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Publications by Jenn Sellers
Protein Stability and in Vivo Concentration of Missense Mutations in Phenylalanine Hydroxylase
Proteins: Structure, Function and Genetics
Biochemistry
Structural Biology
Molecular Biology
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Phosphorylation and Mutations of Ser16in Human Phenylalanine Hydroxylase
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Tetrahydrobiopterin-Responsive Hyperphenylalaninaemia Due to Homozygous Mutations in the Phenylalanine Hydroxylase Gene
European Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Missense Mutations in Dystrophin That Trigger Muscular Dystrophy Decrease Protein Stability and Lead to Cross- Aggregates
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Analysis of Phenylalanine Hydroxylase Genotypes and Hyperphenylalaninemia Phenotypes Using L-[1-13C]Phenylalanine Oxidation Rates in Vivo: A Pilot Study1
Pediatric Research
Child Health
Pediatrics
Perinatology
Caveolin-3 T78M and T78K Missense Mutations Lead to Different Phenotypes in Vivo and in Vitro
Laboratory Investigation
Forensic Medicine
Pathology
Cell Biology
Molecular Biology
Missense Mutations in DYT-TOR1A Dystonia
Neurology: Genetics
Neurology
Genetics
Stabilizing and Destabilizing Effects of Phenylalanine F F5-Phenylalanine Mutations on the Folding of a Small Protein
Tetrahydrobiopterin Responsiveness of Patients With Phenylalanine Hydroxylase Deficiency
Jornal de Pediatria
Child Health
Pediatrics
Perinatology
Structure of Full-Length Human Phenylalanine Hydroxylase in Complex With Tetrahydrobiopterin
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
