|  Help  |  About  |  Contact Us

Search our database by keyword

- or -

Examples

  • Search this entire website. Enter identifiers, names or keywords for genes, diseases, strains, ontology terms, etc. (e.g. Pax6, Parkinson, ataxia)
  • Use OR to search for either of two terms (e.g. OR mus) or quotation marks to search for phrases (e.g. "dna binding").
  • Boolean search syntax is supported: e.g. Balb* for partial matches or mus AND NOT embryo to exclude a term

Search results 1 to 98 out of 98 for Atp7b

Category restricted to Publication (x)

0.03s

Categories

Category: Publication
Type Details Score
Publication
First Author: Ogórek M
Year: 2017
Journal: Metallomics
Title: Atp7a and Atp7b regulate copper homeostasis in developing male germ cells in mice.
Volume: 9
Issue: 9
Pages: 1288-1303
Publication
First Author: Leonhardt K
Year: 2009
Journal: J Biol Chem
Title: Functional interactions of Cu-ATPase ATP7B with cisplatin and the role of ATP7B in the resistance of cells to the drug.
Volume: 284
Issue: 12
Pages: 7793-802
Publication
First Author: Muchenditsi A
Year: 2017
Journal: Am J Physiol Gastrointest Liver Physiol
Title: Targeted inactivation of copper transporter Atp7b in hepatocytes causes liver steatosis and obesity in mice.
Volume: 313
Issue: 1
Pages: G39-G49
Publication
First Author: Terwel D
Year: 2011
Journal: J Neurochem
Title: Neuroinflammatory and behavioural changes in the Atp7B mutant mouse model of Wilson's disease.
Volume: 118
Issue: 1
Pages: 105-12
Publication
First Author: He K
Year: 2011
Journal: Mamm Genome
Title: Identification of high-copper-responsive target pathways in Atp7b knockout mouse liver by GSEA on microarray data sets.
Volume: 22
Issue: 11-12
Pages: 703-13
Publication
First Author: Gerbasi V
Year: 2003
Journal: Neurochem Res
Title: A mutation in the ATP7B copper transporter causes reduced dopamine beta-hydroxylase and norepinephrine in mouse adrenal.
Volume: 28
Issue: 6
Pages: 867-73
Publication
First Author: Buiakova OI
Year: 1999
Journal: Hum Mol Genet
Title: Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation.
Volume: 8
Issue: 9
Pages: 1665-71
Publication
First Author: Muchenditsi A
Year: 2021
Journal: Sci Rep
Title: Systemic deletion of Atp7b modifies the hepatocytes' response to copper overload in the mouse models of Wilson disease.
Volume: 11
Issue: 1
Pages: 5659
Publication
First Author: Wooton-Kee CR
Year: 2020
Journal: Proc Natl Acad Sci U S A
Title: Metabolic dysregulation in the Atp7b -/- Wilson's disease mouse model.
Volume: 117
Issue: 4
Pages: 2076-2083
Publication
First Author: Linz R
Year: 2008
Journal: Am J Physiol Renal Physiol
Title: Intracellular targeting of copper-transporting ATPase ATP7A in a normal and Atp7b-/- kidney.
Volume: 294
Issue: 1
Pages: F53-61
Publication
First Author: Voskoboinik I
Year: 2001
Journal: Biochem Biophys Res Commun
Title: Functional studies on the Wilson copper P-type ATPase and toxic milk mouse mutant.
Volume: 281
Issue: 4
Pages: 966-70
Publication
First Author: Reed V
Year: 1995
Journal: Genomics
Title: Mapping of the mouse homologue of the Wilson disease gene to mouse chromosome 8.
Volume: 28
Issue: 3
Pages: 573-5
Publication
First Author: Gottlieb A
Year: 2022
Journal: Am J Pathol
Title: Hepatic Steatosis in the Mouse Model of Wilson Disease Coincides with a Muted Inflammatory Response.
Volume: 192
Issue: 1
Pages: 146-159
Publication
First Author: Washington-Hughes CL
Year: 2023
Journal: PLoS Genet
Title: Atp7b-dependent choroid plexus dysfunction causes transient copper deficit and metabolic changes in the developing mouse brain.
