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PubMed:28518143 JSONTXT

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LitCoin-entities-OrganismTaxon-PD

Id Subject Object Predicate Lexical cue db_id
T1 554-558 OrganismTaxon denotes rats NCBItxid:10118|NCBItxid:10116|NCBItxid:10114

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T10 1419-1590 Sentence denotes In turn, these effects disrupt the structure and function of the mitochondria and the cell gap junction, result in the reduced ATP synthesis and the increased ATP leakage.
T11 1591-1760 Sentence denotes Stimulation of CaSR significantly attenuates HG-induced abnormal myocardial energy metabolism, suggesting CaSR would be a promising potential therapeutic target for DCM.
T7 981-1162 Sentence denotes In contrast, HG increased extracellular ATP concentration, the expression of gp78, mitochondrial fission proteins (Fis1, Drp1), and the ubiquitination levels of Mfn1, Mfn2 and Cx43.
T8 1163-1241 Sentence denotes Moreover, CaSR agonist and gp78-siRNA significantly reduced the above changes.
T9 1242-1418 Sentence denotes Taken together, these results suggest that HG induces myocardial energy metabolism disorder via decrease of CaSR expression, and activation of gp78-ubiquitin proteasome system.
T1 0-129 Sentence denotes Calcium sensing receptor protects high glucose-induced energy metabolism disorder via blocking gp78-ubiquitin proteasome pathway.
T2 130-230 Sentence denotes Diabetic cardiomyopathy (DCM) is a major complication and fatal cause of the patients with diabetes.
T3 231-409 Sentence denotes The calcium sensing receptor (CaSR) is a G protein-coupled receptor, which is involved in maintaining calcium homeostasis, regulating cell proliferation and apoptosis, and so on.
T4 410-607 Sentence denotes In our previous study, we found that CaSR expression, intracellular calcium levels and cardiac function were all significantly decreased in DCM rats; however, the exact mechanism are not clear yet.
T5 608-769 Sentence denotes The present study revealed the protective role of CaSR in myocardial energy metabolism disorder induced by high glucose (HG) as well as the underlying mechanism.
T6 770-980 Sentence denotes Here, we demonstrated that HG decreased the expression of CaSR, mitochondrial fusion proteins (Mfn1, Mfn2), cell gap junction related proteins (Cx43, β-catenin, N-cadherin), and intracellular ATP concentration.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
13003 0-24 GeneOrGeneProduct denotes Calcium sensing receptor NCBIGene:24247
13004 39-46 ChemicalEntity denotes glucose MESH:D005947
13005 62-81 DiseaseOrPhenotypicFeature denotes metabolism disorder MESH:D008659
