A Dutch family with moderately severe hemophilia B (factor IXHeerde) has a missense mutation identical to that of factor IX London 2.

di Poort, S R, Briët, E, Bertina, R M, Reitsma, P H
Pubblicazione 1989

A Dutch pedigree with mild hemophilia B with a missense mutation in the first EGF domain (factor IXOud en Nieuw Gastel).

di Poort, S R, Briët, E, Bertina, R M, Reitsma, P H
Pubblicazione 1989

Modification of the N-terminus of human factor IX by defective propeptide cleavage or acetylation results in a destabilized calcium-induced conformation: effects on phospholipid bi...

di Wojcik, E G, Van Den Berg, M, Poort, S R, Bertina, R M
Pubblicazione 1997

Factor IX Zutphen: a Cys18-->Arg mutation results in formation of a heterodimer with alpha 1-microglobulin and the inability to form a calcium-induced conformation.

di Wojcik, E G, van den Berg, M, van der Linden, I K, Poort, S R, Cupers, R, Bertina, R M
Pubblicazione 1995

Fulminant meningococcal septic shock in a boy with combined inherited properdin and protein C deficiency.

di Fijen, C A, Derkx, B H, Kuijper, E J, Mannens, M, Poort, S R, Peters, M, Daha, M R, Dankert, J
Pubblicazione 1995

MUC1 (EMA) is preferentially expressed by ALK positive anaplastic large cell lymphoma, in the normally glycosylated or only partly hypoglycosylated form

di Ten, B, Snijdewint, F, von Mensdorff-Pou..., S, Poort-Keesom, R, Oudejans, J, Meijer, J, Willemze, R, Hilgers, J, Meijer, C
Pubblicazione 2001