Volume: 19
Issue: 1
Pages: e1010558
Publication  
First Author: Padula A
Year: 2023
Journal: JCI Insight
Title: Genome editing without nucleases confers proliferative advantage to edited hepatocytes and corrects Wilson disease.
Volume: 8
Issue: 21
Publication
First Author: Mazi TA
Year: 2024
Journal: Biochim Biophys Acta Mol Cell Biol Lipids
Title: Hepatic oxylipin profiles in mouse models of Wilson disease: New insights into early hepatic manifestations.
Volume: 1869
Issue: 2
Pages: 159446
Publication
First Author: Mordaunt CE
Year: 2018
Journal: Hum Mol Genet
Title: Epigenetic changes of the thioredoxin system in the tx-j mouse model and in patients with Wilson disease.
Volume: 27
Issue: 22
Pages: 3854-3869
Publication  
First Author: Michalczyk AA
Year: 2000
Journal: Biochem J
Title: Defective localization of the Wilson disease protein (ATP7B) in the mammary gland of the toxic milk mouse and the effects of copper supplementation.
Volume: 352 Pt 2
Pages: 565-71
Publication
First Author: Chen DB
Year: 2012
Journal: PLoS One
Title: Penicillamine increases free copper and enhances oxidative stress in the brain of toxic milk mice.
Volume: 7
Issue: 5
Pages: e37709
Publication
First Author: Huster D
Year: 2006
Journal: Am J Pathol
Title: Consequences of copper accumulation in the livers of the Atp7b-/- (Wilson disease gene) knockout mice.
Volume: 168
Issue: 2
Pages: 423-34
Publication
First Author: Miyayama T
Year: 2010
Journal: Biochem J
Title: Roles of COMM-domain-containing 1 in stability and recruitment of the copper-transporting ATPase in a mouse hepatoma cell line.
Volume: 429
Issue: 1
Pages: 53-61
Publication
First Author: Barnes N
Year: 2005
Journal: J Biol Chem
Title: The copper-transporting ATPases, menkes and wilson disease proteins, have distinct roles in adult and developing cerebellum.
Volume: 280
Issue: 10
Pages: 9640-5
Publication
First Author: Jończy A
Year: 2019
Journal: Metallomics
Title: Functional iron deficiency in toxic milk mutant mice (tx-J) despite high hepatic ferroportin: a critical role of decreased GPI-ceruloplasmin expression in liver macrophages.
Volume: 11
Issue: 6
Pages: 1079-1092
Publication
First Author: Gray LW
Year: 2012
Journal: PLoS One
Title: Urinary copper elevation in a mouse model of Wilson's disease is a regulated process to specifically decrease the hepatic copper load.
Volume: 7
Issue: 6
Pages: e38327
Publication
First Author: Theophilos MB
Year: 1996
Journal: Hum Mol Genet
Title: The toxic milk mouse is a murine model of Wilson disease.
Volume: 5
Issue: 10
Pages: 1619-24
Publication
First Author: Phinney AL
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: In vivo reduction of amyloid-beta by a mutant copper transporter.
Volume: 100
Issue: 24
Pages: 14193-8
Publication      
First Author: Choi JH
Year: 2018
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for daffodil
Publication
First Author: Rauch H
Year: 1983
Journal: J Hered
Title: Toxic milk, a new mutation affecting cooper metabolism in the mouse.
Volume: 74
Issue: 3
Pages: 141-4
Publication  
First Author: Wei T
Year: 2021
Journal: Front Pharmacol
Title: Comprehensive RNA-Seq Analysis of Potential Therapeutic Targets of Gan-Dou-Fu-Mu Decoction for Treatment of Wilson Disease Using a Toxic Milk Mouse Model.
Volume: 12
Pages: 622268
Publication
First Author: Deng DX
Year: 1998
Journal: Lab Invest
Title: Metallothionein and apoptosis in the toxic milk mutant mouse.
Volume: 78
Issue: 2
Pages: 175-83
Publication
First Author: Howell JM
Year: 1994
Journal: J Comp Pathol
Title: The pathology and trace element status of the toxic milk mutant mouse.
