检索结果 - Neitzel, Heidemarie

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

获取全文 获取全文 获取全文

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

获取全文 获取全文 获取全文

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

获取全文 获取全文 获取全文

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

获取全文 获取全文 获取全文

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

获取全文 获取全文

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

获取全文 获取全文 获取全文

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

获取全文 获取全文 获取全文

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

获取全文 获取全文

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

获取全文 获取全文 获取全文

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

获取全文 获取全文 获取全文

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

获取全文 获取全文 获取全文

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

获取全文 获取全文 获取全文

PUL21a-Cyclin A2 Interaction is Required to Protect Human Cytomegalovirus-Infected Cells from the Deleterious Consequences of Mitotic Entry 由 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

获取全文 获取全文 获取全文

Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation 由 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.

获取全文 获取全文

Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11 由 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

获取全文 获取全文 获取全文

Dosage effect of zero to three functional LBR-genes in vivo and in vitro 由 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

获取全文 获取全文 获取全文

High-throughput sequencing of microdissected chromosomal regions 由 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

获取全文 获取全文 获取全文

Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing 由 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

获取全文 获取全文 获取全文

Establishment of a Mouse Model with Misregulated Chromosome Condensation due to Defective Mcph1 Function 由 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

获取全文 获取全文 获取全文