XRCC2 (X-ray repair cross complementing 2)

por Andreassen, Paul R, Hanenberg, Helmut
Publicado no Atlas Genet Cytogenet Oncol Haematol (2019)

PALB2 (partner and localizer of BRCA2)

por Hanenberg, Helmut, Andreassen, Paul R.
Publicado no Atlas Genet Cytogenet Oncol Haematol (2018)

FANCJ is essential to maintain microsatellite structure genome-wide during replication stress

por Barthelemy, Joanna, Hanenberg, Helmut, Leffak, Michael
Publicado no Nucleic Acids Res (2016)

FANCJ is essential to maintain microsatellite structure genome-wide during replication stress

por Barthelemy, Joanna, Hanenberg, Helmut, Leffak, Michael
Publicado no Nucleic Acids Res (2017)

Understanding BRCA2 Function as a Tumor Suppressor Based on Domain-Specific Activities in DNA Damage Responses

por Andreassen, Paul R., Seo, Joonbae, Wiek, Constanze, Hanenberg, Helmut
Publicado no Genes (Basel) (2021)

FANCD2, FANCJ and BRCA2 cooperate to promote replication fork recovery independently of the Fanconi Anemia core complex

por Raghunandan, Maya, Chaudhury, Indrajit, Kelich, Stephanie L., Hanenberg, Helmut, Sobeck, Alexandra
Publicado no Cell Cycle (2015)

Pregenomic RNA Is Required for Efficient Incorporation of Pol Polyprotein into Foamy Virus Capsids

por Heinkelein, Martin, Leurs, Cordula, Rammling, Matthias, Peters, Katrin, Hanenberg, Helmut, Rethwilm, Axel
Publicado em 2002

CYP4V2 in Bietti's Crystalline Dystrophy: Ocular Localization, Metabolism of ω-3-Polyunsaturated Fatty Acids, and Functional Deficit of the p.H331P Variant

por Nakano, Mariko, Kelly, Edward J., Wiek, Constanze, Hanenberg, Helmut, Rettie, Allan E.
Publicado em 2012

HLA Class I Knockout Converts Allogeneic Primary NK Cells Into Suitable Effectors for “Off-the-Shelf” Immunotherapy

por Hoerster, Keven, Uhrberg, Markus, Wiek, Constanze, Horn, Peter A., Hanenberg, Helmut, Heinrichs, Stefan
Publicado no Front Immunol (2021)

Mutations of the SLX4 gene in Fanconi anemia

por Kim, Yonghwan, Lach, Francis P., Desetty, Rohini, Hanenberg, Helmut, Auerbach, Arleen D., Smogorzewska, Agata
Publicado em 2011

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

Specifically differentiated T cell subset promotes tumor immunity over fatal immunity

por Ramadan, Abdulraouf, Griesenauer, Brad, Adom, Djamilatou, Kapur, Reuben, Hanenberg, Helmut, Liu, Chen, Kaplan, Mark H., Paczesny, Sophie
Publicado no J Exp Med (2017)

High-Efficiency Gene Transfer into Normal and Adenosine Deaminase-Deficient T Lymphocytes Is Mediated by Transduction on Recombinant Fibronectin Fragments

por Pollok, Karen E., Hanenberg, Helmut, Noblitt, Timothy W., Schroeder, Wendy L., Kato, Ikunoshin, Emanuel, David, Williams, David A.
Publicado em 1998

Restriction of Foamy Viruses by Primate Trim5α

por Yap, Melvyn W., Lindemann, Dirk, Stanke, Nicole, Reh, Juliane, Westphal, Dana, Hanenberg, Helmut, Ohkura, Sadayuki, Stoye, Jonathan P.
Publicado em 2008

Multipotent Hematopoietic Progenitors Divide Asymmetrically to Create Progenitors of the Lymphomyeloid and Erythromyeloid Lineages

por Görgens, André, Ludwig, Anna-Kristin, Möllmann, Michael, Krawczyk, Adalbert, Dürig, Jan, Hanenberg, Helmut, Horn, Peter A., Giebel, Bernd
Publicado no Stem Cell Reports (2014)

Multipotent Hematopoietic Progenitors Divide Asymmetrically to Create Progenitors of the Lymphomyeloid and Erythromyeloid Lineages

por Görgens, André, Ludwig, Anna-Kristin, Möllmann, Michael, Krawczyk, Adalbert, Dürig, Jan, Hanenberg, Helmut, Horn, Peter A., Giebel, Bernd
Publicado no Stem Cell Reports (2015)

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

BREAST CANCER-ASSOCIATED MISSENSE MUTANTS OF THE PALB2 WD40 DOMAIN, WHICH DIRECTLY BINDS RAD51C, RAD51 AND BRCA2, DISRUPT DNA REPAIR

por Park, Jung-Young, Singh, Thiyam R., Nassar, Nicolas, Zhang, Fan, Freund, Marcel, Hanenberg, Helmut, Meetei, Amom Ruhikanta, Andreassen, Paul R.
Publicado em 2013

Human Cytomegalovirus Disrupts the Major Histocompatibility Complex Class I Peptide-Loading Complex and Inhibits Tapasin Gene Transcription

por Halenius, Anne, Hauka, Sebastian, Dölken, Lars, Stindt, Jan, Reinhard, Henrike, Wiek, Constanze, Hanenberg, Helmut, Koszinowski, Ulrich H., Momburg, Frank, Hengel, Hartmut
Publicado em 2011

Fanconi anemia signaling network regulates the spindle assembly checkpoint

por Nalepa, Grzegorz, Enzor, Rikki, Sun, Zejin, Marchal, Christophe, Park, Su-Jung, Yang, Yanzhu, Tedeschi, Laura, Kelich, Stephanie, Hanenberg, Helmut, Clapp, D. Wade
Publicado em 2013