New canine models of copper toxicosis: diagnosis, treatment, and genetics.

about

Gene expression patterns in the progression of canine copper-associated chronic hepatitis.Disease Modeling and Gene Therapy of Copper Storage Disease in Canine Hepatic Organoids.

P2860

Q36359677-C0482B1D-B32D-401F-A553-C423409DBF61 Q42144274-E713DD81-7C6E-48D9-BB04-E0BDB63BB909

P2860

New canine models of copper toxicosis: diagnosis, treatment, and genetics.

Item

http://www.wikidata.org/entity/Q46902405

description

2014 nî lūn-bûn

@nan

2014年の論文

@ja

2014年学术文章

@wuu

2014年学术文章

@zh

2014年学术文章

@zh-cn

2014年学术文章

@zh-hans

2014年学术文章

@zh-my

2014年学术文章

@zh-sg

2014年學術文章

@yue

2014年學術文章

@zh-hant

name

New canine models of copper toxicosis: diagnosis, treatment, and genetics.

@en

New canine models of copper toxicosis: diagnosis, treatment, and genetics.

@nl

type

Item

label

New canine models of copper toxicosis: diagnosis, treatment, and genetics.

@en

New canine models of copper toxicosis: diagnosis, treatment, and genetics.

@nl

prefLabel

New canine models of copper toxicosis: diagnosis, treatment, and genetics.

@en

New canine models of copper toxicosis: diagnosis, treatment, and genetics.

@nl

P1476

New canine models of copper toxicosis: diagnosis, treatment, and genetics.

@en

P2093

Hille Fieten

http://www.w3.org/2001/XMLSchema#string

Jan Rothuizen

http://www.w3.org/2001/XMLSchema#string

Louis C Penning

http://www.w3.org/2001/XMLSchema#string

Peter A J Leegwater

http://www.w3.org/2001/XMLSchema#string

P2860

Genome sequence, comparative analysis and haplotype structure of the domestic dog

COMMD proteins, a novel family of structural and functional homologs of MURR1

Identification of Murr1 as a regulator of the human delta epithelial sodium channel

COMMD1 downregulates the epithelial sodium channel through Nedd4-2

COMMD1 regulates the delta epithelial sodium channel (δENaC) through trafficking and ubiquitination

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

COMMD1 promotes the ubiquitination of NF-kappaB subunits through a cullin-containing ubiquitin ligase

The ubiquitously expressed MURR1 protein is absent in canine copper toxicosis

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

Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation

P304

42-48

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1111/NYAS.12442

http://www.w3.org/2001/XMLSchema#string

P478

1314

http://www.w3.org/2001/XMLSchema#string

P577

2014-04-23T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

261804292

http://www.w3.org/2001/XMLSchema#string

P698

24758744

http://www.w3.org/2001/XMLSchema#string

New canine models of copper toxicosis: diagnosis, treatment, and genetics.

about

P2860

P2860

New canine models of copper toxicosis: diagnosis, treatment, and genetics.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P5875

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P5875

P698