Jan Hoeijmakers
Hoeijmakers, Jan 1951-
Hoeijmakers, Jan Hendrik Jozef
Hoeijmakers, Jan
Hoeijmakers, J.H.J. (Jan Hendrik Jozef), 1951-
VIAF ID: 194556749 (Personal)
Permalink: http://viaf.org/viaf/194556749
Preferred Forms
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100 1 _ ‡a Hoeijmakers, J.H.J. ‡q (Jan Hendrik Jozef), ‡d 1951-
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100 1 _ ‡a Hoeijmakers, Jan
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100 1 _
‡a
Hoeijmakers, Jan Hendrik Jozef
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100 1 _
‡a
Hoeijmakers, Jan
‡d
1951-
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100 0 _
‡a
Jan Hoeijmakers
4xx's: Alternate Name Forms (7)
5xx's: Related Names (1)
Works
| Title | Sources |
|---|---|
| Homeostatic imbalance between apoptosis and cell renewal in the liver of premature aging Xpd mice |
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| Homologous and non-homologous recombination differentially affect DNA damage repair in mice |
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| How Relevant is the Escherichia coli UvrABC Model for Excision Repair in Eukaryotes? |
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| Human RAD18 interacts with ubiquitylated chromatin components and facilitates RAD9 recruitment to DNA double strand breaks |
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| The human RAD54 recombinational DNA repair protein is a double-stranded DNA-dependent ATPase |
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| Hybridocytochemistry with 2-acetylaminofluorene-modified probes |
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| Inactivation of the HR6B ubiquitin-conjugating DNA repair enzyme in mice causes male sterility associated with chromatin modification. |
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| Interaction of hHR23 with S5a. The ubiquitin-like domain of hHR23 mediates interaction with S5a subunit of 26 S proteasome |
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| Involvement of global genome repair, transcription coupled repair, and chromatin remodeling in UV DNA damage response changes during development |
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| The isolation of plasmids containing DNA complementary to messenger RNA for variant surface glycoproteins of Trypanosoma brucei |
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| Knockout mouse model and gametogenic failure |
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| Localization of two human homologs, HHR6A and HHR6B, of the yeast DNA repair gene RAD6 to chromosomes Xq24-q25 and 5q23-q31 |
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| A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes |
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| Loss of HR6B ubiquitin-conjugating activity results in damaged synaptonemal complex structure and increased crossing-over frequency during the male meiotic prophase |
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| The major transcripts of the kinetoplast DNA of Trypanosoma brucei are very small ribosomal RNAs. |
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| Mammalian Cry1 and Cry2 are essential for maintenance of circadian rhythms |
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| MARK-AGE biomarkers of ageing |
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| Meningococcal disease in The Netherlands, 1959-1981: the occurrence of serogroups and serotypes 2a and 2b of Neisseria meningitidis |
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| Microinjected photoreactivating enzymes from Anacystis and Saccharomyces monomerize dimers in chromatin of human cells |
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| Molecular and functional analysis of the XPBC/ERCC-3 promoter: transcription activity is dependent on the integrity of an Sp1-binding site |
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| Molecular basis of DNA repair mechanisms and syndromes |
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| Molecular cloning of a human DNA repair gene |
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| Mutation of the mouse Rad17 gene leads to embryonic lethality and reveals a role in DNA damage-dependent recombination |
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| A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis |
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| A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A |
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| Novel expression-linked copies of the genes for variant surface antigens in trypanosomes |
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| Novel functional interactions between nucleotide excision DNA repair proteins influencing the enzymatic activities of TFIIH, XPG, and ERCC1-XPF |
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| A novel regulation mechanism of DNA repair by damage-induced and RAD23-dependent stabilization of xeroderma pigmentosum group C protein |
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| Nucleocytoplasmic shuttling and mCRY-dependent inhibition of ubiquitylation of the mPER2 clock protein |
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| p44 and p34 subunits of the BTF2/TFIIH transcription factor have homologies with SSL1, a yeast protein involved in DNA repair |
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| Phenotypic heterogeneity in nucleotide excision repair mutants of rodent complementation groups 1 and 4 |
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| Photic induction of mPer1 and mPer2 in cry-deficient mice lacking a biological clock |
