List of works - Johan P. De Winter

A Ubiquitin-Binding Protein, FAAP20, Links RNF8-Mediated Ubiquitination to the Fanconi Anemia DNA Repair Network ⬇️

scientific article published on June 14, 2012

A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutations.

scientific article

A histone-fold complex and FANCM form a conserved DNA-remodeling complex to maintain genome stability

scientific article

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 splice site mutation in the noncoding region of BRCA2: implications for Fanconi anemia and familial breast cancer diagnostics

scientific article

A novel ubiquitin ligase is deficient in Fanconi anemia

scientific article (publication date: October 2003)

A protein prioritization approach tailored for the FA/BRCA pathway

scientific article

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

scientific article

Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia

scientific article published on November 2003

Biochemical Characterization of Warsaw Breakage Syndrome Helicase ⬇️

scientific article published on November 18, 2011

Coregulation of FANCA and BRCA1 in human cells

scientific article

Defective sister chromatid cohesion is synthetically lethal with impaired APC/C function.

scientific article

Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis ⬇️

scientific article (publication date: 2012)

Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways

scientific article

FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway

scientific article

Fancf‐deficient mice are prone to develop ovarian tumours ⬇️

scientific article published on November 14, 2011

Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.

scientific article

Genetic reversion in an acute myelogenous leukemia cell line from a Fanconi anemia patient with biallelic mutations in BRCA2 ⬇️

scientific article published on May 15, 2003

Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes

scientific article

Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype

scientific article published on 6 April 2007

Inhibin interferes with activin signaling at the level of the activin receptor complex in Chinese hamster ovary cells

scientific article (publication date: July 1997)

Loss of expression of FANCD2 protein in sporadic and hereditary breast cancer

scientific article

Multiple TPR motifs characterize the Fanconi anemia FANCG protein

scientific article (publication date: 5 January 2004)

Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia

scientific article

Recruitment of fanconi anemia and breast cancer proteins to DNA damage sites is differentially governed by replication

scientific article

The Fanconi anemia gene product FANCF is a flexible adaptor protein

scientific article

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

scientific article

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

scientific article

X-linked inheritance of Fanconi anemia complementation group B

scientific article

List of works by Johan P. De Winter

A Ubiquitin-Binding Protein, FAAP20, Links RNF8-Mediated Ubiquitination to the Fanconi Anemia DNA Repair Network ⬇️

A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutations.

A histone-fold complex and FANCM form a conserved DNA-remodeling complex to maintain genome stability

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

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

A novel splice site mutation in the noncoding region of BRCA2: implications for Fanconi anemia and familial breast cancer diagnostics

A novel ubiquitin ligase is deficient in Fanconi anemia

A protein prioritization approach tailored for the FA/BRCA pathway

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

Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia

Biochemical Characterization of Warsaw Breakage Syndrome Helicase ⬇️

Coregulation of FANCA and BRCA1 in human cells

Defective sister chromatid cohesion is synthetically lethal with impaired APC/C function.

Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis ⬇️

Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways

FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway

Fancf‐deficient mice are prone to develop ovarian tumours ⬇️

Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.

Genetic reversion in an acute myelogenous leukemia cell line from a Fanconi anemia patient with biallelic mutations in BRCA2 ⬇️

Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes

Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype

Inhibin interferes with activin signaling at the level of the activin receptor complex in Chinese hamster ovary cells

Loss of expression of FANCD2 protein in sporadic and hereditary breast cancer

Multiple TPR motifs characterize the Fanconi anemia FANCG protein

Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia

Recruitment of fanconi anemia and breast cancer proteins to DNA damage sites is differentially governed by replication

The Fanconi anemia gene product FANCF is a flexible adaptor protein

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

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

X-linked inheritance of Fanconi anemia complementation group B