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8 el mutated in cystic fibrosis (CF) patients, is opened by ATP binding to two cytosolic nucleotide bin
13 rodotoxin-sensitive sodium ion (Na+) channel is opened by cellular depolarization and favors the pass
14 transient receptor potential (TRPC) channels are opened by classical signal transduction events initi
15 anistic model explaining how the fusion pore is opened by conformational changes in the SNARE complex
18 regulated by sulfonylurea receptor 1 (SUR1), is opened by depletion of ATP and, when opened, causes c
19 f infancy generated KATP channels that could be opened by diazoxide but not in response to metabolic
20 the produced 1-azonia-bicyclo[3.2.0]heptane is opened by different nucleophiles (cyanide, azide, or
21 to the RAM products its double strand region is opened by displacement, therefore, its fluorophore re
24 plugin works with any kind of data that can be opened by jMRUI and outputs in extensible markup lang
27 L encodes a channel in Escherichia coli that is opened by membrane stretch force, probably serving as
28 mechanoelectrical transducer (MET) channels are opened by movement of the bundle in the excitatory d
29 2+ through plasma membrane ion channels that are opened by nicotinic stimulation and/or depolarizatio
30 hen either wild-type MscL or the G22C mutant was opened by osmotic pressure difference; rates of rele
33 When it was applied after the channel had been opened by PKA phosphorylation, cyclophilin A increa
34 the ring-shaped chromosomal cohesin complex is opened by proteolytic cleavage to release pairs of si
41 is present in a secondary structure that can be opened by the wild-type polymerase but not by the mut
42 o the solution of some of these problems has been opened by the discovery of liquid-liquid immiscibil
47 esulted from Ca(2+) entry through VSCCs that were opened by the electrotonic spread of the NMDAR-medi
50 , we demonstrate that the verdoheme ring can be opened by treatment with aqueous formic acid to give
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