المؤلفون: Cristina Capanni, Elisa Schena, Maria Letizia Di Giampietro, Alessandra Montecucco, Elisabetta Mattioli, Giovanna Lattanzi

المصدر: Frontiers in Cell and Developmental Biology, Vol 10 (2022)

مصطلحات موضوعية: lamin A/C, prelamin A, DNA damage repair, laminopathies, premature ageing, Hutchinson-Gilford Progeria Syndrome (HGPS), Biology (General), QH301-705.5

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fcell.2022.1018102/fullTest; https://doaj.org/toc/2296-634XTest

الوصول الحر: https://doaj.org/article/8b102589514c425a97142ec1dfa8d03bTest

المؤلفون: USAI, CHANTAL

مصطلحات موضوعية: Hutchinson-Gilford Progeria Syndrome, HGPS, Biophysics, Microscopy, Expansion Microscopy, Super-resolution Microscopy, Laminopathies

الإتاحة: https://doi.org/10.15167/usai-chantal_phd2024-05-16Test
https://iris.unige.it/handle/11567/1174515Test

المؤلفون: Francesca Chiarini, Camilla Evangelisti, Vittoria Cenni, Antonietta Fazio, Francesca Paganelli, Alberto M. Martelli, Giovanna Lattanzi

المصدر: International Journal of Molecular Sciences; Volume 20; Issue 4; Pages: 847

مصطلحات موضوعية: mTOR, laminopathies, lamin A/C, Emery-Dreifuss muscular dystrophy (EDMD), Hutchinson-Gilford progeria syndrome (HGPS), autophagy, cellular signaling, metabolism, bone remodeling, ageing

جغرافية الموضوع: agris

وصف الملف: application/pdf

العلاقة: Molecular Pathology, Diagnostics, and Therapeutics; https://dx.doi.org/10.3390/ijms20040847Test

الإتاحة: https://doi.org/10.3390/ijms20040847Test

المؤلفون: Dobrzynska, Agnieszka, Gonzalo, Susana, Shanahan, Cathy, Askjaer, Peter

المصدر: Dobrzynska , A , Gonzalo , S , Shanahan , C & Askjaer , P 2016 , ' The nuclear lamina in health and disease ' , Nucleus-Austin , vol. 7 , no. 3 , pp. 233-248 . https://doi.org/10.1080/19491034.2016.1183848Test

مصطلحات موضوعية: chromatin, emerin, farnesylation, Hutchinson-Gilford progeria syndrome, laminopathies, LAP2, LBR, mechanotransduction, metabolism, muscles, nuclear envelope, nuclear lamina

وصف الملف: application/pdf

الإتاحة: https://doi.org/10.1080/19491034.2016.1183848Test
https://kclpure.kcl.ac.uk/portal/en/publications/f9315836-27f1-493e-8699-11a09d3092baTest
https://kclpure.kcl.ac.uk/ws/files/74614435/The_nuclear_lamina_in_DOBRZNSKA_Published9May2017_GOLD_VoR_CC_BY_.pdfTest
http://www.scopus.com/inward/record.url?scp=84976291644&partnerID=8YFLogxKTest

المؤلفون: Silvia Ortega-Gutiérrez, Beatriz Marcos-Ramiro, Jon Macicior

المصدر: International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 7190, p 7190 (2021)

مصطلحات موضوعية: 0301 basic medicine, Aging, Pyridines, Review, medicine.disease_cause, chemistry.chemical_compound, 0302 clinical medicine, Piperidines, Lonafarnib, Biology (General), Hutchinson–Gilford progeria syndrome (HGPS), Spectroscopy, Cellular Senescence, Skin, Progeria, Mutation, integumentary system, rare diseases, Aging, Premature, General Medicine, Progerin, Lamin Type A, Computer Science Applications, Chemistry, Phenotype, 030220 oncology & carcinogenesis, Nuclear lamina, congenital, hereditary, and neonatal diseases and abnormalities, QH301-705.5, Context (language use), Biology, Catalysis, Inorganic Chemistry, Small Molecule Libraries, 03 medical and health sciences, medicine, Humans, Physical and Theoretical Chemistry, Molecular Biology, QD1-999, lamin A, Cell Nucleus, Nuclear Lamina, Point mutation, Organic Chemistry, Laminopathies, Química orgánica, nutritional and metabolic diseases, progeria, Fibroblasts, medicine.disease, 030104 developmental biology, chemistry, progerin, Cancer research, Lamin

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fb1b7093f85929d11daee5c183d56dcTest
http://europepmc.org/articles/PMC8267806Test

المؤلفون: Manuela Teresa Raimondi, Emanuela Jacchetti, Francesca Donnaloja, Federica Carnevali

المصدر: Cells
Cells, Vol 9, Iss 1306, p 1306 (2020)

مصطلحات موضوعية: Emery-Dreyfuss muscular dystrophy, Hutchinson Gilford progeria syndrome, gene regulation, lamin A/C, lamin partners, laminopathy, mechanotransduction, Laminopathy, Review, Biology, Mechanotransduction, Cellular, Chromatin remodeling, 03 medical and health sciences, 0302 clinical medicine, medicine, Animals, Humans, Mechanotransduction, Mitosis, lcsh:QH301-705.5, 030304 developmental biology, Regulation of gene expression, 0303 health sciences, Laminopathies, General Medicine, medicine.disease, Lamin Type A, Chromatin, Cell biology, lcsh:Biology (General), Mutation, Nuclear lamina, 030217 neurology & neurosurgery, Lamin, Protein Binding

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c330e87980ab0ef77345067136eed310Test
http://hdl.handle.net/11311/1137194Test

المؤلفون: Francesca Paganelli, Giovanna Lattanzi, Antonietta Fazio, Camilla Evangelisti, Alberto M. Martelli, Vittoria Cenni, Francesca Chiarini

المساهمون: F. Chiarini, C. Evangelisti, V. Cenni, A. Fazio, F. Paganelli, A. M. Martelli, G. Lattanzi.