13006 95-99 GeneOrGeneProduct denotes gp78 NCBIGene:361367
13007 130-153 DiseaseOrPhenotypicFeature denotes Diabetic cardiomyopathy MESH:D058065
13008 155-158 DiseaseOrPhenotypicFeature denotes DCM MESH:D002311
13009 207-215 OrganismTaxon denotes patients NCBITaxon:9606
13010 221-229 DiseaseOrPhenotypicFeature denotes diabetes MESH:D003920
13011 235-259 GeneOrGeneProduct denotes calcium sensing receptor NCBIGene:24247
13012 261-265 GeneOrGeneProduct denotes CaSR NCBIGene:24247
13013 272-298 GeneOrGeneProduct denotes G protein-coupled receptor NCBIGene:24247
13014 333-340 ChemicalEntity denotes calcium MESH:D002118
13015 447-451 GeneOrGeneProduct denotes CaSR NCBIGene:24247
13016 478-485 ChemicalEntity denotes calcium MESH:D002118
13017 550-553 DiseaseOrPhenotypicFeature denotes DCM MESH:D002311
13018 554-558 OrganismTaxon denotes rats NCBITaxon:10116
13019 658-662 GeneOrGeneProduct denotes CaSR NCBIGene:24247
13020 666-703 DiseaseOrPhenotypicFeature denotes myocardial energy metabolism disorder MESH:D009202
13021 720-727 ChemicalEntity denotes glucose MESH:D005947
13022 828-832 GeneOrGeneProduct denotes CaSR NCBIGene:24247
13023 865-869 GeneOrGeneProduct denotes Mfn1 NCBIGene:192647
13024 871-875 GeneOrGeneProduct denotes Mfn2 NCBIGene:64476
13025 914-918 GeneOrGeneProduct denotes Cx43 NCBIGene:24392
13026 920-929 GeneOrGeneProduct denotes β-catenin NCBIGene:84353
13027 931-941 GeneOrGeneProduct denotes N-cadherin NCBIGene:83501
13028 962-965 ChemicalEntity denotes ATP MESH:D000255
13029 1021-1024 ChemicalEntity denotes ATP MESH:D000255
13030 1058-1062 GeneOrGeneProduct denotes gp78 NCBIGene:361367
13031 1096-1100 GeneOrGeneProduct denotes Fis1 NCBIGene:288584
13032 1102-1106 GeneOrGeneProduct denotes Drp1 NCBIGene:114114
13033 1142-1146 GeneOrGeneProduct denotes Mfn1 NCBIGene:192647
13034 1148-1152 GeneOrGeneProduct denotes Mfn2 NCBIGene:64476
13035 1157-1161 GeneOrGeneProduct denotes Cx43 NCBIGene:24392
13036 1173-1177 GeneOrGeneProduct denotes CaSR NCBIGene:24247
13037 1190-1194 GeneOrGeneProduct denotes gp78 NCBIGene:361367
13038 1296-1333 DiseaseOrPhenotypicFeature denotes myocardial energy metabolism disorder MESH:D009202
13039 1350-1354 GeneOrGeneProduct denotes CaSR NCBIGene:24247
13040 1385-1389 GeneOrGeneProduct denotes gp78 NCBIGene:361367
13041 1546-1549 ChemicalEntity denotes ATP MESH:D000255
13042 1578-1581 ChemicalEntity denotes ATP MESH:D000255
13043 1606-1610 GeneOrGeneProduct denotes CaSR NCBIGene:24247
13044 1647-1684 DiseaseOrPhenotypicFeature denotes abnormal myocardial energy metabolism MESH:D009202
13045 1697-1701 GeneOrGeneProduct denotes CaSR NCBIGene:24247
13046 1756-1759 DiseaseOrPhenotypicFeature denotes DCM MESH:D002311

