Search Results - "Balemans, Monique C M"

Reduced exploration, increased anxiety, and altered social behavior: Autistic-like features of euchromatin histone methyltransferase 1 heterozygous knockout mice by Balemans, Monique C.M., Huibers, Manon M.H., Eikelenboom, Nathalie W.D., Kuipers, Arthur J., van Summeren, Rik C.J., Pijpers, Michael M.C.A., Tachibana, Makoto, Shinkai, Yoichi, van Bokhoven, Hans, Van der Zee, Catharina E.E.M.

“…The 9q34.3 subtelomeric deletion syndrome is a newly defined mental retardation syndrome, caused by haplo-insufficiency of the euchromatin histone…”
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Actual drawing of histological images improves knowledge retention by Balemans, Monique C.M., Kooloos, Jan G.M., Donders, A. Rogier T., Van der Zee, Catharina E.E.M.

“…Medical students have to process a large amount of information during the first years of their study, which has to be retained over long periods of nonuse…”
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Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome by Balemans, Monique C M, Kasri, Nael Nadif, Kopanitsa, Maksym V, Afinowi, Nurudeen O, Ramakers, Ger, Peters, Theo A, Beynon, Andy J, Janssen, Sanne M, van Summeren, Rik C J, Eeftens, Jorine M, Eikelenboom, Nathalie, Benevento, Marco, Tachibana, Makoto, Shinkai, Yoichi, Kleefstra, Tjitske, van Bokhoven, Hans, Van der Zee, Catharina E E M

“…Euchromatin histone methyltransferase 1 (EHMT1) is a highly conserved protein that catalyzes mono- and dimethylation of histone H3 lysine 9, thereby…”
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Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice by Balemans, Monique C.M., Ansar, Muhammad, Oudakker, Astrid R., van Caam, Arjan P.M., Bakker, Brenda, Vitters, Elly L., van der Kraan, Peter M., de Bruijn, Diederik R.H., Janssen, Sanne M., Kuipers, Arthur J., Huibers, Manon M.H., Maliepaard, Eliza M., Walboomers, X. Frank, Benevento, Marco, Nadif Kasri, Nael, Kleefstra, Tjitske, Zhou, Huiqing, Van der Zee, Catharina E.E.M., van Bokhoven, Hans

“…Haploinsufficiency of Euchromatin histone methyltransferase 1 (EHMT1), a chromatin modifying enzyme, is the cause of Kleefstra syndrome (KS). KS is an…”
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