Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease (Q83223721)

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scientific article published on 28 January 2006

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English	Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease	scientific article published on 28 January 2006

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16649058%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease (English)

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20 January 2020

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Zhi-Ying Wu

1

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20 January 2020

Gui-Xian Zhao

2

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20 January 2020

Wan-Jin Chen

3

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20 January 2020

Ning Wang

4

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20 January 2020

Bo Wan

5

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20 January 2020

Min-Ting Lin

6

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20 January 2020

Shen-Xing Murong

7

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20 January 2020

Long Yu

8

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20 January 2020

publication date

28 January 2006

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20 January 2020

Journal of Molecular Medicine

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20 January 2020

84

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20 January 2020

5

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20 January 2020

438-442

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20 January 2020

Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence variation database for the Wilson disease copper transporter, ATP7B

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High frequency of two mutations in codon 778 in exon 8 of the ATP7B gene in Taiwanese families with Wilson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of three novel mutations and a high frequency of the Arg778Leu mutation in Korean patients with Wilson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Wilson disease gene: spectrum of mutations and their consequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of haplotypes associated with copper toxicosis in Bedlington Terriers in Australia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wilson disease and canine copper toxicosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype and mutation analysis in Japanese patients with Wilson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in chinese patients with Wilson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a new copper metabolism gene by positional cloning in a purebred dog population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New haplotypes in the Bedlington terrier indicate complexity in copper toxicosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel ATP7B mutations causing Wilson disease in several Israeli ethnic groups

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SIFT: Predicting amino acid changes that affect protein function

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the human homologue of the canine copper toxicosis gene MURR1 in Wilson disease patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16649058

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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