Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Camilla Enström"'
Autor:
Jonas Carlsson Almlöf, Per Lundmark, Anders Lundmark, Bing Ge, Seraya Maouche, Harald H H Göring, Ulrika Liljedahl, Camilla Enström, Jessy Brocheton, Carole Proust, Tiphaine Godefroy, Jennifer G Sambrook, Jennifer Jolley, Abigail Crisp-Hihn, Nicola Foad, Heather Lloyd-Jones, Jonathan Stephens, Rhian Gwilliam, Catherine M Rice, Christian Hengstenberg, Nilesh J Samani, Jeanette Erdmann, Heribert Schunkert, Tomi Pastinen, Panos Deloukas, Alison H Goodall, Willem H Ouwehand, François Cambien, Ann-Christine Syvänen
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e52260 (2012)
A large number of genome-wide association studies have been performed during the past five years to identify associations between SNPs and human complex diseases and traits. The assignment of a functional role for the identified disease-associated SN
Externí odkaz:
https://doaj.org/article/d0a286581c23430fa9c2b3d1ada6f11f
Autor:
Per Lundmark, Abigail Crisp-Hihn, Seraya Maouche, Tiphaine Godefroy, Harald H H Göring, Nilesh J. Samani, Anders Lundmark, Carole Proust, Jonathan Stephens, François Cambien, Jessy Brocheton, Bing Ge, Nicola S. Foad, Heribert Schunkert, Ulrika Liljedahl, Tomi Pastinen, Panos Deloukas, Camilla Enström, Jennifer Jolley, Rhian Gwilliam, Heather Lloyd-Jones, Ann-Christine Syvänen, Alison H. Goodall, Jonas Carlsson Almlöf, Jeanette Erdmann, Willem H. Ouwehand, Jennifer G. Sambrook, Catherine M. Rice, Christian Hengstenberg
Publikováno v:
PLoS ONE; Vol 7
PLoS ONE
PLoS ONE, Vol 7, Iss 12, p e52260 (2012)
PLoS ONE
PLoS ONE, Vol 7, Iss 12, p e52260 (2012)
A large number of genome-wide association studies have been performed during the past five years to identify associations between SNPs and human complex diseases and traits. The assignment of a functional role for the identified disease-associated SN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c26502286334aa82a5f081f2917b2ea
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-195164
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-195164
Autor:
Anders Isaksson, Meena Kanduri, Fergus Ryan, Camilla Enström, Richard Rosenquist, Hanna Göransson, Nicola Cahill
Publikováno v:
Articles
Global hypomethylation and regional hypermethylation are well-known epigenetic features of cancer; however, in chronic lymphocytic leukemia (CLL), studies on genome-wide epigenetic modifications are limited. Here, we analyzed the global methylation p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0985376db2a66f44934f3a219e3f82b
https://arrow.tudublin.ie/scschbioart/38
https://arrow.tudublin.ie/scschbioart/38
Publikováno v:
Scandinavian journal of clinical and laboratory investigation. 68(5)
Vitamin K epoxide reductase complex subunit 1 (VKORC1) is the site of inhibition by warfarin and other antivitamin K drugs during oral anticoagulant therapy. The SNP rs9934438 in intron 1 of VKORC1 (c.173+1000CT or 1173CT) discriminating the VKORC1*2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c1a843d55a104c53391e5ac319eee01
https://pubmed.ncbi.nlm.nih.gov/19172700
https://pubmed.ncbi.nlm.nih.gov/19172700
Publikováno v:
Thrombosis research. 121(5)
Introduction: A polymorphism (-14 A/T) affecting PAR1 expression on the platelet surface has recently been identified. A two-fold variation in receptor density, which correlated with the platelet response to PAR1-activating peptide (PAR1-AP), has bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::210d45e925192d5abd82f3227a964f69
https://pubmed.ncbi.nlm.nih.gov/17675219
https://pubmed.ncbi.nlm.nih.gov/17675219
Publikováno v:
Journal of thrombosis and haemostasis : JTH. 4(8)
Warfarin was introduced more than 60 years ago and is used worldwide for the prophylaxis of arterial and venous thromboembolism in primary and secondary prevention. The drug is orally administered as a racemic mixture of (R)- and (S)-enantiomers. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::255acec8c21bba155cd9e5a77f8b2b24
https://pubmed.ncbi.nlm.nih.gov/16879214
https://pubmed.ncbi.nlm.nih.gov/16879214
Autor:
Per Kogner, Tommy Martinsson, Rose-Marie Sjöberg, Staffan Nilsson, Camilla Enström, Anna Djos, Helena Carén, Maria Nethander
Publikováno v:
BMC Cancer
BMC Cancer, Vol 11, Iss 1, p 66 (2011)
BMC Cancer, Vol 11, Iss 1, p 66 (2011)
Background Epigenetic mechanisms such as DNA methylation and histone modifications are important regulators of gene expression and are frequently involved in silencing tumor suppressor genes. Methods In order to identify genes that are epigenetically
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b01773b09d76d5d28f44f375bfa42ff6
http://europepmc.org/articles/PMC3045360
http://europepmc.org/articles/PMC3045360
Autor:
Hanna Göransson, Richard Rosenquist, Fergus Ryan, Nicola Cahill, Anders Isaksson, Camilla Enström, Meena Kanduri
Publikováno v:
Blood. 114:364-364
Abstract 364 Introduction: Aberrant DNA methylation has been shown to play a strong role in tumorogenesis, where genome-wide hypomethylation and regional hypermethylation of tumor suppressor gene (TGS) promoters are characteristic hallmarks of many c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccdd35451d7697d7234aad323e99e6af
https://doi.org/10.1182/blood.v114.22.364.364
https://doi.org/10.1182/blood.v114.22.364.364