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المؤلفون: Yohei Asano, Akihiko Takeuchi, Katsuhiro Hayashi, Kentaro Igarashi, Hiroyuki Tsuchiya, Sei Morinaga, Shinji Miwa, Hirotaka Yonezawa, Yoshihiro Araki, Norio Yamamoto
المصدر: World Journal of Clinical Cases
مصطلحات موضوعية: musculoskeletal diseases, Oncology, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Thyroid cancer, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Long term survival, Case report, medicine, Progeria, Osteosarcoma, integumentary system, business.industry, nutritional and metabolic diseases, Biological reconstruction, General Medicine, medicine.disease, Hutchinson-Gilford progeria syndrome, 030220 oncology & carcinogenesis, embryonic structures, 030211 gastroenterology & hepatology, Frozen autograft, business, Hutchinson Gilford Progeria Syndrome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eadf03acda0e03eff75c3df5ed61a48fTest
http://europepmc.org/articles/PMC7852653Test -
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المؤلفون: Ian R. Kill, Wendy Ofosu, Joanna M. Bridger, Craig S. Clements, Evgeny M. Makarov, David Tree, Christopher H. Eskiw, Mehmet U. Bikkul
المصدر: Biogerontology
مصطلحات موضوعية: 0301 basic medicine, Aging, N-acetyl cysteine, Farnesyltransferase, Hutchinson-Gilford Progeria Syndrome, Progerin, LMNA, zoledronic acid, 0302 clinical medicine, Progeria, Enzyme Inhibitors, Pravastatin, farnesyl transferase inhibitors, pravastatin, biology, integumentary system, Chemistry, Lamin Type A, embryonic structures, Mevalonate pathway, medicine.drug, Research Article, congenital, hereditary, and neonatal diseases and abnormalities, Mevalonic Acid, Cell Line, 03 medical and health sciences, Internal lamin foci, medicine, Humans, Rapamycin, PI3K/AKT/mTOR pathway, Zoledronic acid, nuclear lamins, Hutchinson–Gilford progeria syndrome, rapamycin, Farnesyl transferase inhibitors, nutritional and metabolic diseases, medicine.disease, 030104 developmental biology, progerin, biology.protein, Cancer research, Nuclear lamins, Geriatrics and Gerontology, Gerontology, 030217 neurology & neurosurgery, Lamin
وصف الملف: Print-Electronic
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f6b2fd09330521c2ec71ca71051a6afTest
http://europepmc.org/articles/PMC6535420Test -
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المؤلفون: Meenakshi Wadhwani
المصدر: Journal of Optometry and Ophthalmology.
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, integumentary system, business.industry, embryonic structures, nutritional and metabolic diseases, Medicine, business, Dermatology, Hutchinson Gilford Progeria Syndrome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::0cd8de8912eed4652ba65079284bf09bTest
https://doi.org/10.37191/mapsci-joo-1-009Test -
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المؤلفون: Cristiano Petrini, Chiara Lanzuolo, Gennaro Oliva, Endre Sebestyén, Federica Lucini, Sara Valsoni, Francesco Ferrari, Louis Antonelli, Andrea Bianchi, Francesco Gregoretti, Fabrizia Marullo, Ilaria Olivieri
المصدر: Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
Nature communications 11 (2020): 6274. doi:10.1038/s41467-020-20048-9
info:cnr-pdr/source/autori:Sebestyen E, Marullo F, Lucini F, Petrini C, Bianchi A, Valsoni S, Olivieri I, Antonelli L, Gregoretti F, Oliva G, Ferrari F, Lanzuolo C./titolo:SAMMY-seq reveals early alteration of heterochromatin and deregulation of bivalent genes in Hutchinson-Gilford Progeria Syndrome/doi:10.1038%2Fs41467-020-20048-9/rivista:Nature communications/anno:2020/pagina_da:6274/pagina_a:/intervallo_pagine:6274/volume:11مصطلحات موضوعية: 0301 basic medicine, General Physics and Astronomy, Datasets as Topic, Polycomb-Group Proteins, Hutchinson-Gilford Progeria Syndrome, Histones, 0302 clinical medicine, Progeria, Heterochromatin, Histone post-translational modifications, RNA-Seq, Child, Cells, Cultured, Skin, Multidisciplinary, integumentary system, SAMMY-seq, Lamin Type A, Chromatin, Cell biology, Histone Code, Child, Preschool, embryonic structures, Chromatin Immunoprecipitation Sequencing, Transcriptional Activation, congenital, hereditary, and neonatal diseases and abnormalities, Science, Primary Cell Culture, Biology, General Biochemistry, Genetics and Molecular Biology, Chromatin remodeling, Bivalent (genetics), Article, 03 medical and health sciences, Chromatin analysis, medicine, Humans, Psychological repression, Gene, Nuclear organization, fungi, nutritional and metabolic diseases, General Chemistry, Fibroblasts, medicine.disease, Gene regulation, 030104 developmental biology, 030217 neurology & neurosurgery, Lamin
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca8574e26d8af1183ec0f4c4f1005097Test
