Additive Manufacturing of Cu Using Graphene-Oxide-Treated Powder

por Tidén, Simon, Taher, Mamoun, Vennström, Marie, Jansson, Ulf
Publicado 2023

A near-wearless and extremely long lifetime amorphous carbon film under high vacuum

por Wang, Liping, Zhang, Renhui, Jansson, Ulf, Nedfors, Nils
Publicado 2015

Superior hydrogen storage in high entropy alloys

por Sahlberg, Martin, Karlsson, Dennis, Zlotea, Claudia, Jansson, Ulf
Publicado 2016

Potential blood-based markers of celiac disease

por Bragde, Hanna, Jansson, Ulf, Fredrikson, Mats, Grodzinsky, Ewa, Söderman, Jan
Publicado 2014

Celiac disease biomarkers identified by transcriptome analysis of small intestinal biopsies

por Bragde, Hanna, Jansson, Ulf, Fredrikson, Mats, Grodzinsky, Ewa, Söderman, Jan
Publicado 2018

Prophylactic anticoagulants to prevent venous thromboembolism in patients with nephrotic syndrome—A retrospective observational study

por Welander, Frida, Holmberg, Henrik, Dimény, Emöke, Jansson, Ulf, Själander, Anders
Publicado 2021

Characterisation of gene and pathway expression in stabilised blood from children with coeliac disease

por Bragde, Hanna Gustafsson, Jansson, Ulf, Fredrikson, Mats, Grodzinsky, Ewa, Söderman, Jan
Publicado 2020

Convective Flow Redistribution of Oxygen by Laser Melting of a Zr-Based Amorphous Alloy

por Goetz, Inga K., Pacheco, Victor, Hassila, Carl J., Jansson, Ulf, Schneider, Jochen M., Hans, Marcus
Publicado 2023

Synthesis and Characterisation of Nanocomposite Mo-Fe-B Thin Films Deposited by Magnetron Sputtering

por Malinovskis, Paulius, Fritze, Stefan, Palisaitis, Justinas, Lewin, Erik, Patscheider, Jörg, Persson, Per O. Å., Jansson, Ulf
Publicado 2021

Influence of Deposition Temperature on the Phase Evolution of HfNbTiVZr High-Entropy Thin Films

por Fritze, Stefan, Koller, Christian M., von Fieandt, Linus, Malinovskis, Paulius, Johansson, Kristina, Lewin, Erik, Mayrhofer, Paul H., Jansson, Ulf
Publicado 2019

Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 gen...

por Olsson, K. Sigvard, Wålinder, Olof, Jansson, Ulf, Wilbe, Maria, Bondeson, Marie-Louise, Stattin, Eva-Lena, Raha-Chowdhury, Ruma, Williams, Roger
Publicado 2017