|  Help  |  About  |  Contact Us

Search our database by keyword

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 100 out of 501 for Atp7a

<< First    < Previous  |  Next >    Last >>
0.036s
Type Details Score
Gene
Type: gene
Organism: human
Gene
Type: gene
Organism: cattle
Gene
Type: gene
Organism: chimpanzee
Gene
Type: gene
Organism: zebrafish
Gene
Type: gene
Organism: macaque, rhesus
Gene
Type: gene
Organism: chicken
Gene
Type: gene
Organism: frog, western clawed
Gene
Type: gene
Organism: rat
Gene
Type: gene
Organism: dog, domestic
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Publication
First Author: Cunliffe P
Year: 2001
Journal: Genomics
Title: Intragenic deletions at Atp7a in mouse models for Menkes disease.
Volume: 74
Issue: 2
Pages: 155-62
Publication
First Author: El Meskini R
Year: 2007
Journal: Mol Cell Neurosci
Title: ATP7A (Menkes protein) functions in axonal targeting and synaptogenesis.
Volume: 34
Issue: 3
Pages: 409-21
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: Lenartowicz M
Year: 2004
Journal: Folia Biol (Krakow)
Title: Alternative splicing in the Atp7a gene in the Cu deficient mosaic mutation in mice.
Volume: 52
Issue: 3-4
Pages: 219-23
Publication
First Author: Niciu MJ
Year: 2007
Journal: Neurobiol Dis
Title: Altered ATP7A expression and other compensatory responses in a murine model of Menkes disease.
Volume: 27
Issue: 3
Pages: 278-91
Publication
First Author: Chun H
Year: 2017
Journal: Sci Rep
Title: Organ-specific regulation of ATP7A abundance is coordinated with systemic copper homeostasis.
Volume: 7
Issue: 1
Pages: 12001
Publication
First Author: Cecchi C
Year: 1997
Journal: Hum Mol Genet
Title: The mottled mouse as a model for human Menkes disease: identification of mutations in the Atp7a gene.
Volume: 6
Issue: 3
Pages: 425-33
Publication
First Author: Monty JF
Year: 2005
Journal: J Nutr
Title: Copper exposure induces trafficking of the menkes protein in intestinal epithelium of ATP7A transgenic mice.
Volume: 135
Issue: 12
Pages: 2762-6
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: Wadwa J
Year: 2014
Journal: Physiol Rep
Title: Effects of ATP7A overexpression in mice on copper transport and metabolism in lactation and gestation.
Volume: 2
Issue: 1
Pages: e00195
Publication
First Author: Levinson B
Year: 1997
Journal: Nat Genet
Title: Deletion of the promoter region in the Atp7a gene of the mottled dappled mouse.
Volume: 16
Issue: 3
Pages: 224-5
Publication
First Author: Lenartowicz M
Year: 2011
Journal: Gene Expr Patterns
Title: Alterations in the expression of the Atp7a gene in the early postnatal development of the mosaic mutant mice (Atp7a mo-ms) - An animal model for Menkes disease.
Volume: 11
Issue: 1-2
Pages: 41-7
Publication
First Author: Ash D
Year: 2021
Journal: Nat Commun
Title: The P-type ATPase transporter ATP7A promotes angiogenesis by limiting autophagic degradation of VEGFR2.
Volume: 12
Issue: 1
Pages: 3091
Publication
First Author: Hodgkinson VL
Year: 2015
Journal: J Pathol
Title: X-linked spinal muscular atrophy in mice caused by autonomous loss of ATP7A in the motor neuron.
Volume: 236
Issue: 2
Pages: 241-50
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: Zhu S
Year: 2016
Journal: Metallomics
Title: Multiple di-leucines in the ATP7A copper transporter are required for retrograde trafficking to the trans-Golgi network.
Volume: 8
Issue: 9
Pages: 993-1001
Publication
First Author: Gudekar N
Year: 2020
Journal: Sci Rep
Title: Metallothioneins regulate ATP7A trafficking and control cell viability during copper deficiency and excess.
Volume: 10
Issue: 1
Pages: 7856
Publication
First Author: Siggs OM
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: Disruption of copper homeostasis due to a mutation of Atp7a delays the onset of prion disease.