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 139-153 DiseaseOrPhenotypicFeature denotes cardiomyopathy 0004994

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 16-24 GeneOrGeneProduct denotes receptor
T2 34-38 GeneOrGeneProduct denotes high
T3 47-54 GeneOrGeneProduct denotes induced
T4 86-94 GeneOrGeneProduct denotes blocking
T5 95-99 GeneOrGeneProduct denotes gp78
T6 100-109 GeneOrGeneProduct denotes ubiquitin
T7 110-120 GeneOrGeneProduct denotes proteasome
T8 130-138 GeneOrGeneProduct denotes Diabetic
T9 155-158 GeneOrGeneProduct denotes DCM
T10 165-170 GeneOrGeneProduct denotes major
T11 221-229 GeneOrGeneProduct denotes diabetes
T12 235-259 GeneOrGeneProduct denotes calcium sensing receptor
T13 261-265 GeneOrGeneProduct denotes CaSR
T14 272-298 GeneOrGeneProduct denotes G protein-coupled receptor
T15 333-364 GeneOrGeneProduct denotes calcium homeostasis, regulating
T16 365-369 GeneOrGeneProduct denotes cell
T17 388-397 GeneOrGeneProduct denotes apoptosis
T18 447-451 GeneOrGeneProduct denotes CaSR
T19 478-492 GeneOrGeneProduct denotes calcium levels
T20 519-522 GeneOrGeneProduct denotes all
T21 550-553 GeneOrGeneProduct denotes DCM
T22 658-662 GeneOrGeneProduct denotes CaSR
T23 704-711 GeneOrGeneProduct denotes induced
T24 715-719 GeneOrGeneProduct denotes high
T25 828-832 GeneOrGeneProduct denotes CaSR
T26 834-847 GeneOrGeneProduct denotes mitochondrial
T27 848-854 GeneOrGeneProduct denotes fusion
T28 855-863 GeneOrGeneProduct denotes proteins
T29 865-869 GeneOrGeneProduct denotes Mfn1
T30 871-875 GeneOrGeneProduct denotes Mfn2
T31 878-882 GeneOrGeneProduct denotes cell
T32 896-912 GeneOrGeneProduct denotes related proteins
T33 914-918 GeneOrGeneProduct denotes Cx43
T34 922-929 GeneOrGeneProduct denotes catenin
T35 931-941 GeneOrGeneProduct denotes N-cadherin
T36 962-965 GeneOrGeneProduct denotes ATP
T37 984-992 GeneOrGeneProduct denotes contrast
T38 1007-1020 GeneOrGeneProduct denotes extracellular
T39 1021-1024 GeneOrGeneProduct denotes ATP
T40 1058-1062 GeneOrGeneProduct denotes gp78
T41 1064-1077 GeneOrGeneProduct denotes mitochondrial
T42 1086-1094 GeneOrGeneProduct denotes proteins
T43 1096-1100 GeneOrGeneProduct denotes Fis1
T44 1102-1106 GeneOrGeneProduct denotes Drp1
T45 1117-1131 GeneOrGeneProduct denotes ubiquitination
T46 1142-1146 GeneOrGeneProduct denotes Mfn1
T47 1148-1152 GeneOrGeneProduct denotes Mfn2
T48 1157-1161 GeneOrGeneProduct denotes Cx43
T49 1173-1177 GeneOrGeneProduct denotes CaSR
T50 1190-1194 GeneOrGeneProduct denotes gp78
T51 1215-1222 GeneOrGeneProduct denotes reduced
T52 1288-1295 GeneOrGeneProduct denotes induces
T53 1350-1354 GeneOrGeneProduct denotes CaSR
T54 1371-1381 GeneOrGeneProduct denotes activation
T55 1385-1389 GeneOrGeneProduct denotes gp78
T56 1390-1399 GeneOrGeneProduct denotes ubiquitin
T57 1400-1410 GeneOrGeneProduct denotes proteasome
T58 1442-1449 GeneOrGeneProduct denotes disrupt
T59 1484-1496 GeneOrGeneProduct denotes mitochondria
T60 1505-1509 GeneOrGeneProduct denotes cell
T61 1538-1545 GeneOrGeneProduct denotes reduced
T62 1546-1549 GeneOrGeneProduct denotes ATP
T63 1578-1581 GeneOrGeneProduct denotes ATP
T64 1606-1610 GeneOrGeneProduct denotes CaSR
T65 1625-1635 GeneOrGeneProduct denotes attenuates
T66 1639-1646 GeneOrGeneProduct denotes induced
T67 1697-1701 GeneOrGeneProduct denotes CaSR
T68 1756-1759 GeneOrGeneProduct denotes DCM

