Associated Papers
Current Understanding of DDX41 Mutations in Myeloid Neoplasms.
Kim K et al.
Cancers, 2023
Genotypes and Phenotypes of MEF2C Haploinsufficiency Syndrome: New Cases and Novel Point Mutations.
Wan L et al.
Frontiers in Pediatrics, 2021
Nucleotide variation of sFRP5 gene is not associated with obesity in children and adolescents.
Van Camp JK et al.
Molecular Biology Reports, 2016
Conserved glycine residues in the fusion peptide of the paramyxovirus fusion protein regulate activation of the native state.
Russell CJ et al.
Journal of Virology, 2004
O-helix mutant T664P of Thermus aquaticus DNA polymerase I: altered catalytic properties for incorporation of incorrect nucleotides but not correct nucleotides.
Tosaka A et al.
The Journal of Biological Chemistry, 2001
Biochemical analysis of mutations in palmitoyl-protein thioesterase causing infantile and late-onset forms of neuronal ceroid lipofuscinosis.
Das AK et al.
Human Molecular Genetics, 2001
A novel nucleolar G-protein conserved in eukaryotes.
Park JH et al.
Journal of Cell Science, 2001
Nephrogenic diabetes insipidus: functional analysis of new AVPR2 mutations identified in Italian families.
Albertazzi E et al.
Journal of the American Society of Nephrology : Jasn, 2000
Mutant alleles of the MRS2 gene of yeast nuclear DNA suppress mutations in the catalytic core of a mitochondrial group II intron.
Schmidt U et al.
Journal of Molecular Biology, 1998
A glycine to alanine substitution in the paramyxovirus SV5 fusion peptide increases the initial rate of fusion.
Bagai S et al.
Virology, 1997
Molecular analysis of mutated thyroid peroxidase detected in patients with total iodide organification defects.
Bikker H et al.
The Journal of Clinical Endocrinology and Metabolism, 1997
Studies on the fusion peptide of a paramyxovirus fusion glycoprotein: roles of conserved residues in cell fusion.
Horvath CM et al.
Journal of Virology, 1992
Select a paper to view details