Volume: 110
Issue: 1
Pages: 37-47
Publication  
First Author: Koropatnick J
Year: 1993
Journal: Biochem J
Title: A mutant mouse (tx) with increased hepatic metallothionein stability and accumulation.
Volume: 296 ( Pt 2)
Pages: 443-9
Publication  
First Author: Mercer JF
Year: 1994
Journal: Biochem J
Title: The toxic milk mouse does have elevated hepatic metallothionein mRNA.
Volume: 304 ( Pt 1)
Pages: 317-8
Publication
First Author: Koropatnick J
Year: 1994
Journal: Biochem J
Title: Metallothionein protein and mRNA in the toxic milk mouse.
Volume: 304
Issue: Pt 1
Pages: 318-9
Publication
First Author: Biempica L
Year: 1988
Journal: Lab Invest
Title: Morphologic and chemical studies on a murine mutation (toxic milk mice) resulting in hepatic copper toxicosis.
Volume: 59
Issue: 4
Pages: 500-8
Publication  
First Author: Rauch H
Year: 1977
Journal: Mouse News Lett
Title: tx - toxic milk
Volume: 56
Pages: 48
Publication
First Author: Zhang JW
Year: 2015
Journal: Biochem Biophys Res Commun
Title: Effects of tetrathiomolybdate and penicillamine on brain hydroxyl radical and free copper levels: a microdialysis study in vivo.
Volume: 458
Issue: 1
Pages: 82-5
Publication
First Author: Huster D
Year: 2007
Journal: J Biol Chem
Title: High copper selectively alters lipid metabolism and cell cycle machinery in the mouse model of Wilson disease.
Volume: 282
Issue: 11
Pages: 8343-55
Publication
First Author: Coronado V
Year: 2001
Journal: Mamm Genome
Title: The Jackson toxic milk mouse as a model for copper loading.
Volume: 12
Issue: 10
Pages: 793-5
Publication
First Author: Bronson RT
Year: 1995
Journal: Mouse Genome
Title: Short papers: Acute cerebral neuronal necrosis in copper deficient offspring of female mice with the toxic milk mutation.
Volume: 93
Issue: 1
Pages: 152-154
Publication
First Author: Roberts EA
Year: 2008
Journal: Mol Genet Metab
Title: Mitochondrial structure and function in the untreated Jackson toxic milk (tx-j) mouse, a model for Wilson disease.
Volume: 93
Issue: 1
Pages: 54-65
Publication
First Author: Krishnan N
Year: 2018
Journal: Genes Dev
Title: DPM-1001 decreased copper levels and ameliorated deficits in a mouse model of Wilson's disease.
Volume: 32
Issue: 13-14
Pages: 944-952
Publication  
First Author: Sweet HO
Year: 1989
Journal: Mouse News Lett
Title: Toxic milk-J (txJ)
Volume: 84
Pages: 89
Publication
First Author: Stephenson GF
Year: 1994
Journal: Toxicol Appl Pharmacol
Title: Copper-metallothionein from the toxic milk mutant mouse enhances lipid peroxidation initiated by an organic hydroperoxide.
Volume: 125
Issue: 1
Pages: 90-6
Publication  
First Author: Strader CD
Year: 1994
Journal: Annu Rev Biochem
Title: Structure and function of G protein-coupled receptors.
Volume: 63
Pages: 101-32
Publication
First Author: Rauch H
Year: 1995
Journal: Genomics
Title: The toxic milk mutation, tx, which results in a condition resembling Wilson disease in humans, is linked to mouse chromosome 8.
Volume: 29
Issue: 2
Pages: 551-2
Publication
First Author: Hirayama T
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: Near-infrared fluorescent sensor for in vivo copper imaging in a murine Wilson disease model.
Volume: 109
Issue: 7
Pages: 2228-33
Publication
First Author: Mercer JF
Year: 1992
Journal: J Nutr
Title: Hepatic metallothionein gene expression in toxic milk mice.
Volume: 122
Issue: 6
Pages: 1254-9
Publication  
First Author: Grimes A
Year: 1997
Journal: Biochem J
Title: Decreased carbonic anhydrase III levels in the liver of the mouse mutant 'toxic milk' (tx) due to copper accumulation.
