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1
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 -
2
المؤلفون: Coppedè F
المصدر: The Application of Clinical Genetics, Vol Volume 14, Pp 279-295 (2021)
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Medicine (General), R5-920, integumentary system, hutchinson–gilford progeria syndrome, atypical progeroid syndromes, Genetics, nutritional and metabolic diseases, néstor-guillermo progeria syndrome, QH426-470, restrictive dermopathy, mandibuloacral dysplasia, werner syndrome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doajarticles::2b7bbb87f2c44dccbf90922e44423f28Test
https://www.dovepress.com/mutations-involved-in-premature-ageing-syndromes-peer-reviewed-fulltext-article-TACGTest -
3
المؤلفون: Bridger, JM, Torres Pereira, R, Pina, C, Tosi, S, Lewis, A
المساهمون: Kloc, M, Kubiak, J
المصدر: Nuclear, Chromosomal, and Genomic Architecture in Biology and Medicine ISBN: 9783031065729
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, genome organisation, integumentary system, topologically associated domains, nutritional and metabolic diseases, colorectal cancer, differentiation, Hutchinson-Gilford progeria syndrome, nucleolar associated domains, childhood leukaemia, stem cells, lamina associated domains, cellular senescence, embryogenesis
وصف الملف: Print-Electronic
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb272e8e66634b4cd7b2c74c9e844ef2Test
https://doi.org/10.1007/978-3-031-06573-6_3Test -
4
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 -
5
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: Vicente Andrés, Magda R. Hamczyk
المساهمون: Ministerio de Ciencia, Innovación y Universidades (España), European Regional Development Fund (ERDF/FEDER), Progeria Research Foundation, Fundacio La Marato, Fundación ProCNIC, Instituto de Salud Carlos III
المصدر: Nucleus, Vol 10, Iss 1, Pp 48-54 (2019)
Nucleus
Repisalud
Instituto de Salud Carlos III (ISCIII)
Scopus
RUO. Repositorio Institucional de la Universidad de Oviedo
instnameمصطلحات موضوعية: Premature aging, congenital, hereditary, and neonatal diseases and abnormalities, Vascular smooth muscle, lcsh:QH426-470, Cellular differentiation, Disease, Muscle, Smooth, Vascular, LMNA, 03 medical and health sciences, Progeria, medicine, Animals, Humans, vascular smooth muscle cells, lcsh:QH573-671, 030304 developmental biology, lamin A, 0303 health sciences, integumentary system, business.industry, lcsh:Cytology, Extra View, 030302 biochemistry & molecular biology, nutritional and metabolic diseases, Cell Biology, medicine.disease, Progerin, Lamin Type A, Atherosclerosis, Hutchinson-Gilford progeria syndrome, lcsh:Genetics, progerin, Cancer research, atherosclerosis, business, Lamin, hutchinson-gilford progeria syndrome, lamin a
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2f615358e3f276e90d7de7571bb59ceTest
https://doaj.org/article/f44fdf8a65c245f1b6a1e4410d172064Test -
7
المؤلفون: Ricardo Villa-Bellosta
المصدر: Proc Natl Acad Sci U S A
مصطلحات موضوعية: Male, 0301 basic medicine, 030204 cardiovascular system & hematology, Pyrophosphate, Mice, chemistry.chemical_compound, Adenosine Triphosphate, Progeria, 0302 clinical medicine, Gene Knock-In Techniques, Pyrophosphatases, RNA, Small Interfering, media_common, Multidisciplinary, integumentary system, Apyrase, Longevity, Calcinosis, Biological Sciences, Lamin Type A, Diphosphates, RNA Interference, Hutchinson Gilford Progeria Syndrome, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, media_common.quotation_subject, Myocytes, Smooth Muscle, Aortic Diseases, Mice, Transgenic, Real-Time Polymerase Chain Reaction, 03 medical and health sciences, Antigens, CD, Internal medicine, medicine, Animals, Humans, Vascular calcification, Phosphoric Diester Hydrolases, business.industry, nutritional and metabolic diseases, Alkaline Phosphatase, medicine.disease, Disease Models, Animal, 030104 developmental biology, Endocrinology, Levamisole, chemistry, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fc5d2c846386409bed45f6b6a6f47f5Test
https://doi.org/10.1073/pnas.1910972116Test -
8
المؤلفون: Richa Shukla, Veena Sharma
المصدر: Indian J Clin Biochem
مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Progeria, integumentary system, Genetic syndromes, business.industry, Clinical Biochemistry, nutritional and metabolic diseases, A protein, Review Article, Disease, PRELAMIN A, medicine.disease, Progerin, Bioinformatics, LMNA, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, 030220 oncology & carcinogenesis, Medicine, business, Hutchinson Gilford Progeria Syndrome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d44766e5c9eef04490fc8b17b0a4ea6Test
https://doi.org/10.1007/s12291-019-00849-6Test -
9
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 -
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المؤلفون: Francesco Musumeci, Antonio Giovanni Cammardella, Andrea Montalto, Carmine Musto, Vincenzo Polizzi, Federico Ranocchi, Mauro Cassese, Antonio Lio, Marina Comisso, Vitaliano Buffa
المصدر: The Annals of Thoracic Surgery. 110:e365-e367
مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Premature aging, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Transcatheter aortic, medicine.medical_treatment, Disease, 030204 cardiovascular system & hematology, 03 medical and health sciences, 0302 clinical medicine, Valve replacement, Internal medicine, medicine, Progeria, integumentary system, business.industry, nutritional and metabolic diseases, medicine.disease, Stenosis, 030228 respiratory system, Aortic valve stenosis, Cardiology, Surgery, Cardiology and Cardiovascular Medicine, business, Hutchinson Gilford Progeria Syndrome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::a6bd7b95b5906cc5039fb7e952d1f7f0Test
https://doi.org/10.1016/j.athoracsur.2020.03.067Test