Ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)

Ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)

Item
http://www.wikidata.org/entity/Q14905130
Cln3
P688
CLN3 protein is targeted to neuronal synapses but excluded from synaptic vesicles: new clues to Batten diseaseMembrane trafficking and mitochondrial abnormalities precede subunit c deposition in a cerebellar cell model of juvenile neuronal ceroid lipofuscinosisIncreased expression of lysosomal acid phosphatase in CLN3-defective cells and mouse brain tissueNovel interactions of CLN5 support molecular networking between Neuronal Ceroid Lipofuscinosis proteinsNeuronal vulnerability of CLN3 deletion to calcium-induced cytotoxicity is mediated by calsenilinA mouse gene knockout model for juvenile ceroid-lipofuscinosis (Batten disease)High resolution 1H NMR-based metabolomics indicates a neurotransmitter cycling deficit in cerebral tissue from a mouse model of Batten diseaseSelectively increased sensitivity of cerebellar granule cells to AMPA receptor-mediated excitotoxicity in a mouse model of Batten diseaseCLN3 deficient cells display defects in the ARF1-Cdc42 pathway and actin-dependent eventsBehavioral assessment in mouse models of neuronal ceroid lipofuscinosis using a light-cued T-mazeA murine model for juvenile NCL: gene targeting of mouse Cln3Autophagy is disrupted in a knock-in mouse model of juvenile neuronal ceroid lipofuscinosisVisual deficits in a mouse model of Batten disease are the result of optic nerve degeneration and loss of dorsal lateral geniculate thalamic neuronsTargeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]Unbiased Cell-based Screening in a Neuronal Cell Model of Batten Disease Highlights an Interaction between Ca2+ Homeostasis, Autophagy, and CLN3 Protein Function.Photoreceptor phagosome processing defects and disturbed autophagy in retinal pigment epithelium of Cln3Δex1-6 mice modelling juvenile neuronal ceroid lipofuscinosis (Batten disease).Antigen presenting cell abnormalities in the Cln3(-/-) mouse model of juvenile neuronal ceroid lipofuscinosisOsmoregulation of ceroid neuronal lipofuscinosis type 3 in the renal medullaCLN3 loss disturbs membrane microdomain properties and protein transport in brain endothelial cells.CLN3 defines a novel antiapoptotic pathway operative in neurodegeneration and mediated by ceramide.Novel interactions of CLN3 protein link Batten disease to dysregulation of fodrin-Na+, K+ ATPase complex.Altered arginine metabolism in the central nervous system (CNS) of the Cln3-/- mouse model of juvenile Batten disease.Defective synaptic transmission causes disease signs in a mouse model of juvenile neuronal ceroid lipofuscinosis.Altered Cerebellar Short-Term Plasticity but No Change in Postsynaptic AMPA-Type Glutamate Receptors in a Mouse Model of Juvenile Batten Disease.A knock-in reporter model of Batten disease
P921
Q24291761-FDC0F406-A85D-4527-80B5-D2F24F0FB0B6Q24791822-7E999CEE-2062-44A4-A113-32B66088BF00Q28114924-DF8A61D4-1228-4E1E-B994-C988DAAD93A8Q28115540-08FA344E-BF7E-4C7D-AD99-1E0E0AB4C0DBQ28504443-896BF911-D51C-4C56-8D84-CFC7C17EF7A8Q28504695-3670B049-EE23-48BD-A410-53EF9E32D81AQ28505711-2EE2523C-8447-453D-9C85-8E9C87B2B6CBQ28511406-C706C152-6877-4A59-92B5-B41D87726B68Q28513970-83201108-91D6-4DFC-A772-0CBF41B5EEFFQ28586963-ED17C2B1-FD34-4215-B3A7-BEE585A60E53Q28588743-7FCBB583-D14E-40D7-8E3A-2C46BA036AB7Q28591948-8EDFAA4F-FEDA-4B57-9122-8116BE4E742CQ28592401-704D59A2-B2D4-41CE-B220-EFC4F657FE30Q28593659-A06043FD-DED7-450D-88D2-D3A13F64C145Q35860759-0278351B-4402-4799-A14E-C6B67C6A2CF9Q36302113-F906169F-2F8C-4584-9A3F-61FF61954A0AQ36986268-38AEC801-9576-4DBE-B1DF-0E066B857660Q37174221-3D449642-427D-47AD-B73A-1B2BC32C77AAQ37309514-D7CCA089-9D5E-4958-AA3B-70869F8B41B4Q40962723-72503E6E-9997-4695-94F1-2EDDA5051D84Q42438650-23301B16-EB7C-4AEC-917D-E3A93619A715Q46089492-21159023-0C2C-4A0E-B4FF-A6D6EA1A6172Q47140069-4060F180-708C-4844-9FA2-10FAE8B27691Q54942202-53404E4F-E0FB-4276-ACC9-9F428906731DQ81250919-F4E780C2-E786-4AF8-8F36-DB60327FE6BD
P921

Ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)

Item
http://www.wikidata.org/entity/Q14905130
description
mammalian protein found in Mus musculus
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)
@nl
protèin
@ace
protéine
@fr
بروتين في فأر المنازل
@ar
name
Ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)
@en
Ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)
@nl
type
label
Ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)
@en
Ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)
@nl
altLabel
Cln3
@en
Protein CLN3
@en
battenin
@en
prefLabel
Ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)
@en
Ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)
@nl
P31
P352
P361
P637
P680
P681
P682
P702
P703
P705
P7260
P352
P637
P31
P352
P361
P637
P680
P681
P682
P702
P703
P705
P7260