Zobrazeno 1 - 10
of 15
pro vyhledávání: '"A M Jonsdottir"'
Publikováno v:
Bioengineering, Vol 7, Iss 3, p 75 (2020)
Human embryonic stem cell-derived mesenchymal progenitor (hES-MP) cells are mesenchymal-like cells, derived from human embryonic stem cells without the aid of feeder cells. They have been suggested as a potential alternative to mesenchymal stromal ce
Externí odkaz:
https://doaj.org/article/44eb1c6612014720ab09689b68e5701b
Autor:
Gudlaug M. Jonsdottir, Hjortur Oddsson, David O. Arnar, Gustav Arnar Davidsson, Sigrun H. Lund
Publikováno v:
JAMA Intern Med
This study compares outcomes of a recalled implantable cardioverter/defibrillator lead with a control lead in individuals in Iceland.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0ab6c7d449f5d021be06bc1f81d8146
https://europepmc.org/articles/PMC6990945/
https://europepmc.org/articles/PMC6990945/
Autor:
Neel T. Shah, Kelly N. Wright, Gudrun M. Jonsdottir, Selena Jorgensen, Jon I. Einarsson, Michael G. Muto
Publikováno v:
Obstetrics and Gynecology International, Vol 2011 (2011)
Objectives. We assess whether it is feasible for robotic hysterectomy for endometrial cancer to be less expensive to society than traditional laparoscopic hysterectomy or abdominal hysterectomy. Methods. We performed a retrospective cohort analysis o
Externí odkaz:
https://doaj.org/article/9da0a8777ef240699452c45ab3414da5
Autor:
D. Strunk, M. Lozano, D. C. Marks, Y. S. Loh, G. Gstraunthaler, H. Schennach, E. Rohde, S. Laner-Plamberger, M. Öller, J. Nystedt, R. Lotfi, M. Rojewski, H. Schrezenmeier, K. Bieback, R. Schäfer, T. Bakchoul, M. Waidmann, S. M. Jonsdottir-Buch, H. Montazeri, O. E. Sigurjonsson, P. Iudicone, D. Fioravanti, L. Pierelli, M. Introna, C. Capelli, A. Falanga, M. Takanashi, O. López-Villar, T. Burnouf, J. A. Reems, J. Pierce, A. M. Preslar, K. Schallmoser
Publikováno v:
Vox sanguinis. 113(1)
Autor:
Ingibjorg Eiriksdottir, Ronald E. Kleinman, Jona M. Jonsdottir, Inga Thorsdottir, Mary Fewtrell, Alma M. Rognvaldsdottir, Olof H Jonsdottir, Geir Gunnlaugsson, Patricia L. Hibberd
Publikováno v:
Breastfeeding Medicine. 9:196-202
Breastfeeding has several advantages for both mother and child. Lactation consultants may promote prolonged breastfeeding, but little is known about their impact on the initiation of complementary feeding.Dietary intake during the initial complementa
Autor:
Daniel F. Gudbjartsson, Michael L. Frigge, Agnar Helgason, Unnur Thorsteinsdottir, Gudrun M. Jonsdottir, Theodora Thorlacius, Aslaug Jonasdottir, Gisli Masson, Stefan T Palsson, Augustine Kong, Sverrir T. Sverrisson, Hreinn Stefansson, Gudmundur A. Hardarson, Sigurjon A. Gudjonsson, Jeffrey R. Gulcher, Kari Stefansson, Gudmar Thorleifsson
Publikováno v:
Science. 319:1398-1401
The genome-wide recombination rate varies between individuals, but the mechanism controlling this variation in humans has remained elusive. A genome-wide search identified sequence variants in the 4p16.3 region correlated with recombination rate in b
Autor:
Daniel F. Gudbjartsson, Neil E. Lamb, Jonina Jonsdottir, Sigrun Sigurdardottir, Jeffrey R. Gulcher, Augustine Kong, Gudmar Thorleifsson, Thorgeir E. Thorgeirsson, John Barnard, Kari Stefansson, Stephanie L. Sherman, Gudrun M. Jonsdottir, Bjorgvin Richardsson, Michael L. Frigge
Publikováno v:
Nature Genetics. 36:1203-1206
Intergenerational mixing of DNA through meiotic recombinations of homologous chromosomes during gametogenesis is a major event that generates diversity in the eukaryotic genome. We examined genome-wide microsatellite data for 23,066 individuals, prov
Autor:
