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Latest publications

Quality of life and visual perception in anophthalmic/microphthalmic children treated with ocular prosthesis
Beatrice Casslén, Ylva Jugård, R Taha Najim, Marie Odersjö, Alexandra Topa et al.
Svenska Ögonläkarföreningens (SÖF) årsmöte, Stockholm, Sverige, 8-10 okt, 2018, Poster 2018
Poster

BATLAS: Deconvoluting Brown Adipose Tissue
A. Perdikari, G. G. Leparc, M. Balaz, N. D. Pires, Martin Lidell et al.
Cell Reports, Journal article 2018
Journal article

STK25 regulates oxidative capacity and metabolic efficiency in adipose tissue
Silva Sütt, Emmelie Cansby, A. Paul, M. Amrutkar, Esther Nuñez Durán et al.
Journal of Endocrinology, Journal article 2018
Journal article

Molecular mechanisms and therapeutic targets in neuroblastoma
J. I. Johnsen, C. Dyberg, Susanne Fransson, M. Wickstrom, American Journal Of Pathology V. P. Stle Vp
Pharmacological Research, Journal article 2018
Journal article

Showing 31 - 40 of 317

2016

The ALK inhibitor PF-06463922 is effective as a single agent in neuroblastoma driven by expression of ALK and MYCN
Jikui Guan, E. R. Tucker, Haiying Wang, Damini Chand, L. S. Danielson et al.
DMM Disease Models and Mechanisms, Journal article 2016
Journal article

A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts
C. M. Middeldorp, A. R. Hammerschlag, K. G. Ouwens, M. M. Groen-Blokhuis, B. St. Pourcain et al.
Journal of the American Academy of Child and Adolescent Psychiatry, Journal article 2016
Journal article

Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
SL Pulit, PF McArdle, Q Wong, R Malik, K Gwinn et al.
The Lancet. Neurology, Journal article 2016
Journal article

A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.
Mariona Bustamante, Marie Standl, Quique Bassat, Natalia Vilor-Tejedor, Carolina Medina-Gomez et al.
Human molecular genetics, Journal article 2016
Journal article

Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population
K. Lagerstedt-Robinson, Anna Rohlin, C. Aravidis, B. Melin, Margareta Nordling et al.
Oncology Reports, Journal article 2016
Journal article

GREM1 and POLE variants in hereditary colorectal cancer syndromes
Anna Rohlin, Frida Eiengård, Ulf Lundstam, Theofanis Zagoras, Staffan Nilsson et al.
Genes, Chromosomes and Cancer, Journal article 2016
Journal article

Showing 31 - 40 of 317

Page Manager: Webmaster|Last update: 9/12/2012
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