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Showing 1 to 12 of 93 entries
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American College of Toxicology 2015 Poster Abstracts.

International journal of toxicology

[No authors listed]
PMID: 26957539
Int J Toxicol. 2016 Jan-Feb;35(1):52-84. doi: 10.1177/1091581815623753.

No abstract available.

Cite
American College of Toxicology 2015 Poster Abstracts. Int J Toxicol. 2016;35(1):52-84doi: 10.1177/1091581815623753.
(2016). American College of Toxicology 2015 Poster Abstracts. International journal of toxicology, 35(1), 52-84. https://doi.org/10.1177/1091581815623753
"American College of Toxicology 2015 Poster Abstracts." International journal of toxicology vol. 35,1 (2016): 52-84. doi: https://doi.org/10.1177/1091581815623753
American College of Toxicology 2015 Poster Abstracts. Int J Toxicol. 2016 Jan-Feb;35(1):52-84. doi: 10.1177/1091581815623753. PMID: 26957539.
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Progression of Serosal Vascular Proliferative Lesions to Hemangiosarcomas in the Uterus of the 26-Week Tg.rasH2 Mice Carcinogenicity Studies.

International journal of toxicology

Paranjpe MG, Belich JL, Richardson DR, Vidmar T, Mann PC, McKeon ME, Elbekai RH.
PMID: 27440821
Int J Toxicol. 2017 Jan 01;36(1):29-34. doi: 10.1177/1091581816659068. Epub 2016 Jul 20.

Tg.rasH2 mice are predisposed to hemangiosarcomas. Following the spleen, the uterus is the second most commonly affected organ in the female mice. Female mice are also predisposed to spontaneous vascular proliferative lesions on the serosal surface of the uterus,...

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Paranjpe MG, Belich JL, Richardson DR, et al. Progression of Serosal Vascular Proliferative Lesions to Hemangiosarcomas in the Uterus of the 26-Week Tg.rasH2 Mice Carcinogenicity Studies. Int J Toxicol. 2016;36(1):29-34doi: 10.1177/1091581816659068.
Paranjpe, M. G., Belich, J. L., Richardson, D. R., Vidmar, T., Mann, P. C., McKeon, M. E., & Elbekai, R. H. (2017). Progression of Serosal Vascular Proliferative Lesions to Hemangiosarcomas in the Uterus of the 26-Week Tg.rasH2 Mice Carcinogenicity Studies. International journal of toxicology, 36(1), 29-34. https://doi.org/10.1177/1091581816659068
Paranjpe, Madhav G, et al. "Progression of Serosal Vascular Proliferative Lesions to Hemangiosarcomas in the Uterus of the 26-Week Tg.rasH2 Mice Carcinogenicity Studies." International journal of toxicology vol. 36,1 (2017): 29-34. doi: https://doi.org/10.1177/1091581816659068
Paranjpe MG, Belich JL, Richardson DR, Vidmar T, Mann PC, McKeon ME, Elbekai RH. Progression of Serosal Vascular Proliferative Lesions to Hemangiosarcomas in the Uterus of the 26-Week Tg.rasH2 Mice Carcinogenicity Studies. Int J Toxicol. 2017 Jan 01;36(1):29-34. doi: 10.1177/1091581816659068. Epub 2016 Jul 20. PMID: 27440821.
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Safety Assessment of Cucumis sativus (Cucumber)-Derived Ingredients as Used in Cosmetics.

International journal of toxicology

Fiume MM, Bergfeld WF, Belsito DV, Hill RA, Klaassen CD, Liebler DC, Marks JG, Shank RC, Slaga TJ, Snyder PW, Andersen FA.
PMID: 24861368
Int J Toxicol. 2014 May;33(2):47S-64S. doi: 10.1177/1091581814526892. Epub 2014 May 26.

The CIR Expert Panel assessed the safety of 6 Cucumis sativus (cucumber)-derived ingredients and found them safe in cosmetic formulations in the present practices of use and concentration. These ingredients are reported to function in cosmetics as skin-conditioning agents....

