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Journal articles on the topic 'CPTX'

Author: Grafiati

Published: 5 June 2025

Last updated: 25 June 2025

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1

Suzuki, Kunimichi, Jonathan Elegheert, Inseon Song, et al. "A synthetic synaptic organizer protein restores glutamatergic neuronal circuits." Science 369, no. 6507 (2020): eabb4853. http://dx.doi.org/10.1126/science.abb4853.

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Neuronal synapses undergo structural and functional changes throughout life, which are essential for nervous system physiology. However, these changes may also perturb the excitatory–inhibitory neurotransmission balance and trigger neuropsychiatric and neurological disorders. Molecular tools to restore this balance are highly desirable. Here, we designed and characterized CPTX, a synthetic synaptic organizer combining structural elements from cerebellin-1 and neuronal pentraxin-1. CPTX can interact with presynaptic neurexins and postsynaptic AMPA-type ionotropic glutamate receptors and induced the formation of excitatory synapses both in vitro and in vivo. CPTX restored synaptic functions, motor coordination, spatial and contextual memories, and locomotion in mouse models for cerebellar ataxia, Alzheimer’s disease, and spinal cord injury, respectively. Thus, CPTX represents a prototype for structure-guided biologics that can efficiently repair or remodel neuronal circuits.

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2

Stearns, Mark E., Greg Kim, Fernando Garcia, and Min Wang. "Interleukin-10 Induced Activating Transcription Factor 3 Transcriptional Suppression of Matrix Metalloproteinase-2 Gene Expression in Human Prostate CPTX-1532 Cells." Molecular Cancer Research 2, no. 7 (2004): 403–16. http://dx.doi.org/10.1158/1541-7786.403.2.7.

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Abstract Aberrant expression of the 72-kDa type IV collagenase [matrix metalloproteinase (MMP)-2] is implicated in the invasion and angiogenesis process of malignant tumors. We investigated the effects of interleukin (IL)-10 on MMP-2 expression in CPTX-1532 human prostate tumor cells. Our results demonstrate that IL-10 significantly inhibited MMP-2 transcription and protein expression induced by a phorbol ester, phorbol 12-myristate 13-acetate. The inhibitory effects of IL-10 on MMP-2 expression correlated with the suppression of MMP-2 promoter activity. To determine the mechanism of IL-10 action, we examined IL-10–dependent promoter activity with luciferase constructs from a 2-kbp promoter region of the human MMP-2 gene. We functionally characterized the promoter fragments by transient transfection experiments with CPTX-1532 cells. The experiments revealed that a cAMP responsive element binding protein (CREB) consensus domain was identified upstream of the 5′ transcriptional start site, which was highly responsive to IL-10–dependent down-regulation of promoter luciferase activity. Electrophoretic mobility shift assays combined with antibody “supershift assays” confirmed the data from the luciferase assays. Immunoblot assays of activating transcription factor (ATF) 3 immunoprecipitates with tyrosine specific antibodies revealed that IL-10 stimulated tyrosine phosphorylation of ATF3 to activate binding to the CREB domain and suppress MMP-2 expression. Studies with stable, IL-10 transfected CPTX-1532 subclones further showed that IL-10 failed to suppress MMP-2 expression in ATF3-deficient CPTX-1532 cells, where the ATF3 mRNA was destroyed with a DNAzyme oligonucleotide targeting the 5′ region of the mRNA. Finally, reconstitution of ATF3 successfully restored the inhibitory effects of IL-10 on MMP-2 gene expression. Taken together, these data demonstrate the critical role of tyrosine phosphorylated ATF3 and the CREB consensus domain in IL-10 suppression of MMP-2 gene expression in primary human prostate tumor cells.

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3

Kapanci, Tugba, Sarah Merks, Thomas H. Rammsayer, and Stefan J. Troche. "On the Relationship between P3 Latency and Mental Ability as a Function of Increasing Demands in a Selective Attention Task." Brain Sciences 9, no. 2 (2019): 28. http://dx.doi.org/10.3390/brainsci9020028.

