Výsledky vyhledávání - Neitzel, Heidemarie

Chromosomal Aberrations Associated with Clonal Evolution and Leukemic Transformation in Fanconi Anemia: Clinical and Biological Implications Autor Meyer, Stefan, Neitzel, Heidemarie, Tönnies, Holger

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

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Holoprosencephaly–polydactyly/pseudotrisomy 13: a presentation of two new cases and a review of the literature Autor Bous, Sophia M., Solomon, Benjamin D., Graul-Neumann, Luitgard, Neitzel, Heidemarie, Hardisty, Emily E., Muenke, Maximilian

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

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Creation of monosomic derivatives of human cultured cell lines Autor Clarke, Duncan J., Giménez-Abián, Juan F., Tönnies, Holger, Neitzel, Heidemarie, Sperling, Karl, Downes, C. Stephen, Johnson, Robert T.

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MCPH1 patient cells exhibit delayed release from DNA damage-induced G(2)/M checkpoint arrest Autor Gavvovidis, Ioannis, Pöhlmann, Charlotte, Marchal, Juan Alberto, Stumm, Markus, Yamashita, Daisuke, Hirano, Tatsuya, Schindler, Detlev, Neitzel, Heidemarie, Trimborn, Marc

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A Novel MCPH1 Isoform Complements the Defective Chromosome Condensation of Human MCPH1-Deficient Cells Autor Gavvovidis, Ioannis, Rost, Isabell, Trimborn, Marc, Kaiser, Frank J., Purps, Josephine, Wiek, Constanze, Hanenberg, Helmut, Neitzel, Heidemarie, Schindler, Detlev

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

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Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder deli... Autor Polityko, Anna, Khurs, Olga, Rumyantseva, Natalia, Naumchik, Irina, Kosyakova, Nadezda, Tönnies, Holger, Sperling, Karl, Neitzel, Heidemarie, Weise, Anja, Liehr, Thomas

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Evidence for a pre-malignant cell line in a skin biopsy from a patient with Nijmegen breakage syndrome Autor Habib, Raneem, Neitzel, Heidemarie, Ernst, Aurelie, Wong, John K. L., Goryluk-Kozakiewicz, Bozenna, Gerlach, Antje, Demuth, Ilja, Sperling, Karl, Chrzanowska, Krystyna

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

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Telomere attrition and dysfunction: a potential trigger of the progeroid phenotype in nijmegen breakage syndrome Autor Habib, Raneem, Kim, Ryong, Neitzel, Heidemarie, Demuth, Ilja, Chrzanowska, Krystyna, Seemanova, Eva, Faber, Renaldo, Digweed, Martin, Voss, Reinhard, Jäger, Kathrin, Sperling, Karl, Walter, Michael

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PUL21a-Cyclin A2 Interaction is Required to Protect Human Cytomegalovirus-Infected Cells from the Deleterious Consequences of Mitotic Entry Autor Eifler, Martin, Uecker, Ralf, Weisbach, Henry, Bogdanow, Boris, Richter, Ellen, König, Lydia, Vetter, Barbara, Lenac-Rovis, Tihana, Jonjic, Stipan, Neitzel, Heidemarie, Hagemeier, Christian, Wiebusch, Lüder

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

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Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11 Autor Tzschach, Andreas, Bisgaard, Anne-Marie, Kirchhoff, Maria, Graul-Neumann, Luitgard M, Neitzel, Heidemarie, Page, Stephanie, Ahmed, Alischo, Müller, Ines, Erdogan, Fikret, Ropers, Hans-Hilger, Kalscheuer, Vera M, Ullmann, Reinhard

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Dosage effect of zero to three functional LBR-genes in vivo and in vitro Autor Gravemann, Sophia, Schnipper, Nele, Meyer, Hannes, Vaya, Amparo, Nowaczyk, Malgorzata JM, Rajab, Anna, Hofmann, Wolf-Karsten, Salewsky, Bastian, Tönnies, Holger, Neitzel, Heidemarie, Stassen, Hans H, Sperling, Karl, Hoffmann, Katrin

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High-throughput sequencing of microdissected chromosomal regions Autor Weise, Anja, Timmermann, Bernd, Grabherr, Manfred, Werber, Martin, Heyn, Patricia, Kosyakova, Nadezda, Liehr, Thomas, Neitzel, Heidemarie, Konrat, Kateryna, Bommer, Christiane, Dietrich, Carola, Rajab, Anna, Reinhardt, Richard, Mundlos, Stefan, Lindner, Tom H, Hoffmann, Katrin

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

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Establishment of a Mouse Model with Misregulated Chromosome Condensation due to Defective Mcph1 Function Autor Trimborn, Marc, Ghani, Mahdi, Walther, Diego J., Dopatka, Monika, Dutrannoy, Véronique, Busche, Andreas, Meyer, Franziska, Nowak, Stefanie, Nowak, Jean, Zabel, Claus, Klose, Joachim, Esquitino, Veronica, Garshasbi, Masoud, Kuss, Andreas W., Ropers, Hans-Hilger, Mueller, Susanne, Poehlmann, Charlotte, Gavvovidis, Ioannis, Schindler, Detlev, Sperling, Karl, Neitzel, Heidemarie

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