17 results on '"Sorrentino, Vincenzo"'
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2. A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia
3. Cardiac expression of ryanodine receptor subtype 3; a strategic component in the intracellular Ca2 + release system of Purkinje fibers in large mammalian heart
4. Chapter 2 - Power converters as interface and integration systems in hybrid AC/DC smart grids
5. PPARδ Promotes Running Endurance by Preserving Glucose
6. MECP2 mutation in male patients with non-specific X-linked mental retardation
7. A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog–Scott syndrome)
8. ATP-induced activation of expressed RyR3 at low free calcium
9. Expression of the Ryanodine Receptor Type 3 in Skeletal Muscle: A New Partner in Excitation-Contraction Coupling?
10. Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c
11. List of contributors
12. Correction to the sequence of the donor splice site of intron 2 of the GSD1b gene
13. Genomic structure and chromosomal location of the human TGFβ-receptor interacting protein-1 (TRIP-1) gene to 1p34.1
14. Structure and mutation analysis of the glycogen storage disease type 1b gene
15. Contractile impairment and structural alterations of skeletal muscles from knockout mice lacking type 1 and type 3 ryanodine receptors
16. cDNA cloning reveals a tissue specific expression of alternatively spliced transcripts of the ryanodine receptor type 3 (RyR3) calcium release channel
17. The Ryanodine Receptor Family of Intracellular Calcium Release Channels
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