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 16-24 GeneOrGeneProduct denotes receptor
T2 34-38 GeneOrGeneProduct denotes high
T3 95-99 GeneOrGeneProduct denotes gp78
T4 100-109 GeneOrGeneProduct denotes ubiquitin
T5 110-120 GeneOrGeneProduct denotes proteasome
T6 165-170 GeneOrGeneProduct denotes major
T7 221-229 GeneOrGeneProduct denotes diabetes
T8 235-259 GeneOrGeneProduct denotes calcium sensing receptor
T9 261-265 GeneOrGeneProduct denotes CaSR
T10 272-298 GeneOrGeneProduct denotes G protein-coupled receptor
T11 333-364 GeneOrGeneProduct denotes calcium homeostasis, regulating
T12 365-369 GeneOrGeneProduct denotes cell
T13 388-397 GeneOrGeneProduct denotes apoptosis
T14 447-451 GeneOrGeneProduct denotes CaSR
T15 478-492 GeneOrGeneProduct denotes calcium levels
T16 658-662 GeneOrGeneProduct denotes CaSR
T17 715-719 GeneOrGeneProduct denotes high
T18 828-832 GeneOrGeneProduct denotes CaSR
T19 834-847 GeneOrGeneProduct denotes mitochondrial
T20 848-854 GeneOrGeneProduct denotes fusion
T21 865-869 GeneOrGeneProduct denotes Mfn1
T22 871-875 GeneOrGeneProduct denotes Mfn2
T23 878-882 GeneOrGeneProduct denotes cell
T24 896-912 GeneOrGeneProduct denotes related proteins
T25 914-918 GeneOrGeneProduct denotes Cx43
T26 922-929 GeneOrGeneProduct denotes catenin
T27 931-941 GeneOrGeneProduct denotes N-cadherin
T28 1007-1020 GeneOrGeneProduct denotes extracellular
T29 1058-1062 GeneOrGeneProduct denotes gp78
T30 1064-1077 GeneOrGeneProduct denotes mitochondrial
T31 1096-1100 GeneOrGeneProduct denotes Fis1
T32 1102-1106 GeneOrGeneProduct denotes Drp1
T33 1142-1146 GeneOrGeneProduct denotes Mfn1
T34 1148-1152 GeneOrGeneProduct denotes Mfn2
T35 1157-1161 GeneOrGeneProduct denotes Cx43
T36 1173-1177 GeneOrGeneProduct denotes CaSR
T37 1190-1194 GeneOrGeneProduct denotes gp78
T38 1215-1222 GeneOrGeneProduct denotes reduced
T39 1350-1354 GeneOrGeneProduct denotes CaSR
T40 1385-1389 GeneOrGeneProduct denotes gp78
T41 1390-1399 GeneOrGeneProduct denotes ubiquitin
T42 1400-1410 GeneOrGeneProduct denotes proteasome
T43 1484-1496 GeneOrGeneProduct denotes mitochondria
T44 1505-1509 GeneOrGeneProduct denotes cell
T45 1538-1545 GeneOrGeneProduct denotes reduced
T46 1606-1610 GeneOrGeneProduct denotes CaSR
T47 1697-1701 GeneOrGeneProduct denotes CaSR

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 130-153 DiseaseOrPhenotypicFeature denotes Diabetic cardiomyopathy D058065
T2 155-158 DiseaseOrPhenotypicFeature denotes DCM D058065
T3 221-229 DiseaseOrPhenotypicFeature denotes diabetes DISEASE
T4 550-553 DiseaseOrPhenotypicFeature denotes DCM D058065
T5 1756-1759 DiseaseOrPhenotypicFeature denotes DCM D058065

