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6. Comparative analyses reveal potential uses of Brachypodium distachyon as a model for cold stress responses in temperate grasses

7. Evolution of drought and frost responses in cool season grasses (Pooideae): was drought tolerance a precursor to frost tolerance?

8. Responsiveness to long days for flowering is reduced in Arabidopsis by yearly variation in growing season temperatures.

9. Testing the chilling- before drought-tolerance hypothesis in Pooideae grasses.

10. Independent recruitment of FRUITFULL-like transcription factors in the convergent origins of vernalization-responsive grass flowering.

11. Convergent evolution of the annual life history syndrome from perennial ancestors.

12. Flowering time runs hot and cold.

13. Major niche transitions in Pooideae correlate with variation in photoperiodic flowering and evolution of CCT domain genes.

14. Phenotypic responses to light, water, and nutrient conditions in the allopolyploid Arabidopsis suecica and its parent species A. thaliana and A. arenosa : Does the allopolyploid outrange its parents?

15. Flowering Times of Wild Arabidopsis Accessions From Across Norway Correlate With Expression Levels of FT , CO , and FLC Genes.

16. A Vernalization Response in a Winter Safflower ( Carthamus tinctorius ) Involves the Upregulation of Homologs of FT , FUL , and MAF .

17. Increased above-ground resource allocation is a likely precursor for independent evolutionary origins of annuality in the Pooideae grass subfamily.

18. Discrimination of grass pollen of different species by FTIR spectroscopy of individual pollen grains.

19. Understanding Past, and Predicting Future, Niche Transitions based on Grass Flowering Time Variation.

20. Combining Chemical Information From Grass Pollen in Multimodal Characterization.

21. Importance of Individual Germination Receptor Subunits in the Cooperative Function between GerA and Ynd.

22. Evolution of Cold Acclimation and Its Role in Niche Transition in the Temperate Grass Subfamily Pooideae.

23. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) shows adaptation of grass pollen composition.

25. A high-throughput FTIR spectroscopy approach to assess adaptive variation in the chemical composition of pollen.

26. Evolution of the miR5200-FLOWERING LOCUS T flowering time regulon in the temperate grass subfamily Pooideae.

27. Local Populations of Arabidopsis thaliana Show Clear Relationship between Photoperiodic Sensitivity of Flowering Time and Altitude.

28. Evidence for an Early Origin of Vernalization Responsiveness in Temperate Pooideae Grasses.

29. Introduced Scotch broom (Cytisus scoparius) invades the genome of native populations in vulnerable heathland habitats.

30. What's the meaning of local? Using molecular markers to define seed transfer zones for ecological restoration in Norway.

31. Population Structure, Genetic Variation, and Linkage Disequilibrium in Perennial Ryegrass Populations Divergently Selected for Freezing Tolerance.

32. The role of seasonal flowering responses in adaptation of grasses to temperate climates.

33. Evidence for adaptive evolution of low-temperature stress response genes in a Pooideae grass ancestor.

34. Genome wide transcriptional profiling of acclimation to photoperiod in high-latitude accessions of Arabidopsis thaliana.

35. Molecular mechanisms underlying frost tolerance in perennial grasses adapted to cold climates.

36. Did gene family expansions during the Eocene-Oligocene boundary climate cooling play a role in Pooideae adaptation to cool climates?

38. Molecules and morphology in concert. II. The Festuca brachyphylla complex (Poaceae) in Svalbard.

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