
Hans A. Heemskerk, MSc.
Hans
Heemskerk is PhD-student in the DMD Genetic Therapy Group at the Human Genetics
Department (LUMC) since May 2005. He studied Biomedical Science at the
University of Leiden.
He is
focusing on the
development of safe and efficient antisense formulations for
the body-wide treatment of muscle tissue in Duchenne Muscular Dystrophy
patients, under supervision of Dr. Annemieke Aartsma-Rus and Prof. Dr. Gert-Jan
B van Ommen. Currently he is a postdoc in the group of Jenny Morgan at the
Institute of Child Health (London, UK).
Publication list
Aartsma-Rus,A., Janson,A.A.,
Heemskerk,J.A.,
De Winter,C.L., van Ommen,G.J., and van Deutekom,J.C. (2006) Therapeutic
modulation of DMD splicing by blocking exonic splicing enhancer sites with
antisense oligonucleotides. Ann.N.Y.Acad.Sci., 1082, 74-76.
Aartsma-Rus A, van Vliet L, Hirschi M, Janson, A.A., Heemskerk, J.A.
et al. (2008) Guidelines for antisense oligonucleotide design and
insight in splice modulating mechanisms. Mol Ther; epub 23 Sept
Heemskerk JA, de Winter CL, De Kimpe S...and Aartsma-Rus A (2009) In vivo comparison of 2'O-methyl-PS and morpholino antisense oligonucleotides for DMD exon skipping. J Gene Med ; 11:257-66
Heemskerk JA, de Winter CL, van Ommen G-J, van Deutekom JCT and Aartsma-Rus A: Development of antisense-mediated exon skipping as a treatment for Duchenne muscular dystrophy. Annals of the NY Acad Science 2009; 1175: 71-9.
Heemskerk JA, de Winter CL, van Kuik P….Aartsma-Rus A, and van Deutekom JCT: Pre-clinical PK and PD Studies on 2’O-Methyl-Phosphorothioate RNA Antisense Oligonucleotides in the mdx mouse model. Mol Ther 2010; 18: 1210-7
Spitali P, Heemskerk JA, Vossen RHAM, Ferlini A, den Dunnen JT, 't Hoen PAC and Aartsma-Rus A: Accurate quantification of dystrophin mRNA and exon skipping levels in Duchenne Muscular Dystrophy. Lab Invest 2010; 90: 1396-402