(Q36574973)

15 August 2017

1 reference

title

Syndromes with genetic instability: model diseases for (skin) cancerogenesis (English)

1 reference

15 August 2017

Steffen Emmert

1

1 reference

PubMed ID

16928240

15 August 2017

Diana Leibeling

series ordinal

2

1 reference

PubMed ID

16928240

15 August 2017

Thomas M Rünger

series ordinal

3

1 reference

15 August 2017

1 September 2006

1 reference

15 August 2017

1 reference

15 August 2017

4

1 reference

15 August 2017

9

1 reference

15 August 2017

721-731

1 reference

Genome maintenance mechanisms for preventing cancer

15 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Replication of damaged DNA by translesion synthesis in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

The xeroderma pigmentosum group C gene leads to selective repair of cyclobutane pyrimidine dimers rather than 6-4 photoproducts

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Nucleotide excision repair and human syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Xeroderma pigmentosum and the role of UV-induced DNA damage in skin cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

DNA double strand break repair and chromosomal translocation: lessons from animal models

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

The inherited basis of human radiosensitivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

DNA double-strand breaks: signaling, repair and the cancer connection

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Xeroderma pigmentosum: children of the moon

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Role of DNA mismatch repair defects in the pathogenesis of human cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

The hereditary nonpolyposis colorectal cancer syndrome: genetics and clinical implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Recombinational DNA repair and human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Nijmegen breakage syndrome. The International Nijmegen Breakage Syndrome Study Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Positional cloning of the gene for Nijmegen breakage syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Squamous cell carcinoma of the tongue in a patient with Rothmund-Thomson syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Cancer in Fanconi anemia, 1927-2001

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

The Fanconi anaemia/BRCA pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

An overview of three new disorders associated with genetic instability: LIG4 syndrome, RS-SCID and ATR-Seckel syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Assessment of 3 xeroderma pigmentosum group C gene polymorphisms and risk of cutaneous melanoma: a case-control study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

How disruption of cell cycle regulating genes might predispose to sun-induced skin cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

Antiproliferative activity of ecteinascidin 743 is dependent upon transcription-coupled nucleotide-excision repair.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1610-0387.2006.06047.X

10.1111/J.1610-0387.2006.06047.X

21 January 2018

Identifiers

DOI

1 reference

15 August 2017

1 reference

PubMed ID

16928240