المؤلفون: Vogiatzis S., Celestino M., Trevisan M., Magro G., Del Vecchio C., Erdengiz D., Palu G., Parolin C., Maguire-Zeiss K., Calistri A.

المساهمون: Vogiatzis, S., Celestino, M., Trevisan, M., Magro, G., Del Vecchio, C., Erdengiz, D., Palu, G., Parolin, C., Maguire-Zeiss, K., Calistri, A.

مصطلحات موضوعية: Alpha-synuclein, NEDD4, Parkinson’s disease, Ubiquibodie, Animal, Cell Line, Tumor, Dopaminergic Neuron, Genetic Vector, HEK293 Cell, Human, Intracellular Space, Lentiviru, Mice, Nedd4 Ubiquitin Protein Ligase, Neural Stem Cell, Parkinson Disease, Recombinant Protein, Ubiquitination

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34831478; info:eu-repo/semantics/altIdentifier/wos/WOS:000725125000001; volume:10; issue:11; firstpage:3256; journal:CELLS; http://hdl.handle.net/11577/3421192Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85119297039

الإتاحة: https://doi.org/10.3390/cells10113256Test
http://hdl.handle.net/11577/3421192Test

المؤلفون: Rusmini, Paola, Polanco, Maria Josefa, Cristofani, Riccardo, Cicardi, Maria Elena, Meroni, Marco, Galbiati, Mariarita, Piccolella, Margherita, Messi, Elio, Giorgetti, Elisa, Lieberman, Andrew P., Milioto, Carmelo, Rocchi, Anna, Aggarwal, Tanya, Pennuto, Maria, Crippa, Valeria, Poletti, Angelo

المساهمون: Rusmini, Paola, Polanco, Maria Josefa, Cristofani, Riccardo, Cicardi, Maria Elena, Meroni, Marco, Galbiati, Mariarita, Piccolella, Margherita, Messi, Elio, Giorgetti, Elisa, Lieberman, Andrew P., Milioto, Carmelo, Rocchi, Anna, Aggarwal, Tanya, Pennuto, Maria, Crippa, Valeria, Poletti, Angelo

مصطلحات موضوعية: Animal, Autophagy, Disease Models, Gene Expression Regulation, Gene Knock-In Technique, HSP27 Heat-Shock Protein, Human, Mice, Muscular Disorders, Atrophic, Protein Folding, Receptors, Androgen, Ubiquitin, Ubiquitin-Protein Ligase, Multidisciplinary

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26490709; info:eu-repo/semantics/altIdentifier/wos/WOS:000363129100001; volume:5; issue:1; firstpage:15174; journal:SCIENTIFIC REPORTS; http://hdl.handle.net/11577/3257869Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84944937332; www.nature.com/srep/index.html

الإتاحة: https://doi.org/10.1038/srep15174Test
http://hdl.handle.net/11577/3257869Test

المؤلفون: Vogiatzis S., Celestino M., Trevisan M., Magro G., Del Vecchio C., Erdengiz D., Palu G., Parolin C., Maguire-Zeiss K., Calistri A.

المساهمون: Vogiatzis, S., Celestino, M., Trevisan, M., Magro, G., Del Vecchio, C., Erdengiz, D., Palu, G., Parolin, C., Maguire-Zeiss, K., Calistri, A.

مصطلحات موضوعية: Alpha-synuclein, NEDD4, Parkinson’s disease, Ubiquibodie, Animal, Cell Line, Tumor, Dopaminergic Neuron, Genetic Vector, HEK293 Cell, Human, Intracellular Space, Lentiviru, Mice, Nedd4 Ubiquitin Protein Ligase, Neural Stem Cell, Parkinson Disease, Recombinant Protein, Ubiquitination

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34831478; info:eu-repo/semantics/altIdentifier/wos/WOS:000725125000001; volume:10; issue:11; firstpage:3256; journal:CELLS; https://hdl.handle.net/11577/3421466Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85119297039

الإتاحة: https://doi.org/10.3390/cells10113256Test
https://hdl.handle.net/11577/3421466Test

المؤلفون: Raimundo L., Paterna A., Calheiros J., Ribeiro J., Cardoso D. S. P., Piga I., Neto S. J., Hegan D., Glazer P. M., Indraccolo S., Mulhovo S., Costa J. L., Ferreira M. -J. U., Saraiva L.

المساهمون: Raimundo, L., Paterna, A., Calheiros, J., Ribeiro, J., Cardoso, D. S. P., Piga, I., Neto, S. J., Hegan, D., Glazer, P. M., Indraccolo, S., Mulhovo, S., Costa, J. L., Ferreira, M. -J. U., Saraiva, L.

