about
Lysosomal dysfunction and impaired autophagy in a novel mouse model deficient for the lysosomal membrane protein Cln7Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship.Retinal Degeneration in Mice Deficient in the Lysosomal Membrane Protein CLN7.Loss of CLN7 results in depletion of soluble lysosomal proteins and impaired mTOR reactivation.A newly generated neuronal cell model of CLN7 disease reveals aberrant lysosome motility and impaired cell survivalCurrent and Emerging Treatment Strategies for Neuronal Ceroid LipofuscinosesDisease-Linked Glutarylation Impairs Function and Interactions of Mitochondrial Proteins and Contributes to Mitochondrial Heterogeneity
P50
Q28510746-D294ECD4-CEB9-4BD3-AC94-DA8F1294A371Q39868934-2F0F3AC1-C80E-49FB-B2CF-0A8DBB0EA2F5Q51478423-46425C52-BABF-4468-A27C-CC168F529304Q52364277-305133E9-5E9B-4D11-B67E-7D7CAE313191Q57299362-57DC2F1B-E050-48B4-98EE-92DF3F3CE90DQ64086235-94049135-13F1-4902-97B5-21FAA43C8D97Q91405018-3A0C9CBF-5DF3-4878-A813-D16854D04440
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Stephan Storch
@ast
Stephan Storch
@en
Stephan Storch
@es
Stephan Storch
@nl
type
label
Stephan Storch
@ast
Stephan Storch
@en
Stephan Storch
@es
Stephan Storch
@nl
prefLabel
Stephan Storch
@ast
Stephan Storch
@en
Stephan Storch
@es
Stephan Storch
@nl
P106
P21
P31
P496
0000-0002-8807-5917