Volume: 321 ( Pt 2)
Pages: 341-6
Publication
First Author: Roberts EA
Year: 2007
Journal: Biochem Biophys Res Commun
Title: Developmental expression of Commd1 in the liver of the Jackson toxic milk mouse.
Volume: 363
Issue: 4
Pages: 921-5
Publication
First Author: Paynter JA
Year: 1994
Journal: FEBS Lett
Title: Expression of the Menkes gene homologue in mouse tissues lack of effect of copper on the mRNA levels.
Volume: 351
Issue: 2
Pages: 186-90
Publication
First Author: Dong J
Year: 2021
Journal: Cell Death Dis
Title: Inhibiting NLRP3 inflammasome activation prevents copper-induced neuropathology in a murine model of Wilson's disease.
Volume: 12
Issue: 1
Pages: 87
Publication
First Author: Tümer Z
Year: 1996
Journal: Ann Med
Title: Menkes disease: recent advances and new insights into copper metabolism.
Volume: 28
Issue: 2
Pages: 121-9
Publication
First Author: Kuo YM
Year: 1997
Journal: Hum Mol Genet
Title: Developmental expression of the mouse mottled and toxic milk genes suggests distinct functions for the Menkes and Wilson disease copper transporters.
Volume: 6
Issue: 7
Pages: 1043-9
Publication
First Author: Harris ED
Year: 1998
Journal: Mol Cell Biochem
Title: Genes regulating copper metabolism.
Volume: 188
Issue: 1-2
Pages: 57-62
Publication
First Author: Ono S
Year: 1997
Journal: Toxicology
Title: Regional brain distribution of metallothionein, zinc and copper in toxic milk mutant and transgenic mice.
Volume: 124
Issue: 1
Pages: 1-10
Publication
First Author: Wooton-Kee CR
Year: 2015
Journal: J Clin Invest
Title: Elevated copper impairs hepatic nuclear receptor function in Wilson's disease.
Volume: 125
Issue: 9
Pages: 3449-60
Publication
First Author: Cecchi C
Year: 1996
Journal: Genomics
Title: Genomic organization of the mottled gene, the mouse homologue of the human Menkes disease gene.
Volume: 37
Issue: 1
Pages: 96-104
Publication
First Author: Morrison GM
Year: 2003
Journal: Mol Biol Evol
Title: Signal sequence conservation and mature peptide divergence within subgroups of the murine beta-defensin gene family.
Volume: 20
Issue: 3
Pages: 460-70
Publication
First Author: Sebastiani G
Year: 2006
Journal: Hum Mol Genet
Title: Mapping genetic modulators of amyloid plaque deposition in TgCRND8 transgenic mice.
Volume: 15
Issue: 15
Pages: 2313-23
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: Mouse Genome Informatics Scientific Curators
Year: 2001
Title: Gene Ontology Annotation by the MGI Curatorial Staff
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: Wellcome Trust Sanger Institute
Year: 2009
Journal: MGI Direct Data Submission
Title: Alleles produced for the KOMP project by the Wellcome Trust Sanger Institute
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Title: Rat to Mouse ISO GO annotation transfer
Publication
First Author: Skarnes WC
Year: 2011
Journal: Nature
Title: A conditional knockout resource for the genome-wide study of mouse gene function.
Volume: 474
Issue: 7351
Pages: 337-42
Publication        
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2001
Title: Gene Ontology Annotation by the MGI Curatorial Staff
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2000
Title: Gene Ontology Annotation by electronic association of SwissProt Keywords with GO terms
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Title: Human to Mouse ISO GO annotation transfer
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: 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: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Mouse Genome Informatics Computational Sequence to Gene Associations
