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Human Mutation|August 31, 2002
TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathiesStefanie Katzke, Patrick Booms, Frank Tiecke, et al.
European Journal of Cell Biology|March 14, 2022
HS1 deficiency protects against sepsis by attenuating neutrophil-inflicted lung damageIdaira M Guerrero-Fonseca, Alexander García-Ponce, Eduardo Vadillo, et al.
Journal of Hematology & Oncology|September 24, 2016
Silencing of GATA3 defines a novel stem cell-like subgroup of ETP-ALLL Fransecky, M Neumann, S Heesch, et al.
Journal of the American Academy of Dermatology|May 4, 2024
Extramammary Paget disease. Part I. epidemiology, pathogenesis, clinical features, and diagnosisRohan R Shah, Kalee Shah, Britney N Wilson, et al.
Neurology|April 18, 2007
Cognitive and motor assessment in autopsy-proven corticobasal degenerationR Murray, M Neumann, M S Forman, et al.
BMC Cancer|October 1, 2018
Cross-sectional increase of adherence to multidisciplinary tumor board decisionsS Hollunder, U Herrlinger, M Zipfel, et al.
Cancer Medicine|December 30, 2025
Identifying Factors of Organoid Establishment in Pancreatic Cancer: A Prospective Observational StudyKatharina Wansch, François Schneider, Florian Dölvers, et al.
Scientific Reports|April 14, 2026
Impact of culture dimensionality and matrix composition on morphology, phenotype and drug response in pancreatic cancer modelsFlorian Doelvers, Katharina Wansch, Anna Kuehn, et al.
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