Associated Papers
The co-chaperone DNAJA2 buffers proteasomal degradation of cytosolic proteins with missense mