, Perinatology and Child Health

    الإتاحة: https://doi.org/10.1016/j.nmd.2017.06.063Test
    https://api.elsevier.com/content/article/PII:S0960896617306363?httpAccept=text/xmlTest
    https://api.elsevier.com/content/article/PII:S0960896617306363?httpAccept=text/plainTest

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