These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 19941669)

  • 1. Natural selection drives the fine-scale divergence of a coevolutionary arms race involving a long-mouthed weevil and its obligate host plant.
    Toju H
    BMC Evol Biol; 2009 Nov; 9():273. PubMed ID: 19941669
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fine-scale local adaptation of weevil mouthpart length and camellia pericarp thickness: altitudinal gradient of a putative arms race.
    Toju H
    Evolution; 2008 May; 62(5):1086-102. PubMed ID: 18266990
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Phylogeography and the geographic cline in the armament of a seed-predatory weevil: effects of historical events vs. natural selection from the host plant.
    Toju H; Sota T
    Mol Ecol; 2006 Nov; 15(13):4161-73. PubMed ID: 17054510
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Climatic gradients of arms race coevolution.
    Toju H; Abe H; Ueno S; Miyazawa Y; Taniguchi F; Sota T; Yahara T
    Am Nat; 2011 May; 177(5):562-73. PubMed ID: 21508604
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Adaptive divergence of scaling relationships mediates the arms race between a weevil and its host plant.
    Toju H; Sota T
    Biol Lett; 2006 Dec; 2(4):539-42. PubMed ID: 17148283
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Metapopulation structure of a seed-predator weevil and its host plant in arms race coevolution.
    Toju H; Ueno S; Taniguchi F; Sota T
    Evolution; 2011 Jun; 65(6):1707-22. PubMed ID: 21644958
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Imbalance of predator and prey armament: geographic clines in phenotypic interface and natural selection.
    Toju H; Sota T
    Am Nat; 2006 Jan; 167(1):105-17. PubMed ID: 16475103
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Interpopulation variation in predator foraging behaviour promotes the evolutionary divergence of prey.
    Toju H
    J Evol Biol; 2007 Jul; 20(4):1544-53. PubMed ID: 17584247
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Arms race between weevil rostrum length and camellia pericarp thickness: Geographical cline and theory.
    Iseki N; Sasaki A; Toju H
    J Theor Biol; 2011 Sep; 285(1):1-9. PubMed ID: 21651915
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Approximate Bayesian estimation of coevolutionary arms races.
    Nuismer SL; Week B
    PLoS Comput Biol; 2019 Apr; 15(4):e1006988. PubMed ID: 30986245
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Coevolution: the geographic mosaic of coevolutionary arms races.
    Thompson JN
    Curr Biol; 2005 Dec; 15(24):R992-4. PubMed ID: 16360677
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Do arms races punctuate evolutionary stasis? Unified insights from phylogeny, phylogeography and microevolutionary processes.
    Toju H; Sota T
    Mol Ecol; 2009 Sep; 18(18):3940-54. PubMed ID: 19732333
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Geographic structure and dynamics of coevolutionary selection.
    Thompson JN; Cunningham BM
    Nature; 2002 Jun; 417(6890):735-8. PubMed ID: 12066183
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The evolutionary response of predators to dangerous prey: hotspots and coldspots in the geographic mosaic of coevolution between garter snakes and newts.
    Brodie ED; Ridenhour BJ; Brodie ED
    Evolution; 2002 Oct; 56(10):2067-82. PubMed ID: 12449493
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Resilient plant-bird interactions in a volcanic island ecosystem: pollination of Japanese Camellia mediated by the Japanese White-eye.
    Abe H; Ueno S; Takahashi T; Tsumura Y; Hasegawa M
    PLoS One; 2013; 8(4):e62696. PubMed ID: 23646136
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tolerance to seed predation mediated by seed size increases at lower latitudes in a Mediterranean oak.
    Bogdziewicz M; Espelta JM; Bonal R
    Ann Bot; 2019 Mar; 123(4):707-714. PubMed ID: 30452531
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phylogeographical patterns of a generalist acorn weevil: insight into the biogeographical history of broadleaved deciduous and evergreen forests.
    Aoki K; Kato M; Murakami N
    BMC Evol Biol; 2009 May; 9():103. PubMed ID: 19445688
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Local, geographic and phylogenetic scales of coevolution in Drosophila-parasitoid interactions.
    Dupas S; Dubuffet A; Carton Y; Poirié M
    Adv Parasitol; 2009; 70():281-95. PubMed ID: 19773075
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Gut Microbiota in Camellia Weevils Are Influenced by Plant Secondary Metabolites and Contribute to Saponin Degradation.
    Zhang S; Shu J; Xue H; Zhang W; Zhang Y; Liu Y; Fang L; Wang Y; Wang H
    mSystems; 2020 Mar; 5(2):. PubMed ID: 32184361
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Associations of plant fitness, leaf chemistry, and damage suggest selection mosaic in plant-herbivore interactions.
    Muola A; Mutikainen P; Lilley M; Laukkanen L; Salminen JP; Leimu R
    Ecology; 2010 Sep; 91(9):2650-9. PubMed ID: 20957959
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.