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The mental speed approach to individual differences in mental ability (MA) is based on the assumption of higher speed of information processing in individuals with higher than those with lower MA. Empirical support of this assumption has been inconsistent when speed was measured by means of the P3 latency in the event-related potential (ERP). The present study investigated the association between MA and P3 latency as a function of task demands on selective attention. For this purpose, 20 men and 90 women performed on a standard continuous performance test (CPT1 condition) as well as on two further task conditions with lower (CPT0) and higher demands (CPT2) on selective attention. MA and P3 latency negatively correlated in the standard CPT, and this negative relationship even increased systematically from the CPT1 to the CPT2 condition but was absent in the CPT0 condition. The present results indicate that task demands on selective attention are decisive to observe the expected shorter P3 latency in individuals with higher compared to those with lower MA.

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4

Guzmán, M., and M. J. H. Geelen. "Activity of carnitine palmitoyltransferase in mitochondrial outer membranes and peroxisomes in digitonin-permeabilized hepatocytes. Selective modulation of mitochondrial enzyme activity by okadaic acid." Biochemical Journal 287, no. 2 (1992): 487–92. http://dx.doi.org/10.1042/bj2870487.

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A procedure is described for the rapid measurement of the activity of mitochondrial-outer-membrane carnitine palmitoyltransferase (CPTo) and peroxisomal carnitine palmitoyltransferase (CPTp) in digitonin-permeabilized hepatocytes. CPTo activity was determined as the tetradecylglycidate (TDGA)-sensitive malonyl-CoA-sensitive CPT activity, whereas CPTp activity was monitored as the TDGA-insensitive malonyl-CoA-sensitive CPT activity. Under these experimental conditions, the respective contributions of CPTo and CPTp to total hepatocellular malonyl-CoA-sensitive CPT activity were 74.6 and 25.4%, which correlated well with the values of 76.9 and 23.1% for the respective contributions of the mitochondrial and the peroxisomal compartment to total hepatocellular palmitate oxidation. The sensitivity of CPTo to inhibition by malonyl-CoA was very similar to that of CPTp; thus 50% inhibition of CPTo and CPTp activities was achieved with malonyl-CoA concentrations of 2.6 +/- 0.5 and 3.0 +/- 0.4 microM respectively. Short-term incubation of hepatocytes with the phosphatase inhibitor okadaic acid (i) increased the activity of CPTo and the rate of mitochondrial palmitate oxidation, (ii) decreased the affinity of CPTo for palmitoyl-CoA substrate, and (iii) decreased the sensitivity of CPTo to inhibition by malonyl-CoA. By contrast, neither the properties of CPTp nor the rate of peroxisomal palmitate oxidation were changed upon incubation of cells with okadaic acid. Results indicate therefore that CPTo, but not CPTp, may be regulated by a mechanism of phosphorylation/dephosphorylation. The physiological relevance of these findings is discussed.

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5

Murthy, M. S., and S. V. Pande. "Some differences in the properties of carnitine palmitoyltransferase activities of the mitochondrial outer and inner membranes." Biochemical Journal 248, no. 3 (1987): 727–33. http://dx.doi.org/10.1042/bj2480727.

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Recent evidence has shown that the outer, overt, malonyl-CoA-inhibitable carnitine palmitoyltransferase (CPTo) activity resides in the mitochondrial outer membrane [Murthy & Pande (1987) Proc. Natl. Acad. Sci. U.S.A. 84, 378-382]. A comparison of CPTo activity of rat liver mitochondria with the inner, initially latent, carnitine palmitoyltransferase (CPTi) of the mitochondrial inner membrane has revealed that the presence of digitonin and several other detergents inactivates CPTo activity. The CPTi activity, in contrast, was markedly stimulated by various detergents and phospholipid liposomes. These findings explain why in previous studies, which used digitonin or other detergents to expose, separate and purify the CPT activities, the inferences were drawn that (a) the ratio of latent to overt CPT was quite high, (b) both the CPT activities could be ascribed to one active protein recovered, and (c) the observed lack of malonyl-CoA inhibition indicated possible loss/separation of a putative malonyl-CoA-inhibition-conferring protein. Although both CPTo and CPTi were found to catalyse the forward and the backward reactions, CPTo showed greater capacity for the forward reaction and CPTi for the backward reaction. The easily solubilizable CPT, released on sonication of mitoplasts or of intact mitochondria under hypo-osmotic conditions, resembled CPTi in its properties. When octyl glucoside was used under appropriate conditions, 40-50% of the CPTo of outer membranes became solubilized, but it showed limited stability and decreased malonyl-CoA sensitivity. Malonyl-CoA-inhibitability of CPTo was decreased also on exposure of outer membranes to phospholipase C. When outer membranes that had been exposed to octyl glucoside or to phospholipase C were subjected to a reconstitution procedure using asolectin liposomes, the malonyl-CoA-inhibitability of CPTo was restored. A role of phospholipids in the malonyl-CoA sensitivity of CPTo is thus indicated.

