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 *

244 related articles for article (PubMed ID: 29797563)

  • 21. Biogeography in deep time - What do phylogenetics, geology, and paleoclimate tell us about early platyrrhine evolution?
    Kay RF
    Mol Phylogenet Evol; 2015 Jan; 82 Pt B():358-74. PubMed ID: 24333920
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cretaceous origin of dogwoods: an anatomically preserved
    Atkinson BA; Stockey RA; Rothwell GW
    PeerJ; 2016; 4():e2808. PubMed ID: 28028474
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Phylogenetic analyses of Cornales based on 26S rRNA and combined 26S rDNA-MATK-RBCL sequence data.
    Fan C; Xiang QY
    Am J Bot; 2003 Sep; 90(9):1357-72. PubMed ID: 21659236
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Lineage Diversity and Size Disparity in Musteloidea: Testing Patterns of Adaptive Radiation Using Molecular and Fossil-Based Methods.
    Law CJ; Slater GJ; Mehta RS
    Syst Biol; 2018 Jan; 67(1):127-144. PubMed ID: 28472434
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Glandulocalyx upatoiensis, a fossil flower of Ericales (Actinidiaceae/Clethraceae) from the Late Cretaceous (Santonian) of Georgia, USA.
    Schönenberger J; von Balthazar M; Takahashi M; Xiao X; Crane PR; Herendeen PS
    Ann Bot; 2012 Apr; 109(5):921-36. PubMed ID: 22442339
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Extant-only comparative methods fail to recover the disparity preserved in the bird fossil record.
    Mitchell JS
    Evolution; 2015 Sep; 69(9):2414-24. PubMed ID: 26257156
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Do different disparity proxies converge on a common signal? Insights from the cranial morphometrics and evolutionary history of Pterosauria (Diapsida: Archosauria).
    Foth C; Brusatte SL; Butler RJ
    J Evol Biol; 2012 May; 25(5):904-15. PubMed ID: 22356676
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Leaf surface development and the plant fossil record: stomatal patterning in Bennettitales.
    Rudall PJ; Bateman RM
    Biol Rev Camb Philos Soc; 2019 Jun; 94(3):1179-1194. PubMed ID: 30714286
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Tanispermum, a new genus of hemi-orthotropous to hemi-anatropous angiosperm seeds from the Early Cretaceous of eastern North America.
    Friis EM; Crane PR; Pedersen KR
    Am J Bot; 2018 Aug; 105(8):1369-1388. PubMed ID: 30080239
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Rates of morphological evolution are heterogeneous in Early Cretaceous birds.
    Wang M; Lloyd GT
    Proc Biol Sci; 2016 Apr; 283(1828):. PubMed ID: 27053742
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Angiosperm flowers reached their highest morphological diversity early in their evolutionary history.
    López-Martínez AM; Magallón S; von Balthazar M; Schönenberger J; Sauquet H; Chartier M
    New Phytol; 2024 Feb; 241(3):1348-1360. PubMed ID: 38029781
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mid-Cretaceous angiosperm radiation and an asterid origin of bilaterality: diverse and extinct "Ericales" from New Jersey.
    Crepet WL; Nixon KC; Weeks A
    Am J Bot; 2018 Aug; 105(8):1412-1423. PubMed ID: 30075046
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Character evolution and missing (morphological) data across Asteridae.
    Stull GW; Schori M; Soltis DE; Soltis PS
    Am J Bot; 2018 Mar; 105(3):470-479. PubMed ID: 29656519
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Phylogenetic analysis of fossil flowers using an angiosperm-wide data set: proof-of-concept and challenges ahead.
    Schönenberger J; von Balthazar M; López Martínez A; Albert B; Prieu C; Magallón S; Sauquet H
    Am J Bot; 2020 Oct; 107(10):1433-1448. PubMed ID: 33026116
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Origin of Equisetum: Evolution of horsetails (Equisetales) within the major euphyllophyte clade Sphenopsida.
    Elgorriaga A; Escapa IH; Rothwell GW; Tomescu AMF; Rubén Cúneo N
    Am J Bot; 2018 Aug; 105(8):1286-1303. PubMed ID: 30025163
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Icacinaceae fossil provides evidence for a Cretaceous origin of the lamiids.
    Atkinson BA
    Nat Plants; 2022 Dec; 8(12):1374-1377. PubMed ID: 36376504
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Comparative and Phylogenetic Analyses of the Complete Chloroplast Genomes of Three Arcto-Tertiary Relicts:
    Yang Z; Ji Y
    Front Plant Sci; 2017; 8():1536. PubMed ID: 28955348
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Phylogenetic analysis of pelecaniformes (aves) based on osteological data: implications for waterbird phylogeny and fossil calibration studies.
    Smith ND
    PLoS One; 2010 Oct; 5(10):e13354. PubMed ID: 20976229
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fossil evidence of core monocots in the Early Cretaceous.
    Coiffard C; Kardjilov N; Manke I; Bernardes-de-Oliveira MEC
    Nat Plants; 2019 Jul; 5(7):691-696. PubMed ID: 31285562
    [TBL] [Abstract][Full Text] [Related]  

  • 40. An overview of extant conifer evolution from the perspective of the fossil record.
    Leslie AB; Beaulieu J; Holman G; Campbell CS; Mei W; Raubeson LR; Mathews S
    Am J Bot; 2018 Sep; 105(9):1531-1544. PubMed ID: 30157290
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.