(Q48784329)

15 February 2018

title

From xeroderma pigmentosum to the biological clock contributions of Dirk Bootsma to human genetics. (English)

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15 February 2018

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xeroderma pigmentosum

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1

J H Hoeijmakers

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15 February 2018

language of work or name

English

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publication date

1 February 2001

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15 February 2018

published in

Mutation Research

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15 February 2018

volume

485

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15 February 2018

issue

1

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15 February 2018

page(s)

43-59

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15 February 2018

STUDIES ON SYNCHRONOUS DIVISION OF TISSUE CULTURE CELLS INITIATED BY EXCESS THYMIDINE

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CHANGES INDUCED IN THE FIRST POST-IRRADIATION GENERATION CYCLE OF HUMAN CELLS STUDIES BY DOUBLE LABELING

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The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta

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hRAD30 mutations in the variant form of xeroderma pigmentosum

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Synteny of the human loci for fumarate hydratase and UDPG pyrophosphorylase with chromosome 1 markers in somatic cell hybrids

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Regional mapping of the human No. 1 and X chromosome in interspecific cell hybrids using an X/1 translocation

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Assignment of the AK1:Np:ABO linkage group to human chromosome 9

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A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia

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7 January 2021

Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia

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7 January 2021

Unique fusion of bcr and c-abl genes in Philadelphia chromosome positive acute lymphoblastic leukemia.

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7 January 2021

Differences between rodent and human cell lines in the amount of integrated DNA after transfection

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7 January 2021

Repair capability and the cellular age response for killing and mutation induction after UV.

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7 January 2021

Molecular cloning of a human DNA repair gene

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7 January 2021

The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I

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7 January 2021

Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10.

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7 January 2021

Molecular cloning and biological characterization of the human excision repair gene ERCC-3

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7 January 2021

Molecular cloning of the human DNA excision repair gene ERCC-6

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7 January 2021

Structural and functional conservation of two human homologs of the yeast DNA repair gene RAD6

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7 January 2021

Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease

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7 January 2021

Cloning of a human homolog of the yeast nucleotide excision repair gene MMS19 and interaction with transcription repair factor TFIIH via the XPB and XPD helicases

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7 January 2021

Disruption of mouse SNM1 causes increased sensitivity to the DNA interstrand cross-linking agent mitomycin C

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7 January 2021

RAD25 (SSL2), the yeast homolog of the human xeroderma pigmentosum group B DNA repair gene, is essential for viability

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7 January 2021

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

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7 January 2021

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

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7 January 2021

ERCC2: cDNA cloning and molecular characterization of a human nucleotide excision repair gene with high homology to yeast RAD3

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7 January 2021

Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene

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7 January 2021

Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain

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7 January 2021

Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C

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7 January 2021

Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2

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7 January 2021

Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5

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7 January 2021

Isolation of the functional human excision repair gene ERCC5 by intercosmid recombination

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7 January 2021

The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH

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7 January 2021

Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome complementation group A.

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7 January 2021

Xeroderma pigmentosum group E cells lack a nuclear factor that binds to damaged DNA

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7 January 2021

Correction of the DNA repair defect in xeroderma pigmentosum group E by injection of a DNA damage-binding protein

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7 January 2021

Complementation of the xeroderma pigmentosum DNA repair defect in cell-free extracts.

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7 January 2021

Human nucleotide excision repair in vitro: repair of pyrimidine dimers, psoralen and cisplatin adducts by HeLa cell-free extract.

1 reference

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7 January 2021

ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor.

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https://api.crossref.org/works/10.1016%2FS0921-8777%2800%2900079-3

7 January 2021

The human RAD54 recombinational DNA repair protein is a double-stranded DNA-dependent ATPase

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7 January 2021

Cloning, comparative mapping, and RNA expression of the mouse homologues of the Saccharomyces cerevisiae nucleotide excision repair gene RAD23

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7 January 2021

Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair

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7 January 2021

DNA structural elements required for ERCC1-XPF endonuclease activity.

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7 January 2021

DNA-binding polarity of human replication protein A positions nucleases in nucleotide excision repair

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7 January 2021

DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor

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7 January 2021

Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome

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7 January 2021

Molecular mechanism of nucleotide excision repair.

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7 January 2021

DNA repair. The bases for Cockayne syndrome.

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7 January 2021

Transcription-coupled repair of 8-oxoguanine: requirement for XPG, TFIIH, and CSB and implications for Cockayne syndrome

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7 January 2021

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

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7 January 2021

Open complex formation around a lesion during nucleotide excision repair provides a structure for cleavage by human XPG protein

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7 January 2021

Action of DNA repair endonuclease ERCC1/XPF in living cells

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7 January 2021

DNA repair. Engagement with transcription

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7 January 2021

Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence

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7 January 2021

Disruption of mouse RAD54 reduces ionizing radiation resistance and homologous recombination.

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7 January 2021

Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition

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7 January 2021

Inactivation of the HR6B ubiquitin-conjugating DNA repair enzyme in mice causes male sterility associated with chromatin modification.

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7 January 2021

A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy

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7 January 2021

Base excision repair deficient mice lacking the Aag alkyladenine DNA glycosylase.

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7 January 2021

DNA repair methyltransferase (Mgmt) knockout mice are sensitive to the lethal effects of chemotherapeutic alkylating agents

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7 January 2021

Cancer from the outside, aging from the inside: mouse models to study the consequences of defective nucleotide excision repair

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7 January 2021

Cloning, tissue expression, and mapping of a human photolyase homolog with similarity to plant blue-light receptors

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7 January 2021

Mammalian Cry1 and Cry2 are essential for maintenance of circadian rhythms

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7 January 2021

10.1016/S0921-8777(00)00079-3

Identifiers

DOI

1 reference

15 February 2018

PubMed ID

11341993

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15 February 2018