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Experimental Cell Research|January 1, 1995
Maintenance of vascular endothelial cell-specific properties after immortalization with an amphotrophic replication-deficient retrovirus containing human papilloma virus 16 E6/E7 DNAR Fontijn, C Hop, H J Brinkman, et al.
Journal of Rehabilitation Medicine|April 18, 2015
Arm cranking versus wheelchair propulsion for testing aerobic fitness in children with spina bifida who are wheelchair dependentManon A T Bloemen, Janke F de Groot, Frank J G Backx, et al.
Oncogene|October 17, 1996
Lack of class I HLA expression in neuroblastoma is associated with high N-myc expression and hypomethylation due to loss of the MEMO-1 locusN C Cheng, M Beitsma, A Chan, et al.
British Journal of Cancer|October 1, 1994
Allele loss on chromosomes 10 and 17p and epidermal growth factor receptor gene amplification in human malignant astrocytoma related to prognosisS Leenstra, E K Bijlsma, D Troost, et al.
International Journal of Cancer|April 1, 1991
Differences in patterns of allelic loss between two common types of adult cancer, breast and colon carcinoma, and Wilms' tumor of childhoodP Devilee, M van den Broek, M Mannens, et al.
Human Molecular Genetics|February 22, 2001
Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWSJ Bliek, S M Maas, J M Ruijter, et al.
Experimental Cell Research|April 1, 1987
Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1W Keijzer, M Stefanini, D Bootsma, et al.
Human Genetics|November 16, 1978
A new immunochemical method for the quantitative measurement of specific gene products in man-rodent somatic cell hybridsP G de Groot, M N Hamers, A Westerveld, et al.
Genes, Chromosomes & Cancer|April 1, 1997
Malignant astrocytoma-derived region of common amplification in chromosomal band 17p12 is frequently amplified in high-grade osteosarcomasT J Hulsebos, E H Bijleveld, N T Oskam, et al.
Cancer Research|June 1, 1990
Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11M Mannens, P Devilee, J Bliek, et al.
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