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6

Silva, Filomena S. G., Irina G. Starostina, Vilena V. Ivanova, Albert A. Rizvanov, Paulo J. Oliveira, and Susana P. Pereira. "Determination of Metabolic Viability and Cell Mass Using a Tandem Resazurin/Sulforhodamine B Assay." Current Protocols in Toxicology 68, no. 1 (2016): 2.24.1–2.24.15. http://dx.doi.org/10.1002/cptx.1.

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7

Mahalingaiah, Prathap Kumar, Tammy Palenski, and Terry R. Van Vleet. "An In Vitro Model of Hematotoxicity: Differentiation of Bone Marrow-Derived Stem/Progenitor Cells into Hematopoietic Lineages and Evaluation of Lineage-Specific Hematotoxicity." Current Protocols in Toxicology 76, no. 1 (2018): e45. http://dx.doi.org/10.1002/cptx.45.

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8

Loelius, Shannon G., Sherry L. Spinelli, Katie L. Lannan, and Richard P. Phipps. "In Vitro Methods to Characterize the Effects of Tobacco and Nontobacco Products on Human Platelet Function." Current Protocols in Toxicology 76, no. 1 (2018): e46. http://dx.doi.org/10.1002/cptx.46.

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9

Smith, Andrew, Justin Dowis, and Deborah French. "Quantification of Serum Voriconazole, Isavuconazole, and Posaconazole by Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)." Current Protocols in Toxicology 76, no. 1 (2018): e47. http://dx.doi.org/10.1002/cptx.47.

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10

Tamehiro, Norimasa, Reiko Adachi, Yoshie Kimura, Shinobu Sakai, Reiko Teshima, and Kazunari Kondo. "Determining Food Allergens by Skin Sensitization in Mice." Current Protocols in Toxicology 76, no. 1 (2018): e48. http://dx.doi.org/10.1002/cptx.48.

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11

Sanders, Laurie H., Jeremy P. Rouanet, Evan H. Howlett, et al. "Newly Revised Quantitative PCR-Based Assay for Mitochondrial and Nuclear DNA Damage." Current Protocols in Toxicology 76, no. 1 (2018): e50. http://dx.doi.org/10.1002/cptx.50.

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12

Radi, Zaher A., Zachary S. Stewart, and Shawn P. O'Neil. "Accidental and Programmed Cell Death in Investigative and Toxicologic Pathology." Current Protocols in Toxicology 76, no. 1 (2018): e51. http://dx.doi.org/10.1002/cptx.51.

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13

Kietz, Christa, Vilma Pollari, and Annika Meinander. "Generating Germ-Free Drosophila to Study Gut-Microbe Interactions: Protocol to Rear Drosophila Under Axenic Conditions." Current Protocols in Toxicology 77, no. 1 (2018): e52. http://dx.doi.org/10.1002/cptx.52.

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14

Benjamino, Jacquelynn, Lidia Beka, and Joerg Graf. "Microbiome Analyses for Toxicological Studies." Current Protocols in Toxicology 77, no. 1 (2018): e53. http://dx.doi.org/10.1002/cptx.53.

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15

Nichols, Robert G., Jingwei Cai, Iain A. Murray, et al. "Structural and Functional Analysis of the Gut Microbiome for Toxicologists." Current Protocols in Toxicology 78, no. 1 (2018): e54. http://dx.doi.org/10.1002/cptx.54.

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16

Pellizzon, Michael A., and Matthew R. Ricci. "Effects of Rodent Diet Choice and Fiber Type on Data Interpretation of Gut Microbiome and Metabolic Disease Research." Current Protocols in Toxicology 77, no. 1 (2018): e55. http://dx.doi.org/10.1002/cptx.55.

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17

Hilander, Taru, Svetlana Konovalova, Mügen Terzioglu, and Henna Tyynismaa. "Analysis of Mitochondrial Protein Synthesis: De Novo Translation, Steady-State Levels, and Assembled OXPHOS Complexes." Current Protocols in Toxicology 77, no. 1 (2018): e56. http://dx.doi.org/10.1002/cptx.56.

