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Optical monitoring of stress-related changes in the brain tissues and vessels associated with hemorrhagic stroke in newborn rats.

Biomedical optics express

Semyachkina-Glushkovskaya O, Pavlov A, Kurths J, Borisova E, Gisbrecht A, Sindeeva O, Abdurashitov A, Shirokov A, Navolokin N, Zinchenko E, Gekalyuk A, Ulanova M, Zhu D, Luo Q, Tuchin V.
PMID: 26504656
Biomed Opt Express. 2015 Sep 24;6(10):4088-97. doi: 10.1364/BOE.6.004088. eCollection 2015 Oct 01.

Stress is a major factor for a risk of cerebrovascular catastrophes. Studying of mechanisms underlying stress-related brain-injures in neonates is crucial for development of strategy to prevent of neonatal stroke. Here, using a model of sound-stress-induced intracranial hemorrhages in...

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Semyachkina-Glushkovskaya O, Pavlov A, Kurths J, et al. Optical monitoring of stress-related changes in the brain tissues and vessels associated with hemorrhagic stroke in newborn rats. Biomed Opt Express. 2015;6(10):4088-97doi: 10.1364/BOE.6.004088.
Semyachkina-Glushkovskaya, O., Pavlov, A., Kurths, J., Borisova, E., Gisbrecht, A., Sindeeva, O., Abdurashitov, A., Shirokov, A., Navolokin, N., Zinchenko, E., Gekalyuk, A., Ulanova, M., Zhu, D., Luo, Q., & Tuchin, V. (2015). Optical monitoring of stress-related changes in the brain tissues and vessels associated with hemorrhagic stroke in newborn rats. Biomedical optics express, 6(10), 4088-97. https://doi.org/10.1364/BOE.6.004088
Semyachkina-Glushkovskaya, Oxana, et al. "Optical monitoring of stress-related changes in the brain tissues and vessels associated with hemorrhagic stroke in newborn rats." Biomedical optics express vol. 6,10 (2015): 4088-97. doi: https://doi.org/10.1364/BOE.6.004088
Semyachkina-Glushkovskaya O, Pavlov A, Kurths J, Borisova E, Gisbrecht A, Sindeeva O, Abdurashitov A, Shirokov A, Navolokin N, Zinchenko E, Gekalyuk A, Ulanova M, Zhu D, Luo Q, Tuchin V. Optical monitoring of stress-related changes in the brain tissues and vessels associated with hemorrhagic stroke in newborn rats. Biomed Opt Express. 2015 Sep 24;6(10):4088-97. doi: 10.1364/BOE.6.004088. eCollection 2015 Oct 01. PMID: 26504656; PMCID: PMC4605065.
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Beta-Arrestin 1 Mediates Liver Thyrotropin Regulation of Cholesterol Conversion Metabolism via the Akt-Dependent Pathway.

International journal of endocrinology

Niu S, Li H, Chen W, Zhao J, Gao L, Bo T.
PMID: 29853881
Int J Endocrinol. 2018 May 02;2018:4371396. doi: 10.1155/2018/4371396. eCollection 2018.

After activation, G protein-coupled receptors (GPCRs) are desensitized by

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Niu S, Li H, Chen W, et al. Beta-Arrestin 1 Mediates Liver Thyrotropin Regulation of Cholesterol Conversion Metabolism via the Akt-Dependent Pathway. Int J Endocrinol. 2018;2018:4371396doi: 10.1155/2018/4371396.
Niu, S., Li, H., Chen, W., Zhao, J., Gao, L., & Bo, T. (2018). Beta-Arrestin 1 Mediates Liver Thyrotropin Regulation of Cholesterol Conversion Metabolism via the Akt-Dependent Pathway. International journal of endocrinology, 20184371396. https://doi.org/10.1155/2018/4371396
Niu, Shaona, et al. "Beta-Arrestin 1 Mediates Liver Thyrotropin Regulation of Cholesterol Conversion Metabolism via the Akt-Dependent Pathway." International journal of endocrinology vol. 2018 (2018): 4371396. doi: https://doi.org/10.1155/2018/4371396
Niu S, Li H, Chen W, Zhao J, Gao L, Bo T. Beta-Arrestin 1 Mediates Liver Thyrotropin Regulation of Cholesterol Conversion Metabolism via the Akt-Dependent Pathway. Int J Endocrinol. 2018 May 02;2018:4371396. doi: 10.1155/2018/4371396. eCollection 2018. PMID: 29853881; PMCID: PMC5954953.
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Correction: Single-molecule FRET and conformational analysis of beta-arrestin-1 through genetic code expansion and a Se-click reaction.

