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 *

167 related articles for article (PubMed ID: 21847691)

  • 1. DNA content variation in monilophytes and lycophytes: large genomes that are not endopolyploid.
    Bainard JD; Henry TA; Bainard LD; Newmaster SG
    Chromosome Res; 2011 Aug; 19(6):763-75. PubMed ID: 21847691
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Complete plastid genomes from Ophioglossum californicum, Psilotum nudum, and Equisetum hyemale reveal an ancestral land plant genome structure and resolve the position of Equisetales among monilophytes.
    Grewe F; Guo W; Gubbels EA; Hansen AK; Mower JP
    BMC Evol Biol; 2013 Jan; 13():8. PubMed ID: 23311954
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Horsetails are the sister group to all other monilophytes and Marattiales are sister to leptosporangiate ferns.
    Knie N; Fischer S; Grewe F; Polsakiewicz M; Knoop V
    Mol Phylogenet Evol; 2015 Sep; 90():140-9. PubMed ID: 25999055
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Complete plastome sequences of Equisetum arvense and Isoetes flaccida: implications for phylogeny and plastid genome evolution of early land plant lineages.
    Karol KG; Arumuganathan K; Boore JL; Duffy AM; Everett KD; Hall JD; Hansen SK; Kuehl JV; Mandoli DF; Mishler BD; Olmstead RG; Renzaglia KS; Wolf PG
    BMC Evol Biol; 2010 Oct; 10():321. PubMed ID: 20969798
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The first homosporous lycophyte genome revealed the association between the recent dynamic accumulation of LTR-RTs and genome size variation.
    Yu JG; Tang JY; Wei R; Lan MF; Xiang RC; Zhang XC; Xiang QP
    Plant Mol Biol; 2023 Aug; 112(6):325-340. PubMed ID: 37380791
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evaluating the spore genome sizes of ferns and lycophytes: a flow cytometry approach.
    Kuo LY; Huang YJ; Chang J; Chiou WL; Huang YM
    New Phytol; 2017 Mar; 213(4):1974-1983. PubMed ID: 28164337
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genome size and endopolyploidy evolution across the moss phylogeny.
    Bainard JD; Newmaster SG; Budke JM
    Ann Bot; 2020 Mar; 125(4):543-555. PubMed ID: 31777923
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evolution of DNA amounts across land plants (embryophyta).
    Leitch IJ; Soltis DE; Soltis PS; Bennett MD
    Ann Bot; 2005 Jan; 95(1):207-17. PubMed ID: 15596468
    [TBL] [Abstract][Full Text] [Related]  

  • 9. New reports of nuclear DNA content for 407 vascular plant taxa from the United States.
    Bai C; Alverson WS; Follansbee A; Waller DM
    Ann Bot; 2012 Dec; 110(8):1623-9. PubMed ID: 23100602
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Reverse U-to-C editing exceeds C-to-U RNA editing in some ferns - a monilophyte-wide comparison of chloroplast and mitochondrial RNA editing suggests independent evolution of the two processes in both organelles.
    Knie N; Grewe F; Fischer S; Knoop V
    BMC Evol Biol; 2016 Jun; 16(1):134. PubMed ID: 27329857
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Monilophyte mitochondrial rps1 genes carry a unique group II intron that likely originated from an ancient paralog in rpl2.
    Knie N; Grewe F; Knoop V
    RNA; 2016 Sep; 22(9):1338-48. PubMed ID: 27354706
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome size evolution in Ontario ferns (Polypodiidae): evolutionary correlations with cell size, spore size, and habitat type and an absence of genome downsizing.
    Henry TA; Bainard JD; Newmaster SG
    Genome; 2014 Oct; 57(10):555-66. PubMed ID: 25727714
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genome size variation and species relationships in Hieracium sub-genus Pilosella (Asteraceae) as inferred by flow cytometry.
    Suda J; Krahulcová A; Trávnícek P; Rosenbaumová R; Peckert T; Krahulec F
    Ann Bot; 2007 Dec; 100(6):1323-35. PubMed ID: 17921526
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Challenges of flow-cytometric estimation of nuclear genome size in orchids, a plant group with both whole-genome and progressively partial endoreplication.
    Trávníček P; Ponert J; Urfus T; Jersáková J; Vrána J; Hřibová E; Doležel J; Suda J
    Cytometry A; 2015 Oct; 87(10):958-66. PubMed ID: 25929591
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The variability of nuclear DNA content of different Pelargonium species estimated by flow cytometry.
    Plaschil S; Abel S; Klocke E
    PLoS One; 2022; 17(4):e0267496. PubMed ID: 35482804
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Incongruence between primary sequence data and the distribution of a mitochondrial atp1 group II intron among ferns and horsetails.
    Wikström N; Pryer KM
    Mol Phylogenet Evol; 2005 Sep; 36(3):484-93. PubMed ID: 15922630
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Nuclear DNA content variation and evolution in liverworts.
    Bainard JD; Forrest LL; Goffinet B; Newmaster SG
    Mol Phylogenet Evol; 2013 Sep; 68(3):619-27. PubMed ID: 23624193
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mycorrhizal symbiosis stimulates endoreduplication in angiosperms.
    Bainard LD; Bainard JD; Newmaster SG; Klironomos JN
    Plant Cell Environ; 2011 Sep; 34(9):1577-85. PubMed ID: 21707648
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An Exploration into Fern Genome Space.
    Wolf PG; Sessa EB; Marchant DB; Li FW; Rothfels CJ; Sigel EM; Gitzendanner MA; Visger CJ; Banks JA; Soltis DE; Soltis PS; Pryer KM; Der JP
    Genome Biol Evol; 2015 Aug; 7(9):2533-44. PubMed ID: 26311176
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Structures of xyloglucans in primary cell walls of gymnosperms, monilophytes (ferns sensu lato) and lycophytes.
    Hsieh YS; Harris PJ
    Phytochemistry; 2012 Jul; 79():87-101. PubMed ID: 22537406
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.