Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ólöf Sigurðardóttir"'
Autor:
Emil L. Sigurðsson, Unnur Thorsteinsdottir, Valgerður Steinthórsdóttir, Davíð O. Arnar, Karl Andersen, Ásgeir Sigurðsson, G. Thorleifsson, Magnús Baldvinsson, Patrick Sulem, Stefan E Matthiasson, Kari Stefansson, G Sveinbjörnsson, Aslaug Jonasdottir, Ólöf Sigurðardóttir, Ragnar Bjarnason, Aðalbjörg Jónasdóttir, Ingileif Jonsdottir, Thórarinn Guðnason, Eythór Björnsson, Bjorn L. Thorarinsson, Isleifur Olafsson, Solveig Gretarsdottir, Ragnar Danielsen, Brynjar Viðarsson, Snaedis Kristmundsdottir, Daníel F. Guðbjartsson, Hakon Jonsson, Anna Helgadottir, Bjarni V. Halldorsson, Guðmundur Thorgeirsson, Hilma Holm
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology
Supplemental Digital Content is available in the text.
Objective: Familial hypercholesterolemia (FH) is traditionally defined as a monogenic disease characterized by severely elevated LDL-C (low-density lipoprotein cholesterol) levels. In practi
Objective: Familial hypercholesterolemia (FH) is traditionally defined as a monogenic disease characterized by severely elevated LDL-C (low-density lipoprotein cholesterol) levels. In practi
Autor:
Bhairavi Swaminathan, Daniel F. Gudbjartsson, Ellinor Johnsson, Hlif Steingrimsdottir, Ulla Vogel, Ram Ajore, Ingemar Turesson, Ólöf Sigurðardóttir, Anna K. Kähler, Markus Hansson, Thorunn Rafnar, Isleifur Olafsson, Mina Ali, Magnus Jöud, Britt-Marie Halvarsson, Patrick Sulem, Urban Gullberg, Kari Stefansson, Guðmar Thorleifsson, Unnur Thorsteinsdottir, Annette Juul Vangsted, Sven Nelander, Robert Månsson, Anders Waage, Guðmundur I Eyjólfsson, Ulf-Henrik Mellqvist, Sigurður Yngvi Kristinsson, Christina M. Hultman, Björn Nilsson, Hareth Nahi, Erik Ingelsson, Stig Lenhoff, Gisli Masson, Vilhelmina Haraldsdottir
Publikováno v:
Nature Communications
Nature Communications; 6, pp 1-8 (2015)
Nature Communications; 6, pp 1-8 (2015)
Multiple myeloma (MM) is characterized by an uninhibited, clonal growth of plasma cells. While first-degree relatives of patients with MM show an increased risk of MM, the genetic basis of inherited MM susceptibility is incompletely understood. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::839481e59b5fd934fb8b9089289865d3
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-257040
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-257040