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Готові списки джерел за темами / Inhibitory effects / Книги

Книги з теми "Inhibitory effects"

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: Inhibitory effects.

Автор: Grafiati

Опубліковано: 10 грудня 2022

Оновлено: 28 січня 2023

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1

Patel, Sunit Mohanlal. The effects of the inhibitory amino acid gamma-aminobutyric acid (GABA) on food intake in the rat. Portsmouth: University of Portsmouth, 2003.

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2

Hann, Brad. The Inhibitory effects of alpha-cyano-4-hydroxycinnamic acid on the lactate transporter of H69 small cell lung cancer cells. Sudbury, Ont: Laurentian University, 1995.

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3

Mooney, Mark H. Glucagon-like peptide-1 and gastric inhibitory polypeptide: Effects of N-terminal glycation on hormone degradation, insulin secretion and antihyperglycaemic activity. [S.l: The Author], 2000.

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4

William Harvey Conference (1995 London, England). Improved non-steroid anti-inflammatory drugs: COX-2 enzyme inhibitors : proceedings of a conference held on October 10-11, 1995, at Regent's College, London. Dordrecht: Kluwer Academic, 1996.

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5

Khongčharœ̄nsunthō̜n, Wisātrī. Rāingān wičhai rư̄ang kānsưksā khunnasombat kāntān čhulinsī dư̄ yā læ kāntān mareng khō̜ng sānsakat čhāk samunphrai Thai bāng chanit =: Inhibitory effects of some Thai herb extracts on the growth of some drug resistant microorganisms and cancer cell lines. [Chon Buri]: Phāk Wichā Chīwawitthayā, Khana Witthayāsāt, Mahāwitthayālai Būraphā, 2006.

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6

J, Cragoe Edward, Kleyman Thomas R, and Simchowitz Louis, eds. Amiloride and its analogs: Unique cation transport inhibitors. New York, N.Y: VCH, 1992.

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7

F, James Lynn, United States. Agricultural Research Service., and Swainsonine and Related Glycosidase Inhibitors Symposium (1987 : Logan, Utah), eds. Swainsonine and related glycosidase inhibitors. Ames: Iowa State University Press, 1989.

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8

Vane, John R. Improved non-steroid anti-flammatory drugs COX-2 enzyme inhibitors: Proceedings of a conference held on October 10-11, 1995, at Regent's College, London. Dordrecht: Kluwer Academic Publishers, 1996.

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9

E, Stütz Arnold, ed. Iminosugars as glycosidase inhibitors: Nojirimycin and beyond. Weinheim: Wiley-VCH, 1999.

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10

J, Whalley Lawrence, ed. ACE inhibitors: Central actions. New York: Raven Press, 1994.

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11

Teijeiro, Isabel. Effects of oxidative phosphorylation inhibitors on the growth and viability of Saccharmomyces cerevisiae. Sudbury, Ont: Laurentian University, 1997.

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12

Ogwen-Jones, S. The effects of inhibitors on the environmental cracking of a drill collar steel. Manchester: UMIST, 1994.

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13

Hidir, Saadiah Mohd. The inhibitory effect of cyclic 3',5' adenosine monophosphate and putrescine in inflammation. Birmingham: University of Aston. Department of Pharmacy, 1985.

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14

Georgiev, Bojidor. Serpins and protein kinase inhibitors: Novel functions, structural features and molecular mechanisms. New York: Nova Science Publishers, 2010.

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15

MD, Giordano Antonio, and Soprano Kenneth J, eds. Cell cycle inhibitors in cancer therapy: Current strategies. Totowa, N.J: Humana Press, 2003.

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16

Clute, Paul. The effect of microtubule inhibitors on chromosome cycles of Xenopus laevis blastomeres. Ottawa: National Library of Canada, 1990.

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17

M. A. M. Abou Zour. Inhibitive effects of thiourea and mixed inhibitor systems on mild steel in CO2 solutions. Manchester: UMIST, 1997.

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18

Winegarden, Neil Anthony. The effect of inhibitors of oxidative phosphorylation on the dorsophila heat shock response. Ottawa: National Library of Canada, 1997.

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19

Elaghtaa, A. R. Effect of the presence of precorrosion on the efficiency of inhibitor in CO2 corrosion. Manchester: UMIST, 1995.

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20

Anchors, Michael. Safer than Phen-Fen! Rocklin, CA: Prima Pub., 1997.

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21

International, Amine Oxidases Workshop (4th 1990 Würzburg Germany). Amine oxidases and their impact on neurobiology: Proceedings of the 4th International Amine Oxidases Workshop, Würzburg, Federal Republic of Germany, July 7-10, 1990. Wien: Springer-Verlag, 1990.