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 0-24 GeneOrGeneProduct denotes Calcium sensing receptor
T2 95-99 GeneOrGeneProduct denotes gp78
T3 100-109 GeneOrGeneProduct denotes ubiquitin
T4 110-120 GeneOrGeneProduct denotes proteasome
T5 235-259 GeneOrGeneProduct denotes calcium sensing receptor
T6 261-265 GeneOrGeneProduct denotes CaSR
T7 272-298 GeneOrGeneProduct denotes G protein-coupled receptor
T8 333-364 GeneOrGeneProduct denotes calcium homeostasis, regulating
T9 447-451 GeneOrGeneProduct denotes CaSR
T10 658-662 GeneOrGeneProduct denotes CaSR
T11 828-832 GeneOrGeneProduct denotes CaSR
T12 834-863 GeneOrGeneProduct denotes mitochondrial fusion proteins
T13 865-869 GeneOrGeneProduct denotes Mfn1
T14 871-875 GeneOrGeneProduct denotes Mfn2
T15 914-918 GeneOrGeneProduct denotes Cx43
T16 922-929 GeneOrGeneProduct denotes catenin
T17 931-941 GeneOrGeneProduct denotes N-cadherin
T18 1058-1062 GeneOrGeneProduct denotes gp78
T19 1064-1094 GeneOrGeneProduct denotes mitochondrial fission proteins
T20 1096-1100 GeneOrGeneProduct denotes Fis1
T21 1102-1106 GeneOrGeneProduct denotes Drp1
T22 1142-1146 GeneOrGeneProduct denotes Mfn1
T23 1148-1152 GeneOrGeneProduct denotes Mfn2
T24 1157-1161 GeneOrGeneProduct denotes Cx43
T25 1173-1177 GeneOrGeneProduct denotes CaSR
T26 1190-1194 GeneOrGeneProduct denotes gp78
T27 1350-1354 GeneOrGeneProduct denotes CaSR
T28 1385-1389 GeneOrGeneProduct denotes gp78
T29 1390-1399 GeneOrGeneProduct denotes ubiquitin
T30 1400-1410 GeneOrGeneProduct denotes proteasome
T31 1606-1610 GeneOrGeneProduct denotes CaSR
T32 1697-1701 GeneOrGeneProduct denotes CaSR

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 139-153 DiseaseOrPhenotypicFeature denotes cardiomyopathy 0004994
T2 155-158 DiseaseOrPhenotypicFeature denotes DCM 0019315|0016333
T4 221-229 DiseaseOrPhenotypicFeature denotes diabetes 0005015
T5 550-553 DiseaseOrPhenotypicFeature denotes DCM 0019315|0016333
T7 1756-1759 DiseaseOrPhenotypicFeature denotes DCM 0019315|0016333

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 62-81 DiseaseOrPhenotypicFeature denotes metabolism disorder DISEASE
T2 130-153 DiseaseOrPhenotypicFeature denotes Diabetic cardiomyopathy D058065
T3 155-158 DiseaseOrPhenotypicFeature denotes DCM D058065
T4 221-229 DiseaseOrPhenotypicFeature denotes diabetes DISEASE
T5 550-553 DiseaseOrPhenotypicFeature denotes DCM D058065
T6 666-703 DiseaseOrPhenotypicFeature denotes myocardial energy metabolism disorder DISEASE
T7 1296-1333 DiseaseOrPhenotypicFeature denotes myocardial energy metabolism disorder DISEASE
T8 1647-1684 DiseaseOrPhenotypicFeature denotes abnormal myocardial energy metabolism DISEASE
T9 1756-1759 DiseaseOrPhenotypicFeature denotes DCM D058065

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 62-81 DiseaseOrPhenotypicFeature denotes metabolism disorder DISEASE
T2 130-153 DiseaseOrPhenotypicFeature denotes Diabetic cardiomyopathy D058065
T3 155-158 DiseaseOrPhenotypicFeature denotes DCM D058065
T4 221-229 DiseaseOrPhenotypicFeature denotes diabetes DISEASE
T5 550-553 DiseaseOrPhenotypicFeature denotes DCM D058065
T6 666-703 DiseaseOrPhenotypicFeature denotes myocardial energy metabolism disorder DISEASE
T7 1296-1333 DiseaseOrPhenotypicFeature denotes myocardial energy metabolism disorder DISEASE
T8 1647-1684 DiseaseOrPhenotypicFeature denotes abnormal myocardial energy metabolism DISEASE
T9 1756-1759 DiseaseOrPhenotypicFeature denotes DCM D058065