مصطلحات موضوعية: BRCA1, homologous recombination, indole alkaloid, targeted anticancer therapy, Animal, BRCA1 Protein, Cell Line, Tumor, DNA Repair, Drug Synergism, Female, Human, Mice, Tumor Suppressor Protein, Ubiquitin-Protein Ligase, Ovarian Neoplasm, Poly(ADP-ribose) Polymerase Inhibitors

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33899955; info:eu-repo/semantics/altIdentifier/wos/WOS:000660445100001; volume:178; issue:18; firstpage:3627; lastpage:3647; numberofpages:21; journal:BRITISH JOURNAL OF PHARMACOLOGY; http://hdl.handle.net/11577/3410909Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85107640582

الإتاحة: https://doi.org/10.1111/bph.15506Test
http://hdl.handle.net/11577/3410909Test

المؤلفون: Roux T., Barbier M., Papin M., Davoine C. -S., Sayah S., Coarelli G., Charles P., Marelli C., Parodi L., Tranchant C., Goizet C., Klebe S., Lohmann E., Van Maldergen L., van Broeckhoven C., Coutelier M., Tesson C., Stevanin G., Duyckaerts C., Brice A., Durr A., Darios F., Forlani S., Site P. -S., Banneau G., Cazeneuve C., Fontaine B., Azulay J. -P., Boesfplug-Tanguy O., Hannequin D., Hazan J., Burgo A., Verny C., Koenig M., Labauge P., N'guyen K., Rodriguez D., Belarbi S., Hamri A., Tazir M., Boesch S., Pandolfo M., Laura J., Guergueltcheva V., Tournev I., Pedraza Linares O. L., Nielsen J. E., Svenstrup K., Zaki M., Bauer P., Schols L., Schule R., Lossos A., Bassi M. -T., Basso M., Bertini E., Brusco A., Casali C., Casari G., Criscuolo C., Filla A., Orsi L., Santorelli F. M., Valente E. M., Vavla M., Vazza G., Megarbane A., Benomar A., Kremer B., Van Roon-Mom W., Roxburgh R., Erichsen A. K., Tallaksen C., Alonso I., Coutinho P., Loureiro J. L., Sequeiros J., Salih M., Kostic V. S., Rouco Axpe I., Elsayed L., Paucar M. A., Roumani S., Bing-Wen S., Reid E., Suran N., Warner T., Wood N.

المساهمون: Roux, T., Barbier, M., Papin, M., Davoine, C. -S., Sayah, S., Coarelli, G., Charles, P., Marelli, C., Parodi, L., Tranchant, C., Goizet, C., Klebe, S., Lohmann, E., Van Maldergen, L., van Broeckhoven, C., Coutelier, M., Tesson, C., Stevanin, G., Duyckaerts, C., Brice, A., Durr, A., Darios, F., Forlani, S., Site, P. -S., Banneau, G., Cazeneuve, C., Fontaine, B., Azulay, J. -P., Boesfplug-Tanguy, O., Hannequin, D., Hazan, J., Burgo, A., Verny, C., Koenig, M., Labauge, P., N'Guyen, K., Rodriguez, D., Belarbi, S., Hamri, A., Tazir, M., Boesch, S., Pandolfo, M., Laura, J., Guergueltcheva, V., Tournev, I., Pedraza Linares, O. L., Nielsen, J. E., Svenstrup, K., Zaki, M., Bauer, P., Schols, L., Schule, R., Lossos, A., Bassi, M. -T., Basso, M., Bertini, E., Brusco, A., Casali, C., Casari, G., Criscuolo, C., Filla, A., Orsi, L., Santorelli, F. M., Valente, E. M., Vavla, M., Vazza, G., Megarbane, A., Benomar, A., Kremer, B., Van Roon-Mom, W., Roxburgh, R., Erichsen, A. K., Tallaksen, C., Alonso, I., Coutinho, P., Loureiro, J. L., Sequeiros, J., Salih, M., Kostic, V. S., Rouco Axpe, I., Elsayed, L., Paucar, M. A., Roumani, S., Bing-Wen, S., Reid, E., Suran, N., Warner, T., Wood, N.