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18

Velez-Quinones, Maria A., Hanna Xu, Nhu Vo, et al. "Determination of Thirteen Trace and Toxic Elements in Urine Using Inductively Coupled Mass Spectrometry." Current Protocols in Toxicology 78, no. 1 (2018): e58. http://dx.doi.org/10.1002/cptx.58.

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19

Velez-Quinones, Maria A., Hanna Xu, Nhu Vo, et al. "Simultaneous Determination of Uranium and Depleted Uranium Isotopic Ratio Using Inductively Coupled Mass Spectrometry." Current Protocols in Toxicology 78, no. 1 (2018): e59. http://dx.doi.org/10.1002/cptx.59.

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20

Herron, Josi, Kelly M. Hines, and Libin Xu. "Assessment of Altered Cholesterol Homeostasis by Xenobiotics Using Ultra-High Performance Liquid Chromatography-Tandem Mass Spectrometry." Current Protocols in Toxicology 78, no. 1 (2018): e65. http://dx.doi.org/10.1002/cptx.65.

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21

Joshi, Pranav, Soo-Yeon Kang, Akshata Datar, and Moo-Yeal Lee. "High-Throughput Assessment of Mechanistic Toxicity of Chemicals in Miniaturized 3D Cell Culture." Current Protocols in Toxicology 79, no. 1 (2018): e66. http://dx.doi.org/10.1002/cptx.66.

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22

Bradley, Jenifer A., and Christopher J. Strock. "Screening for Neurotoxicity with Microelectrode Array." Current Protocols in Toxicology 79, no. 1 (2018): e67. http://dx.doi.org/10.1002/cptx.67.

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23

Narayanan, Padma Kumar, and Nianyu Li. "In Vitro Monocyte/Macrophage Phagocytosis Assay for the Prediction of Drug-Induced Thrombocytopenia." Current Protocols in Toxicology 79, no. 1 (2019): e68. http://dx.doi.org/10.1002/cptx.68.

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24

Ghadiminejad, I., and E. D. Saggerson. "The relationship of rat liver overt carnitine palmitoyltransferase to the mitochondrial malonyl-CoA binding entity and to the latent palmitoyltransferase." Biochemical Journal 270, no. 3 (1990): 787–94. http://dx.doi.org/10.1042/bj2700787.

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1. Confirming previous work [Murthy & Pande (1987) Proc. Natl. Acad. Sci. U.S.A. 84, 378-382], malonyl-CoA-inhibitable carnitine palmitoyltransferase (CPT1) from rat liver was found to be localized in outer rather than in inner mitochondrial membranes. 2. Antisera were raised against a liver mitochondrial CPT of Mr 68,000, which was presumed to be the latent from of the enzyme (CPT2). These antisera cross-reacted with solubilized CPT extracted from liver inner mitochondrial membranes and with polypeptides of Mr 68,000 and 60,000 in immunoblots of both inner and outer mitochondrial membranes. The antisera also precipitated CPT activity from detergent-treated total membrane and outer-membrane preparations. 3. The antisera did not precipitate [14C]malonyl-CoA binding material obtained either from total membranes or from outer membranes. 4. It was concluded that liver CPT1 and CPT2 have some epitopes in common and may have a similar subunit size. In addition, CPT1 and the entity that binds malonyl-CoA must be separated polypeptides.

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25

Murthy, M. S. R., and S. V. Pande. "Characterization of a solubilized malonyl-CoA-sensitive carnitine palmitoyltransferase from the mitochondrial outer membrane as a protein distinct from the malonyl-CoA-insensitive carnitine palmitoyltransferase of the inner membrane." Biochemical Journal 268, no. 3 (1990): 599–604. http://dx.doi.org/10.1042/bj2680599.

