(Q38470686)

English

Identification of master genes involved in liver key functions through transcriptomics and epigenomics of methyl donor deficiency in rat: relevance to nonalcoholic liver disease

scientific article published on 09 December 2014

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Identification of master genes involved in liver key functions through transcriptomics and epigenomics of methyl donor deficiency in rat: relevance to nonalcoholic liver disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

0 references

transcriptomics

1 reference

based on heuristic

inferred from title

author name string

Gaili Chen

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25380481%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Julien Broséus

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25380481%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Audrey Donnart

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25380481%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Catherine Chevalier

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25380481%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Francisco Bolaños-Jiménez

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25380481%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Jean-Louis Guéant

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25380481%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

language of work or name

1 reference

based on heuristic

inferred from title

publication date

9 December 2014

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Molecular Nutrition and Food Research

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25380481%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

59

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25380481%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25380481%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

293-302

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25380481%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Methyl donor deficiency affects fetal programming of gastric ghrelin cell organization and function in the rat.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Homocysteine and related genetic polymorphisms in Down's syndrome IQ.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Effects of folate and vitamin B12 deficiencies during pregnancy on fetal, infant, and child development

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Methyl donor deficiency induces cardiomyopathy through altered methylation/acetylation of PGC-1α by PRMT1 and SIRT1.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Folate and homocysteine metabolism in neural plasticity and neurodegenerative disorders

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Association of IL-1 RN*2 allele and methionine synthase 2756 AA genotype with dementia severity of sporadic Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Fetal programming: link between early nutrition, DNA methylation, and complex diseases

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Comprehensive analysis of DNA-methylation in mammalian tissues using MeDIP-chip

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

DNA methylation profiling identifies epigenetic dysregulation in pancreatic islets from type 2 diabetic patients

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Genome-wide survey reveals dynamic widespread tissue-specific changes in DNA methylation during development.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Differential methylation in visceral adipose tissue of obese men discordant for metabolic disturbances

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Epigenetic regulation of depot-specific gene expression in adipose tissue

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Normalization for cDNA microarray data: a robust composite method addressing single and multiple slide systematic variation

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Meta-analysis of muscle transcriptome data using the MADMuscle database reveals biologically relevant gene patterns

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Novel molecular subtypes of serous and endometrioid ovarian cancer linked to clinical outcome

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Open source clustering software

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Java Treeview--extensible visualization of microarray data

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Genome-wide screen of DNA methylation changes induced by low dose X-ray radiation in mice.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Gene ontology: tool for the unification of biology

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

GoMiner: a resource for biological interpretation of genomic and proteomic data

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

KEGG Atlas mapping for global analysis of metabolic pathways

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Inflammatory stress exacerbates hepatic cholesterol accumulation via disrupting cellular cholesterol export

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

β(1) Adrenergic receptor is key to cold- and diet-induced thermogenesis in mice

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Association between angiotensin II type 1 receptor polymorphisms and the occurrence of nonalcoholic fatty liver disease.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Susceptibility and gene interaction study of the angiotensin II type 1 receptor (AGTR1) gene polymorphisms with non-alcoholic fatty liver disease in a multi-ethnic population

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

The human liver fatty acid binding protein (FABP1) gene is activated by FOXA1 and PPARα; and repressed by C/EBPα: Implications in FABP1 down-regulation in nonalcoholic fatty liver disease

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Increased expression of enzymes of triglyceride synthesis is essential for the development of hepatic steatosis

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Foxa1 reduces lipid accumulation in human hepatocytes and is down-regulated in nonalcoholic fatty liver

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Association between liver-specific gene polymorphisms and their expression levels with nonalcoholic fatty liver disease

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Loss of Nrf2 markedly exacerbates nonalcoholic steatohepatitis.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Nuclear factor (erythroid-derived 2)-like-2 factor (Nrf2), a key regulator of the antioxidant response to protect against atherosclerosis and nonalcoholic steatohepatitis

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Nrf2 inhibits LXRα-dependent hepatic lipogenesis by competing with FXR for acetylase binding.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Paraoxonase activity and expression is modulated by therapeutics in experimental rat nonalcoholic Fatty liver disease

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Involvement of regucalcin in lipid metabolism and diabetes

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Prothrombotic factors in histologically proven nonalcoholic fatty liver disease and nonalcoholic steatohepatitis

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Bioinformatics-driven identification and examination of candidate genes for non-alcoholic fatty liver disease

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Transcriptomic and epigenetic changes in early liver steatosis associated to obesity: effect of dietary methyl donor supplementation.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Effects of perilipin 2 antisense oligonucleotide treatment on hepatic lipid metabolism and gene expression

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Glucokinase links Krüppel-like factor 6 to the regulation of hepatic insulin sensitivity in nonalcoholic fatty liver disease

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Post-transcriptional activation of PPAR alpha by KLF6 in hepatic steatosis

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Association of nicotinamide-N-methyltransferase gene rs694539 variant with patients with nonalcoholic steatohepatitis

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Poor maternal nutrition leads to alterations in oxidative stress, antioxidant defense capacity, and markers of fibrosis in rat islets: potential underlying mechanisms for development of the diabetic phenotype in later life

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Nutritional programming in the rat is linked to long-lasting changes in nutrient sensing and energy homeostasis in the hypothalamus

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Folic acid supplementation during the juvenile-pubertal period in rats modifies the phenotype and epigenotype induced by prenatal nutrition.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Overview of homocysteine and folate metabolism. With special references to cardiovascular disease and neural tube defects.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome?

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Induction and prevention of cleft lip, alveolus and palate and neural tube defects with special consideration of B vitamins and the methylation cycle

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Low paternal dietary folate alters the mouse sperm epigenome and is associated with negative pregnancy outcomes

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

AGA technical review on nonalcoholic fatty liver disease

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

The genetics of NAFLD.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

The de novo DNA methyltransferase DNMT3A in development and cancer

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Molecular mechanisms of gene silencing mediated by DNA methylation

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Folate and fetal programming: a play in epigenomics?

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Maternal nutrition at conception modulates DNA methylation of human metastable epialleles

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Mutation in folate metabolism causes epigenetic instability and transgenerational effects on development

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

What is an epigenetic transgenerational phenotype? F3 or F2.

1 reference

https://api.crossref.org/works/10.1002%2FMNFR.201400483

21 January 2018

Identifiers

10.1002/MNFR.201400483

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25380481%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25380481%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q38470686&oldid=1783750879"