Gillemans, Nynke

Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

Borg, J., Papadopoulos, P., Georgitsi, M., Gutiérrez, L., Grech, G., Fanis, P., Phylactides, M., Verkerk, A. J. M. H., van der Spek, P. J., Scerri, C. A., et al. (2010) · Nature Genetics

Hemoglobinopathies and Related DisordersKruppel-like factors research

Cited by 371

The active spatial organization of the β-globin locus requires the transcription factor EKLF

Drissen, R., Palstra, R.-J., Gillemans, N., Splinter, E., Grosveld, F., Philipsen, S., & de Laat, W. (2004) · Genes & Development

Genomics and Chromatin DynamicsHemoglobinopathies and Related Disorders

Cited by 352

Expression of cDNA encoding the human “protective protein≓ associated with lysosomal β-galactosidase and neuraminidase: Homology to yeast proteases

Galjart, N. J., Gillemans, N., Harris, A., van der Horst, G. T. J., Verheijen, F. W., Galjaard, H., & d'Azzo, A. (1988) · Cell

Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus

Cited by 220

Human lysosomal protective protein has cathepsin A-like activity distinct from its protective function

Galjart, N. J., Morreau, H., Willemsen, R., Gillemans, N., Bonten, E. J., & d'Azzo, A. (1991) · Journal of Biological Chemistry

Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus

Cited by 158

Mouse "protective protein". cDNA cloning, sequence comparison, and expression.

Galjart, N. J., Gillemans, N., Meijer, D., & d'Azzo, A. (1990) · Journal of Biological Chemistry

Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus

Cited by 76