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Browsing by Author Kok, Y.J.M. de

Full Text	Issue Date	Title	Author(s)
	1995	A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene	Kok, Y.J.M. de; Merkx, G.F.M.; Maarel, S.M. van der, et al
	1995	Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3	Bitner-Glindzicz, M.; Turnpenny, P.; Höglund, P., et al
	1996	Gabaergic inhibition of the pituitary release of adrenocorticotropin and alfa-melanotropin is impaired in dogs with hepatic encephalopathy	Rothuizen, J.; Kok, Y.J.M. de; Slob, A.K., et al
	1987	A genotype-dependent hippocampal dynorphinergic mechanism controls mouse exploration	Daal, J.H.H.M. van; Kok, Y.J.M. de; Jenks, B.G., et al
	1996	Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4	Kok, Y.J.M. de; Vossenaar, E.R.; Cremers, C.W.R.J., et al
	1996	De moleculaire basis van X-gebonden doofheid type 3 (DFN3): identificatie van 6 nieuwe deleties 900 kb proximaal van het DFN3gene, POU3F4	Kok, Y.J.M. de; Cremers, C.W.R.J.; Vossenaar, E.R., et al
	1997	The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases : identification of a somatic mosaicism for a POU3F4 missense mutation	Kok, Y.J.M. de; Cremers, C.W.R.J.; Ropers, H.-H., et al
	1995	Production of native creatine kinase B in insect cells using a baculovirus expression vector	Kok, Y.J.M. de; Geurds, M.P.A.; Usmany, M., et al
	1995	Tissue- and cell-specific distribution of creatine kinase B: A new and highly specific monoclonal antibody for use in immunohistochemistry	Sistermans, E.A.; Kok, Y.J.M. de; Peters, W.J.M, et al
	1995	Tissue- and cell-specific distribution of creatine kinase B: A new and highly specific monoclonal antibody for use in immunohistochemistry.	Sistermans, E.A.; Kok, Y.J.M. de; Peters, W.J.M, et al
	1995	Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardation	Maarel, S.M. van der; Scholten, I.H.J.M.; Maat-Kievit, J.A., et al