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Fiume MM, Bergfeld WF, Belsito DV, et al. Safety Assessment of Cucumis sativus (Cucumber)-Derived Ingredients as Used in Cosmetics. Int J Toxicol. 2014;33(2):47S-64Sdoi: 10.1177/1091581814526892.
Fiume, M. M., Bergfeld, W. F., Belsito, D. V., Hill, R. A., Klaassen, C. D., Liebler, D. C., Marks, J. G., Shank, R. C., Slaga, T. J., Snyder, P. W., & Andersen, F. A. (2014). Safety Assessment of Cucumis sativus (Cucumber)-Derived Ingredients as Used in Cosmetics. International journal of toxicology, 33(2), 47S-64S. https://doi.org/10.1177/1091581814526892
Fiume, Monice M, et al. "Safety Assessment of Cucumis sativus (Cucumber)-Derived Ingredients as Used in Cosmetics." International journal of toxicology vol. 33,2 (2014): 47S-64S. doi: https://doi.org/10.1177/1091581814526892
Fiume MM, Bergfeld WF, Belsito DV, Hill RA, Klaassen CD, Liebler DC, Marks JG, Shank RC, Slaga TJ, Snyder PW, Andersen FA. Safety Assessment of Cucumis sativus (Cucumber)-Derived Ingredients as Used in Cosmetics. Int J Toxicol. 2014 May;33(2):47S-64S. doi: 10.1177/1091581814526892. Epub 2014 May 26. PMID: 24861368.
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Lead neurotoxicity: heme oxygenase and nitric oxide synthase activities in developing rat brain.

Neurotoxicity research

Reddy GR, Suresh A, Murthy KS, Chetty CS.
PMID: 12826491
Neurotox Res. 2002 Feb;4(1):33-9. doi: 10.1080/10298420290007600.

Chronic lead (Pb) exposure has been shown to result in cognitive deficits in children. Diffusible nitric oxide (NO) is a biological messenger known to regulate long-term potentiation (LTP) in the developing nervous system. Carbon monoxide (CO), as in the...

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Reddy GR, Suresh A, Murthy KS, et al. Lead neurotoxicity: heme oxygenase and nitric oxide synthase activities in developing rat brain. Neurotox Res. 2002;4(1):33-9doi: 10.1080/10298420290007600.
Reddy, G. R., Suresh, A., Murthy, K. S., & Chetty, C. S. (2002). Lead neurotoxicity: heme oxygenase and nitric oxide synthase activities in developing rat brain. Neurotoxicity research, 4(1), 33-9. https://doi.org/10.1080/10298420290007600
Reddy, Gottipolu R, et al. "Lead neurotoxicity: heme oxygenase and nitric oxide synthase activities in developing rat brain." Neurotoxicity research vol. 4,1 (2002): 33-9. doi: https://doi.org/10.1080/10298420290007600
Reddy GR, Suresh A, Murthy KS, Chetty CS. Lead neurotoxicity: heme oxygenase and nitric oxide synthase activities in developing rat brain. Neurotox Res. 2002 Feb;4(1):33-9. doi: 10.1080/10298420290007600. PMID: 12826491.
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American College of Toxicology 2017 Annual Meeting Poster Abstracts.

International journal of toxicology

[No authors listed]
PMID: 29382288
Int J Toxicol. 2018 Jan/Feb;37(1):63-104. doi: 10.1177/1091581817749473.

No abstract available.

