المؤلفون: Coppedè F

المصدر: The Application of Clinical Genetics, Vol Volume 14, Pp 279-295 (2021)

مصطلحات موضوعية: hutchinson–gilford progeria syndrome, werner syndrome, restrictive dermopathy, mandibuloacral dysplasia, néstor-guillermo progeria syndrome, atypical progeroid syndromes, Medicine (General), R5-920, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://www.dovepress.com/mutations-involved-in-premature-ageing-syndromes-peer-reviewed-fulltext-article-TACGTest; https://doaj.org/toc/1178-704XTest

الوصول الحر: https://doaj.org/article/e09a001f6c0a430a89323d98b91e9efdTest

المؤلفون: Hisaya Kato, Yoshiro Maezawa

المصدر: Journal of Atherosclerosis and Thrombosis. 2022, 29(4):439

المؤلفون: Lingling Geng, Zunpeng Liu, Weiqi Zhang, Wei Li, Zeming Wu, Wei Wang, Ruotong Ren, Yao Su, Peichang Wang, Liang Sun, Zhenyu Ju, Piu Chan, Moshi Song, Jing Qu, Guang-Hui Liu

المصدر: Protein & Cell, Vol 10, Iss 6, Pp 417-435 (2018)

مصطلحات موضوعية: Quercetin, Stem cell, Aging, Werner syndrome, Hutchinson-Gilford progeria syndrome, Cytology, QH573-671, Animal biochemistry, QP501-801

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1007/s13238-018-0567-yTest; https://doaj.org/toc/1674-800XTest; https://doaj.org/toc/1674-8018Test

الوصول الحر: https://doaj.org/article/3f86cfb2c9364aa486703ea08e753d5eTest

المؤلفون: Coppedè Fabio

المساهمون: Coppede', Fabio

مصطلحات موضوعية: Atypical progeroid syndrome, Hutchinson-gilford progeria syndrome, Mandibuloacral dysplasia, Néstor-guillermo progeria syndrome, Restrictive dermopathy, Werner syndrome

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34103969; info:eu-repo/semantics/altIdentifier/wos/WOS:000657474600001; volume:14; firstpage:279; lastpage:295; numberofpages:17; journal:THE APPLICATION OF CLINICAL GENETICS; https://hdl.handle.net/11568/1106474Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85107925335

الإتاحة: https://doi.org/10.2147/TACG.S273525Test
https://hdl.handle.net/11568/1106474Test

المؤلفون: Coppedè F

المصدر: Clinical Interventions in Aging, Vol Volume 8, Pp 1023-1032 (2013)

مصطلحات موضوعية: Hutchinson–Gilford Progeria Syndrome, Werner syndrome, premature aging disorders, epidemiology, cardiovascular diseases, cancer, atherosclerosis, genetics, sign and symptoms, Geriatrics, RC952-954.6

وصف الملف: electronic resource

العلاقة: https://www.dovepress.com/the-epidemiology-of-premature-aging-and-associated-comorbidities-peer-reviewed-article-CIATest; https://doaj.org/toc/1178-1998Test

الوصول الحر: https://doaj.org/article/7991b857163044eeadb177ba0e3bd180Test

المؤلفون: Fabio Coppedè

المصدر: The Application of Clinical Genetics

مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, DNA repair, Review, Bioinformatics, restrictive dermopathy, Progeroid syndromes, 03 medical and health sciences, 0302 clinical medicine, atypical progeroid syndromes, Genetics, medicine, Genetics (clinical), Werner syndrome, Progeria, Hutchinson–Gilford progeria syndrome, integumentary system, Genetic heterogeneity, business.industry, Néstor-Guillermo progeria syndrome, nutritional and metabolic diseases, Atypical progeroid syndromes, Hutchinson-gilford progeria syndrome, Mandibuloacral dysplasia, Néstor-guillermo progeria syndrome, Restrictive dermopathy, medicine.disease, Hypoplasia, 030104 developmental biology, business, 030217 neurology & neurosurgery, mandibuloacral dysplasia

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb2fe17d6122e15ef63995e77851912bTest
https://pubmed.ncbi.nlm.nih.gov/34103969Test

المؤلفون: Yoshiro Maezawa, Hisaya Kato

المصدر: Journal of atherosclerosis and thrombosis. 29(4)

