Keywords: lipophuscinosis ceroid neuronal; AD; Alzheimer's disease; CNS; central nervous system; CPD; cycles per degree (of visual angle); DLGN; dorsal lateral geniculate nucleus; HD; Huntington's disease; NCL; neuronal ceroid lipofuscinosis; OKR; optokinetic reflex test; OMR; optomotor respon
مقالات ISI lipophuscinosis ceroid neuronal (ترجمه نشده)
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Keywords: lipophuscinosis ceroid neuronal; Aβ; amyloid-β peptide; AD; Alzheimer's disease; APP; amyloid precursor protein; ATP; adenosine triphosphate; BBB; blood-brain barrier; CNS; central nervous system; ECM; extracellular matrix; Hsp; heat shock protein; IFN; interferon; IκB; NF-κB inhib
Keywords: lipophuscinosis ceroid neuronal; Frontotemporal lobar degeneration; Neuronal ceroid lipofuscinosis; Progranulin; Conditional knockout mice; Neuropathology; Nestin;
Keywords: lipophuscinosis ceroid neuronal; FTLD-NCL family; Frontotemporal lobar degeneration; Neuronal ceroid lipofuscinosis; Progranulin mutation; Homozygous or heterozygous state;
Keywords: lipophuscinosis ceroid neuronal; AFR; African; AMR; Latino; BDSRA; Batten Disease Support and Research Association; EAS; East Asian; ExAC; Exome Aggregation Consortium; FIN; Finnish; FTD; frontotemporal dementia; HGMD; Human Gene Mutation Database; NCL; neuronal ceroid lipofuscinosis; NF
Keywords: lipophuscinosis ceroid neuronal; Cysteine cathepsin; Cathepsin D; Cystatin; Neuronal ceroid lipofuscinosis; EPM-1; Aging; Alzheimer's disease;
Keywords: lipophuscinosis ceroid neuronal; gLE; genetic leukoencephalopathy; CNS; central nervous system; MRI; magnetic resonance imaging; MSUD; Maple Syrup Urine Disease; ClC-2; Chloride Ion Channel 2; MLC; Megalencephalic Leukoencephalopathy with subcortical cysts; X-ALD; X-linked Adrenoleukodys
Keywords: lipophuscinosis ceroid neuronal; ERT; enzyme replacement therapy; CLN1; ceroid lipofuscinosis, neuronal-1; CLN2; ceroid lipofuscinosis, neuronal-2; LSD; lysosomal storage disorder; MU-6S-Palm-βGlc; 4-methylumbelliferyl-6-thiopalmitoyl-β-d-glucoside; NCL; neuronal ceroid lipofuscinosis;
Keywords: lipophuscinosis ceroid neuronal; Neuronal ceroid lipofuscinosis; NCL; Neurodegeneration; Model systems;
Keywords: lipophuscinosis ceroid neuronal; NCL, neuronal ceroid lipofuscinosis; CLN11, neuronal ceroid lipofuscinosis-11; ONL, outer nuclear layer; INL, inner nuclear layer; GCL, ganglion cell layerNeurodegeneration; Progranulin; Autofluorescent storage material; Neuronal ceroid lipofuscinosis
Keywords: lipophuscinosis ceroid neuronal; AP-AB; anti-phospholipid antibody(ies); APS; anti-phospholipid syndrome; BMP/LBPA; bis(monoacylglycero)phosphate/lysobisphosphatidic acid; CAD; cationic amphiphilic drug(s); Chol; cholesterol; CL; cardiolipin; ECV/MVB; endosomal carrier vesicle(s)/multive
Keywords: lipophuscinosis ceroid neuronal; NCL; neuronal ceroid lipofuscinosis; CDK; cyclin-dependent kinase; S1P; sphingosine-1-phosphate; GlcCer; glucosylceramide; TLC; thin layer chromatography; FA; fact acid; LacCer; lactosylceramide; Sulf; sulfatide; So; sphingosine; Batten disease; Cell cycl
Keywords: lipophuscinosis ceroid neuronal; retinal degeneration; pupillary light reflex; electroretinogram; neuronal ceroid lipofuscinosis; neurodegeneration; lysosomal storage disease;
Keywords: lipophuscinosis ceroid neuronal; AD; Alzheimer's disease; ALS; amyotrophic lateral sclerosis; EDTA; ethylenediaminetetraacetic acid; FTLD; frontotemporal lobar degeneration; GFAP; glial fibrillary acidic protein; HE; hematoxylin and eosin; HPRT; hypoxanthine phosphoribosyltransferase;