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22

PhD, Henderson Brian, and Bodmer Mark W, eds. Therapeutic modulation of cytokines. Boca Raton, Fla: CRC Press, 1996.

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23

Bartolomeo/Lupi. Inhibitory After-Effects in Spatial Processing: Experimental and Theoretical Issues on Inhibition of Return (Cognitive Neuropsychology). Psychology Press, 2006.

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24

Department of the Environment. Determination of the Inhibitory Effects of Chemicals and Waste Waters on the Anaerobic Digestion of Sewage Sludge (1986). Stationery Office Books, 1987.

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25

Lalman, Jerald David Anthony. Anaerobic degradation of linoleic (C18:2), oleic (C18:1) and stearic (C18:0) acids and their inhibitory effects on acidogens, acetogens and methanogens. 2000.

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26

Kramer, Carolyn, and Emily Blumberg. Immunosuppressants and Antiretroviral Therapy in HIV-Positive Transplant Patients. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190493097.003.0028.

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Анотація:

Protease inhibitors (PIs), especially ritonavir, are inhibitors of CYP3A4 and P-gp1 and can significantly increase levels of calcineurin inhibitors and mammalian target of rapamycin (mTOR) inhibitors. Cobicistat is an inhibitor of CYP3A4, and its effect on levels of calcineurin inhibitors and mTOR inhibitors is likely to be similar to that of ritonavir. Efavirenz may result in lower concentrations of calcineurin inhibitors and mTOR inhibitors. Dose reduction and careful attention to monitoring drug levels are critical to avoid toxicity and maintain therapeutic immunosuppressive concentrations when PIs or cobicistat are coadministered with calcineurin inhibitors or mTOR inhibitors. Although there is no formalized recommendation for the ideal antiretroviral therapy regimen in HIV-positive transplant recipients, a regimen consisting of two nucleoside reverse transcriptase and an integrase inhibitor minimizes the risk of drug–drug interactions and simplifies dosing of immunosuppressive agents while maintaining a high barrier to resistance.

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27

1938-, Cohen Jack S., ed. Oligodeoxynucleotides antisense inhibitors of gene expression. Boca Raton, Fla: CRC Press, 1989.

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28

Nutt, David J., and Liam J. Nestor. The GABA system and addiction. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198797746.003.0008.

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Research points to the potential role of gamma-aminobutyric acid (GABA) in substance addiction. GABA is the major inhibitory neurotransmitter in the brain. Disturbances in the GABA system may predate substance abuse and addiction, whereby its efficacy to modulate other neurotransmitter systems (e.g. dopamine) strongly implicated in substance addiction behaviours is impaired. There are a number of addictive substances that boost GABA functioning, however, such as alcohol and benzodiazepines. Medications that boost the availability of GABA or mimic its effects at receptors may possess some clinical potential in treating addiction, but also have abuse liability.

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29

Ziemann, Ulf. Pharmacology of TMS measures. Edited by Charles M. Epstein, Eric M. Wassermann, and Ulf Ziemann. Oxford University Press, 2012. http://dx.doi.org/10.1093/oxfordhb/9780198568926.013.0013.

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This article discusses various aspects of the pharmacology of transcranial magnetic stimulator (TMS) measures. TMS measures reflect axonal, or excitatory or inhibitory synaptic excitability in distinct interneuron circuits. TMS measures can be employed to study the effects of a drug with unknown or multiple modes of action, and hence to determine its main mode of action at the systems level of the motor cortex. TMS experiments can also study acute drug effects that may be different from chronic drug effects. TMS or repetitive TMS may induce changes in endogenous neurotransmitter or neuromodulator systems. This allows for the study of neurotransmission along defined neuronal projections in health and disease. This article describes pharmacological experiments that have characterized the physiology of TMS measures of motor cortical excitability. Pharmacological challenging of TMS measures has opened a broad window into human cortical physiology.

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30

Carson, Beverly D. Histone Deacetylase Inhibitors: Pharmacology, Uses and Health Effects. Nova Science Publishers, Incorporated, 2015.

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31

Cragoe, Edward J., and Thomas R. Kleyman. Amiloride and Its Analogs: Unique Cation Transport Inhibitors. John Wiley & Sons, 1993.

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32

Topoisomerase Inhibitors: Classification, Mechanisms of Action and Adverse Effects. Nova Science Publishers, Incorporated, 2017.

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33

Fomberstein, Kenneth, Marissa Rubin, Dipan Patel, John-Paul Sara, and Abhishek Gupta. Perioperative Opioid Analgesics of Use in Pain Management for Spine Surgery. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190626761.003.0004.

