Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Maria J. Eriksson"'
Autor:
Andreas Liliequist, Per Agvald, Claes Frostell, Christofer Adding, Joakim Norderfeldt, Per-Arne Lönnqvist, Maria J. Eriksson
Publikováno v:
Acta Anaesthesiologica Scandinavica
Introduction Critically ill Covid‐19 pneumonia patients are likely to develop the sequence of acute pulmonary hypertension, right ventricular (RV) strain, and eventually RV failure due to known pathophysiology (endothelial inflammation plus thrombo
Publikováno v:
Aging Cell. 10:1011-1020
Hutchinson-Gilford progeria syndrome (HGPS or progeria) is a very rare genetic disorder with clinical features suggestive of premature aging. Here, we show that induced expression of the most common HGPS mutation (LMNA c.1824C>T, p.G608G) results in
Publikováno v:
Journal of Hypertension. 27:2257-2264
To assess left ventricular (LV) structure and function in preeclampsia, a serious vascular-related pregnancy disorder, by Doppler tissue imaging (DTI) in combination with the levels of cardiovascular biomarkers.Thirty-five pregnant women with preecla
Publikováno v:
European Journal of Human Genetics. 17:928-937
Most cases of the segmental progeroid syndrome, Hutchinson-Gilford progeria syndrome (HGPS), are caused by a de novo dominant mutation within a single codon of the LMNA gene. This mutation leads to the increased usage of an internal splice site that
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 90:1354-1359
The aim of this study was to evaluate endothelial function measured as flow-mediated dilatation (FMD) of the brachial artery and blood markers of cardiovascular disease in young female endurance athletes with menstrual disturbance. Age- and body mass
Autor:
Brit Corneliussen, Thomas Grundström, Maria J. Eriksson, Juha Saarikettu, Ingela Bergqvist, Björn Eriksson, Dan Holmberg
Publikováno v:
European Journal of Immunology. 30:2857-2863
E2A, HEB and E2-2 genes encode a group of basic helix-loop-helix (bHLH) transcription factors that are structurally and functionally similar. Deletion of the genes encoding either of these proteins leads to early lethality and a block in B lymphocyte
Autor:
Eva Schmidt, Maria J. Eriksson
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 4, Iss 1, p 282 (2011)
BMC Research Notes, Vol 4, Iss 1, p 282 (2011)
Background The tetracycline-controlled transactivator system is a powerful tool to control gene expression in vitro and to generate consistent and conditional transgenic in vivo model organisms. It has been widely used to study gene function and to e
Publikováno v:
PLoS ONE, Vol 4, Iss 1, p e4114 (2009)
PLoS ONE
PLoS ONE
Multiple genetic disorders caused by mutations that affect the proteins lamin A and C show strong skin phenotypes. These disorders include the premature aging disorders Hutchinson-Gilford progeria syndrome and mandibuloacral dysplasia, as well as res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ff26d66a7b9c15cf967cff6f11dd0d5
http://hdl.handle.net/10138/161764
http://hdl.handle.net/10138/161764