Pages that link to "Q34556955"

The following pages link to Phenylalanine hydroxylase misfolding and pharmacological chaperones. (Q34556955):

Displaying 21 items.

• Pharmacological chaperoning: a primer on mechanism and pharmacology (Q27001695) (← links)
• Protein homeostasis disorders of key enzymes of amino acids metabolism: mutation-induced protein kinetic destabilization and new therapeutic strategies. (Q30355120) (← links)
• A commentary on the utility of a new L-DOPA-responsive dystonia mouse model (Q36817843) (← links)
• Protein homeostasis defects of alanine-glyoxylate aminotransferase: new therapeutic strategies in primary hyperoxaluria type I. (Q38129886) (← links)
• Innovative strategies to treat protein misfolding in inborn errors of metabolism: pharmacological chaperones and proteostasis regulators. (Q38200933) (← links)
• Molecular genetics and diagnosis of phenylketonuria: state of the art. (Q38216515) (← links)
• Protein Stability, Folding and Misfolding in Human PGK1 Deficiency. (Q38223684) (← links)
• Genetics of Phenylketonuria: Then and Now. (Q38751728) (← links)
• Tyrosine and tryptophan hydroxylases as therapeutic targets in human disease (Q39038494) (← links)
• Structural basis for ligand-dependent dimerization of phenylalanine hydroxylase regulatory domain (Q39859787) (← links)
• Conformational stabilization as a strategy to prevent nucleophosmin mislocalization in leukemia (Q42635149) (← links)
• Natural (and Unnatural) Small Molecules as Pharmacological Chaperones and Inhibitors in Cancer. (Q47673940) (← links)
• The Effects of PMM2-CDG-Causing Mutations on the Folding, Activity, and Stability of the PMM2 Protein (Q50444478) (← links)
• Co-expression of phenylalanine hydroxylase variants and effects of interallelic complementation on in vitro enzyme activity and genotype-phenotype correlation. (Q53299118) (← links)
• Generation of urine-derived induced pluripotent stem cells from a patient with phenylketonuria. (Q55187124) (← links)
• Identification of 34 novel mutations in propionic acidemia: Functional characterization of missense variants and phenotype associations (Q57069344) (← links)
• Phenylalanine iminoboronates as new phenylalanine hydroxylase modulators (Q57976153) (← links)
• The quaternary structure of human tyrosine hydroxylase: effects of dystonia-associated missense variants on oligomeric state and enzyme activity (Q58566459) (← links)
• EU-OPENSCREEN: A Novel Collaborative Approach to Facilitate Chemical Biology (Q63349863) (← links)
• Toward mechanistic models for genotype-phenotype correlations in phenylketonuria using protein stability calculations (Q91069776) (← links)
• A Pharmacological Chaperone Therapy for Acute Intermittent Porphyria (Q91765565) (← links)