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351. Multi-model evaluation of phenology prediction for wheat in Australia.

352. Uso della modellistica per il monitoraggio e la sostenibilità degli agroecosistemi

353. Rifaximin on epigenetics and autophagy in animal model of hepatocellular carcinoma secondary to metabolic-dysfunction associated steatotic liver disease.

354. Spatial patterns of historical crop yields reveal soil health attributes in US Midwest fields.

355. Baccharis anomala DC. extract reduces inflammation and attenuates hepatic fibrosis in vivo by decreasing NF-kB and extracellular matrix compounds.

356. Bezafibrate reduces the damage, activation and mechanical properties of lung fibroblast cells induced by hydrogen peroxide.

357. Increased sinusoidal pressure impairs liver endothelial mechanosensing, uncovering novel biomarkers of portal hypertension.

358. A simple soil mass correction for a more accurate determination of soil carbon stock changes.

359. Novel technologies for emission reduction complement conservation agriculture to achieve negative emissions from row-crop production.

360. Development of a municipality index of environmental pressure in Campania, Italy.

362. Contrasting long-term temperature trends reveal minor changes in projected potential evapotranspiration in the US Midwest.

363. Subfield crop yields and temporal stability in thousands of US Midwest fields.

364. CPBMF65, a synthetic human uridine phosphorylase-1 inhibitor, reduces HepG2 cell proliferation through cell cycle arrest and senescence.

365. Unstable crop yields reveal opportunities for site-specific adaptations to climate variability.

366. Assessing uncertainties in crop and pasture ensemble model simulations of productivity and N 2 O emissions.

367. Therapeutic ultrasound stimulates MC3T3-E1 cell proliferation through the activation of NF-κB1, p38α, and mTOR.

368. Response of wheat growth, grain yield and water use to elevated CO 2 under a Free-Air CO 2 Enrichment (FACE) experiment and modelling in a semi-arid environment.

369. Can Impacts of Climate Change and Agricultural Adaptation Strategies Be Accurately Quantified if Crop Models Are Annually Re-Initialized?

370. Multimodel ensembles of wheat growth: many models are better than one.

371. How do various maize crop models vary in their responses to climate change factors?

372. (+)-Catechin attenuates activation of hepatic stellate cells.

373. Capsaicin modulates proliferation, migration, and activation of hepatic stellate cells.

374. Fructose-1,6-bisphosphate induces phenotypic reversion of activated hepatic stellate cell.

375. Capsaicin induces de-differentiation of activated hepatic stellate cell.

376. In situ detection of tree root distribution and biomass by multi-electrode resistivity imaging.

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