Anja Capell

researcher

Anja Capell is …
instance of (P31):
humanQ5

External links are
P496ORCID iD0000-0003-3118-911X

P108employerLudwig Maximilian University of MunichQ55044
P735given nameAnjaQ16419555
AnjaQ16419555
P106occupationresearcherQ1650915

Reverse relations

author (P50)
Q40267315A basolateral sorting signal directs ADAM10 to adherens junctions and is required for its function in cell migration
Q40725025A non-amyloidogenic function of BACE-2 in the secretory pathway
Q24630100ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import
Q40763877Apical sorting of beta-secretase limits amyloid beta-peptide production
Q42825763CADASIL-associated Notch3 mutations have differential effects both on ligand binding and ligand-induced Notch3 receptor signaling through RBP-Jk
Q59806735CSF progranulin increases in the course of Alzheimer's disease and is associated with sTREM2, neurodegeneration and cognitive decline
Q45231223Cellular ageing, increased mortality and FTLD-TDP-associated neuropathology in progranulin knockout mice
Q60912714Early increase of CSF sTREM2 in Alzheimer's disease is associated with tau related-neurodegeneration but not with amyloid-β pathology
Q58765250Early lysosomal maturation deficits in microglia triggers enhanced lysosomal activity in other brain cells of progranulin knockout mice
Q40663039Gamma-secretase activity is associated with a conformational change of nicastrin
Q28297818Gamma-secretase complex assembly within the early secretory pathway
Q36013954Impaired protein degradation in FTLD and related disorders
Q99420895Loss of TMEM106B potentiates lysosomal and FTLD-like pathology in progranulin-deficient mice
Q39767438Masking of transmembrane-based retention signals controls ER export of gamma-secretase
Q26824221Mechanisms of granulin deficiency: lessons from cellular and animal models
Q36003800Membrane orientation and subcellular localization of transmembrane protein 106B (TMEM106B), a major risk factor for frontotemporal lobar degeneration
Q51973117Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion.
Q47903554Mutant presenilin 2 transgenic mouse: effect on an age-dependent increase of amyloid beta-protein 42 in the brain
Q40619177Nicastrin interacts with gamma-secretase complex components via the N-terminal part of its transmembrane domain
Q64889283Opposite microglial activation stages upon loss of PGRN or TREM2 result in reduced cerebral glucose metabolism.
Q41889633Presenilin-1 affects trafficking and processing of betaAPP and is targeted in a complex with nicastrin to the plasma membrane
Q34030951Presenilin-1 mutations of leucine 166 equally affect the generation of the Notch and APP intracellular domains independent of their effect on Abeta 42 production
Q28201180Presenilin-dependent intramembrane proteolysis of CD44 leads to the liberation of its intracellular domain and the secretion of an Abeta-like peptide
Q34170826Progranulin transcripts with short and long 5' untranslated regions (UTRs) are differentially expressed via posttranscriptional and translational repression
Q39838808Proteolytic processing of TAR DNA binding protein-43 by caspases produces C-terminal fragments with disease defining properties independent of progranulin
Q35904539Reduced secretion and altered proteolytic processing caused by missense mutations in progranulin
Q39320638Retromer regulates postendocytic sorting of β-secretase in polarized Madin-Darby canine kidney cells
Q58125066Substitution of phenylalanine by proline at position 19 of amyloid β peptide results in an increased production of amyloid β peptides with alternative N-termini after protein kinase C stimulation
Q36366427TREM2 deficiency impairs chemotaxis and microglial responses to neuronal injury.
Q36073450TREM2 deficiency reduces the efficacy of immunotherapeutic amyloid clearance
Q24314869The FTLD risk factor TMEM106B and MAP6 control dendritic trafficking of lysosomes
Q40619751The presenilin C-terminus is required for ER-retention, nicastrin-binding and gamma-secretase activity
Q48177216The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects

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