scholarly article | Q13442814 |
P50 | author | Kelly R Karch | Q84236680 |
P2093 | author name string | Benjamin A Garcia | |
Mariel Coradin | |||
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Increased serine protease activity and cathelicidin promotes skin inflammation in rosacea | Q28239417 | ||
Cathepsin B Expression and the Correlation with Clinical Aspects of Oral Squamous Cell Carcinoma | Q28274479 | ||
Roles of matrix metalloproteinases in cancer progression and their pharmacological targeting | Q28298681 | ||
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A review of COFRADIC techniques targeting protein N-terminal acetylation | Q30872116 | ||
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Sampling the N-terminal proteome of human blood | Q33740667 | ||
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Matrix metalloproteinases in renal development and disease | Q33854879 | ||
Factor Xa subsite mapping by proteome-derived peptide libraries improved using WebPICS, a resource for proteomic identification of cleavage sites | Q33993989 | ||
Isotopic labeling of terminal amines in complex samples identifies protein N-termini and protease cleavage products | Q34102556 | ||
Proteases and proteolysis in Alzheimer disease: a multifactorial view on the disease process | Q34110227 | ||
Biochemical characterization and N-terminomics analysis of leukolysin, the membrane-type 6 matrix metalloprotease (MMP25): chemokine and vimentin cleavages enhance cell migration and macrophage phagocytic activities | Q34172720 | ||
Mapping the active site of papain with the aid of peptide substrates and inhibitors | Q34209275 | ||
Identifying and quantifying proteolytic events and the natural N terminome by terminal amine isotopic labeling of substrates | Q34220314 | ||
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The paracaspase MALT1 cleaves HOIL1 reducing linear ubiquitination by LUBAC to dampen lymphocyte NF-κB signalling | Q34500164 | ||
Histone H3.3 and its proteolytically processed form drive a cellular senescence programme | Q34533167 | ||
Targeting proteases: successes, failures and future prospects | Q34563752 | ||
High-Throughput Sequencing, a VersatileWeapon to Support Genome-Based Diagnosis in Infectious Diseases: Applications to Clinical Bacteriology | Q34569184 | ||
Global analysis of cellular proteolysis by selective enzymatic labeling of protein N-termini | Q34663327 | ||
Histone proteolysis: a proposal for categorization into 'clipping' and 'degradation'. | Q35008882 | ||
Regulated intramembrane proteolysis: from the endoplasmic reticulum to the nucleus | Q35015161 | ||
The tissue kallikrein family of serine proteases: functional roles in human disease and potential as clinical biomarkers | Q35861497 | ||
Comprehensive analysis of protein modifications by top-down mass spectrometry | Q35873932 | ||
Identification of Protease Specificity by Combining Proteome-Derived Peptide Libraries and Quantitative Proteomics | Q36001454 | ||
Secretome protein enrichment identifies physiological BACE1 protease substrates in neurons | Q36103683 | ||
Profiling protease activities by dynamic proteomics workflows | Q36199807 | ||
Matrix metalloproteinases (MMPs) in health and disease: an overview | Q36348231 | ||
Top-down and Middle-down Protein Analysis Reveals that Intact and Clipped Human Histones Differ in Post-translational Modification Patterns | Q36604417 | ||
Decoding protein modifications using top-down mass spectrometry | Q36628274 | ||
Systematic proteomic analysis identifies β-site amyloid precursor protein cleaving enzyme 2 and 1 (BACE2 and BACE1) substrates in pancreatic β-cells | Q36760343 | ||
Matrix metalloproteinase inhibitors as therapy for inflammatory and vascular diseases. | Q36836612 | ||
Human membrane metallo-endopeptidase-like protein degrades both beta-amyloid 42 and beta-amyloid 40. | Q37003261 | ||
Top-down MS, a powerful complement to the high capabilities of proteolysis proteomics. | Q37004962 | ||
Protease proteomics: revealing protease in vivo functions using systems biology approaches | Q37197510 | ||
Proteases: multifunctional enzymes in life and disease | Q37225060 | ||
