A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1.

Autor: Irene Johnsrud, Mari Ann Kulseth, Olaug Kristin Rødningen, Linn Landrø, Per Helsing, Erik Waage Nielsen, Ketil Heimdal

Publikováno v: PLoS ONE, Vol 10, Iss 7, p e0131637 (2015)

Hereditary angioedema with C1 inhibitor deficiency (C1-INH-HAE) is characterized by relapsing, non-pruritic swelling in skin and submucosal tissue. Symptoms can appear in early infancy when diagnosis is more difficult. In the absence of a correct dia

Externí odkaz: https://doaj.org/article/79452fe6ebc34b2db20808dade0678b9

Application of microarray analyses to identify genes involved in radiation-induced fibrosis (RIF)

Autor: Olaug Kristin Rødningen, Jan Alsner, Trevor Hastie, Jens Overgaard, Anne-Lise Børresen-Dale

Publikováno v: Rødningen, O K, Alsner, J, Hastie, T, Overgaard, J & Børresen-Dale, A-L 2005, ' Application of microarray analyses to identify genes involved in radiation-induced fibrosis (RIF) ', The Third International Symposium on The Molecular Biology of Breast Cancer, Molde, Norway, 22/06/2005-26/06/2005 .
Aarhus University
Rødningen, O K, Alsner, J, Hastie, T, Overgaard, J & Børresen-Dale, A-L 2005, Application of microarray analyses to identify genes involved in radiation-induced fibrosis (RIF) . in Breast Cancer Res. . 7(Suppl 2) edn, pp. S42-S43, The Third International Symposium on The Molecular Biology of Breast Cancer, Molde, Norway, 22/06/2005 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0500ea7a8f85c3acb965f691020296f5
https://pure.au.dk/portal/da/publications/application-of-microarray-analyses-to-identify-genes-involved-in-radiationinduced-fibrosis-rif(52c057d0-bf10-11da-bee9-02004c4f4f50).html