Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Soley Bjornsdottir"'
Autor:
Thorbjorg Einarsdottir, Thorunn Soley Bjornsdottir, Heida Maria Sigurdardottir, Elisabet Einarsdottir
Publikováno v:
Fish & Shellfish Immunology. 91:469
Winter ulcer disease, caused by Moritella viscosa, is a significant problem in cold water salmonid farming, although the bacterium can infect and cause disease in a number of other fish species, such as lumpfish (Cyclopterus lumpus). Lumpfish are use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67952767b606695dd7c14ef5432eab1a
https://doi.org/10.1016/j.fsi.2019.04.283
https://doi.org/10.1016/j.fsi.2019.04.283
Autor:
Gardar Johannesson, Greg Lemke, Michael L. Frigge, Daniel F. Gudbjartsson, Donna Lai, Acuna Gonzalo, Vala G. Gudnadottir, Andres Ingason, Valgerdur Steinthorsdottir, Sigmundur Sigfusson, Hronn Hardardottir, Helgi Jonsson, Jesus Sainz, Engilbert Sigurdsson, Mark E. Gurney, Thordur Sigmundsson, Birgitta Birgisdottir, Brynjolfur Ingvarsson, Omar Ivarsson, Steinunn Gunnarsdottir, Jeffrey R. Gulcher, Hannes Petursson, Kari Stefansson, Shyamali Ghosh, Augustine Kong, Andrei Manolescu, Vincent Mutel, Hreinn Stefansson, Mingdong Zhou, J Brynjolfsson, Elsa Gudmundsdottir, Thomas T. Chou, Omar Hjaltason, Asgeir Björnsson, Soley Bjornsdottir, Thorkell Andresson, Daniela Brunner, Richard P. Harvey
Publikováno v:
The American Journal of Human Genetics. 71(4):877-892
The cause of schizophrenia is unknown, but it has a significant genetic component. Pharmacologic studies, studies of gene expression in man, and studies of mouse mutants suggest involvement of glutamate and dopamine neurotransmitter systems. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a74258cbdced69dbb5412cf615d7ef6
Autor:
Shyamali Ghosh, Anne Charlotte Fasquel, Birgitta Birgisdottir, Olafur Olafsson, Hreinn Stefansson, Soley Bjornsdottir, Valgerdur Steinthorsdottir, Kari Stefansson, Jeffrey R. Gulcher
Publikováno v:
Gene. 342(1)
The large neuregulin 1 gene ( NRG1 ) has been mapped to a 1.125 Mb region on chromosome 8p11–21. Three major forms of NRG1 (types I–III), all with distinct amino-termini encoded by unique 5′-exons, have been described. We report here the discov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58d5f816b5b3e490026f03b4916096c3
https://pubmed.ncbi.nlm.nih.gov/15527969
https://pubmed.ncbi.nlm.nih.gov/15527969
Autor:
Anna S. Einarsdóttir, Sigurthoardóttir S, Hreinn Stefansson, Einarsdóttir Ie, Gulcher, Baldursson S, Benedickz J, Mike Frigge, Palmi V. Jonsson, Finnbogi Jakobsson, Soffia M. Hrafnkelsdottir, Ari Karason, Kristleifur Kristjansson, Soley Bjornsdottir, Augustine Kong, Kari Stefansson
Publikováno v:
Nature genetics. 17(1)
Essential tremor (ET), the most common movement disorder in humans, appears to be inherited as an autosomal dominant trait in many families1,2. The familial form is called familial essential tremor (FET), which seems similar to sporadic essential tre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49868ecd2fd3da5ea818a0320b2f9283
https://pubmed.ncbi.nlm.nih.gov/11101830
https://pubmed.ncbi.nlm.nih.gov/11101830