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1                     The ATP7A gene encodes a copper-transporting ATPase.
2 e Menkes disease gene (MNK), which encodes a copper-transporting ATPase.
3  to these disorders encode highly homologous copper transporting ATPases.
4 sh the key catalytic properties of the ATP7B copper-transporting ATPase and provide a foundation for
5 ochaperone Atox1 directly interacts with the copper-transporting ATPases and plays a critical role in
6                                          The copper-transporting ATPase ATP7A has an essential role i
7                                              Copper-transporting ATPase ATP7A is essential for mammal
8                                          The copper-transporting ATPases ATP7A and ATP7B play a centr
9 e for the phenotype has been identified as a copper transporting ATPase ( ATP7A ).
10 of-function mutations in the gene encoding a copper-transporting ATPase (Atp7a) on the X chromosome.
11                                          The copper-transporting ATPase ATP7B has a dual intracellula
12                                              Copper-transporting ATPase ATP7B is essential for human
13                                          The copper-transporting ATPase ATP7B is essential for normal
14                                              Copper-transporting ATPase ATP7B is essential for normal
15  Primary sequence analysis suggests that the copper-transporting ATPase ATP7B or the Wilson's disease
16 load caused by mutations in a liver-specific copper-transporting ATPase, ATP7B.
17 myces cerevisiae deficient in the homologous copper-transporting ATPase CCC2, suggesting that this pr
18        Collectively, these data suggest that copper-transporting ATPases, CopA and ATP7A, in both bac
19                                              Copper-transporting ATPases differ from other P-type ATP
20         Wilson's disease protein (WNDP) is a copper-transporting ATPase essential for normal distribu
21                       The Atp7b protein is a copper-transporting ATPase expressed predominantly in th
22 nding domain of WNDP and is conserved in all copper-transporting ATPases from bacteria to mammals; ho
23         The WD protein functions as a P-type copper transporting ATPase in the Golgi but any action i
24 idating the function and localization of the copper-transporting ATPases in mammalian cells and provi
25                    Human Wilson protein is a copper-transporting ATPase located in the secretory path
26     The Wilson's disease protein (WNDP) is a copper-transporting ATPase regulating distribution of co
27 protein, alpha-catenin, tubulin alpha-chain, copper-transporting ATPase, salivary gland protein SGS-3
28              The Wilson disease protein is a copper transporting ATPase shown to play a critical role
29 escued by knockdown of ATP7A, a trans-Golgi, copper-transporting ATPase that traffics to the plasma m
30  mutant of Escherichia coli lacking the CopA copper-transporting ATPase was hypersensitive to killing
31  is caused by mutations in a gene encoding a copper-transporting ATPase (Wilson's disease protein, WN
32 reshold for copper-dependent movement of the copper-transporting ATPases within the secretory compart

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