Cargando…

Ca(2+) Channels on the Move

Mostrar otras versiones (1)

Detalles Bibliográficos
Autores principales:	Taylor, Colin W., Prole, David L., Rahman, Taufiq
Formato:	Texto
Lenguaje:	English
Publicado:	American Chemical Society 2010
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048451/ http://dx.doi.org/10.1021/bi100823m

Ejemplares similares

Ca(2+) Channels on the Move
por: Taylor, Colin W., et al.
Publicado: (2009)

An NAADP-gated Two-pore Channel Targeted to the Plasma Membrane Uncouples Triggering from Amplifying Ca(2+) Signals
por: Brailoiu, Eugen, et al.
Publicado: (2010)

Identification and Analysis of Cation Channel Homologues in Human Pathogenic Fungi
por: Prole, David L., et al.
Publicado: (2012)

Identification and Analysis of Putative Homologues of Mechanosensitive Channels in Pathogenic Protozoa
por: Prole, David L., et al.
Publicado: (2013)

Identification of Intracellular and Plasma Membrane Calcium Channel Homologues in Pathogenic Parasites
por: Prole, David L., et al.
Publicado: (2011)

Exploration of inositol 1,4,5-trisphosphate (IP(3)) regulated dynamics of N-terminal domain of IP(3) receptor reveals early phase molecular events during receptor activation
por: Chandran, Aneesh, et al.
Publicado: (2019)

Cyclic AMP Recruits a Discrete Intracellular Ca(2+) Store by Unmasking Hypersensitive IP(3) Receptors
por: Konieczny, Vera, et al.
Publicado: (2017)

IP(3) Receptors Preferentially Associate with ER-Lysosome Contact Sites and Selectively Deliver Ca(2+) to Lysosomes
por: Atakpa, Peace, et al.
Publicado: (2018)

Clustering of IP(3) receptors by IP(3) retunes their regulation by IP(3) and Ca(2+)
por: Taufiq-Ur-Rahman,, et al.
Publicado: (2009)

Ca(2+) signals initiate at immobile IP(3) receptors adjacent to ER-plasma membrane junctions
por: Thillaiappan, Nagendra Babu, et al.
Publicado: (2017)

And Yet It Moves: Conformational States of the Ca(2+) Channel Pore
por: Olcese, Riccardo
Publicado: (2007)

hGAAP promotes cell adhesion and migration via the stimulation of store-operated Ca(2+) entry and calpain 2
por: Saraiva, Nuno, et al.
Publicado: (2013)

Inositol 1,4,5‐trisphosphate receptors and their protein partners as signalling hubs
por: Prole, David L., et al.
Publicado: (2016)

A genetically encoded toolkit of functionalized nanobodies against fluorescent proteins for visualizing and manipulating intracellular signalling
por: Prole, David L., et al.
Publicado: (2019)

Golgi Anti-apoptotic Proteins Are Highly Conserved Ion Channels That Affect Apoptosis and Cell Migration
por: Carrara, Guia, et al.
Publicado: (2015)

Identification of Putative Potassium Channel Homologues in Pathogenic Protozoa
por: Prole, David L., et al.
Publicado: (2012)

Unveiling some FDA-approved drugs as inhibitors of the store-operated Ca(2+) entry pathway
por: Rahman, Saifur, et al.
Publicado: (2017)

Quantal Ca(2+) release mediated by very few IP(3) receptors that rapidly inactivate allows graded responses to IP(3)
por: Rossi, Ana M., et al.
Publicado: (2021)

Reversal of HCN Channel Voltage Dependence via Bridging of the S4–S5 Linker and Post-S6
por: Prole, David L., et al.
Publicado: (2006)

Mechanisms Underlying Modulation of Neuronal KCNQ2/KCNQ3 Potassium Channels by Extracellular Protons
por: Prole, David L., et al.
Publicado: (2003)

Red fluorescent genetically encoded Ca(2+) indicators for use in mitochondria and endoplasmic reticulum
por: Wu, Jiahui, et al.
Publicado: (2014)

A Bead Aggregation Assay for Detection of Low-Affinity Protein-Protein Interactions Reveals Interactions between N-Terminal Domains of Inositol 1,4,5-Trisphosphate Receptors
por: Chavda, Alap P., et al.
Publicado: (2013)

Structural changes during HCN channel gating defined by high affinity metal bridges
por: Kwan, Daniel C.H., et al.
Publicado: (2012)

Endolysosomal Ca(2+) Signalling and Cancer Hallmarks: Two-Pore Channels on the Move, TRPML1 Lags Behind!
por: Faris, Pawan, et al.
Publicado: (2018)

Watching Ion Channels on the Move
por: Pardo, Luis A
Publicado: (2022)

On the move, lysosomal CAX drives Ca(2+) transport and motility
por: Lloyd-Evans, Emyr
Publicado: (2016)

Two-pore Channels Enter the Atomic Era: Structure of Plant TPC Revealed
por: Patel, Sandip, et al.
Publicado: (2016)

Acid-sensing ion channel 3: An analgesic target
por: Dulai, Jasdip Singh, et al.
Publicado: (2021)

Activation of IP(3) receptors requires an endogenous 1-8-14 calmodulin-binding motif
por: Sun, Yi, et al.
Publicado: (2012)

The store-operated Ca(2+) entry complex comprises a small cluster of STIM1 associated with one Orai1 channel
por: Shen, Yihan, et al.
Publicado: (2021)

Nanodomain Ca(2+) of Ca(2+) channels detected by a tethered genetically encoded Ca(2+) sensor
por: Tay, Lai Hock, et al.
Publicado: (2012)

K(Ca)2 and K(Ca)3.1 Channels in the Airways: A New Therapeutic Target
por: Orfali, Razan, et al.
Publicado: (2023)

Ca(2+)-dependent Inactivation of Ca(V)1.2 Channels Prevents Gd(3+) Block: Does Ca(2+) Block the Pore of Inactivated Channels?
por: Babich, Olga, et al.
Publicado: (2007)

Isolated pores dissected from human two-pore channel 2 are functional
por: Penny, Christopher J., et al.
Publicado: (2016)

Ca(2+) Influx in T Cells: How Many Ca(2+) Channels?
por: Feske, Stefan
Publicado: (2013)

Differential Interactions of Na(+) Channel Toxins with T-type Ca(2+) Channels
por: Sun, Hui, et al.
Publicado: (2008)

Ca(2+)-Sensitive Potassium Channels
por: Orfali, Razan, et al.
Publicado: (2023)

Comparative Ca(2+) channel contributions to intracellular Ca(2+) levels in the circadian clock
por: Plante, Amber E., et al.
Publicado: (2021)

Divergence of Ca(2+) selectivity and equilibrium Ca(2+) blockade in a Ca(2+) release-activated Ca(2+) channel
por: Yamashita, Megumi, et al.
Publicado: (2014)

Reduction of Ca(V) channel activities by Ca(2+)–CaM: inactivation or deactivation?
por: Cui, Jianmin
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_jkvhoi8prjujdumc322fglga27