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| Polyubiquitination of proliferating cell nuclear antigen by HLTF and SHPRH prevents genomic instability from stalled replication forks |
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| Premature aging in mice deficient in DNA repair and transcription |
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| The progeroid phenotype of Ku80 deficiency is dominant over DNA-PKCS deficiency |
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| RAD25 (SSL2), the yeast homolog of the human xeroderma pigmentosum group B DNA repair gene, is essential for viability |
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| Rec8p, a meiotic recombination and sister chromatid cohesion phosphoprotein of the Rad21p family conserved from fission yeast to humans |
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| Recombination and joining: different means to the same ends |
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| Reduced hematopoietic reserves in DNA interstrand crosslink repair-deficient Ercc1-/- mice |
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| Rescue of progeria in trichothiodystrophy by homozygous lethal Xpd alleles |
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| Retinal degeneration and ionizing radiation hypersensitivity in a mouse model for Cockayne syndrome |
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| The rhp6+ gene of Schizosaccharomyces pombe: a structural and functional homolog of the RAD6 gene from the distantly related yeast Saccharomyces cerevisiae |
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| RNA from the insect trypanosome Crithidia luciliae contains transcripts of the maxi-circle and not of the mini-circle component of kinetoplast DNA. |
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| Sequence conservation of the rad21 Schizosaccharomyces pombe DNA double-strand break repair gene in human and mouse |
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| Silencing of unpaired chromatin and histone H2A ubiquitination in mammalian meiosis |
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| Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome |
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| Structure of the nuclear pore complex in mammalian cells Two annular components |
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| The structure of the XPF-ssDNA complex underscores the distinct roles of the XPF and ERCC1 helix- hairpin-helix domains in ss/ds DNA recognition |
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| The structure-specific endonuclease Ercc1-Xpf is required to resolve DNA interstrand cross-link-induced double-strand breaks |
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| Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorder |
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| Targeted disruption of the cell-cycle checkpoint gene ATR leads to early embryonic lethality in mice |
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| TFIIH with inactive XPD helicase functions in transcription initiation but is defective in DNA repair. |
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| Transcription-coupled and global genome repair differentially influence UV-B-induced acute skin effects and systemic immunosuppression |
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| Transfection of the cloned human excision repair gene ERCC-1 to UV-sensitive CHO mutants only corrects the repair defect in complementation group-2 mutants |
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| Transient correction of excision repair defects in fibroblasts of 9 xeroderma pigmentosum complementation groups by microinjection of crude human cell extracts |
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| Trypanosomes : kinetoplast dna and antigenic variation |
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| The ubiquitin-conjugating DNA repair enzyme HR6A is a maternal factor essential for early embryonic development in mice |
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| Ubiquitin ligase Rad18Sc localizes to the XY body and to other chromosomal regions that are unpaired and transcriptionally silenced during male meiotic prophase |
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| UV-sensitive syndrome protein UVSSA recruits USP7 to regulate transcription-coupled repair |
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| A variant surface glycoprotein of Trypanosoma brucei synthesized with a C-terminal hydrophobic 'tail' absent from purified glycoprotein. |
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| Workshop on DNA repair |
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| XAB2, a novel tetratricopeptide repeat protein involved in transcription-coupled DNA repair and transcription |
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| Xeroderma pigmentosum group A correcting protein from calf thymus |
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| Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair |
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| Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease |
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| The XPB and XPD DNA helicases are components of the p53-mediated apoptosis pathway |
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| XPC and human homologs of RAD23: intracellular localization and relationship to other nucleotide excision repair complexes |
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