A. Oostra

发表

Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis

H. Joenje, J. D. de Winter, A. Nieuwint, 2012, Anemia.

SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype

D. Schindler, J. Rouse, Y. Hilhorst‐Hofstee, 2011, Nature Genetics.

Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype.

M. Buchwald, R. Wegner, H. Joenje, 1995, Blood.

Evidence for at least eight Fanconi anemia genes.

M. Buchwald, F. D. di Summa, H. Joenje, 1997, American journal of human genetics.

Mice with a targeted disruption of the Fanconi anemia homolog Fanca.

A. Berns, A. Berns, H. Joenje, 2000, Human molecular genetics.

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

H. Joenje, F. Arwert, N. C. Cheng, 2002, Human molecular genetics.

HSF2BP negatively regulates homologous recombination in DNA interstrand crosslink repair

R. Kanaar, Koichi Sato, J. Dorsman, 2020, Nucleic acids research.

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

G. M. Taylor, J. Clayton-Smith, Q. Waisfisz, 2005, Genes, chromosomes & cancer.

Evidence for complete epistasis of null mutations in murine Fanconi anemia genes Fanca and Fancg.

H. Joenje, F. Arwert, N. C. Cheng, 2011, DNA repair.

Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia

H. Joenje, F. Arwert, A. Eriksson, 1981, Nature.

Cytogenetic toxicity of D2O in human lymphocyte cultures. Increased sensitivity in Fanconil's anemia

H. Joenje, A. H. Wanamarta, A. Oostra, 1983, Experientia.

Somatic Mosaicism in Fanconi Anemia: Molecular Basis and Clinical Significance

C. Mathew, A. Veerman, R. Gibson, 1997, European journal of human genetics : EJHG.

Some characteristics of hyperoxia-adapted HeLa cells. A tissue culture model for cellular oxygen tolerance.

H. Joenje, P. Van Der Valk, J. Gille, 1985, Laboratory investigation; a journal of technical methods and pathology.

Apparent absence of BRCA2 protein in a proportion of acute myeloid leukemia cell lines

G. Pals, Q. Waisfisz, A. Medhurst, 2004, Leukemia.

Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M.

H. Joenje, J. D. de Winter, M. A. van der Valk, 2009, Human molecular genetics.

HSF2BP Negatively Regulates Homologous Recombination in DNA Interstrand Crosslink Repair in Human Cells by Direct Interaction With BRCA2

J. Lebbink, R. Kanaar, Koichi Sato, 2018, bioRxiv.

WAPL-Dependent Repair of Damaged DNA Replication Forks Underlies Oncogene-Induced Loss of Sister Chromatid Cohesion.

R. Wolthuis, H. Riele, A. Oostra, 2020, Developmental cell.

A novel ubiquitin ligase is deficient in Fanconi anemia

C. Bishop, Q. Waisfisz, Weidong Wang, 2003, Nature Genetics.

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

R. Wolthuis, R. King, J. D. de Winter, 2015, Nature Communications.

Defects in the Fanconi Anemia Pathway and Chromatid Cohesion in Head and Neck Cancer.

S. Feller, B. Ylstra, N. Ameziane, 2015, Cancer research.

Non-redundant roles in sister chromatid cohesion of the DNA helicase DDX11 and the SMC3 acetyl transferases ESCO1 and ESCO2

R. Wolthuis, M. Rooimans, A. Oostra, 2020, PloS one.

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

Hans Joenje, K. Chrzanowska, H. Joenje, 2010, American journal of human genetics.

CHAPTER Chromatid cohesion defects in human cancer cell lines 6

B. Ylstra, N. Ameziane, H. Joenje, 2010 .

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

L. Hood, J. Roach, P. May, 2015, Nature Communications.

Fanconi anemia: adult head and neck cancer and hematopoietic mosaicism.

G. Pals, B. Alter, H. Joenje, 2005, Archives of otolaryngology--head & neck surgery.

Fancf‐deficient mice are prone to develop ovarian tumours

J. Visser, M. van de Ven, P. Kramer, 2012, The Journal of pathology.

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

Q. Waisfisz, A. D’Andrea, M. Sasaki, 2003, Cancer research.

Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion

R. Wolthuis, G. Stewart, N. Ameziane, 2020, Nature Communications.

Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes.

C. Mathew, Q. Waisfisz, H. Joenje, 2004, Blood.

2 Loss of Rb Proteins Causes Genomic Instabilty in the Abence of Mitogenic Signaling

R. Banerjee, M. V. Vugt, F. Foijer, 2013 .

Loss of Rb proteins causes genomic instability in the absence of mitogenic signaling.

R. Banerjee, M. V. van Vugt, F. Foijer, 2010, Genes & development.

mitogenic signaling Loss of Rb proteins causes genomic instability in the absence of Material

R. Banerjee, M. V. Vugt, F. Foijer, 2010 .

Identification of the Fanconi Anemia Complementation Group I Gene, FANCI

C. Mathew, G. Pals, Q. Waisfisz, 2007, Cellular oncology : the official journal of the International Society for Cellular Oncology.

The Cellular Phenotype of Roberts Syndrome Fibroblasts as Revealed by Ectopic Expression of ESCO2

R. Wolthuis, Wouter van Zon, Q. Waisfisz, 2009, PloS one.

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

Weidong Wang, D. Schindler, A. Medhurst, 2007, The EMBO journal.

Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage Syndrome

H. Joenje, J. D. de Winter, M. Rooimans, 2010, Anemia.

Biallelic BUB1 mutations cause microcephaly, developmental delay, and variable effects on cohesion and chromosome segregation

R. Wolthuis, M. Speicher, Q. Waisfisz, 2022, Science advances.

CHAPTER 6 Deficiency of the centrosomal protein CEP 170 is associated with microcephaly

E. Bakker, J. Dorsman, S. Piersma, 2015 .

University of Birmingham Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion

R. Wolthuis, G. Stewart, N. Ameziane, 2020 .

Characterization of an oxygen-tolerant cell line derived from Chinese hamster ovary

E. Roubos, H. Joenje, J. Gille, 2004, Cell and Tissue Research.

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

Weidong Wang, Ting-Yi Lin, A. Stasiak, 2010, Molecular cell.

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

Weidong Wang, D. Schindler, H. Joenje, 2012, Molecular cell.

Cytogenetic toxicity of paraquat and streptonigrin in Fanconi's anemia.

H. D. de Koning, H. Joenje, F. Arwert, 1987, Cancer genetics and cytogenetics.

Clastogenicity of cyclophosphamide in Fanconi's anemia lymphocytes without exogenous metabolic activation.

H. Joenje, A. Oostra, 1986, Cancer genetics and cytogenetics.

Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes.

C. Mathew, Q. Waisfisz, H. Joenje, 2004, Blood.

Non-Redundant Roles in Sister Chromatid Cohesion of the DNA Helicase DDX11 and the SMC3 Acetyl Transferases ESCO1/2

R. Wolthuis, J. D. Lange, M. Rooimans, 2019, bioRxiv.

Chapter 5 A metabolic basis for hyperoxia tolerance in HeLa cells

J. Dorsman, W. Schoonen, A. Oostra, 2017 .

Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes.

C. Mathew, Q. Waisfisz, H. Joenje, 2004, Blood.