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Xeroderma pigmentosum and other diseases of human premature aging and DNA repair: molecules to patients

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title

Xeroderma pigmentosum and other diseases of human premature aging and DNA repair: molecules to patients (English)

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main subject

xeroderma pigmentosum

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2

Vilhelm A Bohr

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author name string

Laura J Niedernhofer

series ordinal

1

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Miriam Sander

series ordinal

3

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Kenneth H Kraemer

series ordinal

4

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language of work or name

English

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publication date

2011

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published in

Mechanisms of Ageing and Development

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volume

132

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issue

6-7

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page(s)

340-7

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cites work

MMXD, a TFIIH-independent XPD-MMS19 protein complex involved in chromosome segregation

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PubMed Central

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7 April 2017

True lies: the double life of the nucleotide excision repair factors in transcription and DNA repair

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7 April 2017

Adverse effects of trichothiodystrophy DNA repair and transcription gene disorder on human fetal development

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PubMed Central

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7 April 2017

Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations

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7 April 2017

XPD helicase structures and activities: insights into the cancer and aging phenotypes from XPD mutations

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7 April 2017

Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship

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PubMed Central

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7 April 2017

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

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7 April 2017

Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair.

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27 September 2017

Cockayne syndrome group B protein promotes mitochondrial DNA stability by supporting the DNA repair association with the mitochondrial membrane

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27 September 2017

Trichothiodystrophy: from basic mechanisms to clinical implications

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27 September 2017

Molecular insights into the recruitment of TFIIH to sites of DNA damage

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27 September 2017

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A Japanese trichothiodystrophy patient with XPD mutations.

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28 November 2018

NER factors are recruited to active promoters and facilitate chromatin modification for transcription in the absence of exogenous genotoxic attack.

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28 November 2018

New areas of focus at workshop on human diseases involving DNA repair deficiency and premature aging

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28 November 2018

Rare diseases provide rare insights into DNA repair pathways, TFIIH, aging and cancer center

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https://pubmed.ncbi.nlm.nih.gov/21708183

retrieved

12 December 2020

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Identifiers

DOI

10.1016/J.MAD.2011.06.004

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PMC publication ID

3474983

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PubMed publication ID

21708183

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ResearchGate publication ID

51252679

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(Q24628121)

Xeroderma pigmentosum and other diseases of human premature aging and DNA repair: molecules to patients

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