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ATP7B gene
Known as:
ATP7B
, ATPase, Cu(2+)-TRANSPORTING, BETA POLYPEPTIDE
, ATPase copper transporting beta
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National Institutes of Health
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Related topics
Related topics
2 relations
Hepatolenticular Degeneration
Wilson disease protein
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Variations in ATP7B in cats with primary copper-associated hepatopathy
Hajime Asada
,
J. Chambers
,
+7 authors
K. Ohno
Journal of feline medicine and surgery
2020
Corpus ID: 207890706
Objectives Primary copper-associated hepatopathy (PCH) has been reported in young cats. Although our group recently reported a…
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2020
2020
p.P1379S, a benign variant with reduced ATP7B protein level in Wilson Disease
Fan Yi
,
Sheri A. Poskanzer
,
+6 authors
S. Hahn
JIMD Reports
2020
Corpus ID: 219442219
Wilson disease (WD) is an autosomal recessive disorder of copper transport caused by inherited defects in the ATP7B gene and…
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2019
2019
ATP7B Binds Ruthenium(II) p-Cymene Half-Sandwich Complexes: Role of Steric Hindrance and Ru-I Coordination in Rescuing the Sequestration.
Kallol Purkait
,
Ruturaj
,
Arindam Mukherjee
,
Arnab Gupta
Inorganic Chemistry
2019
Corpus ID: 204953744
Ruthenium(II/III) complexes are predicted to be efficient alternatives to platinum drug-resistant cancers but have never been…
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2016
2016
Erratum to: Non-Ceruloplasmin Copper Distincts Subtypes in Alzheimer’s Disease: a Genetic Study of ATP7B Frequency
R. Squitti
,
M. Ventriglia
,
+9 authors
C. Bonvicini
Molecular Neurobiology
2016
Corpus ID: 4301587
Meta-analyses show that serum copper non-boundto-ceruloplasmin (non-Cp-Cu) is higher in patients with Alzheimer’s disease (AD…
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2014
2014
Diagnosis of abnormal biliary copper excretion by positron emission tomography with targeting of (64)Copper-asialofetuin complex in LEC rat model of Wilson's disease.
R. Bahde
,
S. Kapoor
,
K. Bhargava
,
C. Palestro
,
Sanjeev Gupta
American Journal of Nuclear Medicine and…
2014
Corpus ID: 39407291
Identification by molecular imaging of key processes in handling of transition state metals, such as copper (Cu), will be of…
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2014
2014
Interactions between Metal-binding Domains Modulate Intracellular Targeting of Cu(I)-ATPase ATP7B, as Revealed by Nanobody Binding*
Yiping Huang
,
S. Nokhrin
,
+8 authors
S. Lutsenko
Journal of Biological Chemistry
2014
Corpus ID: 32639295
Background: Copper regulates the intracellular localization of a copper transporter ATP7B; the molecular mechanism of this…
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2011
2011
A Novel Splice-site Allelic Variant is Responsible for Wilson Disease in an Omani Family.
M. Al-Tobi
,
Masoud Kashoob
,
S. Joshi
,
R. Bayoumi
Sultan Qaboos University Medical Journal
2011
Corpus ID: 46606997
OBJECTIVES The objective of this study was to characterise Wilson's Disease (WD) [OMIM 277900] genetically and test for allelic…
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2011
2011
Involvement of Protein Kinase D in Expression and Trafficking of ATP 7 B ( Copper ATPase ) *
Rajendra Pilankatta
,
D. Lewis
,
G. Inesi
2011
Corpus ID: 46158170
ATP7B is a P-type ATPase involved in copper transport and homeostasis. In experiments with microsomes isolated from COS-1 cells…
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2003
2003
Construction of site-directed mutant variants of ATP7B in vitro and their expression
Murong Shen-xin
2003
Corpus ID: 87091354
Objective To study the expression of normal and variant ATP7B proteins, in order to further find the mechanism of Wilson disease…
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1995
1995
Mapping of the mouse homologue of the Wilson disease gene to mouse chromosome 8.
V. Reed
,
P. Williamson
,
Peter Bull
,
D. Cox
,
Y. Boyd
Genomics
1995
Corpus ID: 12876549
ATP7B, the gene altered in Wilson disease (WD) patients, lies in a block of homology shared between human chromosome 13q14 and…
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