(Q41571756)

3 October 2017

Genome-wide DNA methylation analysis in blood cells from patients with Werner syndrome (English)

1 reference

3 October 2017

0 references

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Maria Giulia Bacalini

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Davide Gentilini

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

author name string

A Marcoccia

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

S Pisoni

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

A M Di Blasio

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

A Corsi

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

C Franceschi

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

D Raimondo

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

A Spanò

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

P Garagnani

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

F Bondanini

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

publication date

30 August 2017

1 reference

3 October 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

volume

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

page(s)

92

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

Accelerated epigenetic aging in Werner syndrome

11 June 2020

cites work

1 reference

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The methylation of nuclear and mitochondrial DNA in ageing phenotypes and longevity

6 June 2018

1 reference

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Novel genetic loci underlying human intracranial volume identified through genome-wide association

6 June 2018

1 reference

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The telomeric protein AKTIP interacts with A- and B-type lamins and is involved in regulation of cellular senescence.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

shinyGEO: a web-based application for analyzing gene expression omnibus datasets

6 June 2018

1 reference

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Erratum: A meta-analysis on age-associated changes in blood DNA methylation: results from an original analysis pipeline for Infinium 450k data

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Enrichr: a comprehensive gene set enrichment analysis web server 2016 update

6 June 2018

1 reference

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DNA methylation in PRDM8 is indicative for dyskeratosis congenita

6 June 2018

1 reference

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Biomarkers in rheumatic diseases: how can they facilitate diagnosis and assessment of disease activity?

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Epigenetic Regulation of Werner Syndrome Gene in Age-Related Cataract

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

The DNA structure and sequence preferences of WRN underlie its function in telomeric recombination events

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Systemic sclerosis-associated fibrosis: an accelerated aging phenotype?

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

AKTIP/Ft1, a New Shelterin-Interacting Factor Required for Telomere Maintenance

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Autoantibodies in systemic sclerosis: unanswered questions

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Identification of a DNA methylation signature in blood cells from persons with Down Syndrome

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Genome-wide DNA methylation analysis in dermal fibroblasts from patients with diffuse and limited systemic sclerosis reveals common and subset-specific DNA methylation aberrancies

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Telomerase protects Werner syndrome lineage-specific stem cells from premature aging.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

2013 classification criteria for systemic sclerosis: an American college of rheumatology/European league against rheumatism collaborative initiative

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

The epidemiology of premature aging and associated comorbidities

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Enrichr: interactive and collaborative HTML5 gene list enrichment analysis tool

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

FOXOs: signalling integrators for homeostasis maintenance

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Aberrant DNA methylation profiles in the premature aging disorders Hutchinson-Gilford Progeria and Werner syndrome

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Loss of ceramide synthase 3 causes lethal skin barrier disruption

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Accumulation of long-chain glycosphingolipids during aging is prevented by caloric restriction.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Interplay between FOXO, TOR, and Akt

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Comparison of Beta-value and M-value methods for quantifying methylation levels by microarray analysis

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

NCBI GEO: archive for functional genomics data sets--10 years on

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Roles of Werner syndrome protein in protection of genome integrity

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

From the rarest to the most common: insights from progeroid syndromes into skin cancer and aging.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Early atherosclerosis in systemic sclerosis and its relation to disease or traditional risk factors

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

FOXO transcription factors in ageing and cancer.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

PI3K/Akt and CREB regulate adult neural hippocampal progenitor proliferation and differentiation

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

The disintegrin and metalloproteinase ADAM12 contributes to TGF-beta signaling through interaction with the type II receptor

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

FOXO transcription factors at the interface between longevity and tumor suppression

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Morphological adjustment of senescent cells by modulating caveolin-1 status.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Systemic sclerosis-scleroderma.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

A comparison of adult and childhood progerias: Werner syndrome and Hutchinson-Gilford progeria syndrome

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Clinical, endocrine and metabolic aspects of the Werner syndrome compared with those of normal aging

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Clinical aspects of systemic sclerosis (scleroderma)

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Diagnostic criteria for Werner syndrome based on Japanese nationwide epidemiological survey

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Serum levels of ADAM12-S: possible association with the initiation and progression of dermal fibrosis and interstitial lung disease in patients with systemic sclerosis

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

[Aging and the control of the insulin-FOXO signaling pathway].

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Significant elevation of IgG anti-WRN (RecQ3 RNA/DNA helicase) antibody in systemic sclerosis

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

European Scleroderma Study Group to define disease activity criteria for systemic sclerosis. IV. Assessment of skin thickening by modified Rodnan skin score

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Biomarkers of oxidative stress are significantly elevated in Down syndrome

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5577832

Hutchinson-Gilford progeria syndrome with scleroderma-like skin changes due to a homozygous missense LMNA mutation

19 August 2018

1 reference

12 December 2020

Generalized morphea in a child with harlequin ichthyosis: a rare association

1 reference

12 December 2020

Werner's syndrome: a quite rare disease for differential diagnosis of scleroderma

1 reference

12 December 2020

EBV transformation and cell culturing destabilizes DNA methylation in human lymphoblastoid cell lines

1 reference

12 December 2020

Chronic leg ulcers in Werner's syndrome

1 reference

12 December 2020

Progeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation

1 reference

12 December 2020

Clinical and metabolic studies on Werner's syndrome: with special reference to disorders of lipid and liver function

1 reference

12 December 2020

Leg ulcers in Werner's syndrome. Report of one case

1 reference

12 December 2020

10.1186/S13148-017-0389-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

11 June 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28861129%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

PubMed publication ID

28861129

1 reference