Zobrazeno 1 - 10
of 132
pro vyhledávání: '"M. Nevado"'
Autor:
F. de-la Morena-López, C. Esteban-Fernández-Zarza, J. M. Esteban, B. Botella-Mateu, J. A. García-García, M. Santiago-Sánchez, M. Nevado-Santos, B. de Cuenca-Morón
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 102, Iss 5, Pp 342-344 (2010)
Externí odkaz:
https://doaj.org/article/dd946de5dcf7415c88999aa3b55784dd
Autor:
Magda R Hamczyk, Ricardo Villa‐Bellosta, Víctor Quesada, Pilar Gonzalo, Sandra Vidak, Rosa M Nevado, María J Andrés‐Manzano, Tom Misteli, Carlos López‐Otín, Vicente Andrés
Publikováno v:
EMBO Molecular Medicine, Vol 11, Iss 4, Pp 1-13 (2019)
Abstract Hutchinson–Gilford progeria syndrome (HGPS) is a rare genetic disorder caused by progerin, a mutant lamin A variant. HGPS patients display accelerated aging and die prematurely, typically from atherosclerosis complications. Recently, we de
Externí odkaz:
https://doaj.org/article/90fa5e8960124fb793cbbc7fdd07bf46
Autor:
Magda R. Hamczyk, Rosa M. Nevado
Publikováno v:
Clínica e Investigación en Arteriosclerosis (English Edition). 35:42-51
Autor:
Álvaro Macías, Rosa M. Nevado, Cristina González-Gómez, Pilar Gonzalo, María Jesús Andrés-Manzano, Beatriz Dorado, Ignacio Benedicto, Vicente Andrés
18 p.-6 fig.-1 tab.
Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare genetic disease caused by expression of progerin, a lamin A variant that is also expressed at low levels in non-HGPS individuals. Although HGPS patients die pre
Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare genetic disease caused by expression of progerin, a lamin A variant that is also expressed at low levels in non-HGPS individuals. Although HGPS patients die pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66987f88295072f3d098ff75bad056be
https://hdl.handle.net/20.500.12105/16218
https://hdl.handle.net/20.500.12105/16218
Publikováno v:
Cells, Vol 9, Iss 10, p 2252 (2020)
Hutchinson–Gilford progeria syndrome (HGPS) is among the most devastating of the laminopathies, rare genetic diseases caused by mutations in genes encoding nuclear lamina proteins. HGPS patients age prematurely and die in adolescence, typically of
Externí odkaz:
https://doaj.org/article/916c15b0db634249ba9b9d708475498d
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2419
Aging is associated with alterations in the arterial wall that promote vascular disease development and its clinical manifestations, including myocardial infarction, stroke, and arterial dissection. The arterial wall is comprised of three layers, int
Publikováno v:
Journal of the American College of Cardiology. 75:919-930
Aging is the main risk factor for vascular disease and ensuing cardiovascular and cerebrovascular events, the leading causes of death worldwide. In a progressively aging population, it is essential to develop early-life biomarkers that efficiently id
Publikováno v:
Methods in Molecular Biology ISBN: 9781071619230
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21e67eaccee8af4136421516dbb11980
https://doi.org/10.1007/978-1-0716-1924-7_38
https://doi.org/10.1007/978-1-0716-1924-7_38
Autor:
Martine de Boer, Frank Rühle, Vicente Andrés, Leon J. De Windt, Erika Hilbold, Christian Bär, Jana-Charlotte Hegenbarth, Monika Stoll, Rosa M Nevado, Blanche Schroen, Leonie Martens, Dirk J. Duncker, Anne-Sophie Armand, Federica De Majo, Thomas Thum, Magda R. Hamczyk
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 118(36):e2022974118. National Academy of Sciences
Proc Natl Acad Sci U S A
Proc Natl Acad Sci U S A
Genomic instability, the unresolved accumulation of DNA variants, is hypothesized as one of the contributors to the natural aging process. We assessed the frequency of unresolved DNA damage reaching the transcriptome of the murine myocardium during t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b2bfad205c1fe062cc23760a694be55
https://cris.maastrichtuniversity.nl/en/publications/cb4a6312-19ed-49a3-b368-2108e21f0804
https://cris.maastrichtuniversity.nl/en/publications/cb4a6312-19ed-49a3-b368-2108e21f0804
Publikováno v:
Scopus
Repisalud
Instituto de Salud Carlos III (ISCIII)
Cells, Vol 9, Iss 2252, p 2252 (2020)
Cells
Volume 9
Issue 10
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
RUO: Repositorio Institucional de la Universidad de Oviedo
Universidad de Oviedo (UNIOVI)
Repisalud
Instituto de Salud Carlos III (ISCIII)
Cells, Vol 9, Iss 2252, p 2252 (2020)
Cells
Volume 9
Issue 10
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
RUO: Repositorio Institucional de la Universidad de Oviedo
Universidad de Oviedo (UNIOVI)
Hutchinson&ndash
Gilford progeria syndrome (HGPS) is among the most devastating of the laminopathies, rare genetic diseases caused by mutations in genes encoding nuclear lamina proteins. HGPS patients age prematurely and die in adolescence, typi
Gilford progeria syndrome (HGPS) is among the most devastating of the laminopathies, rare genetic diseases caused by mutations in genes encoding nuclear lamina proteins. HGPS patients age prematurely and die in adolescence, typi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c8fa17bd3780855690b3b91b0762808
http://hdl.handle.net/10651/58813
http://hdl.handle.net/10651/58813