Hans Joenje

PROF.DR.

1984 …2018

Research output per year

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Research Output

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Meeting Abstract
2010

Ectopic ESCO2 Expression in Roberts Syndrome Fibroblasts Corrects Cohesion Defects and Sensitivity to DNA Damaging Agents

van der Lelij, P., van Gosliga, D., Oostra, A. B., Steltenpool, J., de Groot, J., Waisfisz, Q., Scheper, R. J., Darroudi, F., Godthelp, B. C., Joenje, H. & de Winter, J. P., Jul 2010, In : American Journal of Medical Genetics Part A. 152A, 7, p. 1635-1636

Research output: Contribution to journalMeeting AbstractAcademic

Ectopic ESCO2 Expression in Roberts Syndrome Fibroblasts Corrects Cohesion Defects and Sensitivity to DNA Damaging Agents

van der Lelij, P., van Gosliga, D., Oostra, A. B., Steltenpool, J., de Groot, J., Waisfisz, Q., Scheper, R. J., Darroudi, F., Godthelp, B. C., Joenje, H. & de Winter, J. P., 2010, In : American Journal of Medical Genetics Part A. 152A, 7, p. 1635-1636

Research output: Contribution to journalMeeting AbstractOther research output

2009

Fanconi Anemia: Recent Advances and Perspectives

Joenje, H., Dorsman, J. C., Waisfisz, Q., de Winter, J. P. & Bierings, M., 2009, In : Haematologica. 94, p. S7-S7

Research output: Contribution to journalMeeting AbstractOther research output

2007

Roberts syndrome-SC phocomeliia: Clinical and molecular findings

Vega, H., Jabs, E. W., Gordillo, M., Trainer, A., Luque, R., Kayserili, H., Skovby, F., Hennekam, R., Uzielli, M., Schnur, R., Manouvrier, S., Paznekas, W. A., Chang, S., Waisfisz, Q., Joenje, H., Hou, F. & Zou, H., 15 Jun 2007, In : American Journal of Medical Genetics Part A. 143A, 12, p. 1298-1299

Research output: Contribution to journalMeeting AbstractAcademic

2006

Hypermethylation of FANCC and FANCL resulting in a mitomycine-C (MMC) sensitive cellular phenotype in sporadic acute leukemia.

Hess, C. J., Ameziane, N., Schuurhuis, G. J., Errami, A., Denkers, F., Hubeeck, I., Kaspers, G. J. L., Joenje, H., Reinhardt, D., Ossenkoppele, G. J., Zwaan, C. M. & Waisfisz, Q., 16 Nov 2006, In : Blood. 108, 11, p. 630A-630A

Research output: Contribution to journalMeeting AbstractAcademic

2005

Persistent chromosomal instability and cross-linker sensitivity in Fanconi anaemia derived leukaemia cell lines with bi-allelic FANCD1/BRCA2 mutations

Meyer, S., Tonnies, H., Fergusson, WF., Oostra, AB., Medhurst, AL., Waisfisz, Q., De Winter, JP., Chen, F., Carr, TF., Green, M., Barber, L., Eden, OB., Will, AM., Joenje, H. & Taylor, GM., Apr 2005, In : British Journal of Haematology. 129, p. 81-81

Research output: Contribution to journalMeeting AbstractAcademic

2004

A Fanconi anemia core complex contains a ubiquitin ligase and is required for monoubiquitination of FANCD2

Meetei, A. R., de Winter, J., Medhurst, A., Wallisch, M., Waisfisz, Q., van de Vrugt, H., Oostra, A., Yan, Z., Ling, C., Bishop, C., Hoatlin, M., Joenje, H. & Wang, OW., May 2004, In : CELL STRUCTURE AND FUNCTION. 29, p. 11-11

Research output: Contribution to journalMeeting AbstractAcademic