Výsledky vyhledávání - Geert Weeda

  • Zobrazuji výsledky 1 - 18 z 18
Upřesnit hledání
  1. 1
    A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome

    A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome Autor Geert Weeda, Reinier C.A. van Ham, Wim Vermeulen, D. Bootsma, Alex J. van der Eb, Jan H.J. Hoeijmakers

    Vydáno 1990
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  2. 2
    RAD25 (SSL2), the yeast homolog of the human xeroderma pigmentosum group B DNA repair gene, is essential for viability.

    RAD25 (SSL2), the yeast homolog of the human xeroderma pigmentosum group B DNA repair gene, is essential for viability. Autor Eun‐Ah Park, Sami N. Guzder, Marcel Koken, Iris Jaspers-Dekker, Geert Weeda, Jan H.J. Hoeijmakers, Satya Prakash, Louise Prakash

    Vydáno 1992
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  3. 3
    The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor.

    The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor. Autor Laurent Schaeffer, Vincent Moncollin, Richard Roy, Adrien Staub, M. Mezzina, Alain Sarasin, Geert Weeda, Jan H.J. Hoeijmakers, Jean‐Marc Egly

    Vydáno 1994
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  4. 4
    The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells

    The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells Autor Laura J. Niedernhofer, Jeroen Essers, Geert Weeda, Berna Beverloo, Jan de Wit, Manja Muijtjens, Hanny Odijk, Jan H.J. Hoeijmakers, Roland Kanaar

    Vydáno 2001
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  5. 5
    The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I

    The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I Autor Marcel van Duin, G. Vredeveldt, Lynne V. Mayne, Hanny Odijk, Wim Vermeulen, Binie Klein, Geert Weeda, Jan H.J. Hoeijmakers, D. Bootsma, A. Westerveld

    Vydáno 1989
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  6. 6
    The role of nucleotide excision repair in protecting embryonic stem cells from genotoxic effects of UV-induced DNA damage

    The role of nucleotide excision repair in protecting embryonic stem cells from genotoxic effects of UV-induced DNA damage Autor Petra P. H. Van Sloun, Jacob G. Jansen, Geert Weeda, Leon H.F. Mullenders, A.A. van Zeeland, P.H.M. Lohman, Harry Vrieling

    Vydáno 1999
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  7. 7
    Molecular cloning and biological characterization of the human excision repair gene ERCC-3.

    Molecular cloning and biological characterization of the human excision repair gene ERCC-3. Autor Geert Weeda, R C van Ham, Remco Masurel, A. Westerveld, Hanny Odijk, Jan de Wit, D. Bootsma, A.J. van der Eb, J H Hoeijmakers

    Vydáno 1990
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  8. 8
    The XPB subunit of repair/transcription factor TFIIH directly interacts with SUG1, a subunit of the 26S proteasome and putative transcription factor

    The XPB subunit of repair/transcription factor TFIIH directly interacts with SUG1, a subunit of the 26S proteasome and putative transcription factor Autor Geert Weeda, Mireille Rossignol, R. A. Fräser, G. Sebastiaan Winkler, Wim Vermeulen, Laura J. vanʼt Veer, Lanping Ma, Jan H.J. Hoeijmakers, J.M. Egly

    Vydáno 1997
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  9. 9
    Adenosine deaminase: characterization and expression of a gene with a remarkable promoter.

    Adenosine deaminase: characterization and expression of a gene with a remarkable promoter. Autor D. Valerio, M. G. C. Duyvesteyn, B.M.M. Dekker, Geert Weeda, Th.M. Berkvens, L. van der Voorn, H. van Ormondt, A.J. van der Eb

    Vydáno 1985
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  10. 10
    Base excision repair deficient mice lacking the Aag alkyladenine DNA glycosylase

    Base excision repair deficient mice lacking the Aag alkyladenine DNA glycosylase Autor Bevin P. Engelward, Geert Weeda, Michael D. Wyatt, J. Broekhof, Jan de Wit, I. Donker, James M. Allan, Barry Gold, Jan H.J. Hoeijmakers, Leona D. Samson