مصطلحات موضوعية: Premature aging, congenital, hereditary, and neonatal diseases and abnormalities, Aging, Disease, Bioinformatics, Pediatric Disease, Progeroid syndromes, Pathogenesis, Progeria, Internal Medicine, medicine, Humans, Werner syndrome, integumentary system, business.industry, Biochemistry (medical), nutritional and metabolic diseases, medicine.disease, Atherosclerosis, Cardiovascular Diseases, Child, Preschool, Werner Syndrome, Cardiology and Cardiovascular Medicine, business, Hutchinson Gilford Progeria Syndrome

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3885dff92d0749108d795a96ebd4b597Test
https://pubmed.ncbi.nlm.nih.gov/34511576Test

المؤلفون: Guang-Hui Liu, Jing Qu, Wei Li, Moshi Song, Zhenyu Ju, Lingling Geng, Ruotong Ren, Zeming Wu, Zunpeng Liu, Wei Wang, Weiqi Zhang, Peichang Wang, Yao Su, Piu Chan, Liang Sun

المصدر: Protein & Cell
Protein & Cell, Vol 10, Iss 6, Pp 417-435 (2018)

مصطلحات موضوعية: 0301 basic medicine, Senescence, Premature aging, endocrine system, Aging, lcsh:Animal biochemistry, Ascorbic Acid, Biochemistry, Models, Biological, Cell Line, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Progeria, Drug Discovery, medicine, Humans, heterocyclic compounds, lcsh:QH573-671, lcsh:QP501-801, Cellular Senescence, Werner syndrome, Cell Proliferation, Stem cell, lcsh:Cytology, business.industry, Cell growth, Mesenchymal stem cell, Aging, Premature, Mesenchymal Stem Cells, Cell Biology, medicine.disease, Hutchinson-Gilford progeria syndrome, 030104 developmental biology, chemistry, 030220 oncology & carcinogenesis, Cancer research, Quercetin, business, Biotechnology, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02f1d0269c7221dfdacf3bf541c84868Test
http://europepmc.org/articles/PMC6538594Test

المؤلفون: Samuel Corless, Felix Bormann, Julian Gutekunst, Frank Lyko, Manuel Rodríguez-Paredes, Günter Raddatz, Tanja Musch, Sylvia Erhardt, Anke S. Lonsdorf, Florian Köhler

المصدر: Genome Medicine
Genome Medicine, Vol 12, Iss 1, Pp 1-16 (2020)

مصطلحات موضوعية: Premature aging, congenital, hereditary, and neonatal diseases and abnormalities, Aging, lcsh:QH426-470, Lamina-associated domains (LADs), lcsh:Medicine, Biology, Cell Line, Epigenesis, Genetic, 03 medical and health sciences, Progeria, 0302 clinical medicine, Protein Domains, Genetics, medicine, Humans, Epigenetics, Molecular Biology, Genetics (clinical), 030304 developmental biology, Werner syndrome, Chromatin accessibility, 0303 health sciences, DNA methylation, integumentary system, Research, lcsh:R, nutritional and metabolic diseases, Fibroblasts, Lamin Type A, medicine.disease, Progerin, Hutchinson-Gilford progeria syndrome, 3. Good health, Cell biology, Chromatin, lcsh:Genetics, Gene Expression Regulation, Molecular Medicine, 030217 neurology & neurosurgery, Lamin

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b39b127c01bafb162e01fde300bc71eTest
https://doi.org/10.1186/s13073-020-00749-yTest

المؤلفون: Coppede F.

المساهمون: Coppede, F.

مصطلحات موضوعية: Atypical HGPS, Atypical progeria, Atypical WS, Hutchinson-Gilford Progeria Syndrome, LMNA, Premature aging syndrome, Werner Syndrome, WRN, ZMPSTE24

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/isbn/9780128122006; ispartofbook:Encyclopedia of Endocrine Diseases; firstpage:669; lastpage:674; numberofpages:6; http://hdl.handle.net/11568/1034761Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85079255461; http://dx.doi.org/10.1016/B978-0-12-801238-3.95829-XTest

الإتاحة: https://doi.org/10.1016/B978-0-12-801238-3.95829-XTest
http://hdl.handle.net/11568/1034761Test