View Author
scopus: 35466178900

Burbach, J.P.H.

(Peter Burbach)


ubi-b ␤ app ϩ1 patient expression control neuron uncx 41 protein ␤ app brain transcript development section deletion mutation autism genomic homeobox region duplication vasopressin subject nipa 1 ubi-b ϩ1 immunoreactivities cortex ds patients gain het clone hypothalamus hippocampu primer loss het ubi-b ϩ1 proteins uncx 41 expression ϩ1 proteins probe chromosome adenohypophysi neurohypophysi hybridization dinucleotide magnocellular neurons mouse adult netherland result cyfip 1 level analysis burbach phenotype system wild-type cyfip ubi-b ϩ1 immunoreactivity magnocellular tangle disorder factor utrecht identi fied 11.2 genomic pcr mutant ubi-b ϩ1 exons 9 neuropil threads motor dinucleotide deletions axonal projections immunoreactivity nondemented motif table antibody ubi-b transcripts ad patients control patients zwaag rudolf magnus institute




3 Most Recent Publications

A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder (Article)
Zwaag, B. van der Staal, W.G. Buizer-Voskamp, J.E. Nelen, M.R. Berg, L.H. van den Ploos van Amstel, H.K. Engeland, H. van Burbach, J.P.H. Hochstenbach, R. Poot, M. Spierenburg, H.A. Jonge, M.V. de Verbeek, N.E. Slot, R. van 't Es, M.A. van Freitag, C.M.
2010-06-01
Neurohypophysial dysmorphogenesis in mice lacking the homeobox gene Uncx4·1 (Article)
Asbreuk, C.H.J. Doorninck, J.H. van Mansouri, A. Smidt, M.P. Burbach, J.P.H.
2006-02-01
Frameshift mutants of β amyloid precursor protein and ubiquitin-B are prominent in Alzheimer and Down patients. (Article)
Leeuwen, F.W. van Kleijn, D.P.V. de Burbach, J.P.H. Hol, E.M. Martens, J.W.M. Hurk, H.H. van den Neubauer, A. Sonnemans, M.A.F. Sluijs, J.A. Koycu, S. Ramdjielal, R.D.J. Salehi, A. Grosveld, F.G.
1998-01-09