Keywords: lipophuscinosis ceroid neuronal; AD; Alzheimer's disease; ALS; amyotrophic lateral sclerosis; ANOVA; Analysis of variance; Aβ; amyloid β; bHLH; basic Helix-Loop-Helix; C4; complement C4; CLEAR; coordinated lysosomal expression and regulation; Cyba; cytochrome b-245 light chain; DW; d
Keywords: lipophuscinosis ceroid neuronal; sleep; neuronal ceroid lipofuscinosis; seizures; vision loss; restless leg syndrome
The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal
Keywords: lipophuscinosis ceroid neuronal; P5-ATPase; ATP13A2; Parkinson's disease; Neuronal ceroid lipofuscinosis; Endolysosomal pathway; Lysosome degradation; CHO cells; Chinese hamster ovary cells; EE; Early Endosome; LE; Late Endosome; KRS; Kufor Rakeb Syndrome; MVB; Multi-Vesicular Body; NCL;
Juvenile-onset neuronal ceroid lipofuscinosis (CLN1) disease with a novel deletion and duplication in the PPT1 gene
Keywords: lipophuscinosis ceroid neuronal; Neuronal ceroid lipofuscinosis; Juvenile-onset; Novel mutations; CLN1; PPT1;
Immunogenicity to cerliponase alfa intracerebroventricular enzyme replacement therapy for CLN2 disease: Results from a Phase 1/2 study
Keywords: lipophuscinosis ceroid neuronal; Cerliponase alfa; Enzyme replacement therapy; CLN2; Neuronal ceroid lipofuscinosis; Anti-drug antibodies; Hypersensitivity; Immunogenicity; ADA; anti-drug antibody; ICV; intracerebroventricular.; ML; motor-language.; NAb; neutralizing anti-drug antibody.;
First case of genetically confirmed CLN3 disease in Chinese with cDNA sequencing revealing pathogenicity of a novel splice site variant
Keywords: lipophuscinosis ceroid neuronal; CLN3 disease; Neuronal ceroid lipofuscinosis; Electron microscopy; Splice site mutation; cDNA sequencing;
Cln3 function is linked to osmoregulation in a Dictyostelium model of Batten disease
Keywords: lipophuscinosis ceroid neuronal; Neuronal ceroid lipofuscinosis; Batten disease; CLN3; Dictyostelium discoideum; Osmoregulation; RNA sequencing;
Cln5 is secreted and functions as a glycoside hydrolase in Dictyostelium
Keywords: lipophuscinosis ceroid neuronal; AprA; autocrine proliferation repressor A; CadA; calcium-dependent cell adhesion molecule A; CDC48; cell division cycle protein 48; CfaD; counting factor-associated protein D; CLN5; ceroid lipofuscinosis neuronal 5; CM; conditioned media; CprA; cysteine p
Identification of CLN6 as a molecular entity of endoplasmic reticulum-driven anti-aggregate activity
Keywords: lipophuscinosis ceroid neuronal; αB-crystallin; Aggregate; CLN6; Endoplasmic reticulum; Neuronal ceroid lipofuscinosis;
in vivo localization of the neuronal ceroid lipofuscinosis proteins, CLN3 and CLN7, at endogenous expression levels
Keywords: lipophuscinosis ceroid neuronal; CLN3; CLN7; MFSD8; Localization; Neuronal ceroid lipofuscinosis; Batten disease; Drosophila;
CLN5 is cleaved by members of the SPP/SPPL family to produce a mature soluble protein
Keywords: lipophuscinosis ceroid neuronal; CLN5; Signal Peptide Peptidase-like proteases; Neuronal ceroid lipofuscinosis; Endosomes; Neurodegeneration; Intracellular trafficking;
ReviewCanine neuronal ceroid lipofuscinoses: Promising models for preclinical testing of therapeutic interventions
Keywords: lipophuscinosis ceroid neuronal; Dog; Canine; Retinal degeneration; Neurodegeneration; Heredity; Lysosomal storage disease; Neuronal ceroid lipofuscinosis; Therapy; Genetics;
Characterisation of early changes in ovine CLN5 and CLN6 Batten disease neural cultures for the rapid screening of therapeutics
Keywords: lipophuscinosis ceroid neuronal; Batten disease; Neuronal ceroid lipofuscinosis; CLN5; CLN6; Neuronal cell culture; Gene therapy; Autophagy;
