The zebrafish homeobox gene hox-2.2: transcription unit, potential regulatory regions and in situ localization of transcripts.

Por Njølstad, P R, Molven, A, Apold, J, Fjose, A
Publicado em 1990

Primary structure, developmentally regulated expression and potential duplication of the zebrafish homeobox gene ZF-21.

Por Njølstad, P R, Molven, A, Hordvik, I, Apold, J, Fjose, A
Publicado em 1988

Application of natural and amplification created restriction sites for the diagnosis of PKU mutations.

Por Eiken, H G, Odland, E, Boman, H, Skjelkvåle, L, Engebretsen, L F, Apold, J
Publicado em 1991

A termination mutant prevalent in Norwegian haplotype 7 phenylketonuria genes.

Por Apold, J, Eiken, H G, Odland, E, Fredriksen, A, Bakken, A, Lorens, J B, Boman, H
Publicado em 1990

Screening for germline rearrangements in BRCA1 and BRCA2 in Norwegian families with breast or breast/ovarian cancer

Por Van Ghelue, M, Ingebrigtsen, M, Riise Stensland, HMF, Mæhle, L, Apold, J, Møller, P, Marton, V, Jonsrud, C
Publicado no Breast Cancer Res (2005)

Expression of recombinant human phenylalanine hydroxylase as fusion protein in Escherichia coli circumvents proteolytic degradation by host cell proteases. Isolation and characteri...

Por Martinez, A, Knappskog, P M, Olafsdottir, S, Døskeland, A P, Eiken, H G, Svebak, R M, Bozzini, M, Apold, J, Flatmark, T
Publicado em 1995

Mutation-Specific Survival of Inherited Breast Cancer

Por Møller, P., Borg, Å., Evans, G., Haites, N., Steel, C. M., Vasen, H., Gregory, H., Hodgson, S., Apold, J., Lalloo, F., Mæhle, L., Anderson, E., Heimdal, K., The Biomed 2 Demonstration Programme on Inherited Breast Cancer
Publicado em 1999

Guidelines for Follow-Up of Women at High Risk for Inherited Breast Cancer: Consensus Statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer

Por Møller, P., Evans, G., Haites, N., Vasen, H., Reis, M. M., Anderson, E., Apold, J., Hodgson, S., Eccles, D., Olsson, H., Stoppa-Lyonnet, D., Chang-Claude, J., Morrison, P. J., Bevilacqua, G., Heimdal, K., Mæhle, L., Lalloo, F., Gregory, H., Preece, P., Borg, Å., Nevin, N. C., Caligo, M., Steel, C. M.
Publicado em 1999

Multiple origins for phenylketonuria in Europe

Por Eisensmith, R. C., Okano, Y., Dasovich, M., Wang, T., Güttler, F., Lou, H., Guldberg, P., Lichter-Konecki, U., Konecki, D. S., Svensson, E., Hagenfeldt, L., Rey, F., Munnich, A., Lyonnet, S., Cockburn, F., Connor, J. M., Pembrey, M. E., Smith, I., Gitzelmann, R., Steinmann, B., Apold, J., Eiken, H. G., Giovannini, M., Riva, E., Longhi, R., Romano, C., Cerone, R., Naughten, E. R., Mullins, C., Cahalane, S., Özalp, I., Fekete, G., Schuler, D., Berencsi, G. Y., Nász, I., Brdicka, R., Kamaryt, J., Pijackova, A., Cabalska, B., Boszkowa, K., Schwartz, E., Kalinin, V. N., Jin, L., Chakraborty, R., Woo, S. L. C.
Publicado em 1992