Volume: 109
Issue: 34
Pages: 13733-8
Publication
First Author: Sudhahar V
Year: 2013
Journal: Diabetes
Title: Copper transporter ATP7A protects against endothelial dysfunction in type 1 diabetic mice by regulating extracellular superoxide dismutase.
Volume: 62
Issue: 11
Pages: 3839-50
Publication
First Author: Sudhahar V
Year: 2019
Journal: Arterioscler Thromb Vasc Biol
Title: Copper Transporter ATP7A (Copper-Transporting P-Type ATPase/Menkes ATPase) Limits Vascular Inflammation and Aortic Aneurysm Development: Role of MicroRNA-125b.
Volume: 39
Issue: 11
Pages: 2320-2337
Publication      
First Author: Smart NG
Year: 2008
Journal: MGI Direct Data Submission
Title: Tigrou-like is an allele of the copper transporter Atp7a and causes male lethality
Publication
First Author: Donsante A
Year: 2011
Journal: Mol Ther
Title: ATP7A gene addition to the choroid plexus results in long-term rescue of the lethal copper transport defect in a Menkes disease mouse model.
Volume: 19
Issue: 12
Pages: 2114-23
Publication
First Author: Kim BE
Year: 2007
Journal: J Med Genet
Title: Phenotypic diversity of Menkes disease in mottled mice is associated with defects in localisation and trafficking of the ATP7A protein.
Volume: 44
Issue: 10
Pages: 641-6
Publication  
First Author: Hunsicker PR
Year: 1969
Journal: Mouse News Lett
Title: [Ym = yellow mottled].
Volume: 40
Pages: 42
Publication
First Author: Lenartowicz M
Year: 2012
Journal: PLoS One
Title: Prenatal treatment of mosaic mice (Atp7a mo-ms) mouse model for Menkes disease, with copper combined by dimethyldithiocarbamate (DMDTC).
Volume: 7
Issue: 7
Pages: e40400
Publication
First Author: Lenartowicz M
Year: 2017
Journal: Biochim Biophys Acta
Title: Copper therapy reduces intravascular hemolysis and derepresses ferroportin in mice with mosaic mutation (Atp7amo-ms): An implication for copper-mediated regulation of the Slc40a1 gene expression.
Volume: 1863
Issue: 6
Pages: 1410-1421
Publication  
First Author: Haberkiewicz O
Year: 2022
Journal: Int J Mol Sci
Title: Decreased Expression of the Slc31a1 Gene and Cytoplasmic Relocalization of Membrane CTR1 Protein in Renal Epithelial Cells: A Potent Protective Mechanism against Copper Nephrotoxicity in a Mouse Model of Menkes Disease.
Volume: 23
Issue: 19
Publication
First Author: Lenartowicz M
Year: 2014
Journal: PLoS One
Title: Haemolysis and perturbations in the systemic iron metabolism of suckling, copper-deficient mosaic mutant mice - an animal model of Menkes disease.
Volume: 9
Issue: 9
Pages: e107641
Publication
First Author: Haddad MR
Year: 2014
Journal: Mol Genet Metab
Title: Molecular and biochemical characterization of Mottled-dappled, an embryonic lethal Menkes disease mouse model.
Volume: 113
Issue: 4
Pages: 294-300
Publication
First Author: Guthrie LM
Year: 2020
Journal: Science
Title: Elesclomol alleviates Menkes pathology and mortality by escorting Cu to cuproenzymes in mice.
Volume: 368
Issue: 6491
Pages: 620-625
Publication  
First Author: Krzanowska H
Year: 1966
Journal: Mouse News Lett
Title: Mo
Volume: 35
Pages: 35
Publication
First Author: Krzanowska H
Year: 1971
Journal: Genetica Polonica
Title: Selection for expression of sex-linked gene Ms (Mosaic) in heterozygous mice
Volume: 12
Issue: 4
Pages: 537-44
Publication
First Author: Gajewska A
Year: 2009
Journal: Brain Res Bull
Title: Impaired growth hormone-releasing hormone neurons ultrastructure and peptide accumulation in the arcuate nucleus of mosaic mice with altered copper metabolism.
Volume: 80
Issue: 3
Pages: 128-32
Publication
First Author: Lenartowicz M
Year: 2001
Journal: Folia Histochem Cytobiol
Title: Alterations in kidney morphology in mice with mosaic mutation.
