mws898 mws898

E-mailpia.helene.klausen.01regionhdk

Ole Maaløes Vej 5
2200 København N.

CV

Karriere

2006-
Forskningskoordinator, BRIC

2002-2005
Forsker, Granulocyt Laboratoriet, Rigshospitalet

1998-2001
Ph.D. studerende, Leukemia and Lymphoma Laboratory, Rigshospitalet

2000
Gæsteforsker, Roswell Park Cancer Institute, Buffalo, USA

Interesseområder

Koordinerer forskningsprojekter og administrerer forskningsbevillinger

Ansvarlig for http://www.bric.ku.dk

Emneord

BRIC

7 Tidsskriftartikel

On mouse and man: neutrophil gelatinase associated lipocalin is not involved in apoptosis or acute response.
Klausen, P., Niemann, C. U., Cowland, J. B., Krabbe, K. & Borregaard, N., 2005, I: European Journal of Haematology. 75, 4, s. 332-40 8 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

44 Citationer (Scopus)
Localization of serglycin in human neutrophil granulocytes and their precursors.
Niemann, C. U., Cowland, J. B., Klausen, P., Askaa, J., Calafat, J. & Borregaard, N., 2004, I: Journal of Leukocyte Biology. 76, 2, s. 406-15 9 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

43 Citationer (Scopus)
End-stage differentiation of neutrophil granulocytes in vivo is accompanied by up-regulation of p27kip1 and down-regulation of CDK2, CDK4, and CDK6.
Klausen, P., Bjerregaard, M. D., Borregaard, N. & Cowland, J. B., 2003, I: Journal of Leukocyte Biology. 75, 3, s. 569-78 9 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

52 Citationer (Scopus)
The in vivo profile of transcription factors during neutrophil differentiation in human bone marrow.
Bjerregaard, M. D., Jurlander, J., Klausen, P., Borregaard, N. & Cowland, J. B., 2003, I: Blood. 101, 11, s. 4322-32 10 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

152 Citationer (Scopus)
The chimeric anti-CD20 antibody rituximab induces apoptosis in B-cell chronic lymphocytic leukemia cells through a p38 mitogen activated protein-kinase-dependent mechanism.
Pedersen, I. M., Buhl, A. M., Klausen, P., Geisler, C. H. & Jurlander, J., 2002, I: Blood. 99, 4, s. 1314-9 5 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

212 Citationer (Scopus)
Oncostatin M and interleukin 6 inhibit cell cycle progression by prevention of p27kip1 degradation in HepG2 cells.
Klausen, P., Pedersen, L., Jurlander, J. & Baumann, H., 2000, I: Oncogene. 19, 32, s. 3675-83 8 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

57 Citationer (Scopus)
Ligation of major histocompatability complex (MHC) class I molecules on human T cells induces cell death through PI-3 kinase-induced c-Jun NH2-terminal kinase activity: a novel apoptotic pathway distinct from Fas-induced apoptosis.
Skov, S., Klausen, P. & Claesson, M. H., 1997, I: Journal of Cell Biology. 139, 6, s. 1523-31 8 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

78 Citationer (Scopus)

mws898 mws898

Personlig profil

CV

Karriere

Interesseområder

Emneord

Publikation

On mouse and man: neutrophil gelatinase associated lipocalin is not involved in apoptosis or acute response.

Localization of serglycin in human neutrophil granulocytes and their precursors.

End-stage differentiation of neutrophil granulocytes in vivo is accompanied by up-regulation of p27kip1 and down-regulation of CDK2, CDK4, and CDK6.

The in vivo profile of transcription factors during neutrophil differentiation in human bone marrow.

The chimeric anti-CD20 antibody rituximab induces apoptosis in B-cell chronic lymphocytic leukemia cells through a p38 mitogen activated protein-kinase-dependent mechanism.

Oncostatin M and interleukin 6 inhibit cell cycle progression by prevention of p27kip1 degradation in HepG2 cells.

Ligation of major histocompatability complex (MHC) class I molecules on human T cells induces cell death through PI-3 kinase-induced c-Jun NH2-terminal kinase activity: a novel apoptotic pathway distinct from Fas-induced apoptosis.