المصدر: International Journal of Molecular Sciences, Vol 20, Iss 4, p 847 (2019)
International Journal of Molecular Sciences

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, autophagy, Emery-Dreifuss muscular dystrophy (EDMD), Review, Models, Biological, Muscular Dystrophies, Catalysis, Inorganic Chemistry, LMNA, lcsh:Chemistry, Ageing, Autophagy, Bone remodeling, Cellular signaling, Hutchinson-Gilford progeria syndrome (HGPS), Lamin A/C, Laminopathies, Metabolism, mTOR, medicine, Animals, Humans, Physical and Theoretical Chemistry, Muscular dystrophy, Molecular Biology, Mechanistic target of rapamycin, Protein kinase B, lcsh:QH301-705.5, Spectroscopy, PI3K/AKT/mTOR pathway, bone remodeling, laminopathie, lamin A/C, Progeria, biology, integumentary system, TOR Serine-Threonine Kinases, laminopathies, Organic Chemistry, General Medicine, medicine.disease, Progerin, Lamins, Computer Science Applications, lcsh:Biology (General), lcsh:QD1-999, ageing, biology.protein, Cancer research, cellular signaling, metabolism, Signal Transduction

وصف الملف: ELETTRONICO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbf34c0dc148a81337ecdff07bb56563Test
https://hdl.handle.net/11380/1288373Test

المؤلفون: Benedetti Sara, Bernasconi Pia, Bertini Enrico, Biagini Elena, Boriani Giuseppe, Capanni Cristina, Carboni Nicola, Cenacchi Giovanna, Columbaro Marta, D'Adamo Monica, D’Amico Adele, D’Apice Maria, Fontana Marianna, Gambineri Alessandra, Lattanzi Giovanna, Liguori Rocco, Maraldi Nadir M, Mazzanti Laura, Mercuri Eugenio, Mongini Tiziana, Morandi Lucia O, Neri Iria, Nigro Giovanni, Novelli Giuseppe, Ortolani Michela, Pasquali Renato, Pini Antonella, Petrini Stefania, Politano Luisa, Previtali Stefano, Pucci Lisa, Rapezzi Claudio, Ricci Giulia, Rodolico Carmelo, Sbraccia Paolo, Scarano Emanuela, Siciliano Gabriele, Squarzoni Stefano, Toscano Antonio, Vercelli Liliana, Ziacchi Matteo

المصدر: Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 37 (2012)

مصطلحات موضوعية: Laminopathies, Emery-Dreifuss Muscular Dystrophy, Dilated Cardiomyopathy with Conduction Defects, Mandibuloacral Dysplasia, Familial Partial Lipodystrophy Type 2, Hutchinson-Gilford Progeria Syndrome, Rare Diseases, Networking activity, interdisciplinary approach to diseases, Medicine

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1750-1172Test

الوصول الحر: https://doaj.org/article/a5b1f2c1703844cfbb122a8609d267e6Test

المؤلفون: Gesson, Kevin, Vidak, Sandra, Foisner, Roland

المصدر: Seminars in Cell & Developmental Biology

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, BAF, barrier-to-autointegration factor, MDPSC, muscle-derived stem/progenitor cells, animal structures, ESC, embryonic stem cell, LEM, LAP2-Emerin-Man1, MSC, mesenchymal stem cell, Review, Nuclear envelopathies, FPLD, familial partial lipodystrophy, Retinoblastoma Protein, Muscular Dystrophies, Nuclear envelope, LAD, lamina-associated domain, Mice, Progeria, LAP, lamina-associated polypeptide, Animals, Humans, Nucleoplasmins, Dam, DNA adenine methyltransferase, DCM, dilated cardiomyopathy, Cell Proliferation, Adult stem cells, pRb, retinoblastoma protein, integumentary system, Laminopathies, INM, inner nuclear membrane, Membrane Proteins, Aging, Premature, Cell Differentiation, Cell Biology, Lamin Type A, Chromatin, Lamins, HGPS, Hutchinson–Gilford Progeria Syndrome, DNA-Binding Proteins, stomatognathic diseases, EDMD, Emery Dreifuss muscular dystrophy, Gene Expression Regulation, iPS, induced pluripotent stem cell, embryonic structures, ASC, (somatic) adult stem cell, NE, nuclear envelope, Self-renewal, LRD, lamin rich domain, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::fb352e8dfe077ede289c26cbbb47c377Test

المؤلفون: Wood, Kaitlin M

المساهمون: Espenshade, Peter, Michaelis, Susan, MacFarlane, Elena, Sesaki, Hiromi

مصطلحات موضوعية: Hutchinson-Gilford Progeria Syndrome, progeria, atypical progeria, nuclear lamina, laminopathies, progerin, prelamin A

وصف الملف: application/pdf

العلاقة: http://jhir.library.jhu.edu/handle/1774.2/67189Test

الإتاحة: http://jhir.library.jhu.edu/handle/1774.2/67189Test