2015
DOI: 10.1038/ncomms8740
|View full text |Cite
|
Sign up to set email alerts
|

Correction: Corrigendum: DNA methylation signatures link prenatal famine exposure to growth and metabolism

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
6
0

Year Published

2016
2016
2024
2024

Publication Types

Select...
7
2
1

Relationship

0
10

Authors

Journals

citations
Cited by 14 publications
(6 citation statements)
references
References 0 publications
0
6
0
Order By: Relevance
“…Undernutrition usually develops from inadequate protein and micronutrients intake due to unavailability of food [3,4]. Epigenetic modification during pre- and neo-natal period, such as metabolic imprinting, will also increase the risk of malnutrition and diet-related non-communicable diseases later in life [5,6].…”
Section: Introductionmentioning
confidence: 99%
“…Undernutrition usually develops from inadequate protein and micronutrients intake due to unavailability of food [3,4]. Epigenetic modification during pre- and neo-natal period, such as metabolic imprinting, will also increase the risk of malnutrition and diet-related non-communicable diseases later in life [5,6].…”
Section: Introductionmentioning
confidence: 99%
“…For instance, there is strong evidence that nutritional habits can influence gene transcription epigenetically ( van Dijk et al, 2015 ; Etchegaray and Mostoslavsky, 2016 ) and there are several studies claiming inheritance to the offspring ( Figure 1 ) ( Seki et al, 2012 ; Nicholas et al, 2013 ; Rando and Simmons, 2015 ). A recent genome wide analysis of DNA methylation in children born to parents affected by the Dutch famine showed that 70 years later several DNA regions associated with growth and metabolism were significantly differentially methylated, including genes involved in control of birth weight and LDL cholesterol in later life ( Tobi et al, 2015 ).…”
Section: Introductionmentioning
confidence: 99%
“…Later studies determined that several genes linked to metabolic and cardiovascular disease were perturbed epigenetically in this cohort. In particular, DNA methylation at INSR was positively correlated with birth weight, and methylation at CPT1A was positively correlated with LDL cholesterol levels (194,195). A separate study by the same group demonstrated that several genes linked to CVD were differentially methylated in association with prenatal exposure to famine including INSIGF, GNASAS, MEG3, IL10, LEP, and ABCA1 (196).…”
Section: A Metabolic Syndrome and Related Diseasesmentioning
confidence: 96%