human endothelial progenitor cell line hepc-cb1 (Inserm Transfert)
90
Structured Review
Inserm Transfert
human endothelial progenitor cell line hepc-cb1
Human Endothelial Progenitor Cell Line Hepc Cb1, supplied by Inserm Transfert, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+endothelial+progenitor+cell+line+hepc-cb1/human+endothelial+progenitor+cell+line+hepc+cb1/pm33290062-188-48-86
Average 90 stars, based on 1 article reviews
Human Endothelial Progenitor Cell Line Hepc Cb1, supplied by Inserm Transfert, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+endothelial+progenitor+cell+line+hepc-cb1/human+endothelial+progenitor+cell+line+hepc+cb1/pm33290062-188-48-86
Average 90 stars, based on 1 article reviews
human endothelial progenitor cell line hepc-cb1 - by Bioz Stars,
2026-10
90/100 stars
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Inhibition:Article Title: Soluble Guanylate Cyclase Inhibitors Discovered among Natural Compounds. Article Snippet: Figure S1, example of the screening of 320 natural compounds; Figure S2, inhibition of sGC activity by violastyrene analogues and 2-hydroxy-3,5,8-triaceto-1,4naphthoquinone analogues; Figure S3, chemical structures of violastyrene and its analogues; Figure S4, chemical structure of ODQ, violastyrene, and HTANQ; Figure S5, quantification of angiogenesis triggered in human endothelial progenitor cell line HEPC-CB1 after 13 h of culture on Matrigel in the presence of guanylate cyclase inhibitors 1, 2, 3, 6, and 7 (PDF) ■ AUTHOR INFORMATION Corresponding Author Michel Negrerie − Laboratoire d’Optique et Biosciences, Activity Assay:Article Title: Soluble Guanylate Cyclase Inhibitors Discovered among Natural Compounds. Article Snippet: Figure S1, example of the screening of 320 natural compounds; Figure S2, inhibition of sGC activity by violastyrene analogues and 2-hydroxy-3,5,8-triaceto-1,4naphthoquinone analogues; Figure S3, chemical structures of violastyrene and its analogues; Figure S4, chemical structure of ODQ, violastyrene, and HTANQ; Figure S5, quantification of angiogenesis triggered in human endothelial progenitor cell line HEPC-CB1 after 13 h of culture on Matrigel in the presence of guanylate cyclase inhibitors 1, 2, 3, 6, and 7 (PDF) ■ AUTHOR INFORMATION Corresponding Author Michel Negrerie − Laboratoire d’Optique et Biosciences, Analogues:Article Title: Soluble Guanylate Cyclase Inhibitors Discovered among Natural Compounds. Article Snippet: Figure S1, example of the screening of 320 natural compounds; Figure S2, inhibition of sGC activity by violastyrene analogues and 2-hydroxy-3,5,8-triaceto-1,4naphthoquinone analogues; Figure S3, chemical structures of violastyrene and its analogues; Figure S4, chemical structure of ODQ, violastyrene, and HTANQ; Figure S5, quantification of angiogenesis triggered in human endothelial progenitor cell line HEPC-CB1 after 13 h of culture on Matrigel in the presence of guanylate cyclase inhibitors 1, 2, 3, 6, and 7 (PDF) ■ AUTHOR INFORMATION Corresponding Author Michel Negrerie − Laboratoire d’Optique et Biosciences, |