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 *

117 related articles for article (PubMed ID: 37262368)

  • 1. Differential impacts of ionizing radiation on a sexually dimorphic trait in male and female
    Fuciarelli TM; Patel S; Rollo CD
    Int J Radiat Biol; 2023; 99(11):1749-1759. PubMed ID: 37262368
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Impacts of ionization radiation on the cuticular hydrocarbon profile and mating success of male house crickets (
    Fuciarelli TM; Rollo CD
    Int J Radiat Biol; 2021; 97(4):564-570. PubMed ID: 33471571
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The effect of female wings on male courtship behavior in the cricket Gryllus bimaculatus.
    Itoh MT; Murakami S
    Naturwissenschaften; 2002 May; 89(5):230-2. PubMed ID: 12135089
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Radiation induces stress and transgenerational impacts in the cricket,
    Li X; Rollo CD
    Int J Radiat Biol; 2022; 98(6):1098-1105. PubMed ID: 33428853
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The potential influence of morphology on the evolutionary divergence of an acoustic signal.
    Pitchers WR; Klingenberg CP; Tregenza T; Hunt J; Dworkin I
    J Evol Biol; 2014 Oct; 27(10):2163-76. PubMed ID: 25223712
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The evolutionary genetics of sexual size dimorphism in the cricket Allonemobius socius.
    Fedorka KM; Winterhalter WE; Mousseau TA
    Heredity (Edinb); 2007 Aug; 99(2):218-23. PubMed ID: 17473861
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rapid sexual signal diversification is facilitated by permissive females.
    Zhang R; Rayner JG; Bailey NW
    Curr Biol; 2024 Jan; 34(2):403-409.e3. PubMed ID: 38141618
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Optimization of irradiation dose to Aedes aegypti and Ae. albopictus in a sterile insect technique program.
    Bond JG; Osorio AR; Avila N; Gómez-Simuta Y; Marina CF; Fernández-Salas I; Liedo P; Dor A; Carvalho DO; Bourtzis K; Williams T
    PLoS One; 2019; 14(2):e0212520. PubMed ID: 30779779
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Developing the radiation-based sterile insect technique (SIT) for controlling Aedes aegypti: identification of a sterilizing dose.
    Chen C; Aldridge RL; Gibson S; Kline J; Aryaprema V; Qualls W; Xue RD; Boardman L; Linthicum KJ; Hahn DA
    Pest Manag Sci; 2023 Mar; 79(3):1175-1183. PubMed ID: 36424673
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Development of the Sterile Insect Technique to control the dengue vector Aedes aegypti (Linnaeus) in Sri Lanka.
    Ranathunge T; Harishchandra J; Maiga H; Bouyer J; Gunawardena YINS; Hapugoda M
    PLoS One; 2022; 17(4):e0265244. PubMed ID: 35377897
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Body Size, Fecundity, and Sexual Size Dimorphism in the Neotropical Cricket Macroanaxipha macilenta (Saussure) (Orthoptera: Gryllidae).
    Cueva Del Castillo R
    Neotrop Entomol; 2015 Apr; 44(2):116-22. PubMed ID: 26013128
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Involvement of heat shock protein 40 in the wing dimorphism of the house cricket Acheta domesticus.
    Chen Q; Wen M; Li J; Zhou H; Jin S; Zhou JJ; Wang Y; Ren B
    J Insect Physiol; 2019 Apr; 114():35-44. PubMed ID: 30776423
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sexual dimorphism divergence between sister species is associated with a switch in habitat use and mating system in thorny devil stick insects.
    Boisseau RP; Ero MM; Makai S; Bonneau LJG; Emlen DJ
    Behav Processes; 2020 Dec; 181():104263. PubMed ID: 33049376
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Functional morphology of tegmina-based stridulation in the relict species
    Chivers BD; Béthoux O; Sarria-S FA; Jonsson T; Mason AC; Montealegre-Z F
    J Exp Biol; 2017 Mar; 220(Pt 6):1112-1121. PubMed ID: 28082619
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bite force, body size, and octopamine mediate mating interactions in the house cricket (Acheta domesticus).
    Adeola F; Lailvaux S
    J Evol Biol; 2023 Oct; 36(10):1494-1502. PubMed ID: 37737492
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Why do males emerge before females? Sexual size dimorphism drives sexual bimaturism in insects.
    Teder T; Kaasik A; Taits K; Tammaru T
    Biol Rev Camb Philos Soc; 2021 Dec; 96(6):2461-2475. PubMed ID: 34128582
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Trans-Generational Impacts of Paternal Irradiation in a Cricket: Damage, Life-History Features and Hormesis in F1 Offspring.
    Fuciarelli TM; Rollo CD
    Dose Response; 2020; 18(4):1559325820983214. PubMed ID: 33424519
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Differentiation between left and right wing stridulatory files in the field cricket Gryllus bimaculatus (Orthoptera: Gryllidae).
    Duncan J; Soulsbury CD; Montealegre-Z F
    Arthropod Struct Dev; 2021 Nov; 65():101076. PubMed ID: 34482021
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sexual signal loss: The link between behaviour and rapid evolutionary dynamics in a field cricket.
    Zuk M; Bailey NW; Gray B; Rotenberry JT
    J Anim Ecol; 2018 May; 87(3):623-633. PubMed ID: 29417997
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Size-dependent response to conspecific mating calls by male crickets.
    Kiflawi M; Gray DA
    Proc Biol Sci; 2000 Nov; 267(1458):2157-61. PubMed ID: 11413627
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.