| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-133 |
Sentence |
denotes |
Quantitative phosphoproteomics of murine Fmr1-KO cell lines provides new insights into FMRP-dependent signal transduction mechanisms. |
| T1 |
0-133 |
Sentence |
denotes |
Quantitative phosphoproteomics of murine Fmr1-KO cell lines provides new insights into FMRP-dependent signal transduction mechanisms. |
| TextSentencer_T2 |
134-258 |
Sentence |
denotes |
Fragile X mental retardation protein (FMRP) is an RNA-binding protein that has a major effect on neuronal protein synthesis. |
| T2 |
134-258 |
Sentence |
denotes |
Fragile X mental retardation protein (FMRP) is an RNA-binding protein that has a major effect on neuronal protein synthesis. |
| TextSentencer_T3 |
259-446 |
Sentence |
denotes |
Transcriptional silencing of the FMR1 gene leads to loss of FMRP and development of Fragile X syndrome (FXS), the most common known hereditary cause of intellectual impairment and autism. |
| T3 |
259-446 |
Sentence |
denotes |
Transcriptional silencing of the FMR1 gene leads to loss of FMRP and development of Fragile X syndrome (FXS), the most common known hereditary cause of intellectual impairment and autism. |
| TextSentencer_T4 |
447-687 |
Sentence |
denotes |
Here we utilize SILAC-based quantitative phosphoproteomics to analyze murine FMR1(-) and FMR1(+) fibroblastic cell lines derived from FMR1-KO embryos to identify proteins and phosphorylation sites dysregulated as a consequence of FMRP loss. |
| T4 |
447-687 |
Sentence |
denotes |
Here we utilize SILAC-based quantitative phosphoproteomics to analyze murine FMR1(-) and FMR1(+) fibroblastic cell lines derived from FMR1-KO embryos to identify proteins and phosphorylation sites dysregulated as a consequence of FMRP loss. |
| TextSentencer_T5 |
688-839 |
Sentence |
denotes |
We quantify FMRP-related changes in the levels of 5,023 proteins and 6,133 phosphorylation events and map them onto major signal transduction pathways. |
| T5 |
688-839 |
Sentence |
denotes |
We quantify FMRP-related changes in the levels of 5,023 proteins and 6,133 phosphorylation events and map them onto major signal transduction pathways. |
| TextSentencer_T6 |
840-1037 |
Sentence |
denotes |
Our study confirms global downregulation of the MAPK/ERK pathway and decrease in phosphorylation level of ERK1/2 in the absence of FMRP, which is connected to attenuation of long-term potentiation. |
| T6 |
840-1037 |
Sentence |
denotes |
Our study confirms global downregulation of the MAPK/ERK pathway and decrease in phosphorylation level of ERK1/2 in the absence of FMRP, which is connected to attenuation of long-term potentiation. |
| TextSentencer_T7 |
1038-1205 |
Sentence |
denotes |
We detect differential expression of several key proteins from the p53 pathway, pointing to the involvement of p53 signaling in dysregulated cell cycle control in FXS. |
| T7 |
1038-1205 |
Sentence |
denotes |
We detect differential expression of several key proteins from the p53 pathway, pointing to the involvement of p53 signaling in dysregulated cell cycle control in FXS. |
| TextSentencer_T8 |
1206-1408 |
Sentence |
denotes |
Finally, we detect differential expression and phosphorylation of proteins involved in pre-mRNA processing and nuclear transport, as well as Wnt and calcium signaling, such as PLC, PKC, NFAT, and cPLA2. |
| T8 |
1206-1408 |
Sentence |
denotes |
Finally, we detect differential expression and phosphorylation of proteins involved in pre-mRNA processing and nuclear transport, as well as Wnt and calcium signaling, such as PLC, PKC, NFAT, and cPLA2. |
| TextSentencer_T9 |
1409-1499 |
Sentence |
denotes |
We postulate that calcium homeostasis is likely affected in molecular pathogenesis of FXS. |
| T9 |
1409-1499 |
Sentence |
denotes |
We postulate that calcium homeostasis is likely affected in molecular pathogenesis of FXS. |