مصطلحات موضوعية: cognitive impairment, SCA48, SCAR16, spinocerebellar ataxia, STUB1, ATP-Dependent Protease, ATPases Associated with Diverse Cellular Activitie, Ataxia, Female, Human, Male, Ubiquitin-Protein Ligase, Cerebellar Ataxia, Cognitive Dysfunction, Spinocerebellar Ataxias

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32713943; info:eu-repo/semantics/altIdentifier/wos/WOS:000553063200001; volume:22; issue:11; firstpage:1851; lastpage:1862; numberofpages:12; journal:GENETICS IN MEDICINE; http://hdl.handle.net/11577/3427850Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85088563670

الإتاحة: https://doi.org/10.1038/s41436-020-0899-xTest
http://hdl.handle.net/11577/3427850Test

المؤلفون: Gai X., Ghezzi D., Johnson M. A., Biagosch C. A., Shamseldin H. E., Haack T. B., Reyes A., Tsukikawa M., Sheldon C. A., Srinivasan S., Gorza M., Kremer L. S., Wieland T., Strom T. M., Polyak E., Place E., Consugar M., Ostrovsky J., Vidoni S., Robinson A. J., Wong L. -J., Sondheimer N., Salih M. A., Al-Jishi E., Raab C. P., Bean C., Furlan F., Parini R., Lamperti C., Mayr J. A., Konstantopoulou V., Huemer M., Pierce E. A., Meitinger T., Freisinger P., Sperl W., Prokisch H., Alkuraya F. S., Falk M. J., Zeviani M.

المساهمون: Gai, X., Ghezzi, D., Johnson, M. A., Biagosch, C. A., Shamseldin, H. E., Haack, T. B., Reyes, A., Tsukikawa, M., Sheldon, C. A., Srinivasan, S., Gorza, M., Kremer, L. S., Wieland, T., Strom, T. M., Polyak, E., Place, E., Consugar, M., Ostrovsky, J., Vidoni, S., Robinson, A. J., Wong, L. -J., Sondheimer, N., Salih, M. A., Al-Jishi, E., Raab, C. P., Bean, C., Furlan, F., Parini, R., Lamperti, C., Mayr, J. A., Konstantopoulou, V., Huemer, M., Pierce, E. A., Meitinger, T., Freisinger, P., Sperl, W., Prokisch, H., Alkuraya, F. S., Falk, M. J., Zeviani, M.

مصطلحات موضوعية: Age of Onset, Child, Preschool, Chromosomes, Human, Pair 6, DNA, Complementary, F-Box Protein, Female, Fibroblast, Genes, Recessive, HEK293 Cell, Infant, Newborn, Male, Mitochondria, Mitochondrial Encephalomyopathie, Mitochondrial Protein, Muscle, Skeletal, Mutant Protein, Mutation, Oxidative Phosphorylation, Pedigree, Protein Transport, Subcellular Fraction, Syndrome, Ubiquitin-Protein Ligase

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23993194; info:eu-repo/semantics/altIdentifier/wos/WOS:000330268900007; volume:93; issue:3; firstpage:482; lastpage:495; numberofpages:14; journal:AMERICAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11577/3354222Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84883780647

الإتاحة: https://doi.org/10.1016/j.ajhg.2013.07.016Test
http://hdl.handle.net/11577/3354222Test

المؤلفون: Kojovic M., Parees I., Lampreia T., Pienczk-Reclawowicz K., Xiromerisiou G., Rubio-Agusti I., Kramberger M., Carecchio M., Alazami A. M., Brancati F., Slawek J., Pirtosek Z., Valente E. M., Alkuraya F. S., Edwards M. J., Bhatia K. P.

المساهمون: Kojovic, M., Parees, I., Lampreia, T., Pienczk-Reclawowicz, K., Xiromerisiou, G., Rubio-Agusti, I., Kramberger, M., Carecchio, M., Alazami, A. M., Brancati, F., Slawek, J., Pirtosek, Z., Valente, E. M., Alkuraya, F. S., Edwards, M. J., Bhatia, K. P.

مصطلحات موضوعية: Deafness-dystonia syndrome, Mitochondrial disorder, Mohr-Tranebjaerg syndrome, Woodhouse-Sakati syndrome, Adolescent, Adult, Age of Onset, Apoptosis Regulatory Protein, DNA-Binding Protein, Deaf-Blind Disorder, Disease Progression, Dystonia, Family Health, Female, Genetic Testing, Human, Intellectual Disability, Leviviridae, Male, Membrane Transport Protein, Middle Aged, Mutation, Nuclear Protein, Optic Atrophy, Retrospective Studie, Ubiquitin-Protein Ligase Complexe, Young Adult, Genetic Heterogeneity

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23418071; info:eu-repo/semantics/altIdentifier/wos/WOS:000320941200023; volume:28; issue:6; firstpage:795; lastpage:803; numberofpages:9; journal:MOVEMENT DISORDERS; http://hdl.handle.net/11577/3344734Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84879604371

الإتاحة: https://doi.org/10.1002/mds.25394Test
http://hdl.handle.net/11577/3344734Test

