W. V. D. van den Akker

发表

Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability.

Christian Gilissen, Annette Schenck, Koenraad Devriendt, 2012, American journal of human genetics.

Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling

Monica Frega, Huiqing Zhou, Moritz Negwer, 2019, Nature Communications.

Structure and Biological Activity of the Short-chain Lipopolysaccharide from Bartonella henselae ATCC 49882T*

H. Heine, C. Dehio, B. Lindner, 2004, Journal of Biological Chemistry.

Comparative functional analysis provides evidence for a crucial role for the homeobox gene Nkx2.1/Titf‐1 in forebrain evolution

L. Medina, L. Puelles, A. Durston, 2008, The Journal of comparative neurology.

Lipopolysaccharide expression within the genus Bordetella: influence of temperature and phase variation.

W. V. D. van den Akker, 1998, Microbiology.

A homozygous nonsense mutation in the Fukutin gene causes a Walker-Warburg syndrome phenotype

B. Cormand, W. Dobyns, H. van Bokhoven, 2003, Journal of medical genetics.

Knockdown of the complete Hox paralogous group 1 leads to dramatic hindbrain and neural crest defects

A. Durston, N. Bardine, W. V. D. van den Akker, 2005, Development.

Single-cell RNA-seq identifies a reversible epithelial-mesenchymal transition in abnormally specified epithelia of p63 EEC syndrome

F. Tang, Quan Xu, Huiqing Zhou, 2018, bioRxiv.

Autosomal Recessive Dilated Cardiomyopathy due to DOLK Mutations Results from Abnormal Dystroglycan O-Mannosylation

J. Schuurs-Hoeijmakers, H. Mandel, J. van Reeuwijk, 2011, PLoS genetics.

Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia.

A. V. Vulto-van Silfhout, L. Vissers, J. Schuurs-Hoeijmakers, 2012, American journal of human genetics.

Single-cell RNA-seq identifies a reversible mesodermal activation in abnormally specified epithelia of p63 EEC syndrome

F. Tang, S. V. van Heeringen, Quan Xu, 2019, Proceedings of the National Academy of Sciences.

De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further review

J. Schuurs-Hoeijmakers, R. Pfundt, B. D. de Vries, 2018, Clinical genetics.

Identification of hoxb1b downstream genes: hoxb1b as a regulatory factor controlling transcriptional networks and cell movement during zebrafish gastrulation.

H. Spaink, A. Durston, W. V. D. van den Akker, 2010, The International journal of developmental biology.

Neuronal network dysfunction in a human model for Kleefstra syndrome mediated by enhanced NMDAR signaling

D. Schubert, T. Kleefstra, H. van Bokhoven, 2019, bioRxiv.

Detection of HIV antibodies in saliva as a tool for epidemiological studies

W. V. D. van den Akker, A. V. van Loon, G. Roosendaal, 1992, AIDS.

Sp8 controls the anteroposterior patterning at the midbrain-hindbrain border

A. Simeone, P. Gruss, P. Collombat, 2006, Development.

The filamentous hemagglutinin of Bordetella parapertussis is the major adhesin in the phase-dependent interaction with NCI-H292 human lung epithelial cells.

W. V. D. van den Akker, 1998, Biochemical and biophysical research communications.

Bordetella bronchiseptica has a BvgAS-controlled cytotoxic effect upon interaction with epithelial cells.

W. V. D. van den Akker, 1997, FEMS microbiology letters.

Respiratory Syncytial Virus European Laboratory Network 2022 Survey: Need for Harmonization and Enhanced Molecular Surveillance.

A. Meijer, W. V. D. van den Akker, Lance D Presser, 2023, The Journal of infectious diseases.