Results 191 to 200 of about 7,722 (240)

MetInfilt: A prospective trial highlighting the importance of the histological growth pattern in brain metastases. [PDF]

Transl Oncol
Proescholdt MA, Araceli T, Schebesch KM, Doenitz C, Wendl C, Evert K, Noeva E, Hoehne J, Riemenschneider MJ, Hirsch D, Schmidt NO, Sparrer D, Lüke F, Heudobler D, Pukrop T, Blazquez R.   +15 more
europepmc   +1 more source

Analysis of Beta-Dystroglycan in Different Cell Models of Senescence. [PDF]

Int J Mol Sci
Jimenez-Gutierrez GE, Zavaleta-Vásquez TI, Lizcano-Meneses JA, Garcia-Aguirre IA, Laredo-Cisneros MS, Magaña JJ, Winder SJ, Cordero-Martínez J, Cisneros B.   +8 more
europepmc   +1 more source

Involvement of NRF2 and AMPK signaling in aging and progeria: a digest. [PDF]

Redox Biol
Petsouki E, Gerakopoulos V, Gianniou DD, Heiss EH, Trougakos IP.   +4 more
europepmc   +1 more source

Development and validation of a computed tomography-based radiomics-clinical model to preoperatively predict high-grade patterns within lung invasive adenocarcinoma. [PDF]

J Thorac Dis
Zhang X, Cen T, Wang L, Shi M, Zheng L, Hu W, Pan Y, Liang Z.   +7 more
europepmc   +1 more source

Enhancing the intraoperative identification of high-grade patterns in invasive lung adenocarcinoma via radiomics. [PDF]

Transl Lung Cancer Res
Sun Y, Dong H, Jin W, Xuan H, Yuan Z, Käsmann L, Shen L, Wang T, Ye X, Zeng M.   +9 more
europepmc   +1 more source

A High Throughput Phenotypic Screening reveals compounds that counteract premature osteogenic differentiation of HGPS iPS-derived mesenchymal stem cells [PDF]

Scientific Reports, 2016
Hutchinson-Gilford progeria syndrome (HGPS) is a rare fatal genetic disorder that causes systemic accelerated aging in children. Thanks to the pluripotency and self-renewal properties of induced pluripotent stem cells (iPSC), HGPS iPSC-based modeling ...
Nicolas Levy, Lino Ferreira
exaly   +5 more sources

Role of progerin-induced telomere dysfunction in HGPS premature cellular senescence [PDF]

Journal of Cell Science, 2010
Hutchinson-Gilford Progeria Syndrome (HGPS) is a premature-aging syndrome caused by a dominant mutation in the gene encoding lamin A, which leads to an aberrantly spliced and processed protein termed progerin.
Stuart Aaronson, Lee Sam W, Aaronson Stuart A   +2 more
exaly   +3 more sources

Presence and distribution of progerin in HGPS cells is ameliorated by drugs that impact on the mevalonate and mTOR pathways [PDF]

Biogerontology, 2019
Hutchinson–Gilford progeria syndrome (HGPS) is a rare, premature ageing syndrome in children. HGPS is normally caused by a mutation in the LMNA gene, encoding nuclear lamin A.
Evgeny Makarov, Joanna Bridger, Mehmet Ural Bikkul   +2 more
exaly   +4 more sources