المؤلفون: Murdocca M., Citro G., Romeo I., Lupia A., Miersch S., Amadio B., Bonomo A., Rossi A., Sidhu S. S., Pandolfi P. P., Alcaro S., Sangiuolo F. C., Novelli G.

المساهمون: Murdocca, M., Citro, G., Romeo, I., Lupia, A., Miersch, S., Amadio, B., Bonomo, A., Rossi, A., Sidhu, S. S., Pandolfi, P. P., Alcaro, S., Sangiuolo, F. C., Novelli, G.

مصطلحات موضوعية: Conserved RBD region, COVID-19, Drug design, Peptide, Protein–protein docking, SARS-CoV-2 variant, VSVpp.SARS-2S

Relation: info:eu-repo/semantics/altIdentifier/pmid/34452531; info:eu-repo/semantics/altIdentifier/wos/WOS:000689910800001; volume:13; issue:8; firstpage:1; lastpage:21; numberofpages:21; journal:VIRUSES; https://hdl.handle.net/11584/357501; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85113981614

الاتاحة: https://hdl.handle.net/11584/357501
https://doi.org/10.3390/v13081667

المؤلفون: Camerota L., Ritelli M., Wischmeijer A., Majore S., Cinquina V., Fortugno P., Monetta R., Gigante L., Sangiuolo F. C., Novelli G., Colombi M., Brancati F., Ruvolo G., Bertoldo F., Donzelli C., Polisca P., Salehi L. B., Mancino R., di Carlo E., Bollero P., Cozza P., Lagana G., Farsetti P., de Maio F., de Luna V., Mancini F., Chini L., Graziani S., Floris R., Sperandio M., Infante A., de Stefano A., Chiariello L., Grego S.

المساهمون: Camerota L., Ritelli M., Wischmeijer A., Majore S., Cinquina V., Fortugno P., Monetta R., Gigante L., Sangiuolo F. C., Novelli G., Colombi M., Brancati F., Ruvolo G., Bertoldo F., Donzelli C., Polisca P., Salehi L. B., Mancino R., di Carlo E., Bollero P., Cozza P., Lagana G., Farsetti P., de Maio F., de Luna V., Mancini F., Chini L., Graziani S., Floris R., Sperandio M., Infante A., de Stefano A., Chiariello L., Grego S.

مصطلحات موضوعية: Arterial aneurysm, Ehlers-Danlos syndrome, Hereditary connective tissue disorder, Loeys-Dietz syndrome, SMAD2, SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/31569402; info:eu-repo/semantics/altIdentifier/wos/WOS:000498397100035; volume:10; issue:10; journal:GENES; http://hdl.handle.net/11379/525821; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85072779903; https://www.mdpi.com/2073-4425/10/10/764/pdf

الاتاحة: http://hdl.handle.net/11379/525821
https://doi.org/10.3390/genes10100764
https://www.mdpi.com/2073-4425/10/10/764/pdf

المؤلفون: Ferradini V., Parca L., Martino A., Lanzillo C., Silvetti E., Calo L., Caselli S., Novelli G., Helmer-Citterich M., Sangiuolo F. C., Mango R.

المساهمون: Ferradini, V, Parca, L, Martino, A, Lanzillo, C, Silvetti, E, Calo, L, Caselli, S, Novelli, G, Helmer-Citterich, M, Sangiuolo, Fc, Mango, R

مصطلحات موضوعية: Settore MED/03 - GENETICA MEDICA

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000666548100001; volume:12; issue:6; journal:GENES; http://hdl.handle.net/2108/276236; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85107115523

الاتاحة: http://hdl.handle.net/2108/276236
https://doi.org/10.3390/genes12060793

المؤلفون: Camerota, L., Ritelli, M., Wischmeijer, A., Majore, S., Cinquina, V., Fortugno, P., Monetta, R., Gigante, L., Sangiuolo, F. C., Novelli, G., Colombi, M., Brancati, F., Ruvolo, G., Bertoldo, F., Donzelli, C., Polisca, P., Salehi, L. B., Mancino, R., di Carlo, E., Bollero, P., Cozza, P., Lagana, G., Farsetti, P., de Maio, F., de Luna, V., Mancini, F., Chini, L., Graziani, S., Floris, R., Sperandio, M., Infante, A., de Stefano, A., Chiariello, L., Grego, S.

المصدر: Genes, Vol 10, Iss 10, p 764 (2019)
Genes
Volume 10
Issue 10

مصطلحات موضوعية: 0301 basic medicine, Adult, Connective Tissue Disorder, Adolescent, lcsh:QH426-470, Receptor, Transforming Growth Factor-beta Type I, 030105 genetics & heredity, Bioinformatics, Loeys–Dietz syndrome, Article, 03 medical and health sciences, Transforming Growth Factor beta2, tgfbr1, TGFB3, Genotype, Genetics, Arterial aneurysms, Ehlers-Danlos syndrome, Hereditary connective tissue disorders, Loeys-Dietz syndrome, SMAD2, SMAD3, TGFB2, TGFBR1, TGFBR2, ehlers-danlos syndrome, arterial aneurysms, Medicine, Humans, loeys-dietz syndrome, smad3, smad2, Smad3 Protein, Craniofacial, Child, tgfbr2, Genetics (clinical), business.industry, Genetic heterogeneity, Receptor, Transforming Growth Factor-beta Type II, Infant, Middle Aged, medicine.disease, Penetrance, Pedigree, lcsh:Genetics, 030104 developmental biology, Settore MED/03 - Genetica Medica, Ehlers–Danlos syndrome, Child, Preschool, tgfb3, hereditary connective tissue disorders, Age of onset, tgfb2, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c0f5fe4f57ab02cfe566478c650e8eb
http://hdl.handle.net/2108/226337

المؤلفون: Bertoldo, F., Pisano, C., Nardi, P., Donzelli, C., Laganà, G., Salehi, B., Sangiuolo, F. C., Bollero, P., De Maio, F., Mancino, R., Chiocchi, M., De Stefano, A., Cozza, P., Ruvolo, G., Novelli, G.

المساهمون: Bertoldo, F, Pisano, C, Nardi, P, Donzelli, C, Laganà, G, Salehi, B, Sangiuolo, Fc, Bollero, P, De Maio, F, Mancino, R, Chiocchi, M, De Stefano, A, Cozza, P, Ruvolo, G, Novelli, G

مصطلحات موضوعية: Settore MED/23 - CHIRURGIA CARDIACA

Relation: volume:19; firstpage:e48; lastpage:e49; journal:JOURNAL OF CARDIOVASCULAR MEDICINE; http://hdl.handle.net/2108/252033

الاتاحة: http://hdl.handle.net/2108/252033
https://doi.org/10.2459/01.JCM.0000549994.53432.00

المؤلفون: Di Donna, M. G.^1,2 (AUTHOR) martina.gaia.di.donna@gmail.com, Colona, V. L.^3,4 (AUTHOR), Bagnato, M. R.^2,5 (AUTHOR), Bonomi, C. G. (AUTHOR), Tirrito, L. (AUTHOR), Marchionni, E. (AUTHOR), Motta, C. (AUTHOR), Sangiuolo, F. C. (AUTHOR), Martorana, A. (AUTHOR)

المصدر: Neurological Sciences. Dec2024, p1-10.

مصطلحات موضوعية: *CEREBRAL small vessel diseases, *NEUROPSYCHOLOGICAL tests, *SYMPTOMS, *NEURODEGENERATION, *GENETIC mutation