Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-94 |
Sentence |
denotes |
Urinary β-galactosidase stimulates Ca2+ transport by stabilizing TRPV5 at the plasma membrane. |
T1 |
0-94 |
Sentence |
denotes |
Urinary β-galactosidase stimulates Ca2+ transport by stabilizing TRPV5 at the plasma membrane. |
T1 |
0-94 |
Sentence |
denotes |
Urinary β-galactosidase stimulates Ca2+ transport by stabilizing TRPV5 at the plasma membrane. |
TextSentencer_T2 |
95-319 |
Sentence |
denotes |
Transcellular Ca(2+) transport in the late distal convoluted tubule and connecting tubule (DCT2/CNT) of the kidney is a finely controlled process mediated by the transient receptor potential vanilloid type 5 (TRPV5) channel. |
T2 |
95-319 |
Sentence |
denotes |
Transcellular Ca(2+) transport in the late distal convoluted tubule and connecting tubule (DCT2/CNT) of the kidney is a finely controlled process mediated by the transient receptor potential vanilloid type 5 (TRPV5) channel. |
T2 |
95-319 |
Sentence |
denotes |
Transcellular Ca(2+) transport in the late distal convoluted tubule and connecting tubule (DCT2/CNT) of the kidney is a finely controlled process mediated by the transient receptor potential vanilloid type 5 (TRPV5) channel. |
TextSentencer_T3 |
320-499 |
Sentence |
denotes |
A complex-type-N-glycan bound at the extracellular residue Asn358 of TRPV5 through post-translational glycosylation has been postulated to regulate the activity of TRPV5 channels. |
T3 |
320-499 |
Sentence |
denotes |
A complex-type-N-glycan bound at the extracellular residue Asn358 of TRPV5 through post-translational glycosylation has been postulated to regulate the activity of TRPV5 channels. |
T3 |
320-499 |
Sentence |
denotes |
A complex-type-N-glycan bound at the extracellular residue Asn358 of TRPV5 through post-translational glycosylation has been postulated to regulate the activity of TRPV5 channels. |
TextSentencer_T4 |
500-804 |
Sentence |
denotes |
Using in vitro Ca(2+) transport assays, immunoblot analysis, immunohistochemistry, patch clamp electrophysiology and total internal reflection fluorescence microscopy, it is demonstrated that the glycosidase β-galactosidase (β-gal), an enzyme that hydrolyzes galactose, stimulates TRPV5 channel activity. |
T4 |
500-804 |
Sentence |
denotes |
Using in vitro Ca(2+) transport assays, immunoblot analysis, immunohistochemistry, patch clamp electrophysiology and total internal reflection fluorescence microscopy, it is demonstrated that the glycosidase β-galactosidase (β-gal), an enzyme that hydrolyzes galactose, stimulates TRPV5 channel activity. |
T4 |
500-804 |
Sentence |
denotes |
Using in vitro Ca(2+) transport assays, immunoblot analysis, immunohistochemistry, patch clamp electrophysiology and total internal reflection fluorescence microscopy, it is demonstrated that the glycosidase β-galactosidase (β-gal), an enzyme that hydrolyzes galactose, stimulates TRPV5 channel activity. |
TextSentencer_T5 |
805-992 |
Sentence |
denotes |
However, the activity of the non-glycosylated TRPV(N358Q) mutant was not altered in the presence of β-gal, showing that the stimulation is dependent on the presence of the TRPV5 N-glycan. |
T5 |
805-992 |
Sentence |
denotes |
However, the activity of the non-glycosylated TRPV(N358Q) mutant was not altered in the presence of β-gal, showing that the stimulation is dependent on the presence of the TRPV5 N-glycan. |
T5 |
805-992 |
Sentence |
denotes |
However, the activity of the non-glycosylated TRPV(N358Q) mutant was not altered in the presence of β-gal, showing that the stimulation is dependent on the presence of the TRPV5 N-glycan. |
TextSentencer_T6 |
993-1227 |
Sentence |
denotes |
In addition, β-gal was found to stimulate transcellular Ca(2+) transport in isolated mouse primary DCT2/CNT cells. β-gal expression was detected in the apical membrane of the proximal tubules, and the protein was found in mouse urine. |
T6 |
993-1227 |
Sentence |
denotes |
In addition, β-gal was found to stimulate transcellular Ca(2+) transport in isolated mouse primary DCT2/CNT cells. β-gal expression was detected in the apical membrane of the proximal tubules, and the protein was found in mouse urine. |
T6 |
993-1227 |
Sentence |
denotes |
In addition, β-gal was found to stimulate transcellular Ca(2+) transport in isolated mouse primary DCT2/CNT cells. β-gal expression was detected in the apical membrane of the proximal tubules, and the protein was found in mouse urine. |
TextSentencer_T7 |
1228-1327 |
Sentence |
denotes |
In summary, β-gal is present in the pro-urine from where it is thought to stimulate TRPV5 activity. |
T7 |
1228-1327 |
Sentence |
denotes |
In summary, β-gal is present in the pro-urine from where it is thought to stimulate TRPV5 activity. |
T7 |
1228-1327 |
Sentence |
denotes |
In summary, β-gal is present in the pro-urine from where it is thought to stimulate TRPV5 activity. |