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The Structure-Specific Endonuclease Ercc1-Xpf Is Required To Resolve DNA Interstrand Cross-Link-Induced Double-Strand Breaks

Molecular and Cellular Biology, 2004-07, Vol.24 (13), p.5776-5787

2004

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Neurological symptoms and natural course of xeroderma pigmentosum

Brain (London, England : 1878), 2008-08, Vol.131 (8), p.1979-1989

2008

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Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome

Human mutation, 2006-11, Vol.27 (11), p.1092-1103

2006

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A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase

Science (American Association for the Advancement of Science), 1995-06, Vol.268 (5218), p.1749-1753

1995

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ERCC6 founder mutation identified in Finnish patients with COFS syndrome

Clinical genetics, 2010-12, Vol.78 (6), p.541-547

2010

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Predominance of Null Mutations in Ataxia-Telangiectasia

Human molecular genetics, 1996-04, Vol.5 (4), p.433-439

1996

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A case of Rombo syndrome

British journal of dermatology (1951), 2001-06, Vol.144 (6), p.1215-1218

2001

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Localization of an ataxia-telangiectasia gene to chromosome 11q22-23

Nature (London), 1988-12, Vol.336 (6199), p.577-580

1988

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Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F

The EMBO journal, 1993-09, Vol.12 (9), p.3693-3701

1993

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Ataxia-telangiectasia : linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome

Human genetics, 1992-03, Vol.88 (6), p.619-626

1992

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Xeroderma pigmentosum complementation group G associated with Cockayne syndrome

American journal of human genetics, 1993-07, Vol.53 (1), p.185-192

1993

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Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH)

The EMBO journal, 1994-04, Vol.13 (7), p.1645-1653

1994

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Homozygous R788W Point Mutation in the XPF Gene of a Patient with Xeroderma Pigmentosum and Late-Onset Neurologic Disease

Journal of investigative dermatology, 1998-05, Vol.110 (5), p.832-836

1998

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Xeroderma pigmentosum--Cockayne syndrome complex: a further case

Journal of medical genetics, 1996-07, Vol.33 (7), p.607-610

1996

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Clones of normal keratinocytes and a variety of simultaneously present epidermal neoplastic lesions contain a multitude of p53 gene mutations in a xeroderma pigmentosum patient

Cancer research (Chicago, Ill.), 1998-06, Vol.58 (11), p.2449-2455

1998

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Mammalian nucleotide excision repair and syndromes

Biochemical Society transactions, 1997-02, Vol.25 (1), p.309-315

1997

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Development of laparoscopic instruments

Minimally invasive therapy and allied technologies, 2001-01, Vol.10 (3), p.145-154

2001

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Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients

Cytogenetic and genome research, 1988-01, Vol.49 (4), p.259-263

1988

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DNA repair genes, enzymes, patients, and mouse models

Recent results in cancer research, 1997, Vol.143, p.329

Jaspers, N G

1997

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A gene that regulates DNA replication in response to DNA damage is located on human chromosome 4q

American journal of human genetics, 1995-11, Vol.57 (5), p.1095-1103

1995

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Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: genetic relationship to ataxia telangiectasia

American journal of human genetics, 1988, Vol.42 (1), p.66-73

1988

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Retinoic acid and defective UV light induced DNA excision repair in Xeroderma pigmentosum: absence of ameliorating effect

Archives of Dermatological Research, 1984-01, Vol.276 (3), p.201-202

1984

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Ataxia-telangiectasia-like chinese hamster V79 cell mutants with radioresistant DNA synthesis, chromosomal instability, and normal DNA strand break repair

Cancer research (Chicago, Ill.), 1989-03, Vol.49 (6), p.1481-1485

1989

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Genetic Heterogeneity in Ataxia-Telangiectasia Studied by Cell Fusion

Proceedings of the National Academy of Sciences - PNAS, 1982-04, Vol.79 (8), p.2641-2644

1982

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Studies on phenotypic complementation of ataxia-telangiectasia cells by chromosome transfer

American journal of human genetics, 1995-02, Vol.56 (2), p.438-443

1995

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The Structure-Specific Endonuclease Ercc1-Xpf Is Required To Resolve DNA Interstrand Cross-Link-Induced Double-Strand Breaks

Neurological symptoms and natural course of xeroderma pigmentosum

Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome

A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase

ERCC6 founder mutation identified in Finnish patients with COFS syndrome

Predominance of Null Mutations in Ataxia-Telangiectasia

A case of Rombo syndrome

Localization of an ataxia-telangiectasia gene to chromosome 11q22-23

Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F

Ataxia-telangiectasia : linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome

Xeroderma pigmentosum complementation group G associated with Cockayne syndrome

Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH)

Homozygous R788W Point Mutation in the XPF Gene of a Patient with Xeroderma Pigmentosum and Late-Onset Neurologic Disease

Xeroderma pigmentosum--Cockayne syndrome complex: a further case

Clones of normal keratinocytes and a variety of simultaneously present epidermal neoplastic lesions contain a multitude of p53 gene mutations in a xeroderma pigmentosum patient

Mammalian nucleotide excision repair and syndromes

Development of laparoscopic instruments

Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients

DNA repair genes, enzymes, patients, and mouse models

A gene that regulates DNA replication in response to DNA damage is located on human chromosome 4q

Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: genetic relationship to ataxia telangiectasia

Retinoic acid and defective UV light induced DNA excision repair in Xeroderma pigmentosum: absence of ameliorating effect

Ataxia-telangiectasia-like chinese hamster V79 cell mutants with radioresistant DNA synthesis, chromosomal instability, and normal DNA strand break repair

Genetic Heterogeneity in Ataxia-Telangiectasia Studied by Cell Fusion

Studies on phenotypic complementation of ataxia-telangiectasia cells by chromosome transfer

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