Pages that link to "Q28208481"
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The following pages link to Marked differences between metalloproteases meprin A and B in substrate and peptide bond specificity (Q28208481):
Displaying 50 items.
- Targeted disruption of the meprin beta gene in mice leads to underrepresentation of knockout mice and changes in renal gene expression profiles (Q24541391) (← links)
- Meprins, membrane-bound and secreted astacin metalloproteinases (Q24646365) (← links)
- MEP1A allele for meprin A metalloprotease is a susceptibility gene for inflammatory bowel disease (Q24657607) (← links)
- Intestinal epithelium in inflammatory bowel disease (Q27022092) (← links)
- (Q28179289) (redirect page) (← links)
- A selective interaction between OS-9 and the carboxyl-terminal tail of meprin beta (Q28208244) (← links)
- Structure of homo- and hetero-oligomeric meprin metalloproteases. Dimers, tetramers, and high molecular mass multimers (Q28210655) (← links)
- Multimeric structure of the secreted meprin A metalloproteinase and characterization of the functional protomer (Q28212341) (← links)
- Activation of human meprin-alpha in a cell culture model of colorectal cancer is triggered by the plasminogen-activating system (Q28218647) (← links)
- Proteolysis controls endogenous substance P levels (Q28534739) (← links)
- Evaluation of ¹¹¹in-labelled exendin-4 derivatives containing different meprin β-specific cleavable linkers (Q28545983) (← links)
- Probing the active sites and mechanisms of rat metalloproteases meprin A and B (Q28579711) (← links)
- Compartmentalised expression of meprin in small intestinal mucosa: enhanced expression in lamina propria in coeliac disease (Q33276900) (← links)
- Combinatorial strategies for targeting protein families: application to the proteases (Q33288760) (← links)
- The metalloprotease meprinbeta processes E-cadherin and weakens intercellular adhesion (Q33334334) (← links)
- Metalloprotease meprin beta in rat kidney: glomerular localization and differential expression in glomerulonephritis (Q33338489) (← links)
- ADAM10 is the major sheddase responsible for the release of membrane-associated meprin A. (Q33676656) (← links)
- Role of meprins to protect ileal mucosa of Crohn's disease patients from colonization by adherent-invasive E. coli (Q33940892) (← links)
- Enhanced activity of meprin-α, a pro-migratory and pro-angiogenic protease, in colorectal cancer (Q34077651) (← links)
- The new MATH: homology suggests shared binding surfaces in meprin tetramers and TRAF trimers (Q34155132) (← links)
- Balance of meprin A and B in mice affects the progression of experimental inflammatory bowel disease. (Q34597685) (← links)
- Activation of the epithelial sodium channel by the metalloprotease meprin β subunit (Q34639469) (← links)
- Arabidopsis thaliana BTB/ POZ-MATH proteins interact with members of the ERF/AP2 transcription factor family (Q35008690) (← links)
- Expression of meprins in health and disease (Q35107611) (← links)
- Metalloprotease meprin beta generates nontoxic N-terminal amyloid precursor protein fragments in vivo (Q35145029) (← links)
- Proteomic analyses reveal an acidic prime side specificity for the astacin metalloprotease family reflected by physiological substrates (Q35264713) (← links)
- Villin and actin in the mouse kidney brush-border membrane bind to and are degraded by meprins, an interaction that contributes to injury in ischemia-reperfusion (Q35326081) (← links)
- Actinonin, a meprin A inhibitor, protects the renal microcirculation during sepsis (Q35693793) (← links)
- Meprin metalloprotease expression and regulation in kidney, intestine, urinary tract infections and cancer. (Q36156032) (← links)
- Meprinα transactivates the epidermal growth factor receptor (EGFR) via ligand shedding, thereby enhancing colorectal cancer cell proliferation and migration (Q36318836) (← links)
- The substrate degradome of meprin metalloproteases reveals an unexpected proteolytic link between meprin β and ADAM10. (Q36503385) (← links)
- The metalloproteases meprin α and meprin β: unique enzymes in inflammation, neurodegeneration, cancer and fibrosis (Q36613779) (← links)
- Critical amino acids in the active site of meprin metalloproteinases for substrate and peptide bond specificity (Q36628856) (← links)
- Hepatocyte nuclear factor 4alpha in the intestinal epithelial cells protects against inflammatory bowel disease (Q36732009) (← links)
- Meprin A metalloproteinase and its role in acute kidney injury (Q36836257) (← links)
- The anti-inflammatory peptide Ac-SDKP is released from thymosin-β4 by renal meprin-α and prolyl oligopeptidase. (Q36957095) (← links)
- Prointerleukin-18 is activated by meprin beta in vitro and in vivo in intestinal inflammation (Q36968427) (← links)
- Meprin A and meprin alpha generate biologically functional IL-1beta from pro-IL-1beta (Q36985463) (← links)
- Meprin A metalloproteases enhance renal damage and bladder inflammation after LPS challenge. (Q37086108) (← links)
- Hypoxia Associated Proteolytic Processing of OS-9 by the Metalloproteinase Meprin β. (Q37127955) (← links)
- Meprin A impairs epithelial barrier function, enhances monocyte migration, and cleaves the tight junction protein occludin. (Q37142513) (← links)
- Disruption of the meprin alpha and beta genes in mice alters homeostasis of monocytes and natural killer cells (Q37172385) (← links)
- Mannose-binding lectin codon 54 genetic polymorphism and vaginal protein levels in women with gynecologic malignancies (Q37296509) (← links)
- Meprin metalloproteases inactivate interleukin 6. (Q37635798) (← links)
- Conservation of the egg envelope digestion mechanism of hatching enzyme in euteleostean fishes (Q38339464) (← links)
- Strongyloides stercoralis excretory/secretory protein strongylastacin specifically recognized by IgE antibodies in infected human sera (Q39554016) (← links)
- Activation of the epidermal growth factor receptor (EGFR) by a novel metalloprotease pathway. (Q39943187) (← links)
- A novel 2D-based approach to the discovery of candidate substrates for the metalloendopeptidase meprin (Q39955252) (← links)
- Inhibitors of polyamine biosynthesis decrease the expression of the metalloproteases meprin alpha and MMP-7 in hormone-independent human breast cancer cells. (Q40371630) (← links)
- MEP1A contributes to tumor progression and predicts poor clinical outcome in human hepatocellular carcinoma. (Q41056161) (← links)