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Molecular movements underlying voltage-dependent regulation of the CaV2.1 channel

Biophysical journal, 2022-02, Vol.121 (3), p.25a-25a

2022

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Ginsenoside Rg3 Bile Salt-Phosphatidylcholine-Based Mixed Micelles: Design, Characterization, and Evaluation

Chemical and Pharmaceutical Bulletin, 2015/05/01, Vol.63(5), pp.361-368

2015

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A role for the budding yeast separase, Esp1, in Ty1 element retrotransposition

PLoS genetics, 2015-03, Vol.11 (3), p.e1005109-e1005109

2015

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Efficient removal of aqueous hexavalent chromium by activated carbon derived from Bermuda grass

Journal of colloid and interface science, 2020-02, Vol.560, p.649-658

2020

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Regulation of CaV2.1-channels by the membrane potential

Biophysical journal, 2024-02, Vol.123 (3), p.13a-13a

2024

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Cav2.1 channels divide into two populations at resting membrane potentials

Biophysical journal, 2023-02, Vol.122 (3), p.104a-104a

2023

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Selective G-protein inhibition of CaV2.2 (n-type) calcium channel voltage-sensor domains

Biophysical journal, 2024-02, Vol.123 (3), p.114a-114a

2024

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Investigating Kv7.4 voltage sensor movement with pulsed voltage-clamp fluorometry

Biophysical journal, 2024-02, Vol.123 (3), p.526a-526a

2024

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Synthesis of Ferrosoferric Oxide‐graphene Oxide Nanocomposite by Isoelectric Point Method for the Detection of Catechol

Electroanalysis (New York, N.Y.), 2020-02, Vol.32 (2), p.412-421

2020

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Further characterization of two oppositely acting, epilepsy-associated mutations at position H310 of Kv1.2 (KCNA2) channels

Biophysical journal, 2023-02, Vol.122 (3), p.254a-254a

2023

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Gβγ induces reluctant VSD-I activation in CaV2.2 (n-type) voltage-gated calcium channels

Biophysical journal, 2023-02, Vol.122 (3), p.310a-311a

2023

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Arrhythmia mutations in calmodulin can disrupt cooperativity of Ca2+ binding and cause misfolding

The Journal of physiology, 2020-03, Vol.598 (6), p.1169-1186

2020

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Haplotype-resolved assembly of the mule duck genome using high-fidelity sequencing technology

PloS one, 2024-07, Vol.19 (7), p.e0305914

2024

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A highly selective H/D exchange reaction of 1,4-dihydropyridinesElectronic supplementary information (ESI) available. See DOI: 10.1039/c9ob00575g

2019-04

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Simultaneous determination of catechol and hydroquinone with L-cysteine and nickel cobaltite Co-Functionalised Graphene Oxide Modified Glassy Carbon Electrode

International journal of environmental analytical chemistry, 2023-03, Vol.103 (4), p.899-914

2023

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Arrhythmia mutations in calmodulin can disrupt cooperativity of Ca 2+ binding and cause misfolding

The Journal of physiology, 2020-03, Vol.598 (6), p.1169-1186

2020

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Arrhythmogenic Calmodulin Mutations Can Disrupt the Globular Structure and Uncouple Ca2+ Binding Cooperativity

Biophysical journal, 2020-02, Vol.118 (3), p.106a-106a

2020

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A highly selective H/D exchange reaction of 1,4-dihydropyridines

Organic & biomolecular chemistry, 2019-04, Vol.17 (15), p.3845-3852

2019

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Adsorption of divalent cadmium by calcified iron-embedded carbon beads

RSC advances, 2020-02, Vol.1 (11), p.6277-6286

2020

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An epilepsy-associated K V 1.2 charge-transfer-center mutation impairs K V 1.2 and K V 1.4 trafficking

Proceedings of the National Academy of Sciences - PNAS, 2022-04, Vol.119 (17), p.e2113675119

2022

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Arrhythmia mutations in calmodulin cause conformational changes that affect interactions with the cardiac voltage-gated calcium channel

Proceedings of the National Academy of Sciences - PNAS, 2018-11, Vol.115 (45), p.E10556-E10565

2018

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Ca v 2.1 channels divide into two populations at resting membrane potentials

Biophysical journal, 2023-02, Vol.122 (3S1), p.104a

2023

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Multigenic, dominant-negative loss-of-function caused by an epilepsy-associated mutation in Kv1.2 (KCNA2)

Biophysical journal, 2022-02, Vol.121 (3), p.390a-390a

2022

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An epilepsy-associated KV1.2 charge-transfer-center mutation impairs KV1.2 and KV1.4 trafficking

Proceedings of the National Academy of Sciences - PNAS, 2022-04, Vol.119 (17), p.1-e2113675119

2022

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Synthesis and electrochemical properties of coaxial-cable nanostructure carbon wrapped manganese oxide as anode for lithium ion batteries

Polyhedron, 2020-05, Vol.181, p.114436, Article 114436

2020

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Molecular movements underlying voltage-dependent regulation of the CaV2.1 channel

Ginsenoside Rg3 Bile Salt-Phosphatidylcholine-Based Mixed Micelles: Design, Characterization, and Evaluation

A role for the budding yeast separase, Esp1, in Ty1 element retrotransposition

Efficient removal of aqueous hexavalent chromium by activated carbon derived from Bermuda grass

Regulation of CaV2.1-channels by the membrane potential

Cav2.1 channels divide into two populations at resting membrane potentials

Selective G-protein inhibition of CaV2.2 (n-type) calcium channel voltage-sensor domains

Investigating Kv7.4 voltage sensor movement with pulsed voltage-clamp fluorometry

Synthesis of Ferrosoferric Oxide‐graphene Oxide Nanocomposite by Isoelectric Point Method for the Detection of Catechol

Further characterization of two oppositely acting, epilepsy-associated mutations at position H310 of Kv1.2 (KCNA2) channels

Gβγ induces reluctant VSD-I activation in CaV2.2 (n-type) voltage-gated calcium channels

Arrhythmia mutations in calmodulin can disrupt cooperativity of Ca2+ binding and cause misfolding

Haplotype-resolved assembly of the mule duck genome using high-fidelity sequencing technology

A highly selective H/D exchange reaction of 1,4-dihydropyridinesElectronic supplementary information (ESI) available. See DOI: 10.1039/c9ob00575g

Simultaneous determination of catechol and hydroquinone with L-cysteine and nickel cobaltite Co-Functionalised Graphene Oxide Modified Glassy Carbon Electrode

Arrhythmia mutations in calmodulin can disrupt cooperativity of Ca 2+ binding and cause misfolding

Arrhythmogenic Calmodulin Mutations Can Disrupt the Globular Structure and Uncouple Ca2+ Binding Cooperativity

A highly selective H/D exchange reaction of 1,4-dihydropyridines

Adsorption of divalent cadmium by calcified iron-embedded carbon beads

An epilepsy-associated K V 1.2 charge-transfer-center mutation impairs K V 1.2 and K V 1.4 trafficking

Arrhythmia mutations in calmodulin cause conformational changes that affect interactions with the cardiac voltage-gated calcium channel

Ca v 2.1 channels divide into two populations at resting membrane potentials

Multigenic, dominant-negative loss-of-function caused by an epilepsy-associated mutation in Kv1.2 (KCNA2)

An epilepsy-associated KV1.2 charge-transfer-center mutation impairs KV1.2 and KV1.4 trafficking

Synthesis and electrochemical properties of coaxial-cable nanostructure carbon wrapped manganese oxide as anode for lithium ion batteries

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