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 0-7 ChemicalEntity denotes Calcium http://purl.obolibrary.org/obo/CHEBI_22984
T2 39-46 ChemicalEntity denotes glucose D005947|http://purl.obolibrary.org/obo/CHEBI_4167|http://purl.obolibrary.org/obo/CHEBI_17234
T5 110-120 ChemicalEntity denotes proteasome D046988
T6 155-158 ChemicalEntity denotes DCM http://purl.obolibrary.org/obo/CHEBI_15767
T7 235-242 ChemicalEntity denotes calcium D002118|http://purl.obolibrary.org/obo/CHEBI_29320|http://purl.obolibrary.org/obo/CHEBI_22984
T10 333-340 ChemicalEntity denotes calcium D002118|http://purl.obolibrary.org/obo/CHEBI_29320|http://purl.obolibrary.org/obo/CHEBI_22984
T13 478-485 ChemicalEntity denotes calcium D002118|http://purl.obolibrary.org/obo/CHEBI_29320|http://purl.obolibrary.org/obo/CHEBI_22984
T16 550-553 ChemicalEntity denotes DCM http://purl.obolibrary.org/obo/CHEBI_15767
T17 720-727 ChemicalEntity denotes glucose D005947|http://purl.obolibrary.org/obo/CHEBI_4167|http://purl.obolibrary.org/obo/CHEBI_17234
T20 962-965 ChemicalEntity denotes ATP http://purl.obolibrary.org/obo/CHEBI_30616|http://purl.obolibrary.org/obo/CHEBI_15422
T22 1021-1024 ChemicalEntity denotes ATP http://purl.obolibrary.org/obo/CHEBI_30616|http://purl.obolibrary.org/obo/CHEBI_15422
T24 1400-1410 ChemicalEntity denotes proteasome D046988
T25 1546-1549 ChemicalEntity denotes ATP http://purl.obolibrary.org/obo/CHEBI_30616|http://purl.obolibrary.org/obo/CHEBI_15422
T27 1578-1581 ChemicalEntity denotes ATP http://purl.obolibrary.org/obo/CHEBI_30616|http://purl.obolibrary.org/obo/CHEBI_15422
T29 1756-1759 ChemicalEntity denotes DCM http://purl.obolibrary.org/obo/CHEBI_15767

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 207-215 OrganismTaxon denotes patients
T2 554-558 OrganismTaxon denotes rats