Cite
American College of Toxicology 2017 Annual Meeting Poster Abstracts. Int J Toxicol. 2018;37(1):63-104doi: 10.1177/1091581817749473.
(2018). American College of Toxicology 2017 Annual Meeting Poster Abstracts. International journal of toxicology, 37(1), 63-104. https://doi.org/10.1177/1091581817749473
"American College of Toxicology 2017 Annual Meeting Poster Abstracts." International journal of toxicology vol. 37,1 (2018): 63-104. doi: https://doi.org/10.1177/1091581817749473
American College of Toxicology 2017 Annual Meeting Poster Abstracts. Int J Toxicol. 2018 Jan/Feb;37(1):63-104. doi: 10.1177/1091581817749473. PMID: 29382288.
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Long-Term Systemic Treatment With Methamphetamine Causes Retinal Damage in CD1 Mice.

International journal of toxicology

Yang H, Tao L, Li L.
PMID: 30373422
Int J Toxicol. 2018 Nov/Dec;37(6):448-456. doi: 10.1177/1091581818809356. Epub 2018 Oct 29.

As a powerful psychostimulant with high potential for abuse, methamphetamine (Meth) could cause long-lasting abnormalities in retinas. The purpose of this study was to investigate the effects of systemic administration of Meth at low dose on retinal damage and...

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Yang H, Tao L, Li L. Long-Term Systemic Treatment With Methamphetamine Causes Retinal Damage in CD1 Mice. Int J Toxicol. 2018;37(6):448-456doi: 10.1177/1091581818809356.
Yang, H., Tao, L., & Li, L. (2018). Long-Term Systemic Treatment With Methamphetamine Causes Retinal Damage in CD1 Mice. International journal of toxicology, 37(6), 448-456. https://doi.org/10.1177/1091581818809356
Yang, Haojiang, et al. "Long-Term Systemic Treatment With Methamphetamine Causes Retinal Damage in CD1 Mice." International journal of toxicology vol. 37,6 (2018): 448-456. doi: https://doi.org/10.1177/1091581818809356
Yang H, Tao L, Li L. Long-Term Systemic Treatment With Methamphetamine Causes Retinal Damage in CD1 Mice. Int J Toxicol. 2018 Nov/Dec;37(6):448-456. doi: 10.1177/1091581818809356. Epub 2018 Oct 29. PMID: 30373422.
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Editor's Note.

International journal of toxicology

Genter MB.
PMID: 32022623
Int J Toxicol. 2020 Jan/Feb;39(1):3. doi: 10.1177/1091581819898709.

No abstract available.

Cite
Genter MB. Editor's Note. Int J Toxicol. 2020;39(1):3doi: 10.1177/1091581819898709.
Genter, M. B. (2020). Editor's Note. International journal of toxicology, 39(1), 3. https://doi.org/10.1177/1091581819898709
Genter, Mary Beth. "Editor's Note." International journal of toxicology vol. 39,1 (2020): 3. doi: https://doi.org/10.1177/1091581819898709
Genter MB. Editor's Note. Int J Toxicol. 2020 Jan/Feb;39(1):3. doi: 10.1177/1091581819898709. PMID: 32022623.
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How to Review a Manuscript: Tips and Suggestions.

International journal of toxicology

Genter MB.
PMID: 32153218
Int J Toxicol. 2020 May/Jun;39(3):263. doi: 10.1177/1091581820911280. Epub 2020 Mar 10.

No abstract available.

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Genter MB. How to Review a Manuscript: Tips and Suggestions. Int J Toxicol. 2020;39(3):263doi: 10.1177/1091581820911280.
Genter, M. B. (2020). How to Review a Manuscript: Tips and Suggestions. International journal of toxicology, 39(3), 263. https://doi.org/10.1177/1091581820911280
Genter, Mary Beth. "How to Review a Manuscript: Tips and Suggestions." International journal of toxicology vol. 39,3 (2020): 263. doi: https://doi.org/10.1177/1091581820911280
Genter MB. How to Review a Manuscript: Tips and Suggestions. Int J Toxicol. 2020 May/Jun;39(3):263. doi: 10.1177/1091581820911280. Epub 2020 Mar 10. PMID: 32153218.
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Repeat Dose Toxicity Study of the AV7909 Anthrax Vaccine Candidate in Juvenile Rats.

