Pages that link to "Q28291989"
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The following pages link to The structure of the gene encoding the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3) (Q28291989):
Displaying 15 items.
- Structure and alternative splicing of the gene encoding alpha1I, a human brain T calcium channel alpha1 subunit (Q22003801) (← links)
- Triad proteins and intracellular Ca2+ transients during development of human skeletal muscle cells in aneural and innervated cultures (Q24290849) (← links)
- Malignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscle (Q24676753) (← links)
- Terminal intron dinucleotide sequences do not distinguish between U2- and U12-dependent introns (Q28276093) (← links)
- Parathyroid cells express dihydropyridine-sensitive cation currents and L-type calcium channel subunits (Q30992233) (← links)
- AT-AC pre-mRNA splicing mechanisms and conservation of minor introns in voltage-gated ion channel genes (Q33595931) (← links)
- Genetic disorders of neuromuscular ion channels (Q34811193) (← links)
- Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family (Q35054061) (← links)
- Ethanol regulates calcium channel subunits by protein kinase C delta -dependent and -independent mechanisms. (Q41738910) (← links)
- U1-mediated exon definition interactions between AT-AC and GT-AG introns (Q42525630) (← links)
- Cloning, sequencing and identification of single nucleotide polymorphisms of partial sequence on the porcine CACNA1S gene (Q43866365) (← links)
- A novel mutation in CACNA1S gene associated with hypokalemic periodic paralysis which has a gender difference in the penetrance. (Q45981184) (← links)
- Alternative splicing of a short cassette exon in alpha1B generates functionally distinct N-type calcium channels in central and peripheral neurons (Q47954183) (← links)
- An integrated map of the human regulator of complement activation (RCA) gene cluster on 1q32 (Q59273674) (← links)
- Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis (Q73299439) (← links)