List of works by Hans Joenje

A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome ⬇️

scientific article published on May 1, 2003

A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M

scientific article

A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51

scientific journal article

A novel ubiquitin ligase is deficient in Fanconi anemia

scientific article (publication date: October 2003)

A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair network

scientific article

Analysis of baseline and cisplatin-inducible gene expression in Fanconi anemia cells using oligonucleotide-based microarrays

scientific article

Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2

scientific article published on 21 August 2006

Characterization, expression and complex formation of the murine Fanconi anaemia gene product Fancg

scientific article (publication date: March 2002)

Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis

scientific article (publication date: 2012)

FANCE: the link between Fanconi anaemia complex assembly and activity

scientific article

Impaired DNA damage-induced nuclear Rad51 foci formation uniquely characterizes Fanconi anemia group D1

scientific article (publication date: 25 July 2002)

Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M.

scientific article published on 07 May 2009

Inducibility of nuclear Rad51 foci after DNA damage distinguishes all Fanconi anemia complementation groups from D1/BRCA2.

scientific article published on 8 September 2005

Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice

scientific article (publication date: February 2002)

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

article

The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2

scientific article

Update of the human and mouse Fanconi anemia genes

scientific article

Warsaw breakage syndrome, a cohesinopathy associated with mutations in the XPD helicase family member DDX11/ChlR1

scientific article

Yeast two-hybrid screens imply involvement of Fanconi anemia proteins in transcription regulation, cell signaling, oxidative metabolism, and cellular transport

scientific article (publication date: October 2003)

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