International journal of toxicology

Zmarowski A, Ballin JD, Sharits J, Carrico K, Novak J, Shearer J, Blauth B, Ionin B, Reece J, Savransky V.
PMID: 32691648
Int J Toxicol. 2020 Jul 21;1091581820941412. doi: 10.1177/1091581820941412. Epub 2020 Jul 21.

AV7909 is a next-generation anthrax vaccine candidate indicated for post-exposure prophylaxis of exposure to

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Zmarowski A, Ballin JD, Sharits J, et al. Repeat Dose Toxicity Study of the AV7909 Anthrax Vaccine Candidate in Juvenile Rats. Int J Toxicol. 2020;1091581820941412doi: 10.1177/1091581820941412.
Zmarowski, A., Ballin, J. D., Sharits, J., Carrico, K., Novak, J., Shearer, J., Blauth, B., Ionin, B., Reece, J., & Savransky, V. (2020). Repeat Dose Toxicity Study of the AV7909 Anthrax Vaccine Candidate in Juvenile Rats. International journal of toxicology, 1091581820941412. https://doi.org/10.1177/1091581820941412
Zmarowski, Amy, et al. "Repeat Dose Toxicity Study of the AV7909 Anthrax Vaccine Candidate in Juvenile Rats." International journal of toxicology vol. (2020): 1091581820941412. doi: https://doi.org/10.1177/1091581820941412
Zmarowski A, Ballin JD, Sharits J, Carrico K, Novak J, Shearer J, Blauth B, Ionin B, Reece J, Savransky V. Repeat Dose Toxicity Study of the AV7909 Anthrax Vaccine Candidate in Juvenile Rats. Int J Toxicol. 2020 Jul 21;1091581820941412. doi: 10.1177/1091581820941412. Epub 2020 Jul 21. PMID: 32691648.
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Exposure and Public Health Effects of Polycyclic Aromatic Hydrocarbon Compounds in Sub-Saharan Africa: A Systematic Review.

International journal of toxicology

Ephraim-Emmanuel BC, Ordinioha B.
PMID: 33813922
Int J Toxicol. 2021 May-Jun;40(3):250-269. doi: 10.1177/10915818211002487. Epub 2021 Apr 05.

BACKGROUND AND AIM: In order to achieve improved global health, environmental health risks that could affect this goal have to be reduced as much as possible. This review thus aimed at determining the exposure levels, health risk assessments, and...

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Ephraim-Emmanuel BC, Ordinioha B. Exposure and Public Health Effects of Polycyclic Aromatic Hydrocarbon Compounds in Sub-Saharan Africa: A Systematic Review. Int J Toxicol. 2021;40(3):250-269doi: 10.1177/10915818211002487.
Ephraim-Emmanuel, B. C., & Ordinioha, B. (2021). Exposure and Public Health Effects of Polycyclic Aromatic Hydrocarbon Compounds in Sub-Saharan Africa: A Systematic Review. International journal of toxicology, 40(3), 250-269. https://doi.org/10.1177/10915818211002487
Ephraim-Emmanuel, Benson Chukwunweike, and Ordinioha, Best. "Exposure and Public Health Effects of Polycyclic Aromatic Hydrocarbon Compounds in Sub-Saharan Africa: A Systematic Review." International journal of toxicology vol. 40,3 (2021): 250-269. doi: https://doi.org/10.1177/10915818211002487
Ephraim-Emmanuel BC, Ordinioha B. Exposure and Public Health Effects of Polycyclic Aromatic Hydrocarbon Compounds in Sub-Saharan Africa: A Systematic Review. Int J Toxicol. 2021 May-Jun;40(3):250-269. doi: 10.1177/10915818211002487. Epub 2021 Apr 05. PMID: 33813922.
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Effects of Vanadium Inhalation and Sweetened Beverage Ingestion in Mice: Morphological and Biochemical Changes in the Liver.