    Vydáno 1997
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  11. 11
    Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence

    Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence Autor Geert Weeda, I. Donker, Jan de Wit, Hans Morreau, Roel C. Janssens, C. J. Vissers, Alex L. Nigg, Harry van Steeg, D. Bootsma, Jan H.J. Hoeijmakers

    Vydáno 1997
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  12. 12
    TFIIH with Inactive XPD Helicase Functions in Transcription Initiation but Is Defective in DNA Repair

    TFIIH with Inactive XPD Helicase Functions in Transcription Initiation but Is Defective in DNA Repair Autor G. Sebastiaan Winkler, Sofia J. Araújo, Ulrike Fiedler, Wim Vermeulen, Frédéric Coin, Jean‐Marc Egly, Jan H.J. Hoeijmakers, Richard D. Wood, H. T. Marc Timmers, Geert Weeda

    Vydáno 2000
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  13. 13
    A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy

    A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy Autor Jan de Boer, Jan de Wit, Harry van Steeg, Rob J. W. Berg, Hans Morreau, Pim Visser, Alan R. Lehmann, Marinus Durán, Jane H.J. Hoeijmakers, Geert Weeda

    Vydáno 1998
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  14. 14
    Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH).

    Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH). Autor Anneke J. van Vuuren, Wim Vermeulen, Lanping Ma, Geert Weeda, Esther Appeldoorn, N.G.J. Jaspers, A.J. van der Eb, D. Bootsma, Jan H.J. Hoeijmakers, Sandrine Humbert

    Vydáno 1994
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  15. 15
    Hypermutation of Immunoglobulin Genes in Memory B Cells of DNA Repair–deficient Mice

    Hypermutation of Immunoglobulin Genes in Memory B Cells of DNA Repair–deficient Mice Autor Heinz Jacobs, Yosho Fukita, Gijsbertus T. J. van der Horst, Jan de Boer, Geert Weeda, Jeroen Essers, Niels de Wind, Bevin P. Engelward, L Samson, Sjef Verbeek, Josiane Ménissier de Murcia, Gilbert de Murcia, Hein te Riele, Klaus Rajewsky

    Vydáno 1998
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  16. 16
    p53 modulation of TFIIH–associated nucleotide excision repair activity

    p53 modulation of TFIIH–associated nucleotide excision repair activity Autor Xin Wei Wang, Heidi Yeh, Laurent Schaeffer, Richard Roy, Vincent Moncollin, Jean‐Marc Egly, Z. Wang, E C Friedberg, Michele K. Evans, Bonita G. Taffe, Vilhelm A. Bohr, Geert Weeda, Jan H.J. Hoeijmakers, Kathleen Forrester, Curtis C. Harris

    Vydáno 1995
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  17. 17
    Premature Aging in Mice Deficient in DNA Repair and Transcription

    Premature Aging in Mice Deficient in DNA Repair and Transcription Autor Jan de Boer, Jaan‐Olle Andressoo, Jan de Wit, J. G. M. Huijmans, Rudolph B. Beems, Harry van Steeg, Geert Weeda, Gijsbertus T. J. van der Horst, Wibeke van Leeuwen, Axel P. N. Themmen, M. Meradji, Jan H.J. Hoeijmakers

    Vydáno 2002
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  18. 18
    Defective Transcription-Coupled Repair in Cockayne Syndrome B Mice Is Associated with Skin Cancer Predisposition

    Defective Transcription-Coupled Repair in Cockayne Syndrome B Mice Is Associated with Skin Cancer Predisposition Autor Gijsbertus T. J. van der Horst, Harry van Steeg, Rob J. W. Berg, Alain J. van Gool, Jan de Wit, Geert Weeda, Hans Morreau, Rudolf B. Beems, Coen F. van Kreijl, Frank R. de Gruijl, D. Bootsma, Jan H.J. Hoeijmakers

    Vydáno 1997
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:

Vyhledávací nástroje: