Lista de obras -

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

artículo científico publicado el 14 de junio de 2012

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

artículo científico publicado en 2005

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

artículo científico publicado en 2010

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

artículo científico publicado en 2005

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

artículo científico publicado en 2014

A novel ubiquitin ligase is deficient in Fanconi anemia

artículo científico publicado en 2003

A protein prioritization approach tailored for the FA/BRCA pathway

artículo científico publicado en 2013

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

artículo científico publicado en 2002

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

artículo científico publicado en 2003

Biochemical Characterization of Warsaw Breakage Syndrome Helicase ⬇️

artículo científico publicado el 18 de noviembre de 2011

Coregulation of FANCA and BRCA1 in human cells

artículo científico publicado en 2014

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

artículo científico publicado en 2015

Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis ⬇️

artículo científico publicado el 24 de mayo de 2012

Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways

artículo científico publicado en 2004

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

artículo científico publicado en 2007

Fancf‐deficient mice are prone to develop ovarian tumours ⬇️

artículo científico publicado el 14 de noviembre de 2011

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

artículo científico publicado en 2006

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

artículo científico publicado el 15 de mayo de 2003

Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes

artículo científico publicado en 2003

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

artículo científico publicado en 2007

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

artículo científico publicado en 1997

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

artículo científico publicado en 2007

Multiple TPR motifs characterize the Fanconi anemia FANCG protein

artículo científico publicado en 2004

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

artículo científico publicado en 2013

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

artículo científico publicado en 2009

The Fanconi anemia gene product FANCF is a flexible adaptor protein

artículo científico publicado en 2004

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

artículo científico publicado en 2009

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

artículo científico publicado en 2010

X-linked inheritance of Fanconi anemia complementation group B

artículo científico publicado en 2004

Lista de obras de

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