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1 atography, and fractions were incubated with calcium oxalate monohydrate.
4 ates of microcrystals, most commonly contain calcium oxalate monohydrate (COM) as the primary constit
5 be used to switch the surface morphology of calcium oxalate monohydrate (COM) back and forth, result
7 t study was undertaken to identify potential calcium oxalate monohydrate (COM) crystal-binding protei
9 a monomer, is known to inhibit the growth of calcium oxalate monohydrate (COM) crystals in renal tubu
15 alate kidney stones, the competition between calcium oxalate monohydrate (COM) formation and its inhi
16 which crystallizes in the tubules as either calcium oxalate monohydrate (COM) or calcium oxalate dih
18 of these proteins in the crystallization of calcium oxalate monohydrate (COM), the most prominent co
20 In addition, calcium oxalate dihydrate and calcium oxalate monohydrate crystal aggregates exhibit h
21 correlated with a corresponding increase in calcium oxalate monohydrate crystal attachment to the ce
22 zed in vitro inhibitor of hydroxyapatite and calcium oxalate monohydrate crystal formation, but it is
24 eraction with the positively charged face of calcium-oxalate monohydrate leads to formation of a pept
25 T techniques were able to help differentiate calcium oxalate monohydrate stones with moderate accurac
26 is regularly supersaturated with respect to calcium oxalate monohydrate, the most common solid phase
29 se features include thin concentric rings of calcium oxalate monohydrate within uric acid stones and