(Q34878556)

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Lifespan extension by dietary intervention in a mouse model of Cockayne syndrome uncouples early postnatal development from segmental progeria

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Europe PubMed Central

PubMed publication ID

5 August 2017

Lifespan extension by dietary intervention in a mouse model of Cockayne syndrome uncouples early postnatal development from segmental progeria (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

1 reference

based on heuristic

inferred from title

Cockayne syndrome

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

author name string

Sarah C Vose

2

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Europe PubMed Central

PubMed publication ID

5 August 2017

Dorathy F Vargas

3

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Shuangyun Zhao

4

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Xiu-Ping Wang

5

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

James R Mitchell

6

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

publication date

11 September 2013

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

1144-1147

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Blinded by the UV light: how the focus on transcription-coupled NER has distracted from understanding the mechanisms of Cockayne syndrome neurologic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Cockayne syndrome group B protein prevents the accumulation of damaged mitochondria by promoting mitochondrial autophagy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Repair of persistent strand breaks in the mitochondrial genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Cerebro-oculo-facio-skeletal syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Robinow syndrome, Cockayne syndrome, and Pfeiffer syndrome: an overview of physical, neurological, and oral characteristics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

DNA Damage, Aging, and Cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Transcription-coupled nucleotide excision repair in mammalian cells: molecular mechanisms and biological effects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Impaired genome maintenance suppresses the growth hormone--insulin-like growth factor 1 axis in mice with Cockayne syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Increased apoptosis, p53 up-regulation, and cerebellar neuronal degeneration in repair-deficient Cockayne syndrome mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Extended longevity mechanisms in short-lived progeroid mice: identification of a preservative stress response associated with successful aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Premature aging in mice deficient in DNA repair and transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne syndrome Group B DNA repair genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Postnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XPA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

Cockayne's syndrome: literature review and case report

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266594

8 July 2018

UVB radiation-induced cancer predisposition in Cockayne syndrome group A (Csa) mutant mice.

1 reference

https://api.crossref.org/works/10.1111%2FACEL.12142

21 January 2018

Cockayne's syndrome: dental findings and management

1 reference

https://pubmed.ncbi.nlm.nih.gov/23895664

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comprehensive description of the severity groups in Cockayne syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23895664

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/23895664

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dental findings in a child with Cockayne's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23895664

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/ACEL.12142

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

ResearchGate publication ID

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