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 *

133 related articles for article (PubMed ID: 34294796)

  • 21. King- and queen-specific degradation of uric acid contributes to reproduction in termites.
    Konishi T; Tasaki E; Takata M; Matsuura K
    Proc Biol Sci; 2023 Jan; 290(1990):20221942. PubMed ID: 36598016
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Queen-worker conflicts over male production and sex allocation in a primitively eusocial wasp.
    Tsuchida K; Saigo T; Nagata N; Tsujita S; Takeuchi K; Miyano S
    Evolution; 2003 Oct; 57(10):2365-73. PubMed ID: 14628924
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A heritable component in sex ratio and caste determination in a Cardiocondyla ant.
    Frohschammer S; Heinze J
    Front Zool; 2009 Oct; 6():27. PubMed ID: 19863794
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Alate production and sex ratio in colonies of the Neotropical termite Nasutitermes corniger (Isoptera; Termitidae).
    Thorne BL
    Oecologia; 1983 Apr; 58(1):103-109. PubMed ID: 28310653
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Why and how do termite kings and queens live so long?
    Tasaki E; Takata M; Matsuura K
    Philos Trans R Soc Lond B Biol Sci; 2021 Apr; 376(1823):20190740. PubMed ID: 33678028
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The need for sperm selection may explain why termite colonies have kings and queens, whereas those of ants, wasps and bees have only queens.
    Jaffe K
    Theory Biosci; 2008 Nov; 127(4):359-63. PubMed ID: 18791761
    [TBL] [Abstract][Full Text] [Related]  

  • 27. More effective transposon regulation in fertile, long-lived termite queens than in sterile workers.
    Post F; Bornberg-Bauer E; Vasseur-Cognet M; Harrison MC
    Mol Ecol; 2023 Jan; 32(2):369-380. PubMed ID: 36320186
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Why do some social insect queens mate with several males? Testing the sex-ratio manipulation hypothesis in Lasius niger.
    Fjerdingstad EJ; Gertsch PJ; Keller L
    Evolution; 2002 Mar; 56(3):553-62. PubMed ID: 11989685
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Unique Morphogenesis in the Damp-Wood Termite: Abscission of the Stylus during Female Reproductive Caste Differentiation.
    Oguchi K; Miura T
    Zoolog Sci; 2019 Oct; 36(5):380-386. PubMed ID: 33319961
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Sex-linked genetic influence on caste determination in a termite.
    Hayashi Y; Lo N; Miyata H; Kitade O
    Science; 2007 Nov; 318(5852):985-7. PubMed ID: 17991866
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Higher levels of the lipophilic antioxidants coenzyme Q
    Tasaki E; Yamamoto Y; Iuchi Y
    Insect Sci; 2024 Feb; 31(1):201-210. PubMed ID: 37279723
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Termite queens close the sperm gates of eggs to switch from sexual to asexual reproduction.
    Yashiro T; Matsuura K
    Proc Natl Acad Sci U S A; 2014 Dec; 111(48):17212-7. PubMed ID: 25404335
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic components to caste allocation in a multiple-queen ant species.
    Libbrecht R; Schwander T; Keller L
    Evolution; 2011 Oct; 65(10):2907-15. PubMed ID: 21967431
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Haploidploidy and the evolution of the social insect.
    Trivers RL; Hare H
    Science; 1976 Jan; 191(4224):249-63. PubMed ID: 1108197
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hypoxia adaptation in termites: hypoxic conditions enhance survival and reproductive activity in royals.
    Tasaki E; Matsuura K; Iuchi Y
    Insect Mol Biol; 2018 Dec; 27(6):808-814. PubMed ID: 29989656
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Sex-allocation conflict and sexual selection throughout the lifespan of eusocial colonies.
    Avila P; Fromhage L; Lehmann L
    Evolution; 2019 Jun; 73(6):1116-1132. PubMed ID: 31004345
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Sex investment ratios in eusocial Hymenoptera support inclusive fitness theory.
    Bourke AF
    J Evol Biol; 2015 Nov; 28(11):2106-11. PubMed ID: 26238365
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Long live the queen, the king and the commoner? Transcript expression differences between old and young in the termite Cryptotermes secundus.
    Monroy Kuhn JM; Meusemann K; Korb J
    PLoS One; 2019; 14(2):e0210371. PubMed ID: 30759161
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Influence of environmental conditions on the expression of the sexual dispersal phenotype in a lower termite: implications for the evolution of workers in termites.
    Korb J; Katrantzis S
    Evol Dev; 2004; 6(5):342-52. PubMed ID: 15330867
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Daphnia females adjust sex allocation in response to current sex ratio and density.
    Booksmythe I; Gerber N; Ebert D; Kokko H
    Ecol Lett; 2018 May; 21(5):629-637. PubMed ID: 29484799
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.