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This chapter compares the basic properties of several opioid analgesics and explores their applications in perioperative pain control in spine surgery. Parenteral opioids have long been the cornerstone of treatment for postoperative pain; they work by inhibiting voltage-gated calcium channels and increasing potassium influx, which results in reduced neuronal excitability, thereby inhibiting the ascending transmission of painful stimuli and activating the descending inhibitory pathways. This chapter reviews concepts including opioid conversion and rotation, opioid tolerance, and opioid cross-tolerance. It discusses common opioid side effects, and it explores the perioperative use of several specific opioids including remifentanil, sufentanil, methadone, oxycodone, morphine, and tapentadol and discusses their use in spine surgery. Additionally, this chapter discusses patient-controlled analgesia (PCA) and its importance in postoperative pain control.

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34

Roseberg, Richard J. Chloride fertilizer and soil pH effects on nitrification rate and soil solution constituents. 1985.

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35

1938-, Cohen Jack S., ed. Oligodeoxynucleotides: Antisense inhibitors of gene expression. Houndmills, Basingstoke, Hampshire: Macmillan, 1989.

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36

Sir John R. Vane (Editor) and Jack H. Botting (Editor), eds. Selective COX-2 Inhibitors: Pharmacology, Clinical Effects and Therapeutic Potential. Springer, 1998.

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37

Botting, Jack H., and Sir John R. Vane. Selective COX-2 Inhibitors: Pharmacology, Clinical Effects and Therapeutic Potential. Springer, 2012.

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38

Martin, Harris Warthman. Nitrification inhibitor effects on potato yields and soil inorganic nitrogen. 1990.

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39

Martin, Harris. Nitrification Inhibitor Effects on Potato Yields and Soil Inorganic Nitrogen. Creative Media Partners, LLC, 2019.

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40

Martin, Harris. Nitrification Inhibitor Effects on Potato Yields and Soil Inorganic Nitrogen. Creative Media Partners, LLC, 2019.

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41

Stu, Arnold E. Iminosugars As Glycosidase Inhibitors: Nojirimycin and Beyond. John Wiley & Sons, 1999.

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42

Dickenson, Tony. Endogenous opioids in the CNS. Edited by Paul Farquhar-Smith, Pierre Beaulieu, and Sian Jagger. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198834359.003.0019.

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Анотація:

This short and concise paper was the first to unequivocally reveal that there were endogenous opioids in the central nervous system (CNS), identify their peptide nature and sequence, and show that they exerted physiological inhibitory effects. The idea that there were natural opioids fitted with concurrent reports of opiate-binding sites, and this led to the description of multiple receptors with their own families of peptide transmitters. No truly novel opioid drugs have emerged since, and attempts to protect and manipulate the enkephalins for pain control have yet to be successful. This does not detract from this key study, which made us think about pain modulation in a different way, and subsequent work has clearly shown how endogenous opioid signalling is critical in CNS function, perhaps most importantly in endogenous pain control, such as that harnessed by placebo analgesia.

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43

Stütz, Arnold E., and H. Paulsen. Iminosugars As Glycosidase Inhibitors: Nojirimycin and Beyond. Wiley & Sons, Incorporated, John, 2020.

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44

Stütz, Arnold E., and H. Paulsen. Iminosugars As Glycosidase Inhibitors: Nojirimycin and Beyond. Wiley & Sons, Limited, John, 2004.

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45

The Cheese Effect and New Reversible Mao-A Inhibitors. Springer-Verlag, Austria, 1988.

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46

Marc, Bygdeman, Berger Gary S, and Keith Louis G, eds. Prostaglandins and their inhibitors in clinical obstetrics and gynaecology. Lancaster: MTP Press, 1986.

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47

Bygdeman, Marc. Prostaglandins and their Inhibitors in Clinical Obstetrics and Gynaecology. Springer, 2012.

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48

Hodgkiss, Andrew. Psychiatric consequences of cancer treatments: hormone and cytokine treatments. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198759911.003.0007.

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The antidepressant and neuroprotective effects of oestradiol are described. Psychiatric consequences of oophorectomy, and treatment with tamoxifen and aromatase inhibitors, are then discussed. Androgen-deprivation therapy has temporary effects on cognitive function and mood that reflect the distribution of androgen receptors in the brain. The rapid-onset adverse psychiatric effects of high-dose glucocorticoids are presented (including ‘steroid psychosis’) and a novel, non-genomic molecular mechanism highlighted. In contrast, the depressive effect of chronic glucocorticoid use is then considered.

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49

Wu, Paiyen. Effects of various protease inhibitors on protein degradation of cultured myotubes. 1996.

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50

National Comprehensive Cancer Network® (NCCN®). NCCN Guidelines for Patients® Immunotherapy Side Effects: Immune Checkpoint Inhibitors. National Comprehensive Cancer Network® (NCCN®), 2022.

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