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Publications by Vidar Martin Steen
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
Lipid-Lowering Effects of Tetradecylthioacetic Acid in Antipsychotic-Exposed, Female Rats: Challenges With Long-Term Treatment
PLoS ONE
Multidisciplinary
Related publications
Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome
American Journal of Human Genetics
Genetics
Accumulation of Mutant Lamin a Causes Progressive Changes in Nuclear Architecture in Hutchinson-Gilford Progeria Syndrome
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
The Activating C-Type Lectin-Like Receptor NKp65 Signals Through a Hemi-Immunoreceptor Tyrosine-Based Activation Motif (hemITAM) and Spleen Tyrosine Kinase (Syk)
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Somatic PDGFRB Activating Variants in Fusiform Cerebral Aneurysms
American Journal of Human Genetics
Genetics
Involvement of Tyrosine Kinase and Protein Kinase C in Platelet-Activating-Factor-Inducedc-Fosgene Expression in A-431 Cells
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
FLT3 (FMS-like Tyrosine Kinase 3)
Atlas of Genetics and Cytogenetics in Oncology and Haematology
Cancer Research
Oncology
Genetics
Hematology
Familial Scaphocephaly Syndrome Caused by a Novel Mutation in the FGFR2 Tyrosine Kinase Domain
Journal of Medical Genetics
Genetics
Ranolazine Treatment for Refractory Angina in a Patient With Hutchinson-Gilford Progeria Syndrome and End Stage Aortic Stenosis
Cardiogenetics
A Syndrome Resembling Progeria: A Review of Two Cases
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