Volume: 39
Issue: 3
Pages: 275-81
Publication  
First Author: Styrna J
Year: 1977
Journal: Genetica Polonica
Title: Analysis of causes of lethality in mice with Ms (mosaic) gene.
Volume: 18
Pages: 61-79
Publication
First Author: Krzanowska H
Year: 1973
Journal: Genetica Polonica
Title: Further studies on the expression of sex-linked gene Ms (Mosaic) in heterozygous mice
Volume: 14
Issue: 2
Pages: 193-98
Publication
First Author: Gajkowska B
Year: 2006
Journal: Brain Res Bull
Title: Growth hormone cell phagocytosis in adenohypophysis of mosaic mice: morphological and immunocytochemical electron microscopy study.
Volume: 70
Issue: 1
Pages: 94-8
Publication
First Author: Mori M
Year: 1997
Journal: Mamm Genome
Title: A serine-to-proline mutation in the copper-transporting P-type ATPase gene of the macular mouse.
Volume: 8
Issue: 6
Pages: 407-10
Publication
First Author: Grimes A
Year: 1997
Journal: Hum Mol Genet
Title: Molecular basis of the brindled mouse mutant (Mo(br)): a murine model of Menkes disease.
Volume: 6
Issue: 7
Pages: 1037-42
Publication
First Author: Steveson TC
Year: 2003
Journal: Endocrinology
Title: Menkes protein contributes to the function of peptidylglycine alpha-amidating monooxygenase.
Volume: 144
Issue: 1
Pages: 188-200
Publication
First Author: Hodgkinson VL
Year: 2015
Journal: Am J Physiol Cell Physiol
Title: Autonomous requirements of the Menkes disease protein in the nervous system.
Volume: 309
Issue: 10
Pages: C660-8
Publication
First Author: La Fontaine S
Year: 1999
Journal: Hum Mol Genet
Title: Intracellular localization and loss of copper responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo blo) and brindled (Mo br) mouse mutants.
Volume: 8
Issue: 6
Pages: 1069-75
Publication
First Author: Schlief ML
Year: 2006
Journal: Proc Natl Acad Sci U S A
Title: Role of the Menkes copper-transporting ATPase in NMDA receptor-mediated neuronal toxicity.
Volume: 103
Issue: 40
Pages: 14919-24
Publication
First Author: Llanos RM
Year: 2006
Journal: Biochim Biophys Acta
Title: Correction of a mouse model of Menkes disease by the human Menkes gene.
Volume: 1762
Issue: 4
Pages: 485-93
Publication
First Author: Reed V
Year: 1997
Journal: Hum Mol Genet
Title: Mutation analysis provides additional proof that mottled is the mouse homologue of Menkes' disease.
Volume: 6
Issue: 3
Pages: 417-23
Publication
First Author: Gulec S
Year: 2013
Journal: PLoS One
Title: Investigation of iron metabolism in mice expressing a mutant Menke's copper transporting ATPase (Atp7a) protein with diminished activity (Brindled; Mo (Br) (/y) ).
Volume: 8
Issue: 6
Pages: e66010
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: Kelly EJ
Year: 1996
Journal: Nat Genet
Title: A murine model of Menkes disease reveals a physiological function of metallothionein.
Volume: 13
Issue: 2
Pages: 219-22
Publication
First Author: Perez-Siles G
Year: 2016
Journal: Metallomics
Title: Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX).
Volume: 8
Issue: 9
Pages: 981-92
Publication
First Author: Wang Y
Year: 2012
Journal: PLoS One
Title: Conditional knockout of the Menkes disease copper transporter demonstrates its critical role in embryogenesis.
Volume: 7
Issue: 8
Pages: e43039
Publication
First Author: Wang Y
Year: 2012
Journal: Am J Physiol Gastrointest Liver Physiol
Title: Maternofetal and neonatal copper requirements revealed by enterocyte-specific deletion of the Menkes disease protein.
Volume: 303
Issue: 11
Pages: G1236-44
Publication
First Author: Qian Y
Year: 1998
Journal: J Nutr
Title: Copper efflux from murine microvascular cells requires expression of the menkes disease Cu-ATPase.
