Search Results

There are 17873 results for: content related to: A new mutation in the CSB gene in a C hinese patient with mild C ockayne syndrome

  1. You have full text access to this Open Access content
    BRCA1 contributes to transcription-coupled repair of DNA damage through polyubiquitination and degradation of Cockayne syndrome B protein

    Cancer Science

    Volume 102, Issue 10, October 2011, Pages: 1840–1847, Leizhen Wei, Li Lan, Akira Yasui, Kiyoji Tanaka, Masafumi Saijo, Ayako Matsuzawa, Risa Kashiwagi, Emiko Maseki, Yiheng Hu, Jeffrey D. Parvin, Chikashi Ishioka and Natsuko Chiba

    Article first published online : 17 AUG 2011, DOI: 10.1111/j.1349-7006.2011.02037.x

  2. You have full text access to this Open Access content
    Downregulation of Cockayne syndrome B protein reduces human 8-oxoguanine DNA glycosylase-1 expression and repair of UV radiation-induced 8-oxo-7,8-dihydro-2′-deoxyguanine

    Cancer Science

    Volume 102, Issue 9, September 2011, Pages: 1651–1658, Arash Javeri, James Guy Lyons, Xiao X. Huang and Gary M. Halliday

    Article first published online : 18 JUL 2011, DOI: 10.1111/j.1349-7006.2011.02005.x

  3. Cockayne syndrome group B protein regulates DNA double-strand break repair and checkpoint activation

    The EMBO Journal

    Volume 34, Issue 10, 12 May 2015, Pages: 1399–1416, Nicole L Batenburg, Elizabeth L Thompson, Eric A Hendrickson and Xu-Dong Zhu

    Article first published online : 27 MAR 2015, DOI: 10.15252/embj.201490041

  4. You have free access to this content
    Mutant Cockayne syndrome group B protein inhibits repair of DNA topoisomerase I-DNA covalent complex

    Genes to Cells

    Volume 16, Issue 1, January 2011, Pages: 101–114, Katsuyoshi Horibata, Masafumi Saijo, Mui N. Bay, Li Lan, Isao Kuraoka, Philip J. Brooks, Masamitsu Honma, Takehiko Nohmi, Akira Yasui and Kiyoji Tanaka

    Article first published online : 9 DEC 2010, DOI: 10.1111/j.1365-2443.2010.01467.x

  5. You have free access to this content
    The Cockayne syndrome group B protein is a functional dimer

    The FEBS Journal

    Volume 272, Issue 17, September 2005, Pages: 4306–4314, Mette Christiansen, Tina Thorslund, Bjarne Jochimsen, Vilhelm A. Bohr and Tinna Stevnsner

    Article first published online : 10 AUG 2005, DOI: 10.1111/j.1742-4658.2005.04844.x

  6. You have free access to this content
    The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex

    The EMBO Journal

    Volume 16, Issue 19, October 1, 1997, Pages: 5955–5965, Alain J. van Gool, Elisabetta Citterio, Suzanne Rademakers, Roselinde van Os, Wim Vermeulen, Angelos Constantinou, Jean-Marc Egly, Dirk Bootsma and Jan H.J. Hoeijmakers

    Article first published online : 1 OCT 1997, DOI: 10.1093/emboj/16.19.5955

  7. You have free access to this content
    Defective resolution of pH2AX foci and enhanced DNA breakage in ionizing radiation-treated cockayne syndrome B cells

    IUBMB Life

    Volume 63, Issue 4, April 2011, Pages: 272–276, Monica Ropolo, Enrico Cappelli, Mara Foresta, Alessandro Poggi, Luca Proietti-De-Santis and Guido Frosina

    Article first published online : 24 MAR 2011, DOI: 10.1002/iub.445

  8. Novel missense mutations in a conserved loop between ERCC6 (CSB) helicase motifs V and VI: Insights into Cockayne syndrome

    American Journal of Medical Genetics Part A

    Volume 170, Issue 3, March 2016, Pages: 773–776, Brian T. Wilson, Anneline Lochan, Zornitza Stark and Ruth E. Sutton

    Article first published online : 8 JAN 2016, DOI: 10.1002/ajmg.a.37501

  9. Gender and Cell-Type-Specific Effects of the Transcription-Coupled Repair Protein, ERCC6/CSB, on Repeat Expansion in a Mouse Model of the Fragile X-Related Disorders

    Human Mutation

    Volume 35, Issue 3, March 2014, Pages: 341–349, Xiao-Nan Zhao and Karen Usdin

    Article first published online : 13 JAN 2014, DOI: 10.1002/humu.22495

  10. You have full text access to this Open Access content
    Congenital DNA repair deficiency results in protection against renal ischemia reperfusion injury in mice

    Aging Cell

    Volume 8, Issue 2, April 2009, Pages: 192–200, Denis Susa, James R. Mitchell, Marielle Verweij, Marieke Van De Ven, Henk Roest, Sandra Van Den Engel, Ingeborg Bajema, Kirsten Mangundap, Jan N. M. IJzermans, Jan H. J. Hoeijmakers and Ron W. F. De Bruin