المؤلفون: Parodi, Sara, Di Zanni, Eleonora, Di Lascio, Simona, Bocca, Paola, Prigione, Ignazia, Fornasari, Diego, Pennuto, Maria, Bachetti, Tiziana, Ceccherini, Isabella

المساهمون: Parodi, Sara, Di Zanni, Eleonora, Di Lascio, Simona, Bocca, Paola, Prigione, Ignazia, Fornasari, Diego, Pennuto, Maria, Bachetti, Tiziana, Ceccherini, Isabella

مصطلحات موضوعية: Aggregation, Congenital central hypoventilation syndrome, E3 ubiquitin ligase, Insoluble fraction, PHOX2B, Polyalanine expansion, Ubiquitin-proteasome system, Cell Line, Tumor, HeLa Cell, Homeodomain Protein, Human, Hypoventilation, Mutant Protein, Mutation, Peptide, Proteasome Endopeptidase Complex, Sleep Apnea, Central, Transcription Factor, Transcriptional Activation, Tripartite Motif Protein, Ubiquitin, Ubiquitin-Protein Ligase, Molecular Medicine, Drug Discovery3003 Pharmaceutical Science, Genetics (clinical)

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/22307522; info:eu-repo/semantics/altIdentifier/wos/WOS:000307754700005; volume:90; issue:9; firstpage:1025; lastpage:1035; numberofpages:11; journal:JOURNAL OF MOLECULAR MEDICINE; http://hdl.handle.net/11577/3257876Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84867334353

الإتاحة: https://doi.org/10.1007/s00109-012-0868-1Test
http://hdl.handle.net/11577/3257876Test

المؤلفون: Alazami A. M., Schneider S. A., Bonneau D., Pasquier L., Carecchio M., Kojovic M., Steindl K., De Kerdanet M., Nezarati M. M., Bhatia K. P., Degos B., Goh E., Alkuraya F. S.

المساهمون: Alazami, A. M., Schneider, S. A., Bonneau, D., Pasquier, L., Carecchio, M., Kojovic, M., Steindl, K., De Kerdanet, M., Nezarati, M. M., Bhatia, K. P., Degos, B., Goh, E., Alkuraya, F. S.

مصطلحات موضوعية: Alopecia, Diabete, Hypogonadism, Mental retardation, Woodhouse-Sakati, Adolescent, Adult, Arrhythmias, Cardiac, Basal Ganglia Disease, Base Sequence, Child, Chromosomes, Human, Pair 2, Cohort Studie, Diabetes Mellitu, Intellectual Disability, Male, Molecular Sequence Data, Nuclear Protein, Open Reading Frame, Ubiquitin-Protein Ligase Complexe, Mutation

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/20507343; info:eu-repo/semantics/altIdentifier/wos/WOS:000283947300015; volume:78; issue:6; firstpage:585; lastpage:590; numberofpages:6; journal:CLINICAL GENETICS; http://hdl.handle.net/11577/3344748Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-78149273045

الإتاحة: https://doi.org/10.1111/j.1399-0004.2010.01441.xTest
http://hdl.handle.net/11577/3344748Test

المؤلفون: de Boer, M. D., Selby, A., Atherton, P., Smith, K., Seynnes, O. R., Maganaris, C. N., Maffulli, N., Movin, T., Narici, M., Rennie, M. J.

المساهمون: de Boer, M. D., Selby, A., Atherton, P., Smith, K., Seynnes, O. R., Maganaris, C. N., Maffulli, N., Movin, T., Narici, M., Rennie, M. J.

مصطلحات موضوعية: collagen, focal adhesion kinase, mammalian target of rapamycin, messenger RNA, muscle protein, peptide hydrolase, protein kinase B, proteinase, S6 kinase, tripeptidyl peptidase ii, ubiquitin protein ligase, unclassified drug, atrogin 1, muscle RING finger 1 protein, myosin heavy chain, adult, article, collagen synthesi, controlled study, gene expression, human, human cell, human tissue, hypothesi, male, muscle atrophy, muscle biopsy, muscle fibril, normal human, patella tendon

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000251478300019; volume:585; issue:1; firstpage:241; lastpage:251; numberofpages:11; journal:THE JOURNAL OF PHYSIOLOGY; http://hdl.handle.net/11577/3267160Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-36248952729; https://www.scopus.com/inward/record.uri?eid=2-s2.0-36248952729&doi=10.1113%2fjphysiol.2007.142828&partnerID=40&md5=f446f4898f89ad18e68210faa2c8b508Test

الإتاحة: https://doi.org/10.1113/jphysiol.2007.142828Test
http://hdl.handle.net/11577/3267160Test