Gene Information
Gene symbol: KDR
Gene name: kinase insert domain receptor (a type III receptor tyrosine kinase)
HGNC ID: 6307
Synonyms: FLK1, VEGFR, VEGFR2, CD309
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | FLT1 | 1 hits |
| 2 | IL1RL1 | 1 hits |
| 3 | NRP1 | 1 hits |
| 4 | VEGFA | 1 hits |
| 5 | VWF | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 9603419 | We have used digoxigenin labelled RNA probes to VEGF and the VEGF receptor-2 (Quek1) to investigate the relationship between VEGF expression and vascular events in quail embryos from day 1 to 13 of incubation. |
| 2 | 9621286 | The ability of VEGF to be chemotactic for monocytes and to increase the activity of collagenase and plasminogen activator may have implications for renal development and renal disease. |
| 3 | 9621286 | The ability of VEGF to be chemotactic for monocytes and to increase the activity of collagenase and plasminogen activator may have implications for renal development and renal disease. |
| 4 | 9621286 | The ability of VEGF to be chemotactic for monocytes and to increase the activity of collagenase and plasminogen activator may have implications for renal development and renal disease. |
| 5 | 9621286 | The ability of VEGF to be chemotactic for monocytes and to increase the activity of collagenase and plasminogen activator may have implications for renal development and renal disease. |
| 6 | 9621286 | The ability of VEGF to be chemotactic for monocytes and to increase the activity of collagenase and plasminogen activator may have implications for renal development and renal disease. |
| 7 | 9621286 | The ability of VEGF to be chemotactic for monocytes and to increase the activity of collagenase and plasminogen activator may have implications for renal development and renal disease. |
| 8 | 9621286 | In humans, the cellular actions of VEGF depend on binding to two specific receptors: Flt-1 and KDR. |
| 9 | 9621286 | In humans, the cellular actions of VEGF depend on binding to two specific receptors: Flt-1 and KDR. |
| 10 | 9621286 | In humans, the cellular actions of VEGF depend on binding to two specific receptors: Flt-1 and KDR. |
| 11 | 9621286 | In humans, the cellular actions of VEGF depend on binding to two specific receptors: Flt-1 and KDR. |
| 12 | 9621286 | In humans, the cellular actions of VEGF depend on binding to two specific receptors: Flt-1 and KDR. |
| 13 | 9621286 | In humans, the cellular actions of VEGF depend on binding to two specific receptors: Flt-1 and KDR. |
| 14 | 9621286 | The aims of this study were: (1) to localize VEGF receptor proteins in human renal ontogenesis; (2) to quantify VEGF binding in human fetal and adult kidney; and (3) to dissect the binding into its two known components: the KDR and Flt-1 receptors. |
| 15 | 9621286 | The aims of this study were: (1) to localize VEGF receptor proteins in human renal ontogenesis; (2) to quantify VEGF binding in human fetal and adult kidney; and (3) to dissect the binding into its two known components: the KDR and Flt-1 receptors. |
| 16 | 9621286 | The aims of this study were: (1) to localize VEGF receptor proteins in human renal ontogenesis; (2) to quantify VEGF binding in human fetal and adult kidney; and (3) to dissect the binding into its two known components: the KDR and Flt-1 receptors. |
| 17 | 9621286 | The aims of this study were: (1) to localize VEGF receptor proteins in human renal ontogenesis; (2) to quantify VEGF binding in human fetal and adult kidney; and (3) to dissect the binding into its two known components: the KDR and Flt-1 receptors. |
| 18 | 9621286 | The aims of this study were: (1) to localize VEGF receptor proteins in human renal ontogenesis; (2) to quantify VEGF binding in human fetal and adult kidney; and (3) to dissect the binding into its two known components: the KDR and Flt-1 receptors. |
| 19 | 9621286 | The aims of this study were: (1) to localize VEGF receptor proteins in human renal ontogenesis; (2) to quantify VEGF binding in human fetal and adult kidney; and (3) to dissect the binding into its two known components: the KDR and Flt-1 receptors. |
| 20 | 9621286 | The latter aim was achieved by competitive binding of VEGF and placenta growth factor-2, which only binds to Flt-1. |
| 21 | 9621286 | The latter aim was achieved by competitive binding of VEGF and placenta growth factor-2, which only binds to Flt-1. |
| 22 | 9621286 | The latter aim was achieved by competitive binding of VEGF and placenta growth factor-2, which only binds to Flt-1. |
| 23 | 9621286 | The latter aim was achieved by competitive binding of VEGF and placenta growth factor-2, which only binds to Flt-1. |
| 24 | 9621286 | The latter aim was achieved by competitive binding of VEGF and placenta growth factor-2, which only binds to Flt-1. |
| 25 | 9621286 | The latter aim was achieved by competitive binding of VEGF and placenta growth factor-2, which only binds to Flt-1. |
| 26 | 9621286 | By double-label immunohistochemistry, VEGF receptor proteins were localized solely to endothelial cells of preglomerular vessels, glomeruli, and postglomerular vessels. |
| 27 | 9621286 | By double-label immunohistochemistry, VEGF receptor proteins were localized solely to endothelial cells of preglomerular vessels, glomeruli, and postglomerular vessels. |
| 28 | 9621286 | By double-label immunohistochemistry, VEGF receptor proteins were localized solely to endothelial cells of preglomerular vessels, glomeruli, and postglomerular vessels. |
