Read-through transcript from NM23-H1 into the neighboring NM23-H2 gene encodes a novel protein, NM23-LV von Valentijn, Linda J., Koster, Jan, Versteeg, Rogier

Volltext

Allelotype of pediatric rhabdomyosarcoma von VISSER, M, SIJMONS, C, BRAS, J, ARCECI, R. J, GODFRIED, M, VALENTIJN, L. J, VOUTE, P. A, BAAS, F

Volltext

A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies von Nicholson, Garth A., Valentijn, Linda J., Cherryson, Annia K., Kennerson, Marina L., Bragg, Tara L., DeKroon, Robert M., Ross, David A., Pollard, John D., Mcleod, James G., Bolhuis, Pieter A., Baas, Frank

Volltext

The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1A von Valentijn, L. J., Bolhuis, P. A., Zorn, I., Hoogendijk, J. E., van den Bosch, N., Hensels, G. W., Stanton, V. P., Housman, D. E., Fischbeck, K. H., Ross, D. A., Nicholson, G. A., Meershoek, E. J., Dauwerse, H. G., van Ommen, G. -J. B., Baas, F.

Volltext

Hereditary neuropathy with liability to pressure palsies : Phenotypic differences between patients with the common deletion and a pmp22 frame shift mutation von LENSSEN, P. P. A, GABREËLS-FESTEN, A. A. W. M, VALENTIJN, L. J, JONGEN, P. J. H, VAN BEERSUM, S. E. C, VAN ENGELEN, B. G. M, VAN WENSEN, P. J. M, BOLHUIS, P. A, GABREËLS, F. J. M, MARIMAN, E. C. M

Volltext

Charcot-Marie-Tooth disease type 1A : morphological phenotype of the 17p duplication versus PMP22 point mutations von GABREËLS-FESTEN, A. A. W. M, BOLHUIS, P. A, HOOGENDIJK, J. E, VALENTIJN, L. J, ESHUIS, E. J. H. M, GABREËLS, F. J. M

Volltext

Identical point mutations of PMP–22 in Trembler–J mouse and Charcot–Marie–Tooth disease type 1A von Valentijn, Linda J., Baas, Frank, Wolterman, Ruud A., Hoogendijk, Jessica E., van den Bosch, Norbert H.A., Zorn, Ina, Gabreëls-Festen, Anneke A.W.M., de Visser, Marianne, Bolhuis, Pieter A.

Volltext

De-novo mutation in hereditary motor and sensory neuropathy type I von Hoogendijk, J.E., Hensels, G.W., Janssen, E.A.M., Valentijn, L.J., Baas, F., de Visser, M., Bolhuis, P.A., Gabreels-Festen, A.A.W.M., Gabreels, F.J.M., de onghe, P., Martin, J.-J., van Broeckhoven, C.

Volltext

N-myc enhances the expression of a large set of genes functioning in ribosome biogenesis and protein synthesis von Boon, Kathy, Caron, Huib N., van Asperen, Ronald, Valentijn, Linda, Hermus, Marie-Christine, van Sluis, Peter, Roobeek, Ilja, Weis, Isabel, Voûte, P.A., Schwab, Manfred, Versteeg, Rogier

Volltext

Alternatively sized duplication in Charcot — Marie — Tooth disease type 1A von Valentijn, Linda J., Baas, Frank, Zorn, Ina, Hensels, Gerard W., de Visser, Marianne, Bolhuls, Peter A.

Volltext

Direct regulation of the minichromosome maintenance complex by MYCN in neuroblastoma von Koppen, Arjen, Ait-Aissa, Rachida, Koster, Jan, van Sluis, Peter G, Øra, Ingrid, Caron, Huib N, Volckmann, Richard, Versteeg, Rogier, Valentijn, Linda J

Volltext

Prevalence of the 1.5-Mb 17p deletion in families with hereditary neuropathy with liability to pressure palsies von Mariman, E. C. M., Gabreëls-Festen, A. A. W. M., van Beersum, S. E. C., Valentijn, L. J., Baas, F., Bolhuis, P. A., Jongen, P. J. H., Ropers, H. H., Gabreëls, F. J. M.

Volltext

Inhibition of a new differentiation pathway in neuroblastoma by copy number defects of N-myc, Cdc42, and nm23 genes von VALENTIJN, Linda J, KOPPEN, Arjen, VAN ASPEREN, Ronald, ROOT, Heather A, HANEVELD, Franciska, VERSTEEG, Rogier

Volltext

Déjérine-Sottas neuropathy is associated with a de novo PMP22 mutation von Valentijn, Linda J., Ouvrier, Robert A., Van Den Bosch, Norbert H. A., Bolhuis, Pieter A., Baas, Frank, Nicholson, Garth A.

Volltext

Full transcriptome analysis of rhabdomyosarcoma, normal, and fetal skeletal muscle: statistical comparison of multiple SAGE libraries von Schaaf, Gerben J, Ruijter, Jan M, van Ruissen, Fred, Zwijnenburg, Danny A, Waaijer, Raymond, Valentijn, Linda J, Benit-Deekman, Jennifer, van Kampen, Antoine H. C, Baas, Frank, Kool, Marcel

Volltext

Identification of a functional initiator sequence in the human MDR1 promoter von van Groenigen, Marjon, Valentijn, Linda J., Baas, Frank

Volltext

Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot–Marie–Tooth disease type 1B von Kulkens, Tanja, Bolhuis, Pieter A., Wolterman, Ruud A., Kemp, Stephan, te Nijenhuis, Saskia, Valentijn, Linda J., Hensels, Gerard W., Jennekens, Frans G.I., de Visser, Marianne, Hoogendijk, Jessica E., Baas, Frank

Volltext

Caprine homologue of rodent 5'-AMP-activated protein kinase subunit and yeast SNF4/CAT3 is down-regulated by thyroid hormone von PIOSIK, P. A, VAN GROENIGEN, M, PONNE, N. J, VALENTIJN, L. J, BOLHUIS, P. A, BAAS, F

Volltext

Mededeling: een hangplek voor distelvlinders von L. Valentijn, G. Verschoor

Volltext

The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2 von HOOGENDIJK, J. E, HENSELS, G. W, ZORN, I, VALENTIJN, L, JANSSEN, E. A. M, DE VISSER, M, BARKER, D. F, ONGERBOER DE VISSER, B. W, BAAS, F, BOLHUIS, P. A

Volltext