International journal of toxicology

Cervantes-Valencia ME, González-Villalva A, Cano-Gutiérrez G, Albarrán-Alonso JC, Fortoul TI.
PMID: 34284608
Int J Toxicol. 2021 Oct;40(5):466-474. doi: 10.1177/10915818211030858. Epub 2021 Jul 20.

The aim of this report was to evaluate the morphological and biochemical changes in the liver by the inhalation of vanadium and consumption of sweetened beverages in a subchronic murine model. Forty CD-1 male mice were randomly divided into...

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Cervantes-Valencia ME, González-Villalva A, Cano-Gutiérrez G, et al. Effects of Vanadium Inhalation and Sweetened Beverage Ingestion in Mice: Morphological and Biochemical Changes in the Liver. Int J Toxicol. 2021;40(5):466-474doi: 10.1177/10915818211030858.
Cervantes-Valencia, M. E., González-Villalva, A., Cano-Gutiérrez, G., Albarrán-Alonso, J. C., & Fortoul, T. I. (2021). Effects of Vanadium Inhalation and Sweetened Beverage Ingestion in Mice: Morphological and Biochemical Changes in the Liver. International journal of toxicology, 40(5), 466-474. https://doi.org/10.1177/10915818211030858
Cervantes-Valencia, María Eugenia, et al. "Effects of Vanadium Inhalation and Sweetened Beverage Ingestion in Mice: Morphological and Biochemical Changes in the Liver." International journal of toxicology vol. 40,5 (2021): 466-474. doi: https://doi.org/10.1177/10915818211030858
Cervantes-Valencia ME, González-Villalva A, Cano-Gutiérrez G, Albarrán-Alonso JC, Fortoul TI. Effects of Vanadium Inhalation and Sweetened Beverage Ingestion in Mice: Morphological and Biochemical Changes in the Liver. Int J Toxicol. 2021 Oct;40(5):466-474. doi: 10.1177/10915818211030858. Epub 2021 Jul 20. PMID: 34284608.
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Influences of Unmodified and Carboxylated Carbon Nanotubes on Lipid Profiles in THP-1 Macrophages: A Lipidomics Study.

International journal of toxicology

Pei L, Yang W, Cao Y.
PMID: 34886715
Int J Toxicol. 2021 Dec 10;10915818211056633. doi: 10.1177/10915818211056633. Epub 2021 Dec 10.

Since the possible roles of surface modifications in determining multi-walled carbon nanotube (MWCNT)-promoted endoplasmic reticulum (ER) stress-mediated lipid-laden macrophage foam cell formation are still in debate, we compared unmodified and carboxylated MWCNT-induced cytotoxicity, lipid profile changes, and expression of...

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Pei L, Yang W, Cao Y. Influences of Unmodified and Carboxylated Carbon Nanotubes on Lipid Profiles in THP-1 Macrophages: A Lipidomics Study. Int J Toxicol. 2021;10915818211056633doi: 10.1177/10915818211056633.
Pei, L., Yang, W., & Cao, Y. (2021). Influences of Unmodified and Carboxylated Carbon Nanotubes on Lipid Profiles in THP-1 Macrophages: A Lipidomics Study. International journal of toxicology, 10915818211056633. https://doi.org/10.1177/10915818211056633
Pei, Lanjie, et al. "Influences of Unmodified and Carboxylated Carbon Nanotubes on Lipid Profiles in THP-1 Macrophages: A Lipidomics Study." International journal of toxicology vol. (2021): 10915818211056633. doi: https://doi.org/10.1177/10915818211056633
Pei L, Yang W, Cao Y. Influences of Unmodified and Carboxylated Carbon Nanotubes on Lipid Profiles in THP-1 Macrophages: A Lipidomics Study. Int J Toxicol. 2021 Dec 10;10915818211056633. doi: 10.1177/10915818211056633. Epub 2021 Dec 10. PMID: 34886715.
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Showing 1 to 12 of 93 entries