Chemical science

Han MJ, He QT, Yang M, Chen C, Yao Y, Liu X, Wang Y, Zhu ZL, Zhu KK, Qu C, Yang F, Hu C, Guo X, Zhang D, Chen C, Sun JP, Wang J.
PMID: 34349959
Chem Sci. 2021 Jul 02;12(28):9851. doi: 10.1039/d1sc90143e. eCollection 2021 Jul 21.

[This corrects the article DOI: 10.1039/D1SC02653D.].

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Han MJ, He QT, Yang M, et al. Correction: Single-molecule FRET and conformational analysis of beta-arrestin-1 through genetic code expansion and a Se-click reaction. Chem Sci. 2021;12(28):9851doi: 10.1039/d1sc90143e.
Han, M. J., He, Q. T., Yang, M., Chen, C., Yao, Y., Liu, X., Wang, Y., Zhu, Z. L., Zhu, K. K., Qu, C., Yang, F., Hu, C., Guo, X., Zhang, D., Chen, C., Sun, J. P., & Wang, J. (2021). Correction: Single-molecule FRET and conformational analysis of beta-arrestin-1 through genetic code expansion and a Se-click reaction. Chemical science, 12(28), 9851. https://doi.org/10.1039/d1sc90143e
Han, Ming-Jie, et al. "Correction: Single-molecule FRET and conformational analysis of beta-arrestin-1 through genetic code expansion and a Se-click reaction." Chemical science vol. 12,28 (2021): 9851. doi: https://doi.org/10.1039/d1sc90143e
Han MJ, He QT, Yang M, Chen C, Yao Y, Liu X, Wang Y, Zhu ZL, Zhu KK, Qu C, Yang F, Hu C, Guo X, Zhang D, Chen C, Sun JP, Wang J. Correction: Single-molecule FRET and conformational analysis of beta-arrestin-1 through genetic code expansion and a Se-click reaction. Chem Sci. 2021 Jul 02;12(28):9851. doi: 10.1039/d1sc90143e. eCollection 2021 Jul 21. PMID: 34349959; PMCID: PMC8293806.
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Agonist mediated internalization of M2 mAChR is beta-arrestin-dependent.

Journal of molecular signaling

Jones KT, Echeverry M, Mosser VA, Gates A, Jackson DA.
PMID: 17224084
J Mol Signal. 2006 Dec 05;1:7. doi: 10.1186/1750-2187-1-7.

BACKGROUND: Muscarinic acetylcholine receptors (mAChRs) undergo agonist-promoted internalization, but evidence suggesting that the mechanism of internalization is beta-arrestin dependent has been contradictory and unclear. Previous studies using heterologous over-expression of wild type or dominant-negative forms of beta-arrestins have reported...

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Jones KT, Echeverry M, Mosser VA, et al. Agonist mediated internalization of M2 mAChR is beta-arrestin-dependent. J Mol Signal. 2006;1:7doi: 10.1186/1750-2187-1-7.
Jones, K. T., Echeverry, M., Mosser, V. A., Gates, A., & Jackson, D. A. (2006). Agonist mediated internalization of M2 mAChR is beta-arrestin-dependent. Journal of molecular signaling, 17. https://doi.org/10.1186/1750-2187-1-7
Jones, Kymry T, et al. "Agonist mediated internalization of M2 mAChR is beta-arrestin-dependent." Journal of molecular signaling vol. 1 (2006): 7. doi: https://doi.org/10.1186/1750-2187-1-7
Jones KT, Echeverry M, Mosser VA, Gates A, Jackson DA. Agonist mediated internalization of M2 mAChR is beta-arrestin-dependent. J Mol Signal. 2006 Dec 05;1:7. doi: 10.1186/1750-2187-1-7. PMID: 17224084; PMCID: PMC1769497.
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Angiotensin receptor blocker drugs and inhibition of adrenal beta-arrestin-1-dependent aldosterone production: Implications for heart failure therapy.

