scholarly article | Q13442814 |
P50 | author | Regina Fluhrer | Q63092251 |
Stefan F Lichtenthaler | Q73197474 | ||
Regina Feederle | Q87822177 | ||
Artur Mayerhofer | Q88992184 | ||
Bernd Schröder | Q89671442 | ||
P2093 | author name string | Julia von Blume | |
Martina Haug-Kröper | |||
Merav D Shmueli | |||
Torben Mentrup | |||
Stephan A Müller | |||
Alkmini A Papadopoulou | |||
Johannes Niemeyer | |||
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Molecular characterisation of 'transmembrane protein 192' (TMEM192), a novel protein of the lysosomal membrane | Q24305928 | ||
Substrate requirements for SPPL2b-dependent regulated intramembrane proteolysis | Q24311748 | ||
Signal-peptide-peptidase-like 2a (SPPL2a) is targeted to lysosomes/late endosomes by a tyrosine motif in its C-terminal tail | Q24337321 | ||
Significance analysis of microarrays applied to the ionizing radiation response | Q24606608 | ||
Regulation of intracellular membrane trafficking and cell dynamics by syntaxin-6 | Q24633280 | ||
Maintenance of Golgi structure and function depends on the integrity of ER export | Q24653507 | ||
The syntaxins | Q24806291 | ||
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Requirements for signal peptide peptidase-catalyzed intramembrane proteolysis | Q28213796 | ||
Cell-surface expression of a new splice variant of the mouse signal peptide peptidase | Q28242598 | ||
Human sperm binding is mediated by the sialyl-Lewis(x) oligosaccharide on the zona pellucida | Q28245912 | ||
2016 update of the PRIDE database and its related tools | Q28603110 | ||
The Genotype-Tissue Expression (GTEx) project | Q28657968 | ||
SNAREs--engines for membrane fusion | Q29547230 | ||
Bi-directional protein transport between the ER and Golgi | Q29615233 | ||
The mechanisms of vesicle budding and fusion | Q29615234 | ||
Universal sample preparation method for proteome analysis | Q29615662 | ||
Stop and go extraction tips for matrix-assisted laser desorption/ionization, nanoelectrospray, and LC/MS sample pretreatment in proteomics | Q29615818 | ||
Carbohydrates and fertilization: an overview | Q30428190 | ||
Secretory cargo sorting by Ca2+-dependent Cab45 oligomerization at the trans-Golgi network | Q30755585 | ||
Release of signal peptide fragments into the cytosol requires cleavage in the transmembrane region by a protease activity that is specifically blocked by a novel cysteine protease inhibitor | Q31420350 | ||
VAMP-1: a synaptic vesicle-associated integral membrane protein | Q33583102 | ||
Cleavage by signal peptide peptidase is required for the degradation of selected tail-anchored proteins | Q33797023 | ||
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Accurate proteome-wide label-free quantification by delayed normalization and maximal peptide ratio extraction, termed MaxLFQ. | Q34157715 | ||
Foamy virus envelope protein is a substrate for signal peptide peptidase-like 3 (SPPL3). | Q34310343 | ||
Secretome analysis identifies novel signal Peptide peptidase-like 3 (Sppl3) substrates and reveals a role of Sppl3 in multiple Golgi glycosylation pathways | Q34469573 | ||
Shedding of glycan-modifying enzymes by signal peptide peptidase-like 3 (SPPL3) regulates cellular N-glycosylation | Q34807554 | ||
Sterile inflammation as a factor in human male infertility: Involvement of Toll like receptor 2, biglycan and peritubular cells | Q36193766 | ||
Latest emerging functions of SPP/SPPL intramembrane proteases | Q36331190 | ||
Proteolytic Processing of Neuregulin 1 Type III by Three Intramembrane-cleaving Proteases | Q36419261 | ||
Lectin binding of human sperm associates with DEFB126 mutation and serves as a potential biomarker for subfertility | Q36527122 | ||
Signal peptide peptidases: a family of intramembrane-cleaving proteases that cleave type 2 transmembrane proteins. | Q37476307 | ||
Mechanism, specificity, and physiology of signal peptide peptidase (SPP) and SPP-like proteases | Q38149887 | ||
FANTOM5 CAGE profiles of human and mouse samples | Q38604042 | ||
Signal peptide peptidase-mediated nuclear localization of heme oxygenase-1 promotes cancer cell proliferation and invasion independent of its enzymatic activity | Q38984568 | ||
Protein sorting at the ER-Golgi interface | Q39024908 | ||
Signal peptide peptidase and SPP-like proteases - Possible therapeutic targets? | Q39380083 | ||
Acrosome biogenesis: Revisiting old questions to yield new insights | Q40830245 | ||
Glycine 384 is required for presenilin-1 function and is conserved in bacterial polytopic aspartyl proteases | Q40845419 | ||
Role of vesicle-associated syntaxin 5 in the assembly of pre-Golgi intermediates | Q41064399 | ||
The intramembrane protease SPPL2a promotes B cell development and controls endosomal traffic by cleavage of the invariant chain | Q41881169 | ||
Assessment of spermatogenesis through staging of seminiferous tubules. | Q43437784 | ||
Targeting presenilin-type aspartic protease signal peptide peptidase with gamma-secretase inhibitors | Q44350630 | ||
SNARE proteins in membrane trafficking | Q47878377 | ||
Requirements for presenilin-dependent cleavage of notch and other transmembrane proteins. | Q52583319 | ||
The intramembrane protease SPPL2c promotes male germ cell development by cleaving phospholamban | Q91409250 | ||
P4510 | describes a project that uses | ImageQuant | Q112270642 |
P433 | issue | 3 | |
P577 | publication date | 2019-02-07 | |
P1433 | published in | EMBO Reports | Q5323356 |
P1476 | title | Signal Peptide Peptidase-Like 2c (SPPL2c) impairs vesicular transport and cleavage of SNARE proteins | |
P478 | volume | 20 |
Q91903241 | Regulating the regulator: intramembrane proteolysis of vesicular trafficking proteins and the SERCA regulator phospholamban | cites work | P2860 |
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