Selectivity and types of cell death in the neuronal ceroid lipofuscinoses.
about
Neurodegeneration and Epilepsy in a Zebrafish Model of CLN3 Disease (Batten Disease)Increased expression of lysosomal acid phosphatase in CLN3-defective cells and mouse brain tissueHigh resolution 1H NMR-based metabolomics indicates a neurotransmitter cycling deficit in cerebral tissue from a mouse model of Batten diseaseMurine cathepsin F deficiency causes neuronal lipofuscinosis and late-onset neurological disease.LAMP-2 deficiency leads to hippocampal dysfunction but normal clearance of neuronal substrates of chaperone-mediated autophagy in a mouse model for Danon diseaseA tailored mouse model of CLN2 disease: A nonsense mutant for testing personalized therapies.Combination small molecule PPT1 mimetic and CNS-directed gene therapy as a treatment for infantile neuronal ceroid lipofuscinosis.A metabolomic comparison of mouse models of the Neuronal Ceroid Lipofuscinoses.Disruption of the autophagy-lysosome pathway is involved in neuropathology of the nclf mouse model of neuronal ceroid lipofuscinosisLooking chloride channels straight in the eye: bestrophins, lipofuscinosis, and retinal degeneration.Genetic modifiers of Drosophila palmitoyl-protein thioesterase 1-induced degeneration.Neuroinflammatory paradigms in lysosomal storage diseases.Photoreceptor phagosome processing defects and disturbed autophagy in retinal pigment epithelium of Cln3Δex1-6 mice modelling juvenile neuronal ceroid lipofuscinosis (Batten disease).Biometals in rare neurodegenerative disorders of childhood.Autophagy in neuroprotection and neurodegeneration: A question of balance.Brain Region-Specific Degeneration with Disease Progression in Late Infantile Neuronal Ceroid Lipofuscinosis (CLN2 Disease).Location and connectivity determine GABAergic interneuron survival in the brains of South Hampshire sheep with CLN6 neuronal ceroid lipofuscinosisOsmoregulation of ceroid neuronal lipofuscinosis type 3 in the renal medullaGenetic modulation of apoptotic pathways fails to alter disease course in tripeptidyl-peptidase 1 deficient mice.Vision loss in juvenile neuronal ceroid lipofuscinosis (CLN3 disease)Neuropeptide changes and neuroactive amino acids in CSF from humans and sheep with neuronal ceroid lipofuscinoses (NCLs, Batten disease).Juvenile neuronal ceroid lipofuscinosis (JNCL) and the eye.Pathophysiology of neuropathic lysosomal storage disorders.Treating inflammation in childhood neurodegenerative disorders.Neuronopathic lysosomal storage diseases: clinical and pathologic findings.Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration.A zebrafish model of CLN2 disease is deficient in tripeptidyl peptidase 1 and displays progressive neurodegeneration accompanied by a reduction in proliferation.
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P2860
Selectivity and types of cell death in the neuronal ceroid lipofuscinoses.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Selectivity and types of cell death in the neuronal ceroid lipofuscinoses.
@ast
Selectivity and types of cell death in the neuronal ceroid lipofuscinoses.
@en
type
label
Selectivity and types of cell death in the neuronal ceroid lipofuscinoses.
@ast
Selectivity and types of cell death in the neuronal ceroid lipofuscinoses.
@en
prefLabel
Selectivity and types of cell death in the neuronal ceroid lipofuscinoses.
@ast
Selectivity and types of cell death in the neuronal ceroid lipofuscinoses.
@en
P2093
P2860
P1433
P1476
Selectivity and types of cell death in the neuronal ceroid lipofuscinoses.
@en
P2093
Hannah M Mitchison
Jonathan D Cooper
Ming J Lim
P2860
P356
10.1111/J.1750-3639.2004.TB00502.X
P577
2004-01-01T00:00:00Z