(Q33283626)

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Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13.

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scholarly article

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Europe PubMed Central

PubMed publication ID

25 July 2017

Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13. (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

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Europe PubMed Central

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25 July 2017

Thomas Meitinger

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Europe PubMed Central

PubMed publication ID

25 July 2017

12

object named as

Anke Hinney

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Johannes Hebebrand

13

object named as

Johannes Hebebrand

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Martin Wabitsch

8

object named as

Martin Wabitsch

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Matthias Platzer

10

object named as

Matthias Platzer

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Europe PubMed Central

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25 July 2017

Kathrin Reichwald

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object named as

Kathrin Reichwald

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Europe PubMed Central

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25 July 2017

author name string

Susann Friedel

1

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Europe PubMed Central

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25 July 2017

Harald Brumm

4

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Europe PubMed Central

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25 July 2017

Anne-Kathrin Wermter

5

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Europe PubMed Central

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25 July 2017

Hans-Rudolf Fries

6

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Europe PubMed Central

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25 July 2017

Kerstin Koberwitz

7

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Europe PubMed Central

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25 July 2017

Heike Biebermann

11

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Europe PubMed Central

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25 July 2017

publication date

3 May 2007

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25 July 2017

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Europe PubMed Central

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25 July 2017

8

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25 July 2017

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Europe PubMed Central

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25 July 2017

Lack of support for the association between GAD2 polymorphisms and severe human obesity

1 reference

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Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesity

1 reference

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21 June 2018

Expression of DGAT2 in white adipose tissue is regulated by central leptin action

1 reference

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Polymorphisms in the amino acid transporter solute carrier family 6 (neurotransmitter transporter) member 14 gene contribute to polygenic obesity in French Caucasians

1 reference

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A powerful strategy to account for multiple testing in the context of haplotype analysis

1 reference

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Ghrelin receptor gene: identification of several sequence variants in extremely obese children and adolescents, healthy normal-weight and underweight students, and children with short normal stature

1 reference

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GAD2 on chromosome 10p12 is a candidate gene for human obesity

1 reference

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21 June 2018

Lipopenia and skin barrier abnormalities in DGAT2-deficient mice

1 reference

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21 June 2018

The SLC6A14 gene shows evidence of association with obesity

1 reference

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Sample size requirements to control for stochastic variation in magnitude and location of allele-sharing linkage statistics in affected sibling pairs

1 reference

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An efficient procedure for genotyping single nucleotide polymorphisms.

1 reference

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21 June 2018

Cloning of DGAT2, a second mammalian diacylglycerol acyltransferase, and related family members

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1871603

21 June 2018

DGAT2 is a new diacylglycerol acyltransferase gene family: purification, cloning, and expression in insect cells of two polypeptides from Mortierella ramanniana with diacylglycerol acyltransferase activity

1 reference

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Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height

1 reference

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Peroxisome proliferator-activated receptors: from transcriptional control to clinical practice

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Characterization of a human preadipocyte cell strain with high capacity for adipose differentiation

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The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.

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A test for linkage and association in general pedigrees: the pedigree disequilibrium test

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Obesity resistance and multiple mechanisms of triglyceride synthesis in mice lacking Dgat

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21 June 2018

Several mutations in the melanocortin-4 receptor gene including a nonsense and a frameshift mutation associated with dominantly inherited obesity in humans

1 reference

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21 June 2018

A computer program for aligning a cDNA sequence with a genomic DNA sequence

1 reference

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Screening for variability in the ciliary neurotrophic factor (CNTF) gene: no evidence for association with human obesity

1 reference

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21 June 2018

An autosomal genomic scan for loci linked to prediabetic phenotypes in Pima Indians

1 reference

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21 June 2018

Base-calling of automated sequencer traces using phred. II. Error probabilities

1 reference

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21 June 2018

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

1 reference

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21 June 2018

Genetic and environmental factors in relative body weight and human adiposity

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A mutation in the first transmembrane domain of the lutropin receptor causes male precocious puberty

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21 June 2018

Genomewide search for genes influencing percent body fat in Pima Indians: suggestive linkage at chromosome 11q21-q22. Pima Diabetes Gene Group

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A new DNA sequence assembly program

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Regulation of the apolipoprotein AI gene by ARP-1, a novel member of the steroid receptor superfamily

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Extended clinical phenotype, endocrine investigations and functional studies of a loss-of-function mutation A150V in the thyroid hormone specific transporter MCT8.

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Is glutamate decarboxylase 2 (GAD2) a genetic link between low birth weight and subsequent development of obesity in children?

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Transmembrane domain helix packing stabilizes integrin alphaIIbbeta3 in the low affinity state

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Identification of interactive loci linked to insulin and leptin in mice with genetic insulin resistance

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No evidence for involvement of the promoter polymorphism -866 G/A of the UCP2 gene in childhood-onset obesity in humans.

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Genome scan for childhood and adolescent obesity in German families.

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10.1186/1471-2156-8-17

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Europe PubMed Central

PubMed publication ID

25 July 2017

Dimensions Publication ID

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https://scigraph.springernature.com/pub.10.1186/1471-2156-8-17

9 September 2019

PMC publication ID

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Europe PubMed Central

PubMed publication ID

25 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

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