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 *

310 related articles for article (PubMed ID: 22116756)

  • 21. Oxygen consumption in weakly electric Neotropical fishes.
    Julian D; Crampton WG; Wohlgemuth SE; Albert JS
    Oecologia; 2003 Dec; 137(4):502-11. PubMed ID: 14505027
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The evolutionary origins of electric signal complexity.
    Stoddard PK
    J Physiol Paris; 2002; 96(5-6):485-91. PubMed ID: 14692496
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A model for studying the energetics of sustained high frequency firing.
    Joos B; Markham MR; Lewis JE; Morris CE
    PLoS One; 2018; 13(4):e0196508. PubMed ID: 29708986
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Petrocephalus of Odzala offer insights into evolutionary patterns of signal diversification in the Mormyridae, a family of weakly electrogenic fishes from Africa.
    Lavoué S; Arnegard ME; Sullivan JP; Hopkins CD
    J Physiol Paris; 2008; 102(4-6):322-39. PubMed ID: 18992333
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Structure and sexual dimorphism of the electrocommunication signals of the weakly electric fish, Adontosternarchus devenanzii.
    Zhou M; Smith GT
    J Exp Biol; 2006 Dec; 209(Pt 23):4809-18. PubMed ID: 17114413
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The complexity of high-frequency electric fields degrades electrosensory inputs: implications for the jamming avoidance response in weakly electric fish.
    Shifman AR; Lewis JE
    J R Soc Interface; 2018 Jan; 15(138):. PubMed ID: 29367237
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A sodium-activated potassium channel supports high-frequency firing and reduces energetic costs during rapid modulations of action potential amplitude.
    Markham MR; Kaczmarek LK; Zakon HH
    J Neurophysiol; 2013 Apr; 109(7):1713-23. PubMed ID: 23324315
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Androgen correlates of socially induced changes in the electric organ discharge waveform of a mormyrid fish.
    Carlson BA; Hopkins CD; Thomas P
    Horm Behav; 2000 Nov; 38(3):177-86. PubMed ID: 11038292
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Phylogenetic comparative analysis of electric communication signals in ghost knifefishes (Gymnotiformes: Apteronotidae).
    Turner CR; Derylo M; de Santana CD; Alves-Gomes JA; Smith GT
    J Exp Biol; 2007 Dec; 210(Pt 23):4104-22. PubMed ID: 18025011
    [TBL] [Abstract][Full Text] [Related]  

  • 30. NADPH-diaphorase activity and nitric oxide synthase-like immunoreactivity colocalize in the electromotor system of four species of gymnotiform fish.
    Smith GT; Unguez GA; Reinauer RM
    Brain Behav Evol; 2001; 58(3):122-36. PubMed ID: 11910170
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Ontogeny and evolution of electric organs in gymnotiform fish.
    Kirschbaum F; Schwassmann HO
    J Physiol Paris; 2008; 102(4-6):347-56. PubMed ID: 18984049
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Derived loss of signal complexity and plasticity in a genus of weakly electric fish.
    Saenz DE; Gu T; Ban Y; Winemiller KO; Markham MR
    J Exp Biol; 2021 Jun; 224(12):. PubMed ID: 34109419
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Androgen modulates the kinetics of the delayed rectifying K+ current in the electric organ of a weakly electric fish.
    McAnelly ML; Zakon HH
    Dev Neurobiol; 2007 Oct; 67(12):1589-97. PubMed ID: 17562532
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hormone-induced and maturational changes in electric organ discharges and electroreceptor tuning in the weakly electric fish Apteronotus.
    Meyer JH; Leong M; Keller CH
    J Comp Physiol A; 1987 Mar; 160(3):385-94. PubMed ID: 3572854
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Serotonergic activation of 5HT1A and 5HT2 receptors modulates sexually dimorphic communication signals in the weakly electric fish Apteronotus leptorhynchus.
    Smith GT; Combs N
    Horm Behav; 2008 Jun; 54(1):69-82. PubMed ID: 18336816
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Patterns of electric organ discharge activity in the weakly electric fish Brienomyrus niger L. (Mormyridae).
    Serrier J; Moller P
    Exp Biol; 1989; 48(5):235-44. PubMed ID: 2620705
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Beyond the Jamming Avoidance Response: weakly electric fish respond to the envelope of social electrosensory signals.
    Stamper SA; Madhav MS; Cowan NJ; Fortune ES
    J Exp Biol; 2012 Dec; 215(Pt 23):4196-207. PubMed ID: 23136154
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Proximate and ultimate causes of signal diversity in the electric fish Gymnotus.
    Crampton WG; Rodríguez-Cattáneo A; Lovejoy NR; Caputi AA
    J Exp Biol; 2013 Jul; 216(Pt 13):2523-41. PubMed ID: 23761477
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Intraspecific variability of the pulse-type discharges of the African electric fishes, Pollimyrus isidori and Petrocephalus bovei (Mormyridae, Teleostei), and their dependence on water conductivity.
    Bratton BO; Kramer B
    Exp Biol; 1988; 47(4):227-38. PubMed ID: 3220124
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Time domain processing of electric organ discharge waveforms by pulse-type electric fish.
    Hopkins CD; Westby GW
    Brain Behav Evol; 1986; 29(1-2):77-104. PubMed ID: 3594199
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.