IndraLab

Statements


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sparser
"To further promote Notch activation, TRP120 binds the promoter regions of Notch1 and ADAM17 to promote transcription during infection ( xref )."

sparser
"This study reveals a novel effector-dependent mechanism, which involves interaction with the ADAM17 and Notch1 and activation of canonical Notch signaling pathway in monocytes, a primary target of E. chaffeensis , to modulate ERK1/2 and p38 MAPK pathways and regulate TLR2/4 expression ( xref )."

sparser
"Thus, we generated a spatial neighbourhood network ( xref ), where in health we observed dominant interactions between suprabasal and basal epithelial layers ( MMP9-LRP1; ADAM17-NOTCH1 ) ( xref , xref )."

sparser
"As shown in xref , iNOS overexpression or Pet-cGMP treatment led to serine/threonine phosphorylation of TACE (detected using an antiphosphothreonine antibody) and an interaction between phosphorylated TACE and Notch1 in LCSCs."

sparser
"The activation of Notch signaling, particularly through the DLL4-NOTCH1 and ADAM17-NOTCH1 pathways, was markedly observed transitioning from high-senescence endothelial cells to astrocytes (Fig.  xref F-G), indicating the pivotal role of the Notch pathway in the progression of MDD."

sparser
"This interaction between Notch1 O -glycosylation and cleavage by ADAM17 is involved in the mechanism of heterotaxy."

sparser
"In the healthy mucosa, we detected increased interactions between basal and suprabasal epithelial cells governed by ADAM17 and NOTCH1 ."

reach
"Double immunofluorescence showed strong signals for Notch1 and TACE immunostaining, which were predominantly distributed in CD68 positive macrophages compared with control tissues.In the present study[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

sparser
"These interactions, including the DLL4-NOTCH1 and ADAM17-NOTCH1 receptor pairs, suggest that senescent endothelial cells communicate with astrocytes through pathways critical for immune regulation."

sparser
"In our communication analyses, we detected high probability of interactions between ADAM17-NOTCH1."

sparser
"DSThighM macrophages exhibited a close association with endothelial cells in terms of IL6-IL6ST, MFNG-NOTCH1, OSM-IL6ST, ADAM17-NOTCH1, VEGF1-FLT1, VEGF2-FLT1, and PDGFC-FLT1 ligand-receptor linkages."