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Search results 201 to 300 out of 309 for Ncl

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Type Details Score
Publication
First Author: Kumar V
Year: 2015
Journal: J Cell Biol
Title: A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity.
Volume: 211
Issue: 5
Pages: 1057-75
Publication  
First Author: Hammock EA
Year: 2010
Journal: Neural Dev
Title: Homologs of genes expressed in Caenorhabditis elegans GABAergic neurons are also found in the developing mouse forebrain.
Volume: 5
Pages: 32
Publication
First Author: Tarantino C
Year: 2010
Journal: FASEB J
Title: miRNA 34a, 100, and 137 modulate differentiation of mouse embryonic stem cells.
Volume: 24
Issue: 9
Pages: 3255-63
Publication
First Author: Papin J
Year: 2004
Journal: Curr Opin Biotechnol
Title: Bioinformatics and cellular signaling.
Volume: 15
Issue: 1
Pages: 78-81
Publication
First Author: Ko MS
Year: 1998
Journal: Hum Mol Genet
Title: Genome-wide mapping of unselected transcripts from extraembryonic tissue of 7.5-day mouse embryos reveals enrichment in the t-complex and under-representation on the X chromosome.
Volume: 7
Issue: 12
Pages: 1967-78
Publication      
First Author: Shanghai Model Organisms Center
Year: 2017
Journal: MGI Direct Data Submission
Title: Information obtained from the Shanghai Model Organisms Center (SMOC), Shanghai, China
Publication  
First Author: McKee AE
Year: 2005
Journal: BMC Dev Biol
Title: A genome-wide in situ hybridization map of RNA-binding proteins reveals anatomically restricted expression in the developing mouse brain.
Volume: 5
Pages: 14
Publication
First Author: Cobellis G
Year: 2005
Journal: Nucleic Acids Res
Title: Tagging genes with cassette-exchange sites.
Volume: 33
Issue: 4
Pages: e44
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2001
Title: Gene Ontology Annotation by the MGI Curatorial Staff
Publication
First Author: Hansen J
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: A large-scale, gene-driven mutagenesis approach for the functional analysis of the mouse genome.
Volume: 100
Issue: 17
Pages: 9918-22
Publication
First Author: Visel A
Year: 2004
Journal: Nucleic Acids Res
Title: GenePaint.org: an atlas of gene expression patterns in the mouse embryo.
Volume: 32
Issue: Database issue
Pages: D552-6
Publication
First Author: Stryke D
Year: 2003
Journal: Nucleic Acids Res
Title: BayGenomics: a resource of insertional mutations in mouse embryonic stem cells.
Volume: 31
Issue: 1
Pages: 278-81
Publication  
First Author: Bedogni F
Year: 2021
Journal: Front Mol Neurosci
Title: Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development.
Volume: 14
Pages: 686034
Publication
First Author: Hansen GM
Year: 2008
Journal: Genome Res
Title: Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.
Volume: 18
Issue: 10
Pages: 1670-9
Publication      
First Author: Helmholtz Zentrum Muenchen GmbH
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the EUCOMM and EUCOMMTools projects by the Helmholtz Zentrum Muenchen GmbH (Hmgu)
Publication        
First Author: The Gene Ontology Consortium
Year: 2014
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-rat orthologs
Publication
First Author: Magdaleno S
Year: 2006
Journal: PLoS Biol
Title: BGEM: an in situ hybridization database of gene expression in the embryonic and adult mouse nervous system.
Volume: 4
Issue: 4
Pages: e86
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2003
Title: MGI Sequence Curation Reference
Publication
First Author: Carninci P
Year: 2005
Journal: Science
Title: The transcriptional landscape of the mammalian genome.
Volume: 309
Issue: 5740
Pages: 1559-63
Publication
First Author: Kawai J
Year: 2001
Journal: Nature
Title: Functional annotation of a full-length mouse cDNA collection.
Volume: 409
Issue: 6821
Pages: 685-90
Publication
First Author: Zambrowicz BP
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.
Volume: 100
Issue: 24
Pages: 14109-14
Publication      
First Author: Mouse Genome Informatics (MGI) and National Center for Biotechnology Information (NCBI)
Year: 2008
Journal: Database Download
Title: Mouse Gene Trap Data Load from dbGSS
Publication        
First Author: Cyagen Biosciences Inc.
Year: 2022
Title: Cyagen Biosciences Website.
Publication        
First Author: AgBase, BHF-UCL, Parkinson's UK-UCL, dictyBase, HGNC, Roslin Institute, FlyBase and UniProtKB curators
Year: 2011
Title: Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Publication        
First Author: GOA curators
Year: 2016
Title: Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Publication
First Author: Okazaki Y
Year: 2002
Journal: Nature
Title: Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
Volume: 420
Issue: 6915
Pages: 563-73
Publication        
First Author: The Gene Ontology Consortium
Year: 2010
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs
Publication
First Author: Diez-Roux G
Year: 2011
Journal: PLoS Biol
Title: A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Volume: 9
Issue: 1
Pages: e1000582
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Mouse Genome Informatics Computational Sequence to Gene Associations
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome U74 Array Platform (A, B, C v2).