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By using octyl glucoside in the presence of glycerol, it is possible to obtain a solubilized malonyl-CoA-sensitive carnitine palmitoyltransferase (CPTo) from the outer membranes of rat liver mitochondria. H.p.l.c. on hydroxyapatite column has now allowed a clear separation of the CPTo from the malonyl-CoA-insensitive CPT activity of the inner membranes (CPTi). The separated CPTo activity showed inhibition by low micromolar concentrations of malonyl-CoA, 2-tetradecylglycidyl-CoA and etomoxir-CoA. On solubilization and fractionation, the CPTo rapidly lost activity, unlike the relatively stable CPTi activity. Reconstitution into asolectin liposomes enhanced the activity and the malonyl-CoA-sensitivity of the CPTo fractions, whereas it had no such effect on the activity or malonyl-CoA insensitivity of the CPTi fractions. A polyclonal antibody raised against the malonyl-CoA-insensitive enzyme, purified from the inner membranes, precipitated the CPTi activity, but showed no reactivity with the CPTo fractions. In Western blots, the above antibody did not react with any polypeptide of the CPTo fractions. Incubation of the outer-membrane preparations with [3H]etomoxir, in the presence of ATP and CoA, led to labelling of a 90 kDa polypeptide that in the above hydroxyapatite chromatography was eluted in the same region as the CPTo. No such polypeptide labelling was seen in the CPTi fractions. With heart and skeletal-muscle mitochondria, the correspondingly labelled polypeptide was of about 86 kDa. These results show that the CPTo and CPTi are distinct proteins, that a subunit of 90 kDa for liver and 86 kDa for muscle constitutes a component of their respective CPTo systems, and that the 66 kDa subunit of the CPTi does not constitute a part of the CPTo system.

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26

Allison, Elric Y., Yixue Mei, Geoff B. Coombs, Vanessa Mizzi, Huseyn Ismayilov, and Baraa K. Al-Khazraji. "Effects of single and bilateral limb immersion on systemic and cerebral hemodynamic responses to the cold pressor test." Journal of Applied Physiology, August 1, 2024. http://dx.doi.org/10.1152/japplphysiol.00328.2024.

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The cold pressor test (CPT) involves cold water immersion of either the upper or lower limb(s) and elicits autonomic and hemodynamic increases via stimulation of pain and cutaneous thermoreceptors. It is unclear whether the choice of limb(s) in CPT studies differentially affects systemic and cerebral hemodynamic responses. Herein, we assessed systemic and cerebral hemodynamic and ventilatory responses to different CPT protocols of the hand (CPTH), foot (CPTF), or bilateral feet (CPTBF). We hypothesized CPTBF would elicit greatest physiological responses due to increased exposure area to the cold stimulus. Methods. Twenty-eight (14M;14F) healthy young adults [23.4 (SD: 2.4) years] participated in three 3-minute CPT protocols during a single visit. Mean arterial pressure (MAP), heart rate (HR), middle cerebral artery blood velocity (MCAv) and cerebrovascular conductance index, and end-tidal carbon dioxide (PETCO2), and pain perception were recorded throughout CPT protocols. Results. There was a time-CPT protocol interaction on systolic ( p=0.02) and diastolic blood pressure ( p<0.01), MAP ( p<0.01), HR ( p<0.001), presented as mean(SD). MCAv and cerebrovascular conductance index did not change with CPTs. Peak delta HR from baseline occurred in CPTBF (Δ13.6(15.5)BPM) compared to CPTH (Δ4.85(12.6)BPM; p=0.01) and CPTF (Δ4.04(13.3)BPM; p=0.02). Delta MAP was greater in CPTH (Δ12.3(7.95)mmHg) and CPTBF (Δ12.9(9.24)mmHg) compared to CPTF (Δ8.42(7.12)mmHg; p<0.01). Perceived pain was higher in CPTBF compared to single limb protocols ( p≤0.01). Conclusion. Our findings suggest choice of limb(s) in CPT protocols affects systemic hemodynamic responses and should be considered when designing CPT studies.

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27

Louíse, Nascimento Melgaço, França Tostto Thayse, and Andrade de Jesus Josiene. "SAÚDE PÚBLICA NO SISTEMA PENITENCIÁRIO: UM ESTUDO ACERCA DA SAÚDE DOS DETENTOS DO CONJUNTO PENAL DE TEIXEIRA DE FREITAS." REVISTAFT 27, no. 125 (2023). https://doi.org/10.5281/zenodo.8387470.

