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 *

180 related articles for article (PubMed ID: 32693721)

  • 21. Fossil-based comparative analyses reveal ancient marine ancestry erased by extinction in ray-finned fishes.
    Betancur-R R; Ortí G; Pyron RA
    Ecol Lett; 2015 May; 18(5):441-50. PubMed ID: 25808114
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Foraging habitat determines predator-prey size relationships in marine fishes.
    Griffiths D
    J Fish Biol; 2020 Oct; 97(4):964-973. PubMed ID: 32613622
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Building a Body Shape Morphospace of Teleostean Fishes.
    Price SA; Friedman ST; Corn KA; Martinez CM; Larouche O; Wainwright PC
    Integr Comp Biol; 2019 Sep; 59(3):716-730. PubMed ID: 31241147
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Divergent responses of pelagic and benthic fish body-size structure to remoteness and protection from humans.
    Letessier TB; Mouillot D; Mannocci L; Jabour Christ H; Elamin EM; Elamin SM; Friedlander AM; Hearn A; Juhel JB; Kleiven AR; Moland E; Mouquet N; Nillos-Kleiven PJ; Sala E; Thompson CDH; Velez L; Vigliola L; Meeuwig JJ
    Science; 2024 Mar; 383(6686):976-982. PubMed ID: 38422147
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Habitat coupling writ large: pelagic-derived materials fuel benthivorous macroalgal reef fishes in an upwelling zone.
    Docmac F; Araya M; Hinojosa IA; Dorador C; Harrod C
    Ecology; 2017 Sep; 98(9):2267-2272. PubMed ID: 28632943
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A morphospace for reef fishes: elongation is the dominant axis of body shape evolution.
    Claverie T; Wainwright PC
    PLoS One; 2014; 9(11):e112732. PubMed ID: 25409027
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cross-habitat effects shape the ecosystem consequences of co-invasion by a pelagic and a benthic consumer.
    Fryxell DC; Diluzio AR; Friedman MA; Menge NA; Palkovacs EP
    Oecologia; 2016 Oct; 182(2):519-28. PubMed ID: 27245344
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Explaining the ocean's richest biodiversity hotspot and global patterns of fish diversity.
    Miller EC; Hayashi KT; Song D; Wiens JJ
    Proc Biol Sci; 2018 Oct; 285(1888):. PubMed ID: 30305433
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The role of abiotic and biotic factors in the unequal body shape diversification of a Gondwanan fish radiation (Otophysi: Characiformes).
    Burns MD; Knouft JH; Dillman CB
    Evolution; 2024 Feb; 78(2):253-266. PubMed ID: 37952199
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The evolution of fishes and corals on reefs: form, function and interdependence.
    Bellwood DR; Goatley CH; Bellwood O
    Biol Rev Camb Philos Soc; 2017 May; 92(2):878-901. PubMed ID: 26970292
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Habitat-based polymorphism is common in stream fishes.
    Senay C; Boisclair D; Peres-Neto PR
    J Anim Ecol; 2015 Jan; 84(1):219-27. PubMed ID: 25041645
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A phylogenomic framework for pelagiarian fishes (Acanthomorpha: Percomorpha) highlights mosaic radiation in the open ocean.
    Friedman M; Feilich KL; Beckett HT; Alfaro ME; Faircloth BC; Černý D; Miya M; Near TJ; Harrington RC
    Proc Biol Sci; 2019 Sep; 286(1910):20191502. PubMed ID: 31506051
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Commensal associations and benthic habitats shape macroevolution of the bivalve clade Galeommatoidea.
    Li J; Ó Foighil D; Strong EE
    Proc Biol Sci; 2016 Jul; 283(1834):. PubMed ID: 27383818
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hydroids (Cnidaria, Hydrozoa) from Mauritanian Coral Mounds.
    Gil M; Ramil F; AgÍs JA
    Zootaxa; 2020 Nov; 4878(3):zootaxa.4878.3.2. PubMed ID: 33311142
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The importance of benthic-pelagic coupling for marine ecosystem functioning in a changing world.
    Griffiths JR; Kadin M; Nascimento FJA; Tamelander T; Törnroos A; Bonaglia S; Bonsdorff E; Brüchert V; Gårdmark A; Järnström M; Kotta J; Lindegren M; Nordström MC; Norkko A; Olsson J; Weigel B; Žydelis R; Blenckner T; Niiranen S; Winder M
    Glob Chang Biol; 2017 Jun; 23(6):2179-2196. PubMed ID: 28132408
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Do freshwater fishes diversify faster than marine fishes? A test using state-dependent diversification analyses and molecular phylogenetics of new world silversides (atherinopsidae).
    Bloom DD; Weir JT; Piller KR; Lovejoy NR
    Evolution; 2013 Jul; 67(7):2040-57. PubMed ID: 23815658
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Characterizing ontogenetic habitat shifts in marine fishes: advancing nascent methods for marine spatial management.
    Galaiduk R; Radford BT; Saunders BJ; Newman SJ; Harvey ES
    Ecol Appl; 2017 Sep; 27(6):1776-1788. PubMed ID: 28452413
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Niche diversification follows key innovation in Antarctic fish radiation.
    Ingram T; Mahler D
    Mol Ecol; 2011 Nov; 20(22):4590-1. PubMed ID: 22145162
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Ecological diversification associated with the benthic-to-pelagic transition by North American minnows.
    Burress ED; Holcomb JM; Tan M; Armbruster JW
    J Evol Biol; 2017 Mar; 30(3):549-560. PubMed ID: 27925684
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Maternal investment evolves with larger body size and higher diversification rate in sharks and rays.
    Mull CG; Pennell MW; Yopak KE; Dulvy NK
    Curr Biol; 2024 Jun; 34(12):2773-2781.e3. PubMed ID: 38843829
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.