World journal of cardiology

Lymperopoulos A, Aukszi B.
PMID: 28400916
World J Cardiol. 2017 Mar 26;9(3):200-206. doi: 10.4330/wjc.v9.i3.200.

Aldosterone mediates many of the physiological and pathophysiological/cardio-toxic effects of angiotensin II (AngII). Its synthesis and secretion from the zona glomerulosa cells of the adrenal cortex, elevated in chronic heart failure (HF), is induced by AngII type 1 receptors...

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Lymperopoulos A, Aukszi B. Angiotensin receptor blocker drugs and inhibition of adrenal beta-arrestin-1-dependent aldosterone production: Implications for heart failure therapy. World J Cardiol. 2017;9(3):200-206doi: 10.4330/wjc.v9.i3.200.
Lymperopoulos, A., & Aukszi, B. (2017). Angiotensin receptor blocker drugs and inhibition of adrenal beta-arrestin-1-dependent aldosterone production: Implications for heart failure therapy. World journal of cardiology, 9(3), 200-206. https://doi.org/10.4330/wjc.v9.i3.200
Lymperopoulos, Anastasios, and Aukszi, Beatrix. "Angiotensin receptor blocker drugs and inhibition of adrenal beta-arrestin-1-dependent aldosterone production: Implications for heart failure therapy." World journal of cardiology vol. 9,3 (2017): 200-206. doi: https://doi.org/10.4330/wjc.v9.i3.200
Lymperopoulos A, Aukszi B. Angiotensin receptor blocker drugs and inhibition of adrenal beta-arrestin-1-dependent aldosterone production: Implications for heart failure therapy. World J Cardiol. 2017 Mar 26;9(3):200-206. doi: 10.4330/wjc.v9.i3.200. PMID: 28400916; PMCID: PMC5368669.
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WITHDRAWN:beta-arrestin 1 contributes to primary biliary cirrhosis.

Clinical science (London, England : 1979)

Deng A, Yao D, Chen S, Liu C, Kang J, Zhou Y, Yu H, Qian C, Wu C, Jiang T, Zhong R, Pei G.
PMID: 20025607
Clin Sci (Lond). 2009 Dec 21; doi: 10.1042/CS20090276. Epub 2009 Dec 21.

The Ahead of Print article entitled 'beta-arrestin 1 contributes to primary biliary cirrhosis' was withdrawn by the publisher.

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Deng A, Yao D, Chen S, et al. WITHDRAWN:beta-arrestin 1 contributes to primary biliary cirrhosis. Clin Sci (Lond). 2009;doi: 10.1042/CS20090276.
Deng, A., Yao, D., Chen, S., Liu, C., Kang, J., Zhou, Y., Yu, H., Qian, C., Wu, C., Jiang, T., Zhong, R., & Pei, G. (2009). WITHDRAWN:beta-arrestin 1 contributes to primary biliary cirrhosis. Clinical science (London, England : 1979), . https://doi.org/10.1042/CS20090276
Deng, Anmei, et al. "WITHDRAWN:beta-arrestin 1 contributes to primary biliary cirrhosis." Clinical science (London, England : 1979) vol. (2009). doi: https://doi.org/10.1042/CS20090276
Deng A, Yao D, Chen S, Liu C, Kang J, Zhou Y, Yu H, Qian C, Wu C, Jiang T, Zhong R, Pei G. WITHDRAWN:beta-arrestin 1 contributes to primary biliary cirrhosis. Clin Sci (Lond). 2009 Dec 21; doi: 10.1042/CS20090276. Epub 2009 Dec 21. PMID: 20025607.
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Corrigendum to "Beta-Arrestin 1 Mediates Liver Thyrotropin Regulation of Cholesterol Conversion Metabolism via the Akt-Dependent Pathway".