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O presente estudo trata-se de uma análise sobre a evolução da saúde pública dentro do sistema penitenciário, e como está implementado, esse sistema, dentro do Conjunto Penal de Teixeira de Freitas (CPTX), existe a necessidade de saber o papel do enfermeiro na assistência de saúde dos privados de liberdade, compreender se existe a implementação do Plano Nacional de Saúde no Sistema Prisional (PNSSP), além do  cumprimento do Estatuto Penitenciário do Estado da Bahia e a Política Nacional de Atenção Integral à Saúde das pessoas Privadas de liberdade no Sistema prisional (PNAISP) dentro do CPTX, buscamos contextualizar como foi a evolução da assistência de saúde dentro do sistema prisional brasileiro; identificar o papel do enfermeiro, a assistência prestada e todas medidas de promoção de saúde que são implantadas nas unidades; analisar a prevalência das patologias infecto contagiosas existentes no conjunto penal e como estão sendo direcionados esses detentos infectados. Esse estudo corresponde a uma pesquisa bibliográfica de caráter descritivo e explicativo, direcionado pela abordagem quali-quantitativa, realizado através dos bancos de dados da Biblioteca Virtual de Saúde (BVS), SciELO, google acadêmico, livros, artigos científicos, dissertações, PNSSP, estatuto penitenciário do estado da Bahia, PNAISP, com local de estudo de campo no âmbito do Conjunto Penal de Teixeira de Freitas..

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28

Luz, Anthony L., Cristina Lagido, Matthew D. Hirschey, and Joel N. Meyer. "In Vivo Determination of Mitochondrial Function Using Luciferase‐Expressing Caenorhabditis elegans : Contribution of Oxidative Phosphorylation, Glycolysis, and Fatty Acid Oxidation to Toxicant‐Induced Dysfunction." Current Protocols in Toxicology 69, no. 1 (2016). http://dx.doi.org/10.1002/cptx.10.

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Hamze, Julieta Gabriela, María Jiménez‐Movilla, and Raquel Romar. "Sperm‐Binding Assay Using an In Vitro 3D Model of the Mammalian Cumulus‐Oocyte Complex." Current Protocols in Toxicology 86, no. 1 (2020). http://dx.doi.org/10.1002/cptx.100.

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Zhang, Ziyan, Rajat Singh, and Michael Aschner. "Methods for the Detection of Autophagy in Mammalian Cells." Current Protocols in Toxicology 69, no. 1 (2016). http://dx.doi.org/10.1002/cptx.11.

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Ramm, Susanne, Melanie Adler, and Vishal S. Vaidya. "A High‐Throughput Screening Assay to Identify Kidney Toxic Compounds." Current Protocols in Toxicology 69, no. 1 (2016). http://dx.doi.org/10.1002/cptx.12.

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32

Phelan, Katy, and Kristin M. May. "Basic Techniques in Mammalian Cell Tissue Culture." Current Protocols in Toxicology 70, no. 1 (2016). http://dx.doi.org/10.1002/cptx.13.

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Xue, Yong, Jon G. Wilkes, Ted J. Moskal, Anna J. Williams, Willie M. Cooper, and Dan A. Buzatu. "Flow‐Cytometry‐Based Method to Detect Escherichia coli and Shigella Spp. Using 16S rRNA‐Based Probe." Current Protocols in Toxicology 71, no. 1 (2017). http://dx.doi.org/10.1002/cptx.14.

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Marroquin, Lisa D., Paul D. Bonin, Julie Keefer, and Thomas Schroeter. "Assessment of Bile Salt Export Pump (BSEP) Inhibition in Membrane Vesicles Using Radioactive and LC/MS‐Based Detection Methods." Current Protocols in Toxicology 71, no. 1 (2017). http://dx.doi.org/10.1002/cptx.15.

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35

Wages, Phillip A. "Detecting Protein Sulfenylation in Cells Exposed to a Toxicant." Current Protocols in Toxicology 71, no. 1 (2017). http://dx.doi.org/10.1002/cptx.16.

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36

Bhandari, Sadikshya, Clare Melchiorre, Kristen Dostie, et al. "Detection and Manipulation of the Stress Response Protein Metallothionein." Current Protocols in Toxicology 71, no. 1 (2017). http://dx.doi.org/10.1002/cptx.17.

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37

Winkle, Laura S., Jacklyn S. Kelty, and Charles G. Plopper. "Preparation of Specific Compartments of the Lungs for Pathologic and Biochemical Analysis of Toxicologic Responses." Current Protocols in Toxicology 71, no. 1 (2017). http://dx.doi.org/10.1002/cptx.18.

