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- 2017
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Mark
A low-frequency inactivating AKT2 variant enriched in the finnish population is associated with fasting insulin levels and type 2 diabetes risk
- Contribution to journal › Article
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Mark
Systemic frequencies of T helper 1 and T helper 17 cells in patients with age-related macular degeneration : A case-control study
- Contribution to journal › Article
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Mark
Do group dynamics affect colour morph clines during a range shift?
- Contribution to journal › Article
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Mark
Acute doses of caffeine shift nervous system cell expression profiles toward promotion of neuronal projection growth
- Contribution to journal › Article
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Mark
Knee internal contact force in a varus malaligned phenotype in knee osteoarthritis (KOA)
- Contribution to journal › Article
- 2016
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Mark
Phenotype and genotype in 52 patients with Rubinstein–Taybi syndrome caused by EP300 mutations
- Contribution to journal › Article
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Mark
Heterozygous PINK1 p.G411S mutation increases risk for Parkinson's disease (PD)
(2016) 20th International Congress of Parkinson's Disease and Movement Disorders In Movement Disorders 31(Suppl. S2). p.282-282
- Contribution to journal › Published meeting abstract
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Mark
CCoAOMT Down-Regulation Activates Anthocyanin Biosynthesis in Petunia
- Contribution to journal › Article
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Mark
Synovitis and radiographic progression in non-erosive and erosive hand osteoarthritis : is erosive hand osteoarthritis a separate inflammatory phenotype?
- Contribution to journal › Article
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Mark
Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study
- Contribution to journal › Article
