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Publications by Ove Bruland

Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome

American Journal of Human Genetics
Genetics
2018English

Evidence for Anticipation in Beckwith–Wiedemann Syndrome

European Journal of Human Genetics
Genetics
2013English

Development of Congenital Stromal Corneal Dystrophy Is Dependent on Export and Extracellular Deposition of Truncated Decorin

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2015English

A Tyrosine Kinase-Activating Variant Asn666Ser in PDGFRB Causes a Progeria-Like Condition in the Severe End of Penttinen Syndrome

European Journal of Human Genetics
Genetics
2018English

S100A16 Promotes Differentiation and Contributes to a Less Aggressive Tumor Phenotype in Oral Squamous Cell Carcinoma

BMC Cancer
Cancer ResearchOncologyGenetics
2015English

GBA2 Mutations Cause a Marinesco-Sjögren-Like Syndrome: Genetic and Biochemical Studies

PLoS ONE
Multidisciplinary
2017English

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