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Chang, Yu‐Chi, Toby B. Cole, and Lucio G. Costa. "Behavioral Phenotyping for Autism Spectrum Disorders in Mice." Current Protocols in Toxicology 72, no. 1 (2017). http://dx.doi.org/10.1002/cptx.19.

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39

Tolosa, Laia, M. José Gómez‐Lechón, and M. Teresa Donato. "A Multi‐Parametric Fluorescent Assay for the Screening and Mechanistic Study of Drug‐Induced Steatosis in Liver Cells in Culture." Current Protocols in Toxicology 72, no. 1 (2017). http://dx.doi.org/10.1002/cptx.20.

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40

Kaja, Simon, Andrew J. Payne, Yuliya Naumchuk, and Peter Koulen. "Quantification of Lactate Dehydrogenase for Cell Viability Testing Using Cell Lines and Primary Cultured Astrocytes." Current Protocols in Toxicology 72, no. 1 (2017). http://dx.doi.org/10.1002/cptx.21.

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41

McCullough, Shaun D., Doan M. On, and Emma C. Bowers. "Using Chromatin Immunoprecipitation in Toxicology: A Step‐by‐Step Guide to Increasing Efficiency, Reducing Variability, and Expanding Applications." Current Protocols in Toxicology 72, no. 1 (2017). http://dx.doi.org/10.1002/cptx.22.

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42

Lin, Christine, and Salman R. Khetani. "Micropatterned Co‐Cultures of Human Hepatocytes and Stromal Cells for the Assessment of Drug Clearance and Drug‐Drug Interactions." Current Protocols in Toxicology 72, no. 1 (2017). http://dx.doi.org/10.1002/cptx.23.

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Liu, Cong, Shuichi Sekine, Binbin Song, and Kousei Ito. "Use of Primary Rat Hepatocytes for Prediction of Drug‐Induced Mitochondrial Dysfunction." Current Protocols in Toxicology 72, no. 1 (2017). http://dx.doi.org/10.1002/cptx.24.

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44

Al‐Yousuf, Karamallah, Carl A. Webster, Grant N. Wheeler, Francesca Baldelli Bombelli, and Victoria Sherwood. "Combining Cytotoxicity Assessment and Xenopus laevis Phenotypic Abnormality Assay as a Predictor of Nanomaterial Safety." Current Protocols in Toxicology 73, no. 1 (2017). http://dx.doi.org/10.1002/cptx.25.

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45

Lauer, Fredine T., Jesse L. Denson, Ellen Beswick, and Scott W. Burchiel. "Intracellular Cytokine Detection by Flow Cytometry in Surface Marker‐Defined Human Peripheral Blood Mononuclear T Cells." Current Protocols in Toxicology 73, no. 1 (2017). http://dx.doi.org/10.1002/cptx.26.

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Ness, Kirk P., Shih‐Yu Chang, Elijah J. Weber, Danielle Zumpano, David L. Eaton, and Edward J. Kelly. "Microphysiological Systems to Assess Nonclinical Toxicity." Current Protocols in Toxicology 73, no. 1 (2017). http://dx.doi.org/10.1002/cptx.27.

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Hong, Wei, and Shaopeng Chen. "Optimizing Dual Fluorescent Analysis to Investigate the Toxicity of AgNPs in E. coli." Current Protocols in Toxicology 73, no. 1 (2017). http://dx.doi.org/10.1002/cptx.28.

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Harris, Georgina, Helena Hogberg, Thomas Hartung, and Lena Smirnova. "3D Differentiation of LUHMES Cell Line to Study Recovery and Delayed Neurotoxic Effects." Current Protocols in Toxicology 73, no. 1 (2017). http://dx.doi.org/10.1002/cptx.29.

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Hynes, James, Conn Carey, and Yvonne Will. "Fluorescence‐Based Microplate Assays for In Vitro Assessment of Mitochondrial Toxicity, Metabolic Perturbation, and Cellular Oxygenation." Current Protocols in Toxicology 70, no. 1 (2016). http://dx.doi.org/10.1002/cptx.3.

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Maillet, Agnes, Kim Peng Tan, and Liam R. Brunham. "Use of Human Pluripotent Stem Cell Derived‐Cardiomyocytes to Study Drug‐Induced Cardiotoxicity." Current Protocols in Toxicology 73, no. 1 (2017). http://dx.doi.org/10.1002/cptx.30.

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