CDC5L drives FAH expression to promote metabolic reprogramming in melanoma.

about

CDC5L drives FAH expression to promote metabolic reprogramming in melanoma.

Item

http://www.wikidata.org/entity/Q49476830

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

CDC5L drives FAH expression to promote metabolic reprogramming in melanoma.

@en

CDC5L drives FAH expression to promote metabolic reprogramming in melanoma.

@nl

type

Item

label

CDC5L drives FAH expression to promote metabolic reprogramming in melanoma.

@en

CDC5L drives FAH expression to promote metabolic reprogramming in melanoma.

@nl

prefLabel

CDC5L drives FAH expression to promote metabolic reprogramming in melanoma.

@en

CDC5L drives FAH expression to promote metabolic reprogramming in melanoma.

@nl

P1476

CDC5L drives FAH expression to promote metabolic reprogramming in melanoma.

@en

P2093

Bo Huang

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

Huafeng Zhang

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

Hui Chen

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

Ruimin Cheng

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

Susu Shen

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

Wei Zhang

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

Xiaonan Yin

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

Xiaoyan Zhang

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

Yong Li

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

Yong Zhang

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

P2860

Tyrosinemia type 1: a rare and forgotten cause of reversible hypertrophic cardiomyopathy in infancy

Enhancers: five essential questions

Type 1 hereditary tyrosinemia. Evidence for molecular heterogeneity and identification of a causal mutation in a French Canadian patient

Nucleotide sequence of cDNA encoding human fumarylacetoacetase

Evidence that Myb-related CDC5 proteins are required for pre-mRNA splicing

Cloning and expression of the cDNA encoding human fumarylacetoacetate hydrolase, the enzyme deficient in hereditary tyrosinemia: assignment of the gene to chromosome 15

Targeting mitochondria metabolism for cancer therapy

Overexpression of hypoxia-inducible factor 1alpha in common human cancers and their metastases

P304

114328-114343

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

P31

scholarly article

P356

10.18632/ONCOTARGET.23107

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

P407

English

P433

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

P478

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

P577

2017-12-07T00:00:00Z

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

P698

29371990

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

P932

5768407

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