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T29 1756-1759 ChemicalEntity denotes DCM http://purl.obolibrary.org/obo/CHEBI_15767
T27 1578-1581 ChemicalEntity denotes ATP http://purl.obolibrary.org/obo/CHEBI_15422|http://purl.obolibrary.org/obo/CHEBI_30616
T25 1546-1549 ChemicalEntity denotes ATP http://purl.obolibrary.org/obo/CHEBI_15422|http://purl.obolibrary.org/obo/CHEBI_30616
T24 1400-1410 ChemicalEntity denotes proteasome D046988
T22 1021-1024 ChemicalEntity denotes ATP http://purl.obolibrary.org/obo/CHEBI_15422|http://purl.obolibrary.org/obo/CHEBI_30616
T20 962-965 ChemicalEntity denotes ATP http://purl.obolibrary.org/obo/CHEBI_15422|http://purl.obolibrary.org/obo/CHEBI_30616
T17 720-727 ChemicalEntity denotes glucose http://purl.obolibrary.org/obo/CHEBI_17234|http://purl.obolibrary.org/obo/CHEBI_4167|D005947
T16 550-553 ChemicalEntity denotes DCM http://purl.obolibrary.org/obo/CHEBI_15767
T13 478-485 ChemicalEntity denotes calcium http://purl.obolibrary.org/obo/CHEBI_22984|http://purl.obolibrary.org/obo/CHEBI_29320|D002118
T10 333-340 ChemicalEntity denotes calcium http://purl.obolibrary.org/obo/CHEBI_22984|http://purl.obolibrary.org/obo/CHEBI_29320|D002118
T7 235-242 ChemicalEntity denotes calcium http://purl.obolibrary.org/obo/CHEBI_22984|http://purl.obolibrary.org/obo/CHEBI_29320|D002118
T6 155-158 ChemicalEntity denotes DCM http://purl.obolibrary.org/obo/CHEBI_15767
T5 110-120 ChemicalEntity denotes proteasome D046988
T2 39-46 ChemicalEntity denotes glucose http://purl.obolibrary.org/obo/CHEBI_17234|http://purl.obolibrary.org/obo/CHEBI_4167|D005947
T1 0-7 ChemicalEntity denotes Calcium http://purl.obolibrary.org/obo/CHEBI_22984
T32 1697-1701 GeneOrGeneProduct denotes CaSR
T31 1606-1610 GeneOrGeneProduct denotes CaSR
T30 1400-1410 GeneOrGeneProduct denotes proteasome
T66927 1390-1399 GeneOrGeneProduct denotes ubiquitin
T28 1385-1389 GeneOrGeneProduct denotes gp78
T96083 1350-1354 GeneOrGeneProduct denotes CaSR
T26 1190-1194 GeneOrGeneProduct denotes gp78
T25719 1173-1177 GeneOrGeneProduct denotes CaSR
T8695 1157-1161 GeneOrGeneProduct denotes Cx43
T23 1148-1152 GeneOrGeneProduct denotes Mfn2
T54074 1142-1146 GeneOrGeneProduct denotes Mfn1
T21 1102-1106 GeneOrGeneProduct denotes Drp1
T35725 1096-1100 GeneOrGeneProduct denotes Fis1
T19 1064-1094 GeneOrGeneProduct denotes mitochondrial fission proteins
T18 1058-1062 GeneOrGeneProduct denotes gp78
T94452 931-941 GeneOrGeneProduct denotes N-cadherin
T3107 922-929 GeneOrGeneProduct denotes catenin
T15 914-918 GeneOrGeneProduct denotes Cx43
T14 871-875 GeneOrGeneProduct denotes Mfn2
T1351 865-869 GeneOrGeneProduct denotes Mfn1
T12 834-863 GeneOrGeneProduct denotes mitochondrial fusion proteins
T11 828-832 GeneOrGeneProduct denotes CaSR
T42076 658-662 GeneOrGeneProduct denotes CaSR
T9 447-451 GeneOrGeneProduct denotes CaSR
T8 333-364 GeneOrGeneProduct denotes calcium homeostasis, regulating
T6815 272-298 GeneOrGeneProduct denotes G protein-coupled receptor
T56106 261-265 GeneOrGeneProduct denotes CaSR
T91326 235-259 GeneOrGeneProduct denotes calcium sensing receptor
T4 110-120 GeneOrGeneProduct denotes proteasome
T3 100-109 GeneOrGeneProduct denotes ubiquitin
T8022 95-99 GeneOrGeneProduct denotes gp78
T76220 0-24 GeneOrGeneProduct denotes Calcium sensing receptor
T97009 1756-1759 DiseaseOrPhenotypicFeature denotes DCM D058065
T30387 1647-1684 DiseaseOrPhenotypicFeature denotes abnormal myocardial energy metabolism DISEASE
T12484 1296-1333 DiseaseOrPhenotypicFeature denotes myocardial energy metabolism disorder DISEASE
T38540 666-703 DiseaseOrPhenotypicFeature denotes myocardial energy metabolism disorder DISEASE
T80324 550-553 DiseaseOrPhenotypicFeature denotes DCM D058065
T28042 221-229 DiseaseOrPhenotypicFeature denotes diabetes DISEASE
T80732 155-158 DiseaseOrPhenotypicFeature denotes DCM D058065
T64370 130-153 DiseaseOrPhenotypicFeature denotes Diabetic cardiomyopathy D058065
T35104 62-81 DiseaseOrPhenotypicFeature denotes metabolism disorder DISEASE
T78306 554-558 OrganismTaxon denotes rats
T74485 207-215 OrganismTaxon denotes patients