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1 f the 116-kDa subunit of the bovine vacuolar proton translocating ATPase.
2 alternately spliced form of band 3) and the proton translocating ATPase.
3 f the Saccharomyces cerevisiae mitochondrial proton translocating ATPase.
4 bly of the F0 component of the mitochondrial proton-translocating ATPase.
5 he membrane topography of the yeast vacuolar proton-translocating ATPase a subunit (Vph1p) has been i
6 region between two housekeeping genes, uncC (proton-translocating ATPase) and murA (UDP-N-acetylgluco
9 bound F0 sector of the Escherichia coli F1F0 proton-translocating ATPase can respond to changes in me
20 c nucleotide binding subunit of the vacuolar proton-translocating ATPase (or V-ATPase) and is homolog
21 binding subunit (subunit A) of the vacuolar proton-translocating ATPase (or V-ATPase) is homologous
25 t: the sequence of probe SSA-1 contained the proton-translocating ATPase (uncC) and the entire interg
26 h the catalytic sector (V1) of vacuolar-type proton translocating ATPase (V-ATPase) and sub-58-kDa do
27 Saccharomyces cerevisiae that lack vacuolar proton-translocating ATPase (V-ATPase) activity show a w
29 e Saccharomyces cerevisiae vacuolar membrane proton-translocating ATPase (V-ATPase) can be divided in
30 ed for stable assembly of the yeast vacuolar proton-translocating ATPase (V-ATPase) during both biosy
38 the nucleotide binding sites on the vacuolar proton-translocating ATPase (V-ATPase), the role of arom
40 1 human breast cancer cells express vacuolar proton-translocating ATPase (V-ATPases) at the cell surf
44 ments equivalent to lysosomes where vacuolar proton-translocating ATPases (V-ATPases) are abundant.
48 agments of the genes for the plasma membrane proton-translocating ATPase, vacuole-ATPase, proton-tran
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