Dissecting Receptor-Mediated Ca2+ Influx Pathways: TRP Channels and Their Native Counterparts.
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- Mori Yasuo
- Center for Integrative Bioscience, Okazaki National Research Institutes Departmet of Cell Physiology, National Institute for Physiological Sciences, Okazaki National Research Institutes School of Life Science, The Graduate University for Advanced Studies
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- Inoue Ryuji
- Department of Pharmacology, Faculty of Medicine, Kyushu University
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- Ishii Masakazu
- Center for Integrative Bioscience, Okazaki National Research Institutes Departmet of Cell Physiology, National Institute for Physiological Sciences, Okazaki National Research Institutes
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- Hara Yuji
- Center for Integrative Bioscience, Okazaki National Research Institutes Department of Information Physiology, National Institute for Physiological Sciences, Okazaki National Research Institutes School of Life Science, The Graduate University for Advanced Studies
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- Imoto Keiji
- Department of Information Physiology, National Institute for Physiological Sciences, Okazaki National Research Institutes School of Life Science, The Graduate University for Advanced Studies
Bibliographic Information
- Other Title
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- Dissecting Receptor-Mediated Ca〔2+〕 Influx Pathways: TRP Channels and Their Native Counterparts
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Abstract
Cellular stimulation from the surrounding extracellular environment via receptors and other pathways evoke activation of Ca2+-permeable cation channels that form essential signaling pathways in controlling biological responses. An important clue to understand the molecular mechanisms underlying these cation channels (tentatively termed as receptor-mediated cation channels (RMCC)) was first provided through molecular studies of the transient receptor potential (trp) protein (TRP), which controls light-induced depolarization in Drosophila photoreceptor cells. Use of the genetic information and recombinant expression technique lead to the discovery of numerous mammalian TRP homologues revealing novel RMCCs. In this review, we focus on the dramatic progress in the molecular investigation of RMCC in mammalian systems. The recent findings should provide powerful tools for the development of novel pharmaceutical targets.
Journal
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- The Japanese Journal of Pharmacology
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The Japanese Journal of Pharmacology 87 (4), 245-252, 2001
The Japanese Pharmacological Society
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Details 詳細情報について
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- CRID
- 1390282679263265536
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- NII Article ID
- 10007943949
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- NII Book ID
- AA00691188
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- COI
- 1:CAS:528:DC%2BD3MXptlKkurw%3D
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- ISSN
- 13473506
- 00215198
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- NDL BIB ID
- 6019087
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- PubMed
- 11829143
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- Web Site
- http://id.ndl.go.jp/bib/6019087
- https://ndlsearch.ndl.go.jp/books/R000000004-I6019087
- https://api.elsevier.com/content/article/PII:S0021519819302410?httpAccept=text/xml
- https://api.elsevier.com/content/article/PII:S0021519819302410?httpAccept=text/plain
- https://search.jamas.or.jp/link/ui/2002117909
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed