Evidence map›Paper›PMID 34604220›Full record

ArticleFrontiers in cell and developmental biology2021

Maternal Transmission of Human OGG1 Protects Mice Against Genetically- and Diet-Induced Obesity Through Increased Tissue Mitochondrial Content.

Natalie Burchat, Priyanka Sharma, Hong Ye, Sai Santosh Babu Komakula, Agnieszka Dobrzyn, Vladimir Vartanian, R Stephen Lloyd, Harini Sampath

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Natalie BurchatRutgers Center for Lipid Research, New Jersey Institute for Food, Nutrition, and Health, Rutgers University, New Brunswick, NJ, United States.
Priyanka SharmaRutgers Center for Lipid Research, New Jersey Institute for Food, Nutrition, and Health, Rutgers University, New Brunswick, NJ, United States.
Hong YeRutgers Center for Lipid Research, New Jersey Institute for Food, Nutrition, and Health, Rutgers University, New Brunswick, NJ, United States.
Sai Santosh Babu KomakulaRutgers Center for Lipid Research, New Jersey Institute for Food, Nutrition, and Health, Rutgers University, New Brunswick, NJ, United States.
Agnieszka DobrzynRutgers Center for Lipid Research, New Jersey Institute for Food, Nutrition, and Health, Rutgers University, New Brunswick, NJ, United States.
Vladimir VartanianOregon Institute of Occupational Health Sciences, Oregon Health and Science University, Portland, OR, United States.
R Stephen LloydOregon Institute of Occupational Health Sciences, Oregon Health and Science University, Portland, OR, United States.
Harini SampathRutgers Center for Lipid Research, New Jersey Institute for Food, Nutrition, and Health, Rutgers University, New Brunswick, NJ, United States.
Rutgers, The State University of New Jersey · USOregon Health & Science University · USInstytut Biologii Doświadczalnej im. Marcelego Nenckiego · PL

Funding

Role of oxidative DNA damage in the onset and progression of metabolic syndromeR00DK100640 · NIDDK · RUTGERS, THE STATE UNIV OF N.J. · PI SAMPATH, HARINI · 2016 to 2018
$888k
Role of oxidative DNA damage in the onset and progression of metabolic syndromeK99DK100640 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI SAMPATH, HARINI · 2014 to 2015
$180k
NIDDK NIH HHS K99 DK100640NIDDK NIH HHS R00 DK100640
6 · The paper itself

Abstract

Obesity and related metabolic disorders are pressing public health concerns, raising the risk for a multitude of chronic diseases. Obesity is multi-factorial disease, with both diet and lifestyle, as well as genetic and developmental factors leading to alterations in energy balance. In this regard, a novel role for DNA repair glycosylases in modulating risk for obesity has been previously established. Global deletion of either of two different glycosylases with varying substrate specificities, Nei-like endonuclease 1 (NEIL1) or 8-oxoguanine DNA glycosylase-1 (OGG1), both predispose mice to diet-induced obesity (DIO). Conversely, enhanced expression of the human

Indexed as

developmental origins of diseaseDNA repairmetabolic syndrome (in offspring)mitochondrial functionobesity

Identifiers

PMID34604220
PMCPMC8480284
OpenAlexW3199275167

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.