AbstractMolecular diversity of T-type/Cav3 Ca2+ channels is created by expression of three genes and alternative splicing of those genes. Prompted by the important role of the I–II linker in gating and surface expression of Cav3 channels, we describe here the properties of a novel variant that partially deletes this loop. The variant is abundantly expressed in rat brain, even exceeding transcripts with the complete exon 8. Electrophysiological analysis of the Δ8b variant revealed enhanced current density compared to Cav3.1a, but similar gating. Luminometry experiments revealed an increase in the expression of Δ8b channels at the plasma membrane. We conclude that alternative splicing of Cav3 channels regulates surface expression and may unde...
Cav2.1 P/Q-type voltage-gated calcium channels are essential for neurotransmission in many regions o...
Cav2.1 P/Q-type voltage-gated calcium channels are essential for neurotransmission in many regions o...
Alternative splicing is likely to be the primary source of human proteomic diversity. Our aim was to...
AbstractMolecular diversity of T-type/Cav3 Ca2+ channels is created by expression of three genes and...
Molecular diversity of T-type/Cav3 Ca2+ channels is created by expression of three genes and alterna...
AbstractAt least three genes encode T-type calcium channel α1 subunits, and identification of cDNA t...
AbstractLow voltage-activated T-type calcium channels are encoded by a family of at least three gene...
AbstractT-type calcium channels (T-channels) contribute to a wide variety of physiological functions...
AbstractAt least three genes encode T-type calcium channel α1 subunits, and identification of cDNA t...
An intramolecular interaction between a distal (DCRD) and a proximal regulatory domain (PCRD) within...
ABSTRACTSequence analysis of the human genome permitted cloning of five Ca2+-channel β2 splice varia...
AbstractNeuronal voltage-gated calcium channels generate rapid, transient intracellular calcium sign...
AbstractNeuronal voltage-gated calcium channels generate rapid, transient intracellular calcium sign...
The CACNA1G gene encodes for Cav3.1, the alpha-1G subunit of a low-voltage-activated T-type calcium ...
The CACNA1G gene encodes for Cav3.1, the alpha-1G subunit of a low-voltage-activated T-type calcium ...
Cav2.1 P/Q-type voltage-gated calcium channels are essential for neurotransmission in many regions o...
Cav2.1 P/Q-type voltage-gated calcium channels are essential for neurotransmission in many regions o...
Alternative splicing is likely to be the primary source of human proteomic diversity. Our aim was to...
AbstractMolecular diversity of T-type/Cav3 Ca2+ channels is created by expression of three genes and...
Molecular diversity of T-type/Cav3 Ca2+ channels is created by expression of three genes and alterna...
AbstractAt least three genes encode T-type calcium channel α1 subunits, and identification of cDNA t...
AbstractLow voltage-activated T-type calcium channels are encoded by a family of at least three gene...
AbstractT-type calcium channels (T-channels) contribute to a wide variety of physiological functions...
AbstractAt least three genes encode T-type calcium channel α1 subunits, and identification of cDNA t...
An intramolecular interaction between a distal (DCRD) and a proximal regulatory domain (PCRD) within...
ABSTRACTSequence analysis of the human genome permitted cloning of five Ca2+-channel β2 splice varia...
AbstractNeuronal voltage-gated calcium channels generate rapid, transient intracellular calcium sign...
AbstractNeuronal voltage-gated calcium channels generate rapid, transient intracellular calcium sign...
The CACNA1G gene encodes for Cav3.1, the alpha-1G subunit of a low-voltage-activated T-type calcium ...
The CACNA1G gene encodes for Cav3.1, the alpha-1G subunit of a low-voltage-activated T-type calcium ...
Cav2.1 P/Q-type voltage-gated calcium channels are essential for neurotransmission in many regions o...
Cav2.1 P/Q-type voltage-gated calcium channels are essential for neurotransmission in many regions o...
Alternative splicing is likely to be the primary source of human proteomic diversity. Our aim was to...