Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-48 |
Sentence |
denotes |
A mutation in telethonin alters Nav1.5 function. |
T1 |
0-48 |
Sentence |
denotes |
A mutation in telethonin alters Nav1.5 function. |
TextSentencer_T2 |
49-162 |
Sentence |
denotes |
Excitable cells express a variety of ion channels that allow rapid exchange of ions with the extracellular space. |
T2 |
49-162 |
Sentence |
denotes |
Excitable cells express a variety of ion channels that allow rapid exchange of ions with the extracellular space. |
TextSentencer_T3 |
163-263 |
Sentence |
denotes |
Opening of Na(+) channels in excitable cells results in influx of Na(+) and cellular depolarization. |
T3 |
163-263 |
Sentence |
denotes |
Opening of Na(+) channels in excitable cells results in influx of Na(+) and cellular depolarization. |
TextSentencer_T4 |
264-401 |
Sentence |
denotes |
The function of Na(v)1.5, an Na(+) channel expressed in the heart, brain, and gastrointestinal tract, is altered by interacting proteins. |
T4 |
264-401 |
Sentence |
denotes |
The function of Na(v)1.5, an Na(+) channel expressed in the heart, brain, and gastrointestinal tract, is altered by interacting proteins. |
TextSentencer_T5 |
402-469 |
Sentence |
denotes |
The pore-forming alpha-subunit of this channel is encoded by SCN5A. |
T5 |
402-469 |
Sentence |
denotes |
The pore-forming alpha-subunit of this channel is encoded by SCN5A. |
TextSentencer_T6 |
470-604 |
Sentence |
denotes |
Genetic perturbations in SCN5A cause type 3 long QT syndrome and type 1 Brugada syndrome, two distinct heritable arrhythmia syndromes. |
T6 |
470-604 |
Sentence |
denotes |
Genetic perturbations in SCN5A cause type 3 long QT syndrome and type 1 Brugada syndrome, two distinct heritable arrhythmia syndromes. |
TextSentencer_T7 |
605-840 |
Sentence |
denotes |
Mutations in SCN5A are also associated with increased prevalence of gastrointestinal symptoms, suggesting that the Na(+) channel plays a role in normal gastrointestinal physiology and that alterations in its function may cause disease. |
T7 |
605-840 |
Sentence |
denotes |
Mutations in SCN5A are also associated with increased prevalence of gastrointestinal symptoms, suggesting that the Na(+) channel plays a role in normal gastrointestinal physiology and that alterations in its function may cause disease. |
TextSentencer_T8 |
841-1039 |
Sentence |
denotes |
We collected blood from patients with intestinal pseudo-obstruction (a disease associated with abnormal motility in the gut) and screened for mutations in SCN5A and ion channel-interacting proteins. |
T8 |
841-1039 |
Sentence |
denotes |
We collected blood from patients with intestinal pseudo-obstruction (a disease associated with abnormal motility in the gut) and screened for mutations in SCN5A and ion channel-interacting proteins. |
TextSentencer_T9 |
1040-1156 |
Sentence |
denotes |
A 42-year-old male patient was found to have a mutation in the gene TCAP, encoding for the small protein telethonin. |
T9 |
1040-1156 |
Sentence |
denotes |
A 42-year-old male patient was found to have a mutation in the gene TCAP, encoding for the small protein telethonin. |
TextSentencer_T10 |
1157-1314 |
Sentence |
denotes |
Telethonin was found to be expressed in the human gastrointestinal smooth muscle, co-localized with Na(v)1.5, and co-immunoprecipitated with sodium channels. |
T10 |
1157-1314 |
Sentence |
denotes |
Telethonin was found to be expressed in the human gastrointestinal smooth muscle, co-localized with Na(v)1.5, and co-immunoprecipitated with sodium channels. |
TextSentencer_T11 |
1315-1493 |
Sentence |
denotes |
Expression of mutated telethonin, when co-expressed with SCN5A in HEK 293 cells, altered steady state activation kinetics of SCN5A, resulting in a doubling of the window current. |
T11 |
1315-1493 |
Sentence |
denotes |
Expression of mutated telethonin, when co-expressed with SCN5A in HEK 293 cells, altered steady state activation kinetics of SCN5A, resulting in a doubling of the window current. |
TextSentencer_T12 |
1494-1606 |
Sentence |
denotes |
These results suggest a new role for telethonin, namely that telethonin is a sodium channel-interacting protein. |
T12 |
1494-1606 |
Sentence |
denotes |
These results suggest a new role for telethonin, namely that telethonin is a sodium channel-interacting protein. |
TextSentencer_T13 |
1607-1718 |
Sentence |
denotes |
Also, mutations in telethonin can alter Na(v)1.5 kinetics and may play a role in intestinal pseudo-obstruction. |
T13 |
1607-1718 |
Sentence |
denotes |
Also, mutations in telethonin can alter Na(v)1.5 kinetics and may play a role in intestinal pseudo-obstruction. |