Search Results - Heidemarie Neitzel

  • Showing 1 - 13 results of 13
Refine Results
  1. 1
    Misregulated Chromosome Condensation in MCPH1 Primary Microcephaly is Mediated by Condensin II

    Misregulated Chromosome Condensation in MCPH1 Primary Microcephaly is Mediated by Condensin II by Marc Trimborn, Detlev Schindler, Heidemarie Neitzel, Tatsuya Hirano

    Published 2005
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  2. 2
    Establishment and Characterization of an Immortalized Human Sebaceous Gland Cell Line (SZ95)1

    Establishment and Characterization of an Immortalized Human Sebaceous Gland Cell Line (SZ95)1 by Christos C. Zouboulis, Holger Seltmann, Constantin E. Orfanos, Heidemarie Neitzel

    Published 1999
    Get full text
    Artigo
    Save to List
    Saved in:
  3. 3
    Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factor

    Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factor by Holger Tönnies, Stefanie Teresa Huber, Jörn‐Sven Kühl, Antje Gerlach, Wolfram Ebell, Heidemarie Neitzel

    Published 2003
    Get full text
    Artigo
    Save to List
    Saved in:
  4. 4
    MCPH1 regulates chromosome condensation and shaping as a composite modulator of condensin II

    MCPH1 regulates chromosome condensation and shaping as a composite modulator of condensin II by Daisuke Yamashita, Keishi Shintomi, Takao Ono, Ioannis Gavvovidis, Detlev Schindler, Heidemarie Neitzel, Marc Trimborn, Tatsuya Hirano

    Published 2011
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    Successful bone marrow transplantation in a patient with DNA ligase IV deficiency and bone marrow failure

    Successful bone marrow transplantation in a patient with DNA ligase IV deficiency and bone marrow failure by Bernd Gruhn, J. Seidel, F Zintl, Raymonda Varon, Holger Tönnies, Heidemarie Neitzel, Astrid Bechtold, Holger Hoehn, Detlev Schindler

    Published 2007
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  6. 6
    Premature Chromosome Condensation in Humans Associated with Microcephaly and Mental Retardation: A Novel Autosomal Recessive Condition

    Premature Chromosome Condensation in Humans Associated with Microcephaly and Mental Retardation: A Novel Autosomal Recessive Condition by Heidemarie Neitzel, Luitgard M. Neumann, Detlev Schindler, Andreas Wirges, Holger Tönnies, Marc Trimborn, Alice Krebsová, Reyk Richter, Karl Sperling

    Published 2002
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  7. 7
    Microcephalin and pericentrin regulate mitotic entry via centrosome-associated Chk1

    Microcephalin and pericentrin regulate mitotic entry via centrosome-associated Chk1 by Alexandra Tibelius, Joachim Marhold, Hanswalter Zentgraf, Christoph E. Heilig, Heidemarie Neitzel, Bernard Ducommun, Anita Rauch, Anthony D. Ho, Jiří Bártek, Alwin Krämer

    Published 2009
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  8. 8
    Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation

    Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation by Marc Trimborn, Sandra Bell, Clive Felix, Yasmin Abdul Rashid, Hussain Jafri, Paul Griffiths, Luitgard M. Neumann, Alice Krebs, André Reis, Karl Sperling, Heidemarie Neitzel, Andrew P. Jackson

    Published 2004
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  9. 9
    A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGT

    A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGT by Peter Krawitz, Britta Höchsmann, Yoshiko Murakami, Britta Teubner, Ulrike Krüger, Eva Klopocki, Heidemarie Neitzel, Alexander Hoellein, Christina Schneider, Dmitri Parkhomchuk, Jochen Hecht, Peter N. Robinson, Stefan Mundlos, Taroh Kinoshita, Hubert Schrezenmeier

    Published 2013
    Get full text
    Artigo
    Save to List
    Saved in:
  10. 10
    DNA Ligase IV Mutations Identified in Patients Exhibiting Developmental Delay and Immunodeficiency

    DNA Ligase IV Mutations Identified in Patients Exhibiting Developmental Delay and Immunodeficiency by Mark O’Driscoll, Karen Cerosaletti, Pierre-M Girard, Yan Dai, Markus Stümm, Boris Kysela, Betsy Hirsch, Andrew R. Gennery, S.E. Palmer, Jörg Seidel, Richard A. Gatti, Raymonda Varon, Marjorie A. Oettinger, Heidemarie Neitzel, Penny A. Jeggo, Patrick Concannon

    Published 2001
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  11. 11
    Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing

    Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing by Wei Chen, Reinhard Ullmann, Claudia Langnick, Corinna Menzel, Zofia Wotschofsky, Hao Hu, Andreas Gogol‐Döring, Yuhui Hu, Hui Kang, Andreas Tzschach, Maria Hoeltzenbein, Heidemarie Neitzel, Susanne Markus, Eberhard Wiedersberg, G Kistner, Conny M. A. van Ravenswaaij-Arts, Tjitske Kleefstra, Vera M. Kalscheuer, Hans‐Hilger Ropers

    Published 2009
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  12. 12
    Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1)

    Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1) by Katja Grohmann, Raymonda Varon, Piroschka Stolz, Markus Schuelke, Catrin Janetzki, Enrico Bertini, Kate Bushby, Francesco Muntoni, Robert Ouvrier, Lionel Van Maldergem, Nathalie Goemans, Hanns Lochmüller, S Eichholz, Coleen Adams, Friedrich Bosch, Padraic J. Grattan‐Smith, Carmen Navarro, Heidemarie Neitzel, Tilman Polster, Haluk Topaloğlu, Christina Steglich, Ulf P. Guenther, Klaus Zerres, Sabine Rudnik–Schöneborn, Christoph Hübner

    Published 2003
    Get full text
    Artigo
    Save to List
    Saved in:
  13. 13
    A clinical and molecular genetic study of 112 Iranian families with primary microcephaly

    A clinical and molecular genetic study of 112 Iranian families with primary microcephaly by Hossein Darvish, Sahar Esmaeeli-Nieh, Gholamreza Bahrami Monajemi, Marzieh Mohseni, Saghar Ghasemi-Firouzabadi, Seyedeh Sedigheh Abedini, Ideh Bahman, Payman Jamali, Sarah Azimi, Faezeh Mojahedi, A. Dehghan, Yousef Shafeghati, Aria Jankhah, Masoumeh Falah, Mohammad Javad Soltani Banavandi, Mahdi Ghani, Masoud Garshasbi, Fatemeh Rakhshani, Anoosh Naghavi, Andreas Tzschach, Heidemarie Neitzel, Hans‐Hilger Ropers, Andreas W. Kuß, Farkhondeh Behjati, Kimia Kahrizi, Hossein Najmabadi

    Published 2010
    Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: