Fanconi Anemia Core Complex Gene Promoters Harbor Conserved Transcription Regulatory Elements

Por Meier, Daniel, Schindler, Detlev
Publicado em 2011

Neoplasia, Ageing, and Genetic Instability due to Defective Caretaker Genes

Por Hoehn, Holger, Neveling, Kornelia, Endt, Daniela, Melcher, Ralph, Schindler, Detlev
Publicado no Cell Oncol (2008)

Inhibition of primordial germ cell proliferation by the medaka male determining gene Dmrt1bY

Por Herpin, Amaury, Schindler, Detlev, Kraiss, Anita, Hornung, Ute, Winkler, Christoph, Schartl, Manfred
Publicado em 2007

FANCJ suppresses microsatellite instability and lymphomagenesis independent of the Fanconi anemia pathway

Por Matsuzaki, Kenichiro, Borel, Valerie, Adelman, Carrie A., Schindler, Detlev, Boulton, Simon J.
Publicado no Genes Dev (2015)

Genotyping of Fanconi Anemia Patients by Whole Exome Sequencing: Advantages and Challenges

Por Knies, Kerstin, Schuster, Beatrice, Ameziane, Najim, Rooimans, Martin, Bettecken, Thomas, de Winter, Johan, Schindler, Detlev
Publicado em 2012

Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair

Por Colnaghi, Luca, Jones, Mathew J. K., Cotto-Rios, Xiomaris M., Schindler, Detlev, Hanenberg, Helmut, Huang, Tony T.
Publicado em 2011

MCPH1 regulates chromosome condensation and shaping as a composite modulator of condensin II

Por Yamashita, Daisuke, Shintomi, Keishi, Ono, Takao, Gavvovidis, Ioannis, Schindler, Detlev, Neitzel, Heidemarie, Trimborn, Marc, Hirano, Tatsuya
Publicado em 2011

Acute myeloid leukaemia after treatment for acute lymphoblastic leukaemia in girl with Bloom syndrome

Por Adams, Madeleine, Jenney, Meriel, Lazarou, Laz, White, Rhian, Birdsall, Sanda, Staab, Timo, Schindler, Detlev, Meyer, Stefan
Publicado em 2013

Successful bone marrow transplantation in a patient with DNA ligase IV deficiency and bone marrow failure

Por Gruhn, Bernd, Seidel, Joerg, Zintl, Felix, Varon, Raymonda, Tönnies, Holger, Neitzel, Heidemarie, Bechtold, Astrid, Hoehn, Holger, Schindler, Detlev
Publicado em 2007

Visualization of local DNA unwinding by Mre11/Rad50/Nbs1 using single-molecule FRET

Por Cannon, Brian, Kuhnlein, Jeffrey, Yang, Soo-Hyun, Cheng, Anita, Schindler, Detlev, Stark, Jeremy M., Russell, Rick, Paull, Tanya T.
Publicado em 2013

Distinct functional roles for the two SLX4 ubiquitin-binding UBZ domains mutated in Fanconi anemia

Por Lachaud, Christophe, Castor, Dennis, Hain, Karolina, Muñoz, Ivan, Wilson, Jamie, MacArtney, Thomas J., Schindler, Detlev, Rouse, John
Publicado em 2014

Premature Chromosome Condensation in Humans Associated with Microcephaly and Mental Retardation: A Novel Autosomal Recessive Condition

Por Neitzel, Heidemarie, Neumann, Luitgard M., Schindler, Detlev, Wirges, Andreas, Tönnies, Holger, Trimborn, Marc, Krebsova, Alice, Richter, Reyk, Sperling, Karl
Publicado em 2002

MCPH1 patient cells exhibit delayed release from DNA damage-induced G(2)/M checkpoint arrest

Por Gavvovidis, Ioannis, Pöhlmann, Charlotte, Marchal, Juan Alberto, Stumm, Markus, Yamashita, Daisuke, Hirano, Tatsuya, Schindler, Detlev, Neitzel, Heidemarie, Trimborn, Marc
Publicado em 2010

A Novel MCPH1 Isoform Complements the Defective Chromosome Condensation of Human MCPH1-Deficient Cells

Por Gavvovidis, Ioannis, Rost, Isabell, Trimborn, Marc, Kaiser, Frank J., Purps, Josephine, Wiek, Constanze, Hanenberg, Helmut, Neitzel, Heidemarie, Schindler, Detlev
Publicado em 2012

Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytes

Por Kraemer, Nadine, Ravindran, Ethiraj, Zaqout, Sami, Neubert, Gerda, Schindler, Detlev, Ninnemann, Olaf, Gräf, Ralph, Seiler, Andrea EM, Kaindl, Angela M
Publicado no Cell Cycle (2015)

Immune Thrombocytopenia in Two Unrelated Fanconi Anemia Patients – A Mere Coincidence?

Por Karastaneva, Anna, Lanz, Sofia, Wawer, Angela, Behrends, Uta, Schindler, Detlev, Dietrich, Ralf, Burdach, Stefan, Urban, Christian, Benesch, Martin, Seidel, Markus G.
Publicado no Front Pediatr (2015)

Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation

Por Farag, Heba Gamal, Froehler, Sebastian, Oexle, Konrad, Ravindran, Ethiraj, Schindler, Detlev, Staab, Timo, Huebner, Angela, Kraemer, Nadine, Chen, Wei, Kaindl, Angela M
Publicado no Orphanet J Rare Dis (2013)

Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability

Por Bogliolo, Massimo, Lyakhovich, Alex, Callén, Elsa, Castellà, Maria, Cappelli, Enrico, Ramírez, María J, Creus, Amadeu, Marcos, Ricard, Kalb, Reinhard, Neveling, Kornelia, Schindler, Detlev, Surrallés, Jordi
Publicado em 2007

A novel approach to describe a U1 snRNA binding site

Por Freund, Marcel, Asang, Corinna, Kammler, Susanne, Konermann, Carolin, Krummheuer, Jörg, Hipp, Marianne, Meyer, Imke, Gierling, Wolfram, Theiss, Stephan, Preuss, Thorsten, Schindler, Detlev, Kjems, Jørgen, Schaal, Heiner
Publicado em 2003

Human RAD50 Deficiency in a Nijmegen Breakage Syndrome-like Disorder

Por Waltes, Regina, Kalb, Reinhard, Gatei, Magtouf, Kijas, Amanda W., Stumm, Markus, Sobeck, Alexandra, Wieland, Britta, Varon, Raymonda, Lerenthal, Yaniv, Lavin, Martin F., Schindler, Detlev, Dörk, Thilo
Publicado em 2009