Volume: 128
Issue: 8
Pages: 1276-82
Publication
First Author: White C
Year: 2009
Journal: J Cell Sci
Title: Copper transport into the secretory pathway is regulated by oxygen in macrophages.
Volume: 122
Issue: Pt 9
Pages: 1315-21
Publication        
First Author: Silvers WK
Year: 1979
Title: The Coat Colors of Mice; A Model for Mammalian Gene Action and Interaction
Publication
First Author: Levinson B
Year: 1994
Journal: Nat Genet
Title: The mottled gene is the mouse homologue of the Menkes disease gene.
Volume: 6
Issue: 4
Pages: 369-73
Publication  
First Author: Phillips RJS
Year: 1961
Journal: Genet Res
Title: "Dappled", a new allele at the mottled locus in the house mouse.
Volume: 2
Pages: 290-295
Publication
First Author: Reed V
Year: 1993
Journal: Mouse Genome
Title: Molecular analysis of a series of mutations at the mottled locus
Volume: 91
Issue: 2
Pages: 331-33
Publication  
First Author: Phillips RJS
Year: 1956
Journal: Mouse News Lett
Title: Atp7aMo-dp - dappled
Volume: 15
Pages: 28
Publication
First Author: Reed V
Year: 1994
Journal: Nat Genet
Title: RFLVs in mottled dappled alleles.
Volume: 8
Issue: 1
Pages: 11-2
Publication
First Author: Mototani Y
Year: 2006
Journal: Genomics
Title: Phenotypic and genetic characterization of the Atp7a(Mo-Tohm) mottled mouse: a new murine model of Menkes disease.
Volume: 87
Issue: 2
Pages: 191-9
Publication
First Author: Tao C
Year: 2019
Journal: Diabetologia
Title: Adipocyte-specific disruption of ATPase copper transporting α in mice accelerates lipoatrophy.
Volume: 62
Issue: 12
Pages: 2340-2353
Publication
First Author: Cattanach BM
Year: 1972
Journal: Genet Res
Title: A comparative study of the coats of chimaeric mice and those of heterozygotes for X-linked genes.
Volume: 19
Issue: 3
Pages: 213-28
Publication  
First Author: Chen GF
Year: 2015
Journal: Sci Rep
Title: Copper Transport Protein Antioxidant-1 Promotes Inflammatory Neovascularization via Chaperone and Transcription Factor Function.
Volume: 5
Pages: 14780
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: Masson W
Year: 1996
Journal: Mamm Genome
Title: The use of compound heterozygotes and Hprt selection to analyze X-linked mottled alleles associated with prenatal lethality.
Volume: 7
Issue: 7
Pages: 486-9
Publication
First Author: Schlief ML
Year: 2005
Journal: J Neurosci
Title: NMDA receptor activation mediates copper homeostasis in hippocampal neurons.
Volume: 25
Issue: 1
Pages: 239-46
Publication
First Author: Fraser AS
Year: 1953
Journal: J Genet
Title: Mottled, a sex-modified lethal in the house mouse.
Volume: 51
Issue: 2
Pages: 217-221
Publication
First Author: Nagara H
Year: 1981
Journal: J Neuropathol Exp Neurol
Title: The effect of copper supplementation on the brindled mouse: a clinico-pathological study.
Volume: 40
Issue: 4
Pages: 428-46
Publication
First Author: Hunt DM
Year: 1974
Journal: Nature
Title: Primary defect in copper transport underlies mottled mutants in the mouse.
Volume: 249
Issue: 460
Pages: 852-4
Publication
First Author: Mann JR
Year: 1981
Journal: Biochem J
Title: Copper metabolism in mottled mouse (Mus musculus) mutants. Studies of blotchy (Moblo) mice and a comparison with brindled (Mobr) mice.
Volume: 196
Issue: 1
Pages: 81-8
Publication
First Author: Hunt DM
Year: 1976
Journal: Life Sci
Title: A study of copper treatment and tissue copper levels in the murine congenital copper deficiency, mottled.
Volume: 19
Issue: 12
Pages: 1913-9
Publication
First Author: Piletz JE
Year: 1983
Journal: Biochem Genet
Title: Hepatic metallothionein synthesis in neonatal Mottled-Brindled mutant mice.
Volume: 21
Issue: 5-6
Pages: 465-75
Publication
First Author: Kuznetsov AV
Year: 1996
Journal: J Biol Chem
Title: Increase of flux control of cytochrome c oxidase in copper-deficient mottled brindled mice.
Volume: 271
Issue: 1
Pages: 283-8
Publication
First Author: Martin P
Year: 1994
Journal: Brain Res Dev Brain Res
Title: Heterotypic sprouting of serotonergic forebrain fibers in the brindled mottled mutant mouse.
Volume: 77
Issue: 2
Pages: 215-25
Publication
First Author: Yajima K
Year: 1979
Journal: J Neuropathol Exp Neurol
Title: Neuronal degeneration in the brain of the brindled mouse--a light microscope study.
Volume: 38
Issue: 1
Pages: 35-46
Publication
First Author: Yoshimura N
Year: 1994
Journal: Pathol Int
Title: Histochemical localization of copper in various organs of brindled mice.
Volume: 44
Issue: 1
Pages: 14-9
Publication
First Author: Hunt DM
Year: 1983
Journal: Biochem Genet
Title: Metallothionein and the development of the mottled disorder in the mouse.
Volume: 21
Issue: 11-12
Pages: 1175-94
Publication
First Author: Evans GW
Year: 1978
Journal: J Nutr
Title: Impaired copper homeostasis in neonatal male and adult female Brindled (Mobr) mice.
Volume: 108
Issue: 4
Pages: 554-60
Publication
First Author: Wenk G
Year: 1983
Journal: J Neurochem
Title: Congenital copper deficiency: copper therapy and dopamine-beta-hydroxylase activity in the mottled (brindled) mouse.
Volume: 41
Issue: 6
Pages: 1648-52
Publication
First Author: Kiel-Metzger K
Year: 1984
Journal: Nature
Title: Regional localization of sex-specific Bkm-related sequences on proximal chromosome 17 of mice.
Volume: 310
Issue: 5978
Pages: 579-81
Publication  
First Author: Falconer DS
Year: 1956
Journal: Mouse News Lett
Title: Viable and fertile Brindled male, and new evidence for the allelism of the sex-linked genes, Brindled and Mottled
Volume: 15
Pages: 24-25
Publication
First Author: Hunt DM
Year: 1977
Journal: Comp Biochem Physiol C
Title: Catecholamine biosynthesis and the activity of a number of copper-dependent enzymes in the copper deficient mottled mouse mutants.
Volume: 57
Issue: 1
Pages: 79-83
Publication
First Author: Yoshimura N
Year: 1995
Journal: Pathol Int
Title: Histochemical localization of copper in various organs of brindled mice after copper therapy.
Volume: 45
Issue: 1
Pages: 10-8
Publication
First Author: Martin PM
Year: 1991
Journal: Dev Neurosci
Title: The female brindled mouse as a model of Menkes' disease: the relationship of fur pattern to behavioral and neurochemical abnormalities.
Volume: 13
Issue: 3
Pages: 121-9
Publication
First Author: Hunt DM
Year: 1972
Journal: J Neurochem
Title: An inherited deficiency in noradrenaline biosynthesis in the brindled mouse.
Volume: 19
Issue: 12
Pages: 2811-9
Publication
First Author: Prins HW
Year: 1979
Journal: J Inorg Biochem
Title: Primary biochemical defect in copper metabolism in mice with a recessive X-linked mutation analogous to Menkes' disease in man.
Volume: 10
Issue: 1
Pages: 19-27
Publication
First Author: Falconer DS
Year: 1972
Journal: Genet Res
Title: Sex-linked variegation modified by selection in brindled mice.
Volume: 20
Issue: 3
Pages: 291-316
Publication  
First Author: Sayed AK
Year: 1978
Journal: Fed Proc
Title: 64Cu uptake by cultured fibroblasts from Mobr/Y mice.
Volume: 37
Pages: 746 (Abstr.)
Publication
First Author: Camakaris J
Year: 1979
Journal: Biochem J
Title: Copper metabolism in mottled mouse mutants: copper concentrations in tissues during development.
Volume: 180
Issue: 3
Pages: 597-604
Publication
First Author: Mann JR
Year: 1979
Journal: Biochem J
Title: Copper metabolism in mottled mouse mutants: copper therapy of brindled (Mobr) mice.
Volume: 180
Issue: 3
Pages: 605-12