Ifit2 deficiency results in decreased neuroinflammation upon RSA59 infection. by Jayasri Das Sarma (652473)

TNFα decreases cell NO, and reversal of this effect by adenosine is eNOS-dependent. by Theodore J. Kalogeris (575591)

Decreased extracellular laccase and peroxidase activities in the <i>Moap1</i> mutants. by Min Guo (228787)

IUI+mLPS increases proteolytic activity and decreases collagen IV immunoreactivity. by Brianna Carusillo Theriault (3716470)

Shark liver oil consumption decreases contractility in EDL muscle of trained rats by João Victor Capelli Peixoto (8301123)

“…In the supplemented group, animals were supplemented with SLO (1 g/kg) five times a week for eight weeks. Method: Contractile parameters as maximum isometric twitch force (Tmax), maximum speed of force development (+dF/dt), maximum speed of force decrease (-dF/dt), maximum tetanic force (Fmax) and resistance to fatigue were analyzed in isolated muscle. …”

Total history dependence decreases for small time bins Δ<i>t</i>. by Lucas Rudelt (4059505)

“…The smaller the time bin, the higher the risk that noise in the spike emission reduces the overall predictability or history dependence in the spiking, whereas an overly large time bin holds the risk of destroying coding relevant time information in the spike train. Thus, we chose the smallest time bin Δ<i>t</i> = 5 ms that does not yet show a substantial decrease in <i>R</i>_tot. …”

Supplementary data for "Submandibular gland removal decreases avoidance of bitter taste in mice" by Masataka Narukawa (20599511)

Deficiency of RAC1 in bone marrow-derived macrophages decreases lipid uptake. by Sashidar Bandaru (9389274)

Decreased Polycystin 2 Levels Result in Non-Renal Cardiac Dysfunction with Aging by Ivana Y. Kuo (707543)

“…Here, we examined 1 and 9 month old Pkd2+/- mice to determine if decreased amounts of functional polycystin 2 leads to impaired cardiac function with aging. …”

Fig 6 - by Matthew C. Kochem (18476069)

“…In the present study, our objective was to determine whether TAS1R2-TAS1R3 influences glucose metabolism bidirectionally via hyperactivation with 5 mM sucralose (n = 12) and inhibition with 2 mM sodium lactisole (n = 10) in mixture with 75 g glucose loads during oral glucose tolerance tests (OGTTs) in healthy humans. …”

Fig 2 - by Matthew C. Kochem (18476069)

“…In the present study, our objective was to determine whether TAS1R2-TAS1R3 influences glucose metabolism bidirectionally via hyperactivation with 5 mM sucralose (n = 12) and inhibition with 2 mM sodium lactisole (n = 10) in mixture with 75 g glucose loads during oral glucose tolerance tests (OGTTs) in healthy humans. …”

Fig 1 - by Matthew C. Kochem (18476069)

“…In the present study, our objective was to determine whether TAS1R2-TAS1R3 influences glucose metabolism bidirectionally via hyperactivation with 5 mM sucralose (n = 12) and inhibition with 2 mM sodium lactisole (n = 10) in mixture with 75 g glucose loads during oral glucose tolerance tests (OGTTs) in healthy humans. …”

Participant traits. by Matthew C. Kochem (18476069)

“…In the present study, our objective was to determine whether TAS1R2-TAS1R3 influences glucose metabolism bidirectionally via hyperactivation with 5 mM sucralose (n = 12) and inhibition with 2 mM sodium lactisole (n = 10) in mixture with 75 g glucose loads during oral glucose tolerance tests (OGTTs) in healthy humans. …”

Fig 4 - by Matthew C. Kochem (18476069)

“…In the present study, our objective was to determine whether TAS1R2-TAS1R3 influences glucose metabolism bidirectionally via hyperactivation with 5 mM sucralose (n = 12) and inhibition with 2 mM sodium lactisole (n = 10) in mixture with 75 g glucose loads during oral glucose tolerance tests (OGTTs) in healthy humans. …”

Fig 3 - by Matthew C. Kochem (18476069)

“…In the present study, our objective was to determine whether TAS1R2-TAS1R3 influences glucose metabolism bidirectionally via hyperactivation with 5 mM sucralose (n = 12) and inhibition with 2 mM sodium lactisole (n = 10) in mixture with 75 g glucose loads during oral glucose tolerance tests (OGTTs) in healthy humans. …”

Earlier Migration Timing, Decreasing Phenotypic Variation, and Biocomplexity in Multiple Salmonid Species by Ryan P. Kovach (103840)

“…<div><p>Climate-induced phenological shifts can influence population, evolutionary, and ecological dynamics, but our understanding of these phenomena is hampered by a lack of long-term demographic data. We use a multi-decade census of 5 salmonid species representing 14 life histories in a warming Alaskan stream to address the following key questions about climate change and phenology: How consistent are temporal patterns and drivers of phenology for similar species and alternative life histories? …”

The introduction of mutualisms into assembled communities increases their connectance and complexity while decreasing their richness. by Gui Araujo (22170819)

“…(C) Mutualism also promotes an increase in network connectance when introduced into assembled communities, while stopping mutualistic interactions from entering an assembled system slowly decreases it. (D) As a result, the introduction of mutualistic interactions promotes a growth in complexity in communities where it was once established as low, while stopping the introduction of further mutualistic interactions causes a slight decrease in complexity. …”

GSK343 treatment decreased <i>in vivo</i> tumor volume and growth. by Laura V. Bownes (10276762)

“…Once tumors were palpable (100 mm³), mice were randomized to receive either 100 μL of sterile PBS (vehicle, n = 7) or GSK343 (10 mg/kg/day in 100 μL PBS, n = 7) once daily via intraperitoneal (IP) injection for 21 days. …”

Representative histological images of all 10 piglets obtained 12 weeks after they underwent complete or partial devascularization of the lateral trochlear ridge of the femur. by Ferenc Tóth (665272)

Decreased Sho levels in different animal models infected with diverse prion strains. by Joel C. Watts (195735)

“…<p>(<b>A</b>) Western blot analysis of brain homogenates prepared from wt FVB mice (expressing the PrP-A allotype) infected with RML, 22L, Me7, and 301V prions, and B6.I mice (expressing the PrP-B allotype) infected with 87V and 301V prions. …”