    Article first published online : 10 MAR 2009, DOI: 10.1111/j.1474-9726.2009.00463.x

  11. You have free access to this content
    Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

    The EMBO Journal

    Volume 25, Issue 9, May 3, 2006, Pages: 1915–1923, Luca Proietti-De-Santis, Pascal Drané and Jean-Marc Egly

    Article first published online : 6 APR 2006, DOI: 10.1038/sj.emboj.7601071

  12. You have free access to this content
    The gene expression and deficiency phenotypes of Cockayne syndrome B protein in Caenorhabditis elegans

    FEBS Letters

    Volume 522, Issue 1-3, July 03, 2002, Pages: 47–51, Myon Hee Lee, Byungchan Ahn, In Soon Choi and Hyeon-Sook Koo

    Article first published online : 5 JUN 2002, DOI: 10.1016/S0014-5793(02)02880-6

  13. You have free access to this content
    Accumulation of mitochondrial DNA damage and bioenergetic dysfunction in CSB defective cells

    The FEBS Journal

    Volume 276, Issue 10, May 2009, Pages: 2811–2821, Pia Ø. Osenbroch, Pia Auk-Emblem, Ruth Halsne, Janne Strand, Rune J. Forstrøm, Ingrid van der Pluijm and Lars Eide

    Article first published online : 6 APR 2009, DOI: 10.1111/j.1742-4658.2009.07004.x

  14. Xeroderma Pigmentosum, Cockayne Syndrome and Trichothiodystrophy

    Harper's Textbook of Pediatric Dermatology, Volume 1, 2, Third Edition

    Alan D. Irvine, Peter H. Hoeger, Albert C. Yan, Pages: 135.1–135.24, 2011

    Published Online : 24 MAY 2011, DOI: 10.1002/9781444345384.ch135

  15. You have free access to this content
    CSB protein is (a direct target of HIF-1 and) a critical mediator of the hypoxic response

    The EMBO Journal

    Volume 27, Issue 19, October 8, 2008, Pages: 2545–2556, Silvia Filippi, Paolo Latini, Mattia Frontini, Fabrizio Palitti, Jean-Marc Egly and Luca Proietti-De-Santis

    Article first published online : 11 SEP 2008, DOI: 10.1038/emboj.2008.180

  16. You have free access to this content
    Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome

    Human Mutation

    Volume 31, Issue 2, February 2010, Pages: 113–126, V. Laugel, C. Dalloz, M. Durand, F. Sauvanaud, U. Kristensen, M.C. Vincent, L. Pasquier, S. Odent, V. Cormier-Daire, B. Gener, E.S. Tobias, J.L. Tolmie, D. Martin-Coignard, V. Drouin-Garraud, D. Heron, H. Journel, E. Raffo, J. Vigneron, S. Lyonnet, V. Murday, D. Gubser-Mercati, B. Funalot, L. Brueton, J. Sanchez del Pozo, E. Muñoz, A.R. Gennery, M. Salih, M. Noruzinia, K. Prescott, L. Ramos, Z. Stark, K. Fieggen, B. Chabrol, P. Sarda, P. Edery, A. Bloch-Zupan, H. Fawcett, D. Pham, J.M. Egly, A.R. Lehmann, A. Sarasin and H. Dollfus

    Article first published online : 5 NOV 2009, DOI: 10.1002/humu.21154

  17. Cockayne syndrome – a primary defect in DNA repair, transcription, both or neither?

    BioEssays

    Volume 18, Issue 9, September 1996, Pages: 731–738, Errol C. Friedberg

    Article first published online : 5 FEB 2005, DOI: 10.1002/bies.950180908

  18. Cockayne syndrome, between transcription and DNA repair defects

    Journal of the European Academy of Dermatology and Venereology

    Volume 16, Issue 3, May 2002, Pages: 220–226, S Dubaele and JM Egly

    Article first published online : 27 JUN 2002, DOI: 10.1046/j.1468-3083.2002.00453.x

  19. Cockayne syndrome type II in a Druze isolate in Northern Israel in association with an insertion mutation in ERCC6

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 11, 1 June 2008, Pages: 1423–1429, Tzipora C. Falik-Zaccai, Meital Laskar, Nechama Kfir, Wael Nasser, Hanoch Slor and Morad Khayat

    Article first published online : 29 APR 2008, DOI: 10.1002/ajmg.a.32309

  20. You have full text access to this OnlineOpen article
    Detecting UV-lesions in the genome: The modular CRL4 ubiquitin ligase does it best!

    FEBS Letters

    Volume 585, Issue 18, September 16, 2011, Pages: 2818–2825, Andrea Scrima, Eric S. Fischer, Gondichatnahalli M. Lingaraju, Kerstin Böhm, Simone Cavadini and Nicolas H. Thomä

    Article first published online : 6 MAY 2011, DOI: 10.1016/j.febslet.2011.04.064