GPM #: Keyword: # GPM # proteins Description 1. GPM10100400442 peptide model gel aaa go mh 4603 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 2. GPM10100400443 peptide model gel aaa go mh 3803 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 3. GPM10100400444 peptide model gel aaa go mh 5123 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 4. GPM10100400445 peptide model gel aaa go mh 3484 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 5. GPM10100400446 peptide model gel aaa go mh 4389 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 6. GPM10100400447 peptide model gel aaa go mh 4451 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 7. GPM10100400448 peptide model gel aaa go mh 4385 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 8. GPM10100400449 peptide model gel aaa go mh 3934 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 9. GPM10100400450 peptide model gel aaa go mh 3850 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 10. GPM10100400451 peptide model gel aaa go mh 3087 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 11. GPM10100400452 peptide model gel aaa go mh 3579 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 12. GPM10100400453 peptide model gel aaa go mh 2814 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 13. GPM10100400454 peptide model gel aaa go mh 3402 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 14. GPM10100400455 peptide model gel aaa go mh 3567 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 15. GPM10100400456 peptide model gel aaa go mh 4301 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 16. GPM10100400457 peptide model gel aaa go mh 3696 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 17. GPM10100400458 peptide model gel aaa go mh 4821 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 18. GPM65200010000 peptide model gel aaa go mh 1468 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 19. GPM65200010001 peptide model gel aaa go mh 4195 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. 20. GPM65200010002 peptide model gel aaa go mh 1922 BRENDA cell culture: none BRENDA tissue: none CELL cell type: none GO subcellular: none email: institution: HSCRI, Toronto, Ontario name: Brian Cox, Thomas Kislinger, Andreas I Evangelou, S. L Adamson, Janet Rossant, Vladimir Ignatchenko, Alex Ignatchenko project: PSE115: Comparative analysis of the human and mouse placental transcriptome and proteome project comment: Data obtained from Peptidome PSM1063. Published in "Comparative systems biology of human and mouse as a tool to guide the modeling of human placental pathology", Mol Syst Biol. (2009) 5:279 (PubMed). Placentas from naturally-mated crosses of C57Bl/6J mice on embryonic day 17.5 were cut into thick slices. A scalpel blade was used to isolate the blood-red labyrinth tissue from the more poorly vascularized, and hence paler, spongiotrophoblast tissue, and to remove the superficial chorionic vasculature. From each litter, of the collected labyrinth tissues were set aside for RNA extraction and microarray analysis and for cellular fractionation and proteomic analysis. Page 1 of 2 | 1 | 2 | Key word(s): PSM1063 Total protein ids = 106567 If you do not see a red dot in the square brackets [], you will need Adobe's SVG plugin to view this site properly.

dblist_gpmnotes.pl, v. 2010.07.06