International journal of endocrinology

Niu S, Li H, Chen W, Zhao J, Gao L, Bo T.
PMID: 30275826
Int J Endocrinol. 2018 Sep 10;2018:3029602. doi: 10.1155/2018/3029602. eCollection 2018.

[This corrects the article DOI: 10.1155/2018/4371396.].

Cite
Niu S, Li H, Chen W, et al. Corrigendum to "Beta-Arrestin 1 Mediates Liver Thyrotropin Regulation of Cholesterol Conversion Metabolism via the Akt-Dependent Pathway". Int J Endocrinol. 2018;2018:3029602doi: 10.1155/2018/3029602.
Niu, S., Li, H., Chen, W., Zhao, J., Gao, L., & Bo, T. (2018). Corrigendum to "Beta-Arrestin 1 Mediates Liver Thyrotropin Regulation of Cholesterol Conversion Metabolism via the Akt-Dependent Pathway". International journal of endocrinology, 20183029602. https://doi.org/10.1155/2018/3029602
Niu, Shaona, et al. "Corrigendum to "Beta-Arrestin 1 Mediates Liver Thyrotropin Regulation of Cholesterol Conversion Metabolism via the Akt-Dependent Pathway"." International journal of endocrinology vol. 2018 (2018): 3029602. doi: https://doi.org/10.1155/2018/3029602
Niu S, Li H, Chen W, Zhao J, Gao L, Bo T. Corrigendum to "Beta-Arrestin 1 Mediates Liver Thyrotropin Regulation of Cholesterol Conversion Metabolism via the Akt-Dependent Pathway". Int J Endocrinol. 2018 Sep 10;2018:3029602. doi: 10.1155/2018/3029602. eCollection 2018. PMID: 30275826; PMCID: PMC6151851.
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Single-molecule FRET and conformational analysis of beta-arrestin-1 through genetic code expansion and a Se-click reaction.

Chemical science

Han MJ, He QT, Yang M, Chen C, Yao Y, Liu X, Wang Y, Zhu ZL, Zhu KK, Qu C, Yang F, Hu C, Guo X, Zhang D, Chen C, Sun JP, Wang J.
PMID: 34276941
Chem Sci. 2021 May 31;12(26):9114-9123. doi: 10.1039/d1sc02653d. eCollection 2021 Jul 07.

Single-molecule Förster resonance energy transfer (smFRET) is a powerful tool for investigating the dynamic properties of biomacromolecules. However, the success of protein smFRET relies on the precise and efficient labeling of two or more fluorophores on the protein of...

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Han MJ, He QT, Yang M, et al. Single-molecule FRET and conformational analysis of beta-arrestin-1 through genetic code expansion and a Se-click reaction. Chem Sci. 2021;12(26):9114-9123doi: 10.1039/d1sc02653d.
Han, M. J., He, Q. T., Yang, M., Chen, C., Yao, Y., Liu, X., Wang, Y., Zhu, Z. L., Zhu, K. K., Qu, C., Yang, F., Hu, C., Guo, X., Zhang, D., Chen, C., Sun, J. P., & Wang, J. (2021). Single-molecule FRET and conformational analysis of beta-arrestin-1 through genetic code expansion and a Se-click reaction. Chemical science, 12(26), 9114-9123. https://doi.org/10.1039/d1sc02653d
Han, Ming-Jie, et al. "Single-molecule FRET and conformational analysis of beta-arrestin-1 through genetic code expansion and a Se-click reaction." Chemical science vol. 12,26 (2021): 9114-9123. doi: https://doi.org/10.1039/d1sc02653d
Han MJ, He QT, Yang M, Chen C, Yao Y, Liu X, Wang Y, Zhu ZL, Zhu KK, Qu C, Yang F, Hu C, Guo X, Zhang D, Chen C, Sun JP, Wang J. Single-molecule FRET and conformational analysis of beta-arrestin-1 through genetic code expansion and a Se-click reaction. Chem Sci. 2021 May 31;12(26):9114-9123. doi: 10.1039/d1sc02653d. eCollection 2021 Jul 07. PMID: 34276941; PMCID: PMC8261736.
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Showing 1 to 8 of 8 entries