M. Oortveld

发表

Human Intellectual Disability Genes Form Conserved Functional Modules in Drosophila

M. Huynen, P. Verstreken, Shivakumar Keerthikumar, 2013, PLoS genetics.

Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.

C. Webber, M. Huynen, Shivakumar Keerthikumar, 2016, American journal of human genetics.

Epigenetic Regulation of Learning and Memory by Drosophila EHMT/G9a

Annette Schenck, Huiqing Zhou, Hendrik G. Stunnenberg, 2011, PLoS biology.

CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila.

Annette Schenck, Arif B Ekici, André Reis, 2009, American journal of human genetics.

Drosophila models of early onset cognitive disorders and their clinical applications

M. Oortveld, B. Nijhof, A. Schenck, 2014, Neuroscience & Biobehavioral Reviews.

Terminal keratinocyte differentiation in vitro is associated with a stable DNA methylome

René A. M. Dirks, A. Brinkman, Huiqing Zhou, 2020, Experimental dermatology.

Psoriasis-Associated Late Cornified Envelope (LCE) Proteins Have Antibacterial Activity.

James T. Elder, P. Jansen, J. Bouwstra, 2017, The Journal of investigative dermatology.

CEP89 is required for mitochondrial metabolism and neuronal function in man and fly.

B. V. van Bon, N. de Leeuw, B. D. de Vries, 2013, Human molecular genetics.

CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation

F. Cremers, A. V. van Kessel, H. van Bokhoven, 2010, Human Genetics.

Lifestyle and parental allergen sensitization are reflected in the intrauterine environment at gene expression level

A. Scheynius, M. Joerink, M. Oortveld, 2010, Allergy.

Cathepsin B as a potential cystatin M/E target in the mouse hair follicle

T. Reinheckel, F. Kersten, S. Verbeek, 2017, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration

Y. Hérault, Y. Humeau, P. Verstreken, 2015, Human molecular genetics.

CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation

F. Cremers, A. V. van Kessel, H. van Bokhoven, 2010, Human Genetics.

Psoriasis-Associated Late Cornified Envelope (LCE) Proteins Have Antibacterial Activity.

James T. Elder, P. Jansen, J. Bouwstra, 2017, The Journal of investigative dermatology.