Kristleifur Kristjansson, Laufey T. Amundadottir, Tomas Gudbjartsson, Gudrun M. Jonsdottir, Jeffrey R. Gulcher, Thora J. Jónasdóttir, Sverrir Hardarson, Asgeir Thoroddsen, Gudmundur V. Einarsson, Kjartan Magnússon, Kari Stefansson
Publikováno v:
International Journal of Cancer. 100:476-479
The etiology of RCC is incompletely understood and the inherited genetic contribution uncertain. Although there are rare mendelian forms of RCC stemming from inherited mutations, most cases are thought to be sporadic. We sought to determine the exten
Autor:
Sigurjon A. Gudjonsson, Amanda P. Henry, Eva Halapi, Carolyn Williams, Hyoung Doo Shin, David Gislason, Gudrun M. Jonsdottir, Theodora Thorlacius, Matthias Wjst, Unnur Thorsteinsdottir, Thorarinn Gislason, Soo-Taek Uh, Aslaug Jonasdottir, Janine Altmueller, Dora Ludviksdottir, Ingileif Jonsdottir, Adalbjorg Jonasdottir, Ian P. Hall, Gudmar Thorleifsson, Philip J. Thompson, Choon-Sik Park, Augustine Kong, Thorarinn Blondal, Bjorn R. Ludviksson, Kari Stefansson, Andrea Heinzmann, Hyun Sub Cheong, Klaus A. Deichmann, Hafdis T. Helgadottir, H. Marike Boezen, Dirkje S. Postma, Brynja Jonsdottir, Gerard H. Koppelman, Unnur S. Bjornsdottir, Daniel F. Gudbjartsson, Marcus Krueger
Publikováno v:
Eur. J. Hum. Genet. 18, 902-908 (2010)
European Journal of Human Genetics, 18(8), 902-908. Nature Publishing Group
European Journal of Human Genetics, 18(8), 902-908. Nature Publishing Group
A sequence variant (rs7216389-T) near the ORMDL3 gene on chromosome 17q21 was recently found to be associated with childhood asthma. We sought to evaluate the effect of rs7216389-T on asthma subphenotypes and its correlation with expression levels of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10753f579a6d29466aa935dd63a19872
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=4250
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=4250
Autor:
Lydia Pescollderungg, Wing-Yee So, Andre M. van Rij, David O. Arnar, Bjorn R. Ludviksson, Dora Ludviksdottir, Domenico Girelli, Juliana C.N. Chan, Matthias Wjst, John Beilby, Jeffrey R. Gulcher, Choon-Sik Park, Alan L. James, Daniel F. Gudbjartsson, Eva Halapi, Jennie Hui, H. Marike Boezen, Thomas Werge, Ian P. Hall, Ronald C.W. Ma, Kari Stefansson, Linda M. Rasmussen, Brynja Jonsdottir, Anna Helgadottir, Gudrun M. Jonsdottir, Nicola Martinelli, Augustine Kong, Ulla-Britt Jönsson, Marcus Krueger, Gerard H. Koppelman, David Gislason, Andrea Heinzmann, Ingileif Jonsdottir, Oliviero Olivieri, Hreinn Stefansson, Lyle J. Palmer, Dirkje S. Postma, Thorarinn Gislason, Soo-Taek Uh, Christer Janson, Pier Franco Pignatti, Nicole M. Warrington, Janine Altmüller, Unnur S. Bjornsdottir, Allan I. Levey, Valgerdur Steinthorsdottir, Carolyn Williams, Unnur Thorsteinsdottir, Amanda Wheatley, Daniel J. Rader, Muredach P. Reilly, Gudmundur Thorgeirsson, Jakob Werner Hansen, Hyoung Doo Shin, Attilio Boner, Celeste Porsbjerg, Elisabetta Trabetti, Christopher B. Granger, Vibeke Backer, Philip J. Thompson, Michael J.A. Williams, Maggie C.Y. Ng, Patrick Sulem, Arshed A. Quyyumi, Hyun Sub Cheong, Klaus A. Deichmann, Hafdis T. Helgadottir, Svati H. Shah, Giovanni Malerba, Gregory T. Jones, Gudmundur I. Eyjolfsson, Gudmar Thorleifsson, Viola Vaccarino
Publikováno v:
Nature Genetics, 41(3), 342-347. Nature Publishing Group
Eosinophils are pleiotropic multifunctional leukocytes involved in initiation and propagation of inflammatory responses and thus have important roles in the pathogenesis of inflammatory diseases. Here we describe a genome-wide association scan for se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::287698eef6bf1d823a70d7d0bd01eec9
http://hdl.handle.net/11562/327560
http://hdl.handle.net/11562/327560