Results 141 to 150 of about 1,631,615 (310)
Sheep as a large animal model for hearing research: comparison to common laboratory animals and humans. [PDF]
Lue PY +4 more
europepmc +1 more source
ERα splice variant ERα∆7 lacks the C‐terminus, and its expression may change phenotypes of breast cancers. Our results showed that ERα∆7 is found in the luminal A subtype, and elevated ERα∆7 levels are linked to improved cell survival with lower proliferation and migration.
Long Wai Tsui +10 more
wiley +1 more source
Comprehensive methodology for evaluating the immobility responses in laboratory animals. [PDF]
Estrada-Silva MA +11 more
europepmc +1 more source
Nomenclature for standardized designation of diploid genotypes in genetically modified laboratory animals. [PDF]
Dobrowolski P, Buch T, Nagel-Riedasch S.
europepmc +1 more source
Matrix metalloproteinase‐9 (MMP9) drives ovarian cancer progression. Using MMP9‐null cells (M9‐KO) created from ovarian cancer cells, we found MMP9 loss did not block Epidermal Growth Factor (EGF)‐driven E‐cadherin dissolution or EMT but delayed and reduced EGF‐driven membrane protrusions. Transient MMP9 re‐expression drove membrane protrusion.
Claire Strauel +8 more
wiley +1 more source
How University Students Evaluate the Use of Laboratory Animals: The Role of Species and Individual Differences. [PDF]
Ruiz-Sancho L +3 more
europepmc +1 more source
14‐day casting‐induced immobilization reduced gastrocnemius muscle mass and increased non‐heme iron and ferritin heavy chain levels. Despite iron accumulation, transferrin receptor 1 and iron regulatory protein 2 were paradoxically upregulated. Lipid peroxidation was elevated without compensatory antioxidant responses.
Haruka Yokogawa +2 more
wiley +1 more source
General anesthesia and depth of anesthesia (DoA) evaluation methods in laboratory animals: a comprehensive review. [PDF]
Altınoluk T, Kazdağlı H.
europepmc +1 more source
Reprinted from Laboratory animals 1993 vol 27, pages 301-329Available from British Library Document Supply Centre-DSC:m00/36085 / BLDSC - British Library Document Supply CentreSIGLEGBUnited ...
Laboratory Animals Ltd., London (United Kingdom)
core
This study explores the feasibility of expressing the antitumoral protein Amblyomin‐X through a suicide gene therapy approach and investigates its intracellular fate after gene delivery. Although the gene is efficiently expressed, melanoma cells rapidly degrade the Amblyomin‐X protein via proteasome activity.
Victor Dal Posolo Cinel +4 more
wiley +1 more source

