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Mammalian Cry1 and Cry2 are essential for maintenance of circadian rhythms

Nature (London), 1999-04, Vol.398 (6728), p.627-630

1999

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Disruption of Mouse RAD54 Reduces Ionizing Radiation Resistance and Homologous Recombination

Cell, 1997-04, Vol.89 (2), p.195-204

1997

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ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

Cell, 1992-12, Vol.71 (6), p.939-953

1992

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Identification and characterization of XPC-binding domain of hHR23B

Molecular and Cellular Biology, 1997-12, Vol.17 (12), p.6915-6923

1997

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Two human homologs of Rad23 are functionally interchangeable in complex formation and stimulation of XPC repair activity

Molecular and Cellular Biology, 1997-12, Vol.17 (12), p.6924-6931

1997

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Xeroderma Pigmentosum Group C Protein Complex Is the Initiator of Global Genome Nucleotide Excision Repair

Molecular cell, 1998-08, Vol.2 (2), p.223-232

1998

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Nucleotide excision repair syndromes: molecular basis and clinical symptoms

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 1995-01, Vol.347 (1319), p.75

1995

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Dhr6, a Drosophila homolog of the yeast DNA-repair gene RAD6

Proceedings of the National Academy of Sciences - PNAS, 1991-05, Vol.88 (9), p.3832-3836

1991

Volltextzugriff (PDF)

Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23

The EMBO journal, 1994-04, Vol.13 (8), p.1831-1843

1994

Volltextzugriff (PDF)

Defective Transcription-Coupled Repair in Cockayne Syndrome B Mice Is Associated with Skin Cancer Predisposition

Cell, 1997-05, Vol.89 (3), p.425-435

1997

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The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex

The EMBO journal, 1997-10, Vol.16 (19), p.5955-5965

1997

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HHR23B, a human Rad23 homolog, stimulates XPC protein in nucleotide excision repair in vitro

Molecular and Cellular Biology, 1996-09, Vol.16 (9), p.4852-4861

1996

Volltextzugriff (PDF)

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

DNA repair, 2002-02, Vol.1 (2), p.143-157

2002

Volltextzugriff (PDF)

Sequence Conservation of therad21 Schizosaccharomyces pombeDNA Double-Strand Break Repair Gene in Human and Mouse

Genomics (San Diego, Calif.), 1996-09, Vol.36 (2), p.305-315

1996

Volltextzugriff (PDF)

The genetic defect in DNA repair deficiency syndromes: EACR—Mühlbock Memorial Lecture, 1993

European journal of cancer (1990), 1993, Vol.29 (10), p.1482-1488

Bootsma, Dirk

1993

Volltextzugriff (PDF)

Cloning, Comparative Mapping, and RNA Expression of the Mouse Homologues of theSaccharomyces cerevisiaeNucleotide Excision Repair GeneRAD23

Genomics (San Diego, Calif.), 1996-01, Vol.31 (1), p.20-27

1996

Volltextzugriff (PDF)

A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome

Cell, 1990-08, Vol.62 (4), p.777-791

1990

Volltextzugriff (PDF)

Structural and Functional Conservation of Two Human Homologs of the Yeast DNA Repair Gene RAD6

Proceedings of the National Academy of Sciences - PNAS, 1991-10, Vol.88 (20), p.8865-8869

1991

Volltextzugriff (PDF)

XPC and human homologs of RAD23: intracellular localization and relationship to other nucleotide excision repair complexes

Nucleic acids research, 1996-07, Vol.24 (13), p.2551

1996

Volltextzugriff (PDF)

The genetic defect in DNA repair deficiency syndromes

European journal of cancer (1990), 1993-01, Vol.29 (10), p.1482-1488

Bootsma, Dirk

1993

Volltextzugriff (PDF)

Correction of the DNA Repair Defect in Xeroderma Pigmentosum Group E by Injection of a DNA Damage-Binding Protein

Proceedings of the National Academy of Sciences - PNAS, 1994-04, Vol.91 (9), p.4053-4056

1994

Volltextzugriff (PDF)

Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas

American journal of human genetics, 1994-06, Vol.54 (6), p.1022-1029

1994

Volltextzugriff (PDF)

Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma

Oncogene, 1995-04, Vol.10 (8), p.1521-1528

1995

Volltextzugriff (PDF)

Mutational analysis of the human nucleotide excision repair gene ERCC1

Nucleic acids research, 1996-09, Vol.24 (17), p.3370

1996

Volltextzugriff (PDF)

Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition

Cancer research (Chicago, Ill.), 1999-07, Vol.59 (14), p.3489-3494

1999

Volltextzugriff (PDF)

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Mammalian Cry1 and Cry2 are essential for maintenance of circadian rhythms

Disruption of Mouse RAD54 Reduces Ionizing Radiation Resistance and Homologous Recombination

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

Identification and characterization of XPC-binding domain of hHR23B

Two human homologs of Rad23 are functionally interchangeable in complex formation and stimulation of XPC repair activity

Xeroderma Pigmentosum Group C Protein Complex Is the Initiator of Global Genome Nucleotide Excision Repair

Nucleotide excision repair syndromes: molecular basis and clinical symptoms

Dhr6, a Drosophila homolog of the yeast DNA-repair gene RAD6

Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23

Defective Transcription-Coupled Repair in Cockayne Syndrome B Mice Is Associated with Skin Cancer Predisposition

The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex

HHR23B, a human Rad23 homolog, stimulates XPC protein in nucleotide excision repair in vitro

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

Sequence Conservation of therad21 Schizosaccharomyces pombeDNA Double-Strand Break Repair Gene in Human and Mouse

The genetic defect in DNA repair deficiency syndromes: EACR—Mühlbock Memorial Lecture, 1993

Cloning, Comparative Mapping, and RNA Expression of the Mouse Homologues of theSaccharomyces cerevisiaeNucleotide Excision Repair GeneRAD23

A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome

Structural and Functional Conservation of Two Human Homologs of the Yeast DNA Repair Gene RAD6

XPC and human homologs of RAD23: intracellular localization and relationship to other nucleotide excision repair complexes

The genetic defect in DNA repair deficiency syndromes

Correction of the DNA Repair Defect in Xeroderma Pigmentosum Group E by Injection of a DNA Damage-Binding Protein

Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas

Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma

Mutational analysis of the human nucleotide excision repair gene ERCC1

Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition

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