Cathepsin B as a potential prognostic and therapeutic marker for human lung squamous cell carcinoma | Q37327749 | ||
Proteolytic post-translational modification of proteins: proteomic tools and methodology | Q37388971 | ||
A proteomic approach for the discovery of protease substrates | Q37416084 | ||
Emerging roles of mitochondrial proteases in neurodegeneration | Q37576193 | ||
Quantitative analysis of peptides and proteins in biomedicine by targeted mass spectrometry | Q37618631 | ||
MS-driven protease substrate degradomics | Q37670718 | ||
Series "matrix metalloproteinases in lung health and disease": Biological role of matrix metalloproteinases: a critical balance | Q37823039 | ||
Proteases in autophagy | Q37884674 | ||
Mass spectrometry-based proteomics strategies for protease cleavage site identification. | Q37975970 | ||
Roles of regulated intramembrane proteolysis in virus infection and antiviral immunity | Q38149888 | ||
Identification and interrogation of combinatorial histone modifications. | Q38175981 | ||
Proteolytic clipping of histone tails: the emerging role of histone proteases in regulation of various biological processes. | Q38182451 | ||
Analysis of enzyme kinetics using electrospray ionization mass spectrometry and multiple reaction monitoring: fucosyltransferase V. | Q38302039 | ||
Twenty years of the MEROPS database of proteolytic enzymes, their substrates and inhibitors. | Q38400921 | ||
The kallikrein-related peptidase family: Dysregulation and functions during cancer progression. | Q38581780 | ||
Cysteine cathepsin proteases: regulators of cancer progression and therapeutic response | Q38644547 | ||
Elevated expression of KLK8 predicts poor prognosis in colorectal cancer | Q38718608 | ||
Intramembrane proteases as drug targets | Q38790377 | ||
Systematic substrate identification indicates a central role for the metalloprotease ADAM10 in axon targeting and synapse function | Q38911059 | ||
Middle-down hybrid chromatography/tandem mass spectrometry workflow for characterization of combinatorial post-translational modifications in histones | Q38970543 | ||
Quantitative proteomics to characterize specific histone H2A proteolysis in chronic lymphocytic leukemia and the myeloid THP-1 cell line | Q38990718 | ||
Identifying natural substrates for dipeptidyl peptidases 8 and 9 using terminal amine isotopic labeling of substrates (TAILS) reveals in vivo roles in cellular homeostasis and energy metabolism | Q39177343 | ||
Intracellular proteases | Q39664942 | ||
What does the future hold for Top Down mass spectrometry? | Q39925520 | ||
Prostasin serine protease inhibits breast cancer invasiveness and is transcriptionally regulated by promoter DNA methylation | Q40759567 | ||
Proteolytic removal of core histone amino termini and dephosphorylation of histone H1 correlate with the formation of condensed chromatin and transcriptional silencing during Tetrahymena macronuclear development | Q41899813 | ||
Activation of cell-surface proteases promotes necroptosis, inflammation and cell migration | Q42032616 | ||
Plasma kallikrein and diabetic macular edema | Q43036015 | ||
Prostasin, a potential serum marker for ovarian cancer: identification through microarray technology | Q43754824 | ||
Substrate specificities of the granzyme tryptases A and K. | Q49037235 | ||
Selecting protein N-terminal peptides by combined fractional diagonal chromatography. | Q49052034 | ||
Human macrophage cathepsin B-mediated C-terminal cleavage of apolipoprotein A-I at Ser228 severely impairs antiatherogenic capacity. | Q51163886 | ||
TAILS N-Terminomics and Proteomics Show Protein Degradation Dominates over Proteolytic Processing by Cathepsins in Pancreatic Tumors. | Q51603662 | ||
Prostate Cancer-Associated Kallikrein-Related Peptidase 4 Activates Matrix Metalloproteinase-1 and Thrombospondin-1. | Q51663714 | ||
Emerging roles of proteases in tumour suppression | Q57082634 | ||
P433 | issue | 5 | |
P921 | main subject | proteolysis | Q33123 |
P304 | page(s) | 409-418 | |
P577 | publication date | 2017-04-17 | |
P1433 | published in | Expert Review of Proteomics | Q15749465 |
P1476 | title | Monitoring proteolytic processing events by quantitative mass spectrometry | |
P478 | volume | 14 |
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