| 29 | 9621286 | By double-label immunohistochemistry, VEGF receptor proteins were localized solely to endothelial cells of preglomerular vessels, glomeruli, and postglomerular vessels. |
| 30 | 9621286 | By double-label immunohistochemistry, VEGF receptor proteins were localized solely to endothelial cells of preglomerular vessels, glomeruli, and postglomerular vessels. |
| 31 | 9621286 | By double-label immunohistochemistry, VEGF receptor proteins were localized solely to endothelial cells of preglomerular vessels, glomeruli, and postglomerular vessels. |
| 32 | 9621286 | In developing glomeruli, VEGF receptor protein appeared as soon as endothelial cells were positive for von Willebrand factor. |
| 33 | 9621286 | In developing glomeruli, VEGF receptor protein appeared as soon as endothelial cells were positive for von Willebrand factor. |
| 34 | 9621286 | In developing glomeruli, VEGF receptor protein appeared as soon as endothelial cells were positive for von Willebrand factor. |
| 35 | 9621286 | In developing glomeruli, VEGF receptor protein appeared as soon as endothelial cells were positive for von Willebrand factor. |
| 36 | 9621286 | In developing glomeruli, VEGF receptor protein appeared as soon as endothelial cells were positive for von Willebrand factor. |
| 37 | 9621286 | In developing glomeruli, VEGF receptor protein appeared as soon as endothelial cells were positive for von Willebrand factor. |
| 38 | 9621286 | Placenta growth factor-2 displaced VEGF binding in all renal structures by approximately 60%. |
| 39 | 9621286 | Placenta growth factor-2 displaced VEGF binding in all renal structures by approximately 60%. |
| 40 | 9621286 | Placenta growth factor-2 displaced VEGF binding in all renal structures by approximately 60%. |
| 41 | 9621286 | Placenta growth factor-2 displaced VEGF binding in all renal structures by approximately 60%. |
| 42 | 9621286 | Placenta growth factor-2 displaced VEGF binding in all renal structures by approximately 60%. |
| 43 | 9621286 | Placenta growth factor-2 displaced VEGF binding in all renal structures by approximately 60%. |
| 44 | 9621286 | VEGF receptor proteins thus were found only in renal endothelial cells. |
| 45 | 9621286 | VEGF receptor proteins thus were found only in renal endothelial cells. |
| 46 | 9621286 | VEGF receptor proteins thus were found only in renal endothelial cells. |
| 47 | 9621286 | VEGF receptor proteins thus were found only in renal endothelial cells. |
| 48 | 9621286 | VEGF receptor proteins thus were found only in renal endothelial cells. |
| 49 | 9621286 | VEGF receptor proteins thus were found only in renal endothelial cells. |
| 50 | 9621286 | A coexpression of both VEGF binding sites could be shown, with Flt-1 demonstrating the most abundant VEGF receptor binding sites in the kidney. |
| 51 | 9621286 | A coexpression of both VEGF binding sites could be shown, with Flt-1 demonstrating the most abundant VEGF receptor binding sites in the kidney. |
| 52 | 9621286 | A coexpression of both VEGF binding sites could be shown, with Flt-1 demonstrating the most abundant VEGF receptor binding sites in the kidney. |
| 53 | 9621286 | A coexpression of both VEGF binding sites could be shown, with Flt-1 demonstrating the most abundant VEGF receptor binding sites in the kidney. |
| 54 | 9621286 | A coexpression of both VEGF binding sites could be shown, with Flt-1 demonstrating the most abundant VEGF receptor binding sites in the kidney. |
| 55 | 9621286 | A coexpression of both VEGF binding sites could be shown, with Flt-1 demonstrating the most abundant VEGF receptor binding sites in the kidney. |
| 56 | 9736244 | VEGF receptors 1 and 2 (fit-1 and flk-1) are endothelial-specific receptor tyrosine kinases. |
| 57 | 10864579 | Vascular endothelial growth factor (VEGF), a potent mitogen, is expressed in podocytes in the glomerulus, and VEGF receptors (flt-1, KDR, and neuropilin-1) are present on endothelial cells and other cell types. |
| 58 | 10864579 | Vascular endothelial growth factor (VEGF), a potent mitogen, is expressed in podocytes in the glomerulus, and VEGF receptors (flt-1, KDR, and neuropilin-1) are present on endothelial cells and other cell types. |
| 59 | 10864579 | Vascular endothelial growth factor (VEGF), a potent mitogen, is expressed in podocytes in the glomerulus, and VEGF receptors (flt-1, KDR, and neuropilin-1) are present on endothelial cells and other cell types. |
| 60 | 10864579 | In contrast, mesangial flt-1 and KDR receptor staining were both clearly seen in biopsy samples from proliferative renal diseases. |
| 61 | 10864579 | In contrast, mesangial flt-1 and KDR receptor staining were both clearly seen in biopsy samples from proliferative renal diseases. |
| 62 | 10864579 | In contrast, mesangial flt-1 and KDR receptor staining were both clearly seen in biopsy samples from proliferative renal diseases. |
| 63 | 10864579 | In conclusion, flt-1, KDR, and neuropilin-1 are present on cultured HMC, and VEGF(165) induces HMC proliferation. |
| 64 | 10864579 | In conclusion, flt-1, KDR, and neuropilin-1 are present on cultured HMC, and VEGF(165) induces HMC proliferation. |
| 65 | 10864579 | In conclusion, flt-1, KDR, and neuropilin-1 are present on cultured HMC, and VEGF(165) induces HMC proliferation. |
| 66 | 10864579 | In addition, the flt-1 and KDR receptors are expressed in the mesangium in mesangioproliferative disease. |
| 67 | 10864579 | In addition, the flt-1 and KDR receptors are expressed in the mesangium in mesangioproliferative disease. |
| 68 | 10864579 | In addition, the flt-1 and KDR receptors are expressed in the mesangium in mesangioproliferative disease. |