https://pubmed.ncbi.nlm.nih.gov/33293552Test -
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مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, integumentary system, embryonic structures, nutritional and metabolic diseases, Hutchinson-Gilford Progeria Syndrome, bone deformation, pre-lamin A, Progeroid syndromes
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17ee37e45a3ef49306d62052110d7ac6Test
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المؤلفون: Frédéric Lessard, Olga Moiseeva, Gerardo Ferbeyre, Stéphane Lopes-Paciencia, Geneviève Huot
المصدر: Aging (Albany NY)
مصطلحات موضوعية: 0301 basic medicine, Premature aging, Aging, congenital, hereditary, and neonatal diseases and abnormalities, senescence, Immunoblotting, Protein Prenylation, environment and public health, Serine, 03 medical and health sciences, 0302 clinical medicine, Progeria, Cyclin-dependent kinase, medicine, Humans, Immunoprecipitation, Phosphorylation, Interphase, lamin A, biology, integumentary system, nutritional and metabolic diseases, Cell Biology, medicine.disease, Progerin, Lamin Type A, Cell biology, liquid droplets, Hutchinson-Gilford progeria syndrome, 030104 developmental biology, cyclin dependent kinases, Biochemistry, Microscopy, Fluorescence, 030220 oncology & carcinogenesis, embryonic structures, Mutation, biology.protein, Mutagenesis, Site-Directed, Protein prenylation, Lamin, Research Paper
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0d4f85412c9f8058a3ec46b24d24eaaTest
http://europepmc.org/articles/PMC4789588Test -
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المؤلفون: Lucio Comai, Sita Reddy
المصدر: F1000Research
مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Aging, animal structures, Nuclear Structure & Function, Neurodevelopment, Cell Growth & Division, Physiology, Disease, Review, Biology, General Biochemistry, Genetics and Molecular Biology, Neurobiology of Disease & Regeneration, 03 medical and health sciences, Human health, Muscle & Connective Tissue, medicine, Cell Adhesion, General Pharmacology, Toxicology and Pharmaceutics, Cytoskeleton, Neuronal & Glial Cell Biology, Progeria, General Immunology and Microbiology, integumentary system, General Medicine, Articles, nuclear envelope, medicine.disease, Developmental Molecular Mechanisms, Morphogenesis & Cell Biology, Hutchinson-Gilford progeria syndrome, 030104 developmental biology, Cardiovascular Physiology/Circulation, lamins, Mechanical stability, embryonic structures, Nuclear lamina, Lamin Association Domains, Hutchinson Gilford Progeria Syndrome, Neuroscience, Medical Genetics, Lamin, Control of Gene Expression
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b6ab87e4fc18ef25e5dbcf783032095Test
http://europepmc.org/articles/PMC5074355Test -
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المؤلفون: Liat Apel-Sarid, Praveen Koganti, Gal Levy-Cohen, Nataša Ilić, Aurora Paola Borroni, Michael B. Blank, Pooja Anil Shah, Andrea Emanuelli, Biagio Paolini, Dhanoop Manikoth Ayyathan
المصدر: Aging Cell
مصطلحات موضوعية: 0301 basic medicine, Aging, congenital, hereditary, and neonatal diseases and abnormalities, autophagy, Ubiquitin-Protein Ligases, Regulator, Transfection, ubiquitination, LMNA, 03 medical and health sciences, Hutchinson‐Gilford progeria syndrome, Progeria, Ubiquitin, medicine, Humans, Smurf2, lamin A, biology, integumentary system, Aging, Premature, Cell Biology, Original Articles, medicine.disease, Progerin, Lamin Type A, 3. Good health, Ubiquitin ligase, Cell biology, 030104 developmental biology, progerin, embryonic structures, biology.protein, Nuclear lamina, Original Article, Lysosomes, Lamin
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98a27d9a099dd159f42d05e8779e1daaTest
https://pubmed.ncbi.nlm.nih.gov/29405587Test -
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المصدر: British Journal of Medicine and Medical Research. 5:1527-1533
مصطلحات موضوعية: Premature aging, congenital, hereditary, and neonatal diseases and abnormalities, Progeria, medicine.medical_specialty, Pathology, Environmental Engineering, integumentary system, business.industry, Genetic disorder, nutritional and metabolic diseases, Multidisciplinary team, medicine.disease, Dermatology, Industrial and Manufacturing Engineering, Disease course, Review article, embryonic structures, Medicine, business, Hutchinson Gilford Progeria Syndrome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::65f1d6ca45c31fa71bc4073812153732Test
https://doi.org/10.9734/bjmmr/2015/13452Test -
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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
