例句與造句

1. Common variants of SCN5A, SCN10A, and HEY2 ( this gene ) are associated with Brugada syndrome.
2. More than 10 different splice isoforms have been described for SCN5A, of which several harbour different functional properties.
3. Pathogenic mutations generally exhibit an autosomal dominant inheritance pattern, although recessive forms of SCN5A mutations are also described.
4. Scientists have also associated this syndrome with the gene SCN5A that is mutated and affects the function of the heart.
5. Furthermore, mutations in " SCN5A " can cause Brugada syndrome, cardiac conduction disease, and dilated cardiomyopathy.
6. It's difficult to find scn5a in a sentence. 用scn5a造句挺難的
7. Congenital SSS can be due to mutations of the gene responsible for formation of Alpha subunit of sodium channel ( SCN5A ).
8. Between 1996 and 1998 MMRL published the first gene, SCN5A, to be linked to idiopathic ventricular fibrillation ( IVF ).
9. Two were found to have mutations in the SCN5A gene, which regulates activity of electrically charged molecules involved in maintaining heart rhythms.
10. For a comprehensive list of all mutations see In 2013, Bezzina et al . showed that common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome.
11. Calcium has been suggested as a regulator of SCN5A protein, and the effects of calcium on SCN5A may begin to explain the mechanism by which some these mutations cause LQT3.
12. Calcium has been suggested as a regulator of SCN5A protein, and the effects of calcium on SCN5A may begin to explain the mechanism by which some these mutations cause LQT3.
13. Mutations in SCN5A, which could result in a loss and / or a gain-of-function of the channel, are associated with a spectrum of cardiac diseases.
14. The mutations associated with idiopathic ventricular fibrillation were found in a gene called SCN5A, which had already been associated with another heart disorder known as long QT syndrome, Towbin said.
15. Brugada syndrome is a relatively rare but lethal ventricular arrhythmia most commonly linked to voltage-gated sodium channel gene SCN5A mutations, but also associated with some K v channel gene sequence variants.
16. The defective gene, called SCN5A, is the blueprint for channels that convey sodium ions from outside the cell _ a critical element in the chemical-electrical transfer of energy behind each heartbeat.
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