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Работы, на которые ссылается эта работа

Работ: 102

Работа: Ferula sesquiterpenes, ferutinin, galbanic acid and karatavic acid, suppress thymocyte volume regulation and proliferation by blocking the volume-sensitive anion channel

  1. Influence of plant terpenoids on the permeability of mitochondria and lipid bilayers

    Andrey Y. Abramov, Maria Zamaraeva, Albert Hagelgans +2

    СтатьяPlant chemical constituents analysisBiochimica et Biophysica Acta (BBA) - Biomembranes2001Цитирований: 7
    ABI

  2. Leucine-rich repeat containing 8A (LRRC8A) is essential for T lymphocyte development and function

    Lalit Kumar, Janet Chou, Christina Yee +8

    Статья2014Цитирований: 7
    ABI

  3. Structure of the human volume regulated anion channel

    Jennifer M. Kefauver, Kei Saotome, Adrienne E. Dubin +10

    Статья2018Цитирований: 7
    ABI

  4. Cryo-EM structures of the human volume-regulated anion channel LRRC8

    Go Kasuya, Takanori Nakane, Takeshi Yokoyama +16

    Статья2018Цитирований: 7
    ABI

  5. Ionophoretic properties of ferutinin

    Maria Zamaraeva, Albert Hagelgans, Andrey Y. Abramov +4

    СтатьяBiochemical Analysis and Sensing TechniquesCell Calcium1997Цитирований: 7
    ABI

  6. Sulphonic acid derivatives as probes of pore properties of volume‐regulated anion channels in endothelial cells

    Guy Droogmans, Chantal Maertens, Jean Prenen +1

    Статья1999Цитирований: 7
    ABI

  7. Metabolic Profile, Bioactivities, and Variations in the Chemical Constituents of Essential Oils of the Ferula Genus (Apiaceae)

    Priyankaraj Sonigra, Mukesh Meena

    Обзорная статья2021Цитирований: 7
    ABI

  8. Tannins, novel inhibitors of the volume regulation and the volume-sensitive anion channel

    Nargiza A. Tsiferova, Ozoda J. Khamidova, Anvar Amonov +6

    СтатьяMedicinal Plants and NeuroprotectionEuropean Pharmaceutical Journal2019Цитирований: 7
    ABI

  9. Distinct contributions of LRRC8A and its paralogs to the VSOR anion channel from those of the ASOR anion channel

    Kaori Sato, Tomohiro Numata, Ryuji Inoue +2

    Статья2016Цитирований: 6
    ABI

  10. Chemistry and Sources of Mono- and Bicyclic Sesquiterpenes from Ferula Species

    Antonio G. González, Jaime Bermejo Barrera

    Глава1995Цитирований: 6
    ABI

  11. Voltage-dependent block of endothelial volume-regulated anion channels by calix[4]arenes

    Guy Droogmans, Jean Prenen, Jan Eggermont +2

    Статья1998Цитирований: 6
    ABI

  12. Cell Death Induction and Protection by Activation of Ubiquitously Expressed Anion/Cation Channels. Part 2: Functional and Molecular Properties of ASOR/PAC Channels and Their Roles in Cell Volume Dysregulation and Acidotoxic Cell Death

    Yasunobu Okada, Kaori Sato, Ravshan Z. Sabirov +1

    Обзорная статьяIon channel regulation and functionFrontiers in Cell and Developmental Biology2021Цитирований: 5
    ABI

  13. The ATP-Releasing Maxi-Cl Channel: Its Identity, Molecular Partners, and Physiological/Pathophysiological Implications

    Ravshan Z. Sabirov, Md. Shahidul Islam, Toshiaki Okada +4

    Обзорная статьяIon channel regulation and functionLife2021Цитирований: 5
    ABI

  14. Properties, Structures, and Physiological Roles of Three Types of Anion Channels Molecularly Identified in the 2010’s

    Yasunobu Okada, Ravshan Z. Sabirov, Petr G. Merzlyak +2

    Обзорная статьяIon channel regulation and functionFrontiers in Physiology2021Цитирований: 5
    ABI

  15. Amazing chloride channels: an overview

    B. Nilius, G. Droogmans

    Обзорная статья2003Цитирований: 5
    ABI

  16. Cryo-EM structures of the DCPIB-inhibited volume-regulated anion channel LRRC8A in lipid nanodiscs

    David M. Kern, SeCheol Oh, Richard K. Hite +1

    Статья2019Цитирований: 5
    ABI

  17. Cryo-EM structure of the volume-regulated anion channel LRRC8D isoform identifies features important for substrate permeation

    Ryoki Nakamura, Tomohiro Numata, Go Kasuya +15

    Статья2020Цитирований: 5
    ABI

  18. Natural and synthetic flavonoids, novel blockers of the volume-regulated anion channels, inhibit endothelial cell proliferation

    Yucong Xue, Honglin Li, Yuanyuan Zhang +12

    Статья2018Цитирований: 5
    ABI

  19. Hormonal control of T-cell development in health and disease

    Wilson Savino, Daniella Arêas Mendes‐da‐Cruz, Ailin Lepletier +1

    Обзорная статья2015Цитирований: 5
    ABI

  20. Chronic inflammation in the etiology of disease across the life span

    David Furman, Judith Campisi, Eric Verdin +17

    Обзорная статья2019Цитирований: 5
    ABI

  21. SWELL1 promotes cell growth and metastasis of hepatocellular carcinoma in vitro and in vivo

    Panpan Lu, Qiang Ding, Xin Li +6

    Статья2019Цитирований: 4
    ABI

  22. VRAC: molecular identification as LRRC8 heteromers with differential functions

    Thomas J. Jentsch, Darius Lutter, Rosa Planells‐Cases +2

    Обзорная статья2015Цитирований: 4
    ABI

  23. Annexin A2-S100A10 Represents the Regulatory Component of Maxi-Cl Channel Dependent on Protein Tyrosine Dephosphorylation and Intracellular Ca²⁺

    Md. Rafiqul Islam, Toshiaki Okada, Petr G. Merzlyak +4

    СтатьяS100 Proteins and AnnexinsCellular Physiology and Biochemistry2020Цитирований: 4
    ABI

  24. Blockers of volume-activated Cl? currents inhibit endothelial cell proliferation

    Thomas Voets, Geza Sz�cs, Guy Droogmans +1

    Статья1995Цитирований: 4
    ABI

  25. Cell cycle‐dependent activity of the volume‐ and Ca<sup>2+</sup>‐activated anion currents in Ehrlich lettre ascites cells

    Thomas Kjær Klausen, Andreas Bergdahl, Charlotte Hougaard +3

    Статья2006Цитирований: 3
    ABI