Loss of Cln3 impacts protein secretion in the social amoeba Dictyostelium
Keywords: lipophuscinosis ceroid neuronal; AprA; autocrine proliferation repressor A; CfaD; counting factor-associated protein D; CF; counting factor; CLN3; ceroid lipofuscinosis neuronal 3; CM; conditioned media; CMF; conditioned media factor; CsbA; contact site B protein A; CV; contractile vacuo
Intracerebroventricular gene therapy that delays neurological disease progression is associated with selective preservation of retinal ganglion cells in a canine model of CLN2 disease
Keywords: lipophuscinosis ceroid neuronal; Neuronal ceroid lipofuscinosis; Gene therapy; Retinal degeneration; Optic nerve;
Neuroectoderm-specific deletion of cathepsin D in mice models human inherited neuronal ceroid lipofuscinosis type 10
Keywords: lipophuscinosis ceroid neuronal; Cathepsin D; Neuronal lipofuscinosis; Neurodegenerative disease; Conditional knock-out; CD; cluster of differentiation; CNS; central nervous system; Ctsd; mouse cathepsin D; CTSD; human cathepsin D; NCL; neuronal ceroid lipofuscinosis; P; postnatal day;
Diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2 disease): Expert recommendations for early detection and laboratory diagnosis
Keywords: lipophuscinosis ceroid neuronal; Neuronal ceroid lipofuscinosis; Laboratory diagnosis; Lysosomal storage disorder; Expert recommendations; Neurodegeneration; Genetic cause of epilepsy;
Astrocytes and lysosomal storage diseases
Keywords: lipophuscinosis ceroid neuronal; AD; Alzheimer's disease; DAMP; danger-associated molecular pattern; GBA; glucocerebrosidase; GFAP; glial fibrillary acidic protein; GLD; globoid cell leukodystrophy; INCL; infantile neuronal ceroid lipofuscinosis; JNCL; juvenile neuronal ceroid lipofusc
Antigen presenting cell abnormalities in the Cln3â/â mouse model of juvenile neuronal ceroid lipofuscinosis
Keywords: lipophuscinosis ceroid neuronal; APCs; antigen presenting cells; APhC; allophycocyanin; BM; bone marrow; BMCCs; bone marrow cultured cells; BM-DCs; bone marrow dendritic cells; BM-MÏ; bone marrow macrophages; BSA; bovine serum albumin; CHX; cycloheximide; CTB; cholera toxin B; DCs; dend
Palmitoylation in Alzheimerâ¿¿s disease and other neurodegenerative diseases
Keywords: lipophuscinosis ceroid neuronal; ABCA1; ATP-binding cassette transporter A1; AD; Alzheimer⿿s disease; ADAM17; a disintegrin and metalloproteinase 17; AICD; APP intracellular domain; AKAP79; A-kinase anchoring protein 79; AMPA; α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate; APP; amy
Bridging NCL research gaps
Keywords: lipophuscinosis ceroid neuronal; NCL; neuronal ceroid lipofuscinosis; LSD; lysosomal storage disease; ERT; enzyme replacement therapy; ER; endoplasmic reticulum; PoC; proof-of-concept; iPS cell; induced pluripotent stem cell; PD; Parkinson's disease; NPC; Niemann-Pick type C; SLOS; Smi
Genetics of the neuronal ceroid lipofuscinoses (Batten disease)
Keywords: lipophuscinosis ceroid neuronal; NCL; Neuronal ceroid lipofuscinosis; EPMR; Epilepsy with progressive mental retardation; PME; Progressive myoclonic epilepsy; Batten; CLN; Neuronal ceroid lipofuscinosis; NCL; genetics, mutation;
Towards a new understanding of NCL pathogenesis
Keywords: lipophuscinosis ceroid neuronal; Neuronal ceroid lipofuscinosis; Storage material accumulation; Selective neuron loss; Glial dysfunction; Pathogenesis;
Guidelines for incorporating scientific knowledge and practice on rare diseases into higher education: neuronal ceroid lipofuscinoses as a model disorder
Keywords: lipophuscinosis ceroid neuronal; CEMECO; Centro de Estudio de las MetabolopatÃas Congénitas-Center for Research on Inborn Errors of Metabolism in Córdoba-Argentina; CME; Continuing Medical Education; CPD; Continuing Professional Development; EUCERD; European Union Committee of Experts
Golden Retriever dogs with neuronal ceroid lipofuscinosis have a two-base-pair deletion and frameshift in CLN5
Keywords: lipophuscinosis ceroid neuronal; Whole genome sequence; Neuronal ceroid lipofuscinosis; Canine model; CLN5 mutation; Batten disease; Lysosomal storage disease; Neurodegeneration;
Proteolytic processing of the neuronal ceroid lipofuscinosis related lysosomal protein CLN5
Keywords: lipophuscinosis ceroid neuronal; Neuronal ceroid lipofuscinosis; CLN5; Proteolytic processing; Lysosomal storage disorder;
Experimental therapies in the neuronal ceroid lipofuscinoses
Keywords: lipophuscinosis ceroid neuronal; Neuronal ceroid lipofuscinosis; Batten disease; Small molecule therapy; Cell therapy; Enzyme replacement therapy; Gene therapy;
Multifocal retinopathy in Dachshunds with CLN2 neuronal ceroid lipofuscinosis
Keywords: lipophuscinosis ceroid neuronal; Dog; Canine; Neuronal ceroid lipofuscinosis; Bullous retinopathy; Retinal detachment; TPP1; CLN2; BEST1;
Mutations in MFSD8, Encoding a Lysosomal Membrane Protein, Are Associated with Nonsyndromic Autosomal Recessive Macular Dystrophy
Keywords: lipophuscinosis ceroid neuronal; ACHM; achromatopsia; ar; autosomal recessive; bp; base pair; COD; cone dystrophy; CRD; cone-rod dystrophy; ERG; electroretinography; mfERG; multifocal electroretinography; NCL; neuronal ceroid lipofuscinosis; OCT; optical coherence tomography; PCR; polyme
Compartmentalized zinc deficiency and toxicities caused by ZnT and Zip gene over expression result in specific phenotypes in Drosophila
Keywords: lipophuscinosis ceroid neuronal; ER; endoplasmic reticulum; (e)GFP; (enhanced) green fluorescent protein; RFP; red fluorescent protein; Ztox; zinc toxicity; NCL; neuronal ceroid lipofuscinosis; Drosophila; Zinc homeostasis; Zip; ZnT; Ion transport;
Clinical researchClinico-pathological manifestations of variant late infantile neuronal ceroid lipofuscinosis (vLINCL) caused by a novel mutation in MFSD8 gene
Keywords: lipophuscinosis ceroid neuronal; Neuronal ceroid lipofuscinosis; Autosomal recessive; Retinal degeneration; Lysosomal storage;
Gene disruption of Mfsd8 in mice provides the first animal model for CLN7 disease
Keywords: lipophuscinosis ceroid neuronal; β-gal; β-galactosidase; CtsD; cathepsin D; CD68; cluster of differentiation 68; GFAP; glial fibrillary acidic protein; Lamp1; lysosome-associated membrane protein 1; Lamp2; lysosome-associated membrane protein 2; MFSD8; major facilitator superfamily dom
Case studyCLN6 disease caused by the same mutation originating in Pakistan has varying pathology
Keywords: lipophuscinosis ceroid neuronal; Batten; Neuronal ceroid lipofuscinosis; NCL; CLN6; Pathology; Prenatal;
Pathogenesis and therapies for infantile neuronal ceroid lipofuscinosis (infantile CLN1 disease)
Keywords: lipophuscinosis ceroid neuronal; Neuronal ceroid lipofuscinosis; Batten disease; Neurodegeneration; Neuroinflammation; Lysosomal storage disease; Gene therapy
Genetic basis and phenotypic correlations of the neuronal ceroid lipofusinoses
Keywords: lipophuscinosis ceroid neuronal; NCL, Neuronal ceroid lipofuscinosis; EPMR, progressive epilepsy with mental retardationBatten; CLN; Neuronal ceroid lipofuscinosis; NCL
Bioinformatic perspectives in the neuronal ceroid lipofuscinoses
Keywords: lipophuscinosis ceroid neuronal; Neuronal ceroid lipofuscinosis; Bioinformatics; Linkage analysis; Next generation sequencing; Topology