Deleting the mouse Hsd17b1 gene results in a hypomorphic Naglu allele and a phenotype mimicking a lysosomal storage disease.

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第一作者： Heli,Jokela

第一单位： Research Centre for Integrative Physiology and Pharmacology, Institute of Biomedicine and Turku Center for Disease Modeling, University of Turku, FI-20014, Turku, Finland.

作者： Heli,Jokela ^[1] ; Janne,Hakkarainen ^[1] ; Laura,Kätkänaho ^[1] ; Pirjo,Pakarinen ^[1] ; Suvi T,Ruohonen ^[1] ; Manuel,Tena-Sempere ^[2] ; Fu-Ping,Zhang ^[1] ; Matti,Poutanen ^[3]

作者单位： Research Centre for Integrative Physiology and Pharmacology, Institute of Biomedicine and Turku Center for Disease Modeling, University of Turku, FI-20014, Turku, Finland. ^[1] Research Centre for Integrative Physiology and Pharmacology, Institute of Biomedicine and Turku Center for Disease Modeling, University of Turku, FI-20014, Turku, Finland.;Department of Cell Biology, Physiology and Immunology, and Instituto Maimónides de Investigación Biomédica de Córdoba & Hospital Universitario Reina Sofia (IMIBIC/HURS), ES-14004, Cordoba, Spain. ^[2] Research Centre for Integrative Physiology and Pharmacology, Institute of Biomedicine and Turku Center for Disease Modeling, University of Turku, FI-20014, Turku, Finland. matti.poutanen@utu.fi.;Centre for Bone and Arthritis Research at Institute of Medicine, Sahlgrenska Academy at University of Gothenburg, SE-41345, Gothenburg, Sweden. matti.poutanen@utu.fi. ^[3]