I. Revet

发表

Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity

E. Lam, J. Cleaver, I. Revet, 2009, Nature Reviews Genetics.

ST7-mediated suppression of tumorigenicity of prostate cancer cells is characterized by remodeling of the extracellular matrix

I G Campbell, C. Blancher, I. Campbell, 2006, Oncogene.

Conceptual developments in the causes of Cockayne syndrome

E. Huang, V. Bezrookove, J. Cleaver, 2013, Mechanisms of Ageing and Development.

A minority of foci or pan-nuclear apoptotic staining of γH2AX in the S phase after UV damage contain DNA double-strand breaks

V. Bezrookove, J. Cleaver, I. Revet, 2010, Proceedings of the National Academy of Sciences.

Clinical implications of the basic defects in Cockayne syndrome and xeroderma pigmentosum and the DNA lesions responsible for cancer, neurodegeneration and aging

J. Cleaver, I. Revet, 2008, Mechanisms of Ageing and Development.

Dysmyelination not demyelination causes neurological symptoms in preweaned mice in a murine model of Cockayne syndrome

E. Huang, J. Cleaver, I. Revet, 2012, Proceedings of the National Academy of Sciences.

Homeobox genes in neuroblastoma

I. Revet, 2010 .

MSX1 induces the Wnt pathway antagonist genes DKK1, DKK2, DKK3, and SFRP1 in neuroblastoma cells, but does not block Wnt3 and Wnt5A signalling to DVL3.

D. Geerts, R. Versteeg, J. Koster, 2010, Cancer letters.

Misleading FT4 measurement: Assay-dependent antibody interference

I. Revet, Y. D. de Rijke, Lianne S. M. Boesten, 2016, Biochemia Medica.

UvA-DARE ( Digital Academic Repository ) Homeobox genes in neuroblastoma

Link, R. Versteeg, J. Koster, 2010 .

The MSX1 homeobox transcription factor is a downstream target of PHOX2B and activates the Delta-Notch pathway in neuroblastoma

D. Geerts, R. Versteeg, J. Koster, 2010 .

Characterization of Plasmid pRT1 from Pyrococcus sp. Strain JT1

J. H. Tuttle, J. DiRuggiero, W. D. de Vos, 2002, Journal of bacteriology.

5 MSX 1 is induced by NOTCH 3 and mediates a proliferation arrest module , but not a motility module activated by NOTCH 3 in neuroblastoma

D. Geerts, R. Versteeg, P. Sluis, 2010 .

The DNA damage-binding protein XPC is a frequent target for inactivation in squamous cell carcinomas.

P. Kwok, K. Ridd, J. Cleaver, 2010, The American journal of pathology.

Functional relevance of the histone γH2Ax in the response to DNA damaging agents

D. Dankort, J. Cleaver, I. Revet, 2011, Proceedings of the National Academy of Sciences.

MEIS homeobox genes in neuroblastoma.

D. Geerts, R. Versteeg, N. Schilderink, 2005, Cancer letters.

Phosphorylated H2Ax is not an unambiguous marker for DNA double-strand breaks

J. Cleaver, I. Revet, L. Feeney, 2011, Cell cycle.

Mitochondrial reactive oxygen species are scavenged by Cockayne syndrome B protein in human fibroblasts without nuclear DNA damage

Junjie Chen, R. Swanson, V. Bezrookove, 2014, Proceedings of the National Academy of Sciences.

Falsely decreased ferritin concentrations in two patients with haemophagocytic lymphohistiocytosis: A case report

R. Raymakers, I. Revet, H. Kemperman, 2018, Annals of clinical biochemistry.

The MSX1 homeobox transcription factor is a downstream target of PHOX2B and activates the Delta-Notch pathway in neuroblastoma.

R. Versteeg, I. Revet, R. Volckmann, 2008, Experimental cell research.

The DNA damage-binding protein XPC is a frequent target for inactivation in squamous cell carcinomas.

P. Kwok, K. Ridd, J. Cleaver, 2010, American Journal of Pathology.