Biography and Research Information
OverviewAI-generated summary
Leah E. Latham's research program investigates the neurotoxicological effects of various substances and stresses on neural stem cells and developing brains. Her work includes the establishment of neural stem cell models from nonhuman primate brains for toxicity testing and the assessment of drugs like ketamine and fentanyl on neonatal brain development. Latham has also examined the potential neuroprotective effects of compounds such as carnitine and the impact of cannabidiol and its metabolites on human neural stem cells.
Her research extends to evaluating the effects of environmental stressors and anesthetics like desflurane on neural stem cell models. Additionally, Latham has explored the behavioral deficits and neurotoxicity associated with phencyclidine (PCP). She collaborates with researchers at the National Center for Toxicological Research, including Shuliang Liu, Tucker A. Patterson, William Slikker, and John Talpos, with whom she has co-authored multiple publications. Latham's work contributes to understanding the mechanisms of neurodevelopmental toxicity and identifying potential therapeutic interventions.
Metrics
- h-index: 4
- Publications: 11
- Citations: 54
Selected Publications
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Assessing the developmental effects of fentanyl and impacts on lipidomic profiling using neural stem cell models (2025)
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The effects of cannabidiol and its main metabolites on human neural stem cells (2025)
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Assessing potential desflurane-induced neurotoxicity using nonhuman primate neural stem cell models (2025)
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Establishment of neural stem cells from fetal monkey brain for neurotoxicity testing (2023)
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Development of a primate model to evaluate the effects of ketamine and surgical stress on the neonatal brain (2023)
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Phencyclidine (PCP)-induced neurotoxicity and behavioral deficits (2022)
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ICOS Expression Is Required for Maintenance but Not the Formation of Germinal Centers in the Spleen in Response to Plasmodium yoelii Infection (2022)
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ICOS expression is required for maintenance but not the formation of germinal centers in the spleen in response to <i>P. yoelii</i> infection (2021)
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Neuroprotective Effects of Carnitine and Its Potential Application to Ameliorate Neurotoxicity (2021)
Collaboration Network
Top Collaborators
- Neuroprotective Effects of Carnitine and Its Potential Application to Ameliorate Neurotoxicity
- The effects of cannabidiol and its main metabolites on human neural stem cells
- Development of a primate model to evaluate the effects of ketamine and surgical stress on the neonatal brain
- Establishment of neural stem cells from fetal monkey brain for neurotoxicity testing
- Assessing potential desflurane-induced neurotoxicity using nonhuman primate neural stem cell models
Showing 5 of 7 shared publications
- Neuroprotective Effects of Carnitine and Its Potential Application to Ameliorate Neurotoxicity
- The effects of cannabidiol and its main metabolites on human neural stem cells
- Development of a primate model to evaluate the effects of ketamine and surgical stress on the neonatal brain
- Establishment of neural stem cells from fetal monkey brain for neurotoxicity testing
- Assessing potential desflurane-induced neurotoxicity using nonhuman primate neural stem cell models
Showing 5 of 6 shared publications
- The effects of cannabidiol and its main metabolites on human neural stem cells
- Development of a primate model to evaluate the effects of ketamine and surgical stress on the neonatal brain
- Establishment of neural stem cells from fetal monkey brain for neurotoxicity testing
- Assessing potential desflurane-induced neurotoxicity using nonhuman primate neural stem cell models
- Assessing the developmental effects of fentanyl and impacts on lipidomic profiling using neural stem cell models
Showing 5 of 6 shared publications
- Neuroprotective Effects of Carnitine and Its Potential Application to Ameliorate Neurotoxicity
- Development of a primate model to evaluate the effects of ketamine and surgical stress on the neonatal brain
- Assessing potential desflurane-induced neurotoxicity using nonhuman primate neural stem cell models
- Phencyclidine (PCP)-induced neurotoxicity and behavioral deficits
- Neuroprotective Effects of Carnitine and Its Potential Application to Ameliorate Neurotoxicity
- Development of a primate model to evaluate the effects of ketamine and surgical stress on the neonatal brain
- Establishment of neural stem cells from fetal monkey brain for neurotoxicity testing
- Phencyclidine (PCP)-induced neurotoxicity and behavioral deficits
- Development of a primate model to evaluate the effects of ketamine and surgical stress on the neonatal brain
- Establishment of neural stem cells from fetal monkey brain for neurotoxicity testing
- Assessing potential desflurane-induced neurotoxicity using nonhuman primate neural stem cell models
- Establishment of neural stem cells from fetal monkey brain for neurotoxicity testing
- Assessing potential desflurane-induced neurotoxicity using nonhuman primate neural stem cell models
- Assessing the developmental effects of fentanyl and impacts on lipidomic profiling using neural stem cell models
- ICOS Expression Is Required for Maintenance but Not the Formation of Germinal Centers in the Spleen in Response to Plasmodium yoelii Infection
- ICOS expression is required for maintenance but not the formation of germinal centers in the spleen in response to <i>P. yoelii</i> infection
- ICOS Expression Is Required for Maintenance but Not the Formation of Germinal Centers in the Spleen in Response to Plasmodium yoelii Infection
- ICOS expression is required for maintenance but not the formation of germinal centers in the spleen in response to <i>P. yoelii</i> infection
- ICOS Expression Is Required for Maintenance but Not the Formation of Germinal Centers in the Spleen in Response to Plasmodium yoelii Infection
- ICOS expression is required for maintenance but not the formation of germinal centers in the spleen in response to <i>P. yoelii</i> infection
- ICOS Expression Is Required for Maintenance but Not the Formation of Germinal Centers in the Spleen in Response to Plasmodium yoelii Infection
- ICOS expression is required for maintenance but not the formation of germinal centers in the spleen in response to <i>P. yoelii</i> infection
- Development of a primate model to evaluate the effects of ketamine and surgical stress on the neonatal brain
- Development of a primate model to evaluate the effects of ketamine and surgical stress on the neonatal brain
- Establishment of neural stem cells from fetal monkey brain for neurotoxicity testing
- The effects of cannabidiol and its main metabolites on human neural stem cells
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