Modeling of Tritium Retention in TFTR

Blanchard, W; Brooks, J N; Budny, R V; Hogan, J T; Hosea, J; Skinner, C H

doi:10.2172/2683

Cited by 4 publications

(4 citation statements)

References 2 publications

(4 reference statements)

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“…APETx2 has no effect on ASIC1a or ASIC2a+ASIC3, however, it does potentiate ASIC1b and ASIC2a homomers in the low micromolar range (1-10 μM) [248,250,586]. APETx2 however also inhibits voltage-gated Na + channels [93,836]. IC 50 value for A-317567 was determined using high throughput electrophysiology on human ASIC3 expressed in HEK293 cells [563].…”

Section: Further Reading On Acid-sensing (Proton-gated) Ion Channels ...mentioning

confidence: 99%

THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Ion channels

Alexander

Mathie

Peters

et al. 2021

British J Pharmacology

203

167

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The Concise Guide to PHARMACOLOGY 2021/22 is the fifth in this series of biennial publications. The Concise Guide provides concise overviews, mostly in tabular format, of the key properties of nearly 1900 human drug targets with an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (https://www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. Although the Concise Guide constitutes over 500 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point‐in‐time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/bph.15539. Ion channels are one of the six major pharmacological targets into which the Guide is divided, with the others being: G protein‐coupled receptors, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid‐2021, and supersedes data presented in the 2019/20, 2017/18, 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology (NC‐IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate.

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Section: Further Reading On Acid-sensing (Proton-gated) Ion Channels ...mentioning

confidence: 99%

THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Ion channels

Alexander

Mathie

Peters

et al. 2021

British J Pharmacology

203

167

View full text Add to dashboard Cite

show abstract

“…APETx2 has no effect on ASIC1a or ASIC2a+ASIC3, however, it does potentiate ASIC1b and ASIC2a homomers in the low micromolar range (1-10 μM) [228,230,544]. APETx2 however also inhibits voltage-gated Na + channels [92,776]. IC 50 value for A-317567 was determined using high throughput electrophysiology on human ASIC3 expressed in HEK293 cells [521].…”

Section: Channel Blockersmentioning

confidence: 99%

THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: Ion channels

Alexander

Mathie

Peters

et al. 2019

British J Pharmacology

294

248

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The Concise Guide to PHARMACOLOGY 2019/20 is the fourth in this series of biennial publications. The Concise Guide provides concise overviews of the key properties of nearly 1800 human drug targets with an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (http://www.guidetopharmacology.org/), which provides more detailed views of target and ligand properties. Although the Concise Guide represents approximately 400 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point‐in‐time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/10.1111/bph.14749. Ion channels are one of the six major pharmacological targets into which the Guide is divided, with the others being: G protein‐coupled receptors, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid‐2019, and supersedes data presented in the 2017/18, 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the International Union of Basic and Clinical Pharmacology Committee on Receptor Nomenclature and Drug Classification (NC‐IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate.

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“…To understand the differences seen in the two probing cases, we derived the effective masses for perpendicular and parallel conditions [13], using the definition of the energy band that includes the nonparabolicity factor α [14]. The second order derivation turns out to show a direct difference in the effective masses if one probes the electrons for a position far up in the valley, in the parallel or perpendicular direction.…”

Section: Thz-pump/thz-probe Spectroscopymentioning

confidence: 99%

Terahertz nonlinear spectroscopy of free-carriers in direct bandgap semiconductors

Razzari

Blanchard

et al. 2010

Terahertz Emitters, Receivers, and Applications

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Nonlinear dynamics of free-carriers in direct bandgap semiconductors at terahertz (THz) frequencies is studied using intense few-cycle pulses. Techniques as Z-scan, THz-pump / THz-probe, and optical-pump/ THz-probe are employed to explore nonlinear interactions in both n-doped and photoexcited systems. The physical mechanism that gives rise to such interactions is found to be intervalley scattering.

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Modeling of Tritium Retention in TFTR

Cited by 4 publications

References 2 publications

THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Ion channels

THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Ion channels

THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: Ion channels

Terahertz nonlinear spectroscopy of free-carriers in direct bandgap semiconductors

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