Publication      
First Author: MGI Genome Annotation Group and UniGene Staff
Year: 2015
Journal: Database Download
Title: MGI-UniGene Interconnection Effort
Publication
First Author: Gaudet P
Year: 2011
Journal: Brief Bioinform
Title: Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.
Volume: 12
Issue: 5
Pages: 449-62
Publication      
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
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: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
Publication      
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
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 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
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
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication
First Author: Ibricevic A
Year: 2010
Journal: Toxicol Appl Pharmacol
Title: ATP7B detoxifies silver in ciliated airway epithelial cells.
Volume: 243
Issue: 3
Pages: 315-22
Publication
First Author: Ogiu T
Year: 2000
Journal: Radiat Res
Title: Absence of linkage between radiosensitivity and the predisposing atp7b gene mutation for heritable hepatitis in the LEC rat.
Volume: 154
Issue: 1
Pages: 113-6
Publication
First Author: Lim CM
Year: 2006
Journal: J Biol Chem
Title: Copper-dependent interaction of dynactin subunit p62 with the N terminus of ATP7B but not ATP7A.
Volume: 281
Issue: 20
Pages: 14006-14
Publication
First Author: Chuang LM
Year: 1996
Journal: J Med Genet
Title: High frequency of two mutations in codon 778 in exon 8 of the ATP7B gene in Taiwanese families with Wilson disease.
Volume: 33
Issue: 6
Pages: 521-3
Publication
First Author: Garces JA
Year: 1999
Journal: Curr Biol
Title: Interaction of the p62 subunit of dynactin with Arp1 and the cortical actin cytoskeleton.
Volume: 9
Issue: 24
Pages: 1497-500
Publication  
First Author: Tümer Z
Year: 1999
Journal: Adv Exp Med Biol
Title: Mutation spectrum of ATP7A, the gene defective in Menkes disease.
Volume: 448
Pages: 83-95
Publication
First Author: Hirayama T
Year: 1999
Journal: Cell
Title: RESPONSIVE-TO-ANTAGONIST1, a Menkes/Wilson disease-related copper transporter, is required for ethylene signaling in Arabidopsis.
Volume: 97
Issue: 3
Pages: 383-93
Publication
First Author: Llanos RM
Year: 2008
Journal: Biochem Biophys Res Commun
Title: Copper transport during lactation in transgenic mice expressing the human ATP7A protein.
Volume: 372
Issue: 4
Pages: 613-7
Publication
First Author: Setty SR
Year: 2008
Journal: Nature
Title: Cell-specific ATP7A transport sustains copper-dependent tyrosinase activity in melanosomes.
Volume: 454
Issue: 7208
Pages: 1142-6
Publication      
First Author: Singla A
Year: 2020
Journal: Dis Model Mech
Title: Regulation of copper homeostasis by members of the COMMD protein family.
Publication
First Author: van de Sluis BJ
Year: 1999
Journal: Hum Mol Genet
Title: Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16.
Volume: 8
Issue: 3
Pages: 501-7
Publication
First Author: Ogórek M
Year: 2019
Journal: Biol Reprod
Title: Molecular machinery providing copper bioavailability for spermatozoa along the epididymial tubule in mouse.
Volume: 100
Issue: 6
Pages: 1505-1520
Publication
First Author: Vonk WI
Year: 2011
Journal: PLoS One
Title: Liver-specific Commd1 knockout mice are susceptible to hepatic copper accumulation.
Volume: 6
Issue: 12
Pages: e29183
Publication
First Author: Axelsen KB
Year: 1998
Journal: J Mol Evol
Title: Evolution of substrate specificities in the P-type ATPase superfamily.
Volume: 46
Issue: 1
Pages: 84-101