Publication        
First Author: Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas
Year: 2010
Title: Annotation inferences using phylogenetic trees
Publication      
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
Publication      
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
Publication      
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
Publication      
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
Publication      
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
Interaction Term
Publication
First Author: Cárcel-Trullols J
Year: 2015
Journal: Biochim Biophys Acta
Title: Cell biology of the NCL proteins: What they do and don't do.
Volume: 1852
Issue: 10 Pt B
Pages: 2242-55
Publication
First Author: Jalanko A
Year: 2006
Journal: Biochim Biophys Acta
Title: From genes to systems: new global strategies for the characterization of NCL biology.
Volume: 1762
Issue: 10
Pages: 934-44
Publication  
First Author: von Schantz C
Year: 2008
Journal: BMC Genomics
Title: Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases.
Volume: 9
Pages: 146
Allele
Name: nucleolin; endonuclease-mediated mutation 1, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
HT Experiment  
Experiment Type: transcription profiling by array
Study Type: WT vs. Mutant
Source: ArrayExpress
Strain
Attribute String: coisogenic, mutant strain, endonuclease-mediated mutation
Publication
First Author: Lührig S
Year: 2014
Journal: Stem Cells Dev
Title: Lrrc34, a novel nucleolar protein, interacts with npm1 and ncl and has an impact on pluripotent stem cells.
Volume: 23
Issue: 23
Pages: 2862-74
HT Experiment
Series Id: GSE37643
Experiment Type: transcription profiling by array
Study Type: WT vs. Mutant
Source: ArrayExpress
HT Experiment  
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: GEO
Publication
First Author: Zhou X
Year: 2015
Journal: J Cell Biol
Title: Prosaposin facilitates sortilin-independent lysosomal trafficking of progranulin.
Volume: 210
Issue: 6
Pages: 991-1002
Publication  
First Author: Zhou X
Year: 2017
Journal: Nat Commun
Title: Impaired prosaposin lysosomal trafficking in frontotemporal lobar degeneration due to progranulin mutations.
Volume: 8
Pages: 15277
Publication
First Author: Messer A
Year: 1999
Journal: Mol Genet Metab
Title: An early-onset congenic strain of the motor neuron degeneration (mnd) mouse.
Volume: 66
Issue: 4
Pages: 393-7
Publication
First Author: Seigel GM
Year: 2005
Journal: Eye (Lond)
Title: Progression of early postnatal retinal pathology in a mouse model of neuronal ceroid lipofuscinosis.
Volume: 19
Issue: 12
Pages: 1306-12
Publication
First Author: Elshatory Y
Year: 2003
Journal: FEBS Lett
Title: Early changes in gene expression in two models of Batten disease.
Volume: 538
Issue: 1-3
Pages: 207-12
Publication
First Author: Pontikis CC
Year: 2004
Journal: Brain Res
Title: Late onset neurodegeneration in the Cln3-/- mouse model of juvenile neuronal ceroid lipofuscinosis is preceded by low level glial activation.
Volume: 1023
Issue: 2
Pages: 231-42
Publication
First Author: Wheeler RB
Year: 2002
Journal: Am J Hum Genet
Title: The gene mutated in variant late-infantile neuronal ceroid lipofuscinosis (CLN6) and in nclf mutant mice encodes a novel predicted transmembrane protein.
Volume: 70
Issue: 2
Pages: 537-42
Publication
First Author: Holmberg V
Year: 2004
Journal: Neurobiol Dis
Title: The mouse ortholog of the neuronal ceroid lipofuscinosis CLN5 gene encodes a soluble lysosomal glycoprotein expressed in the developing brain.
Volume: 16
Issue: 1
Pages: 29-40
Publication
First Author: Chang MC
Year: 2017
Journal: J Exp Med
Title: Progranulin deficiency causes impairment of autophagy and TDP-43 accumulation.
Volume: 214
Issue: 9
Pages: 2611-2628
Publication
First Author: Wang L
Year: 2021
Journal: Nat Commun
Title: A novel lncRNA Discn fine-tunes replication protein A (RPA) availability to promote genomic stability.
Volume: 12
Issue: 1
Pages: 5572
Publication
First Author: Wang Y
Year: 2021
Journal: Sci Adv
Title: CLN7 is an organellar chloride channel regulating lysosomal function.
