Emilynn Leigh Banks
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Emilynn Leigh Banks has a total of 15 co-authors. Here are the top co-authors by number of shared publications:
- Ashley Kaskocsak
Wildlife Toxicology Laboratory, Texas Tech University, 1234 Davis Dr., Lubbock, TX 79416, USA
1 shared publication - Benjamin Hames
Wildlife Toxicology Laboratory, Texas Tech University, 1234 Davis Dr., Lubbock, TX 79416, USA
1 shared publication - Hannah N. Suber
Wildlife Toxicology Laboratory, Texas Tech University, Lubbock, TX, USA
1 shared publication - Henry Valencia
Wildlife Toxicology Laboratory, Texas Tech University, 1234 Davis Dr., Lubbock, TX 79416, USA
1 shared publication - Hope Elizabeth Johnson
Department of Chemistry and Biochemistry, The University of Texas at Arlington, Arlington, TX 76019
1 shared publication - Jan Halámek
Department of Environmental Toxicology, The Institute for Forensic Science, Texas Tech University, 1207 Gilbert Drive, Lubbock, Texas 79416, United States
1 shared publication
Latest Publications
- Open Access
- 21 May 2025
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 301 (6) , 110269
Redox response feature and mechanism of Arf1 and their implications for those of Ras and Rho GTPases
- 21 May 2025
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 301 (6) , 110269
Open AccessRedox response feature and mechanism of Arf1 and their implications for those of Ras and Rho GTPases
- Open Access
In Vitro Lethality of Fenbendazole to the Eyeworm Oxyspirura petrowi
Oxyspirura petrowi is a heteroxenous nematode that infects the harderian gland and other ocular tissues in birds. High-intensity infections often cause damage to the infected tissues. Due to the nature of the infection sites, treatment of O. petrowi in these hosts can be difficult. Fenbendazole (FBZ) is a common anthelmintic used to treat birds for helminth infections; however, little information exists as to the efficacy of the drug on O. petrowi infections. The present study aims to estimate lethal concentrations of FBZ to O. petrowi. Adult O. petrowi were maintained in vitro and exposed to doses of 5, 50, 100, and 200 µM concentrations of FBZ and included both negative and vehicle controls. Exposure lasted 7.5 days and lethality was determined for each treatment. Negative and vehicle controls did not differ, and both had 75% survival at the end of the treatment period. The percentage survivorship in ascending order of concentration, corrected for the controls, was 66.67%, 44.44%, 33.33%, and 0%. LC10, LC50, and LC90 estimates were 7.5 ± 0.26, 49.1 ± 1.69, and 163.2 ± 5.63 µM, respectively. In the context of known pharmacokinetics of FBZ in birds, a single oral dose of FBZ can achieve exposure levels that are lethal to O. petrowi, but the drug does not stay in the system long enough. Thus, treatment of O. petrowi infections will require multiple oral doses over several days.
Open AccessIn Vitro Lethality of Fenbendazole to the Eyeworm Oxyspirura petrowi
Oxyspirura petrowi is a heteroxenous nematode that infects the harderian gland and other ocular tissues in birds. High-intensity infections often cause damage to the infected tissues. Due to the nature of the infection sites, treatment of O. petrowi in these hosts can be difficult. Fenbendazole (FBZ) is a common anthelmintic used to treat birds for helminth infections; however, little information exists as to the efficacy of the drug on O. petrowi infections. The present study aims to estimate lethal concentrations of FBZ to O. petrowi. Adult O. petrowi were maintained in vitro and exposed to doses of 5, 50, 100, and 200 µM concentrations of FBZ and included both negative and vehicle controls. Exposure lasted 7.5 days and lethality was determined for each treatment. Negative and vehicle controls did not differ, and both had 75% survival at the end of the treatment period. The percentage survivorship in ascending order of concentration, corrected for the controls, was 66.67%, 44.44%, 33.33%, and 0%. LC10, LC50, and LC90 estimates were 7.5 ± 0.26, 49.1 ± 1.69, and 163.2 ± 5.63 µM, respectively. In the context of known pharmacokinetics of FBZ in birds, a single oral dose of FBZ can achieve exposure levels that are lethal to O. petrowi, but the drug does not stay in the system long enough. Thus, treatment of O. petrowi infections will require multiple oral doses over several days.
- 16 November 2023
- Published by Royal Society of Chemistry (RSC) in The Analyst
- Vol. 149 (2) , 350-356
Metabolite monitoring concept for the biometric identification of individuals from the skin surface
A novel method for metabolite monitoring is presented for diverse applications in biometric identification.
- 16 November 2023
- Published by Royal Society of Chemistry (RSC) in The Analyst
- Vol. 149 (2) , 350-356
Metabolite monitoring concept for the biometric identification of individuals from the skin surface
A novel method for metabolite monitoring is presented for diverse applications in biometric identification.