Fanconi Anemia Core Complex Gene Promoters Harbor Conserved Transcription Regulatory Elements

por Meier, Daniel, Schindler, Detlev
Publicado 2011

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

por Hoehn, Holger, Neveling, Kornelia, Endt, Daniela, Melcher, Ralph, Schindler, Detlev
Publicado 2008

Elevated blood levels of Dickkopf‐1 are associated with acute infections

por Mazon, Melody, Larouche, Valérie, St‐Louis, Maryse, Schindler, Detlev, Carreau, Madeleine
Publicado 2018

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 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 2015

Analysis of global DNA methylation changes in primary human fibroblasts in the early phase following X-ray irradiation

por Maierhofer, Anna, Flunkert, Julia, Dittrich, Marcus, Müller, Tobias, Schindler, Detlev, Nanda, Indrajit, Haaf, Thomas
Publicado 2017

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 2012

Severe reaction to radiotherapy provoked by hypomorphic germline mutations in ATM (ataxia–telangiectasia mutated gene)

por Asadollahi, Reza, Britschgi, Christian, Joset, Pascal, Oneda, Beatrice, Schindler, Detlev, Meier, Urs R., Rauch, Anita
Publicado 2020

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 2011

RPA-Mediated Recruitment of the E3 Ligase RFWD3 Is Vital for Interstrand Crosslink Repair and Human Health

por Feeney, Laura, Muñoz, Ivan M., Lachaud, Christophe, Toth, Rachel, Appleton, Paul L., Schindler, Detlev, Rouse, John
Publicado 2017

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 2007

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 2014

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 2012

MRE11-dependent instability in mitochondrial DNA fork protection activates a cGAS immune signaling pathway

por Luzwick, Jessica W., Dombi, Eszter, Boisvert, Rebecca A., Roy, Sunetra, Park, Soyoung, Kunnimalaiyaan, Selvi, Goffart, Steffi, Schindler, Detlev, Schlacher, Katharina
Publicado 2021

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 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 2013

Cancer in Children With Fanconi Anemia and Ataxia-Telangiectasia—A Nationwide Register-Based Cohort Study in Germany

por Dutzmann, Christina M., Spix, Claudia, Popp, Isabell, Kaiser, Melanie, Erdmann, Friederike, Erlacher, Miriam, Dörk, Thilo, Schindler, Detlev, Kalb, Reinhard, Kratz, Christian P.
Publicado 2022

Infantile fibrosarcoma with TPM3-NTRK1 fusion in a boy with Bloom syndrome

por Huson, Sue M., Staab, Timo, Pereira, Marta, Ward, Heather, Paredes, Roberto, Evans, D. Gareth, Baumhoer, Daniel, O’Sullivan, James, Cheesman, Ed, Schindler, Detlev, Meyer, Stefan
Publicado 2020

Hypomorphic Brca2 and Rad51c double mutant mice display Fanconi anemia, cancer and polygenic replication stress

por Tomaszowski, Karl-Heinz, Roy, Sunetra, Guerrero, Carolina, Shukla, Poojan, Keshvani, Caezaan, Chen, Yue, Ott, Martina, Wu, Xiaogang, Zhang, Jianhua, DiNardo, Courtney D., Schindler, Detlev, Schlacher, Katharina
Publicado 2023

Mutation Analysis of the ERCC4/FANCQ Gene in Hereditary Breast Cancer

por Kohlhase, Sandra, Bogdanova, Natalia V., Schürmann, Peter, Bermisheva, Marina, Khusnutdinova, Elza, Antonenkova, Natalia, Park-Simon, Tjoung-Won, Hillemanns, Peter, Meyer, Andreas, Christiansen, Hans, Schindler, Detlev, Dörk, Thilo
Publicado 2014