Volume: 7
Issue: 51
Pages: eabj9608
Publication  
First Author: Gueiderikh A
Year: 2021
Journal: Sci Adv
Title: Fanconi anemia A protein participates in nucleolar homeostasis maintenance and ribosome biogenesis.
Volume: 7
Issue: 1
Publication  
First Author: Lyly A
Year: 2009
Journal: BMC Cell Biol
Title: Novel interactions of CLN5 support molecular networking between Neuronal Ceroid Lipofuscinosis proteins.
Volume: 10
Pages: 83
Publication
First Author: Staropoli JF
Year: 2012
Journal: Am J Hum Genet
Title: A homozygous mutation in KCTD7 links neuronal ceroid lipofuscinosis to the ubiquitin-proteasome system.
Volume: 91
Issue: 1
Pages: 202-8
Publication
First Author: Poët M
Year: 2006
Journal: Proc Natl Acad Sci U S A
Title: Lysosomal storage disease upon disruption of the neuronal chloride transport protein ClC-6.
Volume: 103
Issue: 37
Pages: 13854-9
Publication
First Author: Ranta S
Year: 1999
Journal: Nat Genet
Title: The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8.
Volume: 23
Issue: 2
Pages: 233-6
Publication
First Author: Geraets RD
Year: 2017
Journal: PLoS One
Title: A tailored mouse model of CLN2 disease: A nonsense mutant for testing personalized therapies.
Volume: 12
Issue: 5
Pages: e0176526
Publication
First Author: Faust JR
Year: 1994
Journal: J Biol Chem
Title: Two related proteolipids and dolichol-linked oligosaccharides accumulate in motor neuron degeneration mice (mnd/mnd), a model for neuronal ceroid lipofuscinosis.
Volume: 269
Issue: 13
Pages: 10150-5
Publication
First Author: Cho SK
Year: 2005
Journal: Glycobiology
Title: Characterization of lipid-linked oligosaccharide accumulation in mouse models of Batten disease.
Volume: 15
Issue: 6
Pages: 637-48
Publication
First Author: Pardo CA
Year: 1994
Journal: Am J Pathol
Title: Accumulation of the adenosine triphosphate synthase subunit C in the mnd mutant mouse. A model for neuronal ceroid lipofuscinosis.
Volume: 144
Issue: 4
Pages: 829-35
Publication
First Author: Wendt KD
Year: 2005
Journal: Behav Brain Res
Title: Behavioral assessment in mouse models of neuronal ceroid lipofuscinosis using a light-cued T-maze.
Volume: 161
Issue: 2
Pages: 175-82
Publication
First Author: Guarneri R
Year: 2004
Journal: Brain Res
Title: Retinal oxidation, apoptosis and age- and sex-differences in the mnd mutant mouse, a model of neuronal ceroid lipofuscinosis.
Volume: 1014
Issue: 1-2
Pages: 209-20
Publication
First Author: Bermingham NA
Year: 1996
Journal: Genomics
Title: The mouse lysosomal membrane protein 1 gene as a candidate for the motorneuron degeneration (mnd) locus.
Volume: 32
Issue: 2
Pages: 266-71
Publication
First Author: Griffin JL
Year: 2002
Journal: Physiol Genomics
Title: Vitamin E deficiency and metabolic deficits in neuronal ceroid lipofuscinosis described by bioinformatics.
Volume: 11
Issue: 3
Pages: 195-203
Publication
First Author: Hersrud SL
Year: 2016
Journal: Biochim Biophys Acta
Title: Antigen presenting cell abnormalities in the Cln3(-/-) mouse model of juvenile neuronal ceroid lipofuscinosis.
Volume: 1862
Issue: 7
Pages: 1324-36
Publication
First Author: Pears MR
Year: 2005
Journal: J Biol Chem
Title: High resolution 1H NMR-based metabolomics indicates a neurotransmitter cycling deficit in cerebral tissue from a mouse model of Batten disease.
Volume: 280
Issue: 52
Pages: 42508-14
Publication  
First Author: Ketscher A
Year: 2016
Journal: Biochimie
Title: Neuroectoderm-specific deletion of cathepsin D in mice models human inherited neuronal ceroid lipofuscinosis type 10.
Volume: 122
Pages: 219-26
Publication
First Author: Kielar C
Year: 2009
Journal: Hum Mol Genet
Title: Molecular correlates of axonal and synaptic pathology in mouse models of Batten disease.
Volume: 18
Issue: 21
Pages: 4066-80
Publication
First Author: Kleine Holthaus SM
Year: 2018
Journal: Mol Ther
Title: Prevention of Photoreceptor Cell Loss in a Cln6nclf Mouse Model of Batten Disease Requires CLN6 Gene Transfer to Bipolar Cells.
Volume: 26
Issue: 5
Pages: 1343-1353
Publication
First Author: Gao H
Year: 2002
Journal: Am J Hum Genet
Title: Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse.
Volume: 70
Issue: 2
Pages: 324-35
Publication
First Author: Morgan JP
Year: 2013
Journal: PLoS One
Title: A murine model of variant late infantile ceroid lipofuscinosis recapitulates behavioral and pathological phenotypes of human disease.
Volume: 8
Issue: 11
Pages: e78694
Publication
First Author: Gorenberg EL
Year: 2022
Journal: PLoS Biol
Title: Identification of substrates of palmitoyl protein thioesterase 1 highlights roles of depalmitoylation in disulfide bond formation and synaptic function.
Volume: 20
Issue: 3
Pages: e3001590
Publication
First Author: Finn R
Year: 2012
Journal: J Neurosci Res
Title: Altered glutamate receptor function in the cerebellum of the Ppt1-/- mouse, a murine model of infantile neuronal ceroid lipofuscinosis.
Volume: 90
Issue: 2
Pages: 367-75
Publication
First Author: Hsu TI
Year: 2015
Journal: Oncogene
Title: MMP7-mediated cleavage of nucleolin at Asp255 induces MMP9 expression to promote tumor malignancy.
Volume: 34
Issue: 7
Pages: 826-37
Publication
First Author: Tsoi H
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: CAG expansion induces nucleolar stress in polyglutamine diseases.
Volume: 109
Issue: 33
Pages: 13428-33
Publication
First Author: Savchenko E
Year: 2017
Journal: Dis Model Mech
Title: Loss of Cln5 causes altered neurogenesis in a mouse model of a childhood neurodegenerative disorder.
Volume: 10
Issue: 9
Pages: 1089-1100
Publication
First Author: Blom T
Year: 2013
Journal: Dis Model Mech
Title: Exacerbated neuronal ceroid lipofuscinosis phenotype in Cln1/5 double-knockout mice.
Volume: 6
Issue: 2
Pages: 342-57
Publication  
First Author: Doccini S
Year: 2022
Journal: Cells
Title: Lysosomal Proteomics Links Disturbances in Lipid Homeostasis and Sphingolipid Metabolism to CLN5 Disease.
Volume: 11
Issue: 11
Publication  
First Author: Hafler BP
Year: 2014
Journal: Brain Res
Title: Progressive retinal degeneration and accumulation of autofluorescent lipopigments in Progranulin deficient mice.
Volume: 1588
Pages: 168-74
Publication  
First Author: Ward ME
Year: 2017
Journal: Sci Transl Med
Title: Individuals with progranulin haploinsufficiency exhibit features of neuronal ceroid lipofuscinosis.
Volume: 9
Issue: 385
Publication
First Author: Schultheis PJ
Year: 2013
Journal: Hum Mol Genet
Title: Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited α-synuclein accumulation and age-dependent sensorimotor deficits.
Volume: 22
Issue: 10
Pages: 2067-82
Publication
First Author: Miller JN
Year: 2015
Journal: Hum Mol Genet
Title: The novel Cln1(R151X) mouse model of infantile neuronal ceroid lipofuscinosis (INCL) for testing nonsense suppression therapy.
Volume: 24
Issue: 1
Pages: 185-96
Publication
First Author: Sharifi A
Year: 2010
Journal: Hum Mol Genet
Title: Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis.
Volume: 19
Issue: 22
Pages: 4497-514
Publication
First Author: Broom MF
Year: 1998
Journal: J Med Genet
Title: Ovine neuronal ceroid lipofuscinosis: a large animal model syntenic with the human neuronal ceroid lipofuscinosis variant CLN6.
Volume: 35
Issue: 9
Pages: 717-21
Publication  
First Author: Lonka L
Year: 2005
Journal: BMC Neurosci
Title: The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy.
Volume: 6
Pages: 27
Publication
First Author: Peddigari S
Year: 2013
Journal: Nucleic Acids Res
Title: hnRNPL and nucleolin bind LINE-1 RNA and function as host factors to modulate retrotransposition.
Volume: 41
Issue: 1
Pages: 575-85
Publication
First Author: Gongol B
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: Shear stress regulation of miR-93 and miR-484 maturation through nucleolin.
Volume: 116
Issue: 26
Pages: 12974-12979
Publication
First Author: Appu AP
Year: 2019
Journal: J Inherit Metab Dis
Title: Cln3-mutations underlying juvenile neuronal ceroid lipofuscinosis cause significantly reduced levels of Palmitoyl-protein thioesterases-1 (Ppt1)-protein and Ppt1-enzyme activity in the lysosome.
Volume: 42
Issue: 5
Pages: 944-954
Publication
First Author: Ookuma YF
Year: 2013
Journal: Histochem Cell Biol
Title: Multiple functional involvement of thymosin beta-4 in tooth germ development.
Volume: 139
Issue: 2
Pages: 355-70