Pages that link to "Q24791822"
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The following pages link to Membrane trafficking and mitochondrial abnormalities precede subunit c deposition in a cerebellar cell model of juvenile neuronal ceroid lipofuscinosis (Q24791822):
Displayed 50 items.
- Ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease) (Q14905130) (← links)
- Early endosome antigen 1 (Q14911544) (← links)
- Lysosomal-associated membrane protein 1 (Q21494692) (← links)
- Cathepsin D (Q21499226) (← links)
- RAB7, member RAS oncogene family (Q21986364) (← links)
- Neuronal ceroid lipofuscinosis protein CLN3 interacts with motor proteins and modifies location of late endosomal compartments (Q24302244) (← links)
- FRET-assisted determination of CLN3 membrane topology (Q27318704) (← links)
- Loss of Cln3 function in the social amoeba Dictyostelium discoideum causes pleiotropic effects that are rescued by human CLN3 (Q27334931) (← links)
- Neurodegeneration and Epilepsy in a Zebrafish Model of CLN3 Disease (Batten Disease) (Q27339580) (← links)
- Distinct early molecular responses to mutations causing vLINCL and JNCL presage ATP synthase subunit C accumulation in cerebellar cells (Q27354870) (← links)
- Abnormally increased surface expression of AMPA receptors in the cerebellum, cortex and striatum of Cln3(-/-) mice (Q28393049) (← links)
- Lysosomal dysfunction and impaired autophagy in a novel mouse model deficient for the lysosomal membrane protein Cln7 (Q28510746) (← links)
- CLN3 deficient cells display defects in the ARF1-Cdc42 pathway and actin-dependent events (Q28513970) (← links)
- Autophagy is disrupted in a knock-in mouse model of juvenile neuronal ceroid lipofuscinosis (Q28591948) (← links)
- Visual deficits in a mouse model of Batten disease are the result of optic nerve degeneration and loss of dorsal lateral geniculate thalamic neurons (Q28592401) (← links)
- Partial correction of the CNS lysosomal storage defect in a mouse model of juvenile neuronal ceroid lipofuscinosis by neonatal CNS administration of an adeno-associated virus serotype rh.10 vector expressing the human CLN3 gene. (Q30574131) (← links)
- Alterations in ROS activity and lysosomal pH account for distinct patterns of macroautophagy in LINCL and JNCL fibroblasts (Q31110961) (← links)
- Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases (Q33326044) (← links)
- The juvenile Batten disease protein, CLN3, and its role in regulating anterograde and retrograde post-Golgi trafficking (Q34271805) (← links)
- A homozygous mutation in KCTD7 links neuronal ceroid lipofuscinosis to the ubiquitin-proteasome system. (Q34285108) (← links)
- An atypical case of neuronal ceroid lipofuscinosis with co-inheritance of a variably penetrant POLG1 mutation (Q34315263) (← links)
- The Batten disease gene CLN3 is required for the response to oxidative stress. (Q34829561) (← links)
- Partial genetic suppression of a loss-of-function mutant of the neuronal ceroid lipofuscinosis-associated protease TPP1 in Dictyostelium discoideum. (Q35041354) (← links)
- Evidence for aberrant astrocyte hemichannel activity in Juvenile Neuronal Ceroid Lipofuscinosis (JNCL). (Q35149204) (← links)
- Genetic modifiers of Drosophila palmitoyl-protein thioesterase 1-induced degeneration (Q35844775) (← links)
- Unbiased Cell-based Screening in a Neuronal Cell Model of Batten Disease Highlights an Interaction between Ca2+ Homeostasis, Autophagy, and CLN3 Protein Function (Q35860759) (← links)
- Analysis of potential biomarkers and modifier genes affecting the clinical course of CLN3 disease (Q35876823) (← links)
- Lithium rescues the impaired autophagy process in CbCln3(Δex7/8/Δex7/8) cerebellar cells and reduces neuronal vulnerability to cell death via IMPase inhibition. (Q35896710) (← links)
- Neuron-astrocyte interactions in neurodegenerative diseases: Role of neuroinflammation (Q36238937) (← links)
- Photoreceptor phagosome processing defects and disturbed autophagy in retinal pigment epithelium of Cln3Δex1-6 mice modelling juvenile neuronal ceroid lipofuscinosis (Batten disease). (Q36302113) (← links)
- Astrocytes and lysosomal storage diseases (Q36332588) (← links)
- RANK Ligand Modulation of Autophagy in Oral Squamous Cell Carcinoma Tumor Cells (Q36362955) (← links)
- A new large animal model of CLN5 neuronal ceroid lipofuscinosis in Borderdale sheep is caused by a nucleotide substitution at a consensus splice site (c.571+1G>A) leading to excision of exon 3. (Q36473670) (← links)
- Alterations in striatal dopamine catabolism precede loss of substantia nigra neurons in a mouse model of juvenile neuronal ceroid lipofuscinosis (Q36682820) (← links)
- Lysosomal Storage Diseases-Regulating Neurodegeneration (Q36771137) (← links)
- Antigen presenting cell abnormalities in the Cln3(-/-) mouse model of juvenile neuronal ceroid lipofuscinosis (Q36986268) (← links)
- Location and connectivity determine GABAergic interneuron survival in the brains of South Hampshire sheep with CLN6 neuronal ceroid lipofuscinosis (Q37109009) (← links)
- Monitoring autophagy in lysosomal storage disorders (Q37159173) (← links)
- Osmoregulation of ceroid neuronal lipofuscinosis type 3 in the renal medulla (Q37174221) (← links)
- Vision loss in juvenile neuronal ceroid lipofuscinosis (CLN3 disease) (Q37260497) (← links)
- CLN3 loss disturbs membrane microdomain properties and protein transport in brain endothelial cells (Q37309514) (← links)
- Neuropeptide changes and neuroactive amino acids in CSF from humans and sheep with neuronal ceroid lipofuscinoses (NCLs, Batten disease). (Q37394217) (← links)
- Efficacy of phosphodiesterase-4 inhibitors in juvenile Batten disease (CLN3). (Q37561375) (← links)
- Human iPSC models of neuronal ceroid lipofuscinosis capture distinct effects of TPP1 and CLN3 mutations on the endocytic pathway (Q37649077) (← links)
- Congenic fine-mapping identifies a major causal locus for variation in the native collateral circulation and ischemic injury in brain and lower extremity (Q37663600) (← links)
- Neuronal ceroid lipofuscinosis: impact of recent genetic advances and expansion of the clinicopathologic spectrum (Q38115191) (← links)
- NCLs and ER: A stressful relationship. (Q39229073) (← links)
- Linking mitochondrial dysfunction to neurodegeneration in lysosomal storage diseases. (Q39287167) (← links)
- btn1 affects endocytosis, polarization of sterol-rich membrane domains and polarized growth in Schizosaccharomyces pombe (Q39598497) (← links)
- Aberrant adhesion impacts early development in a Dictyostelium model for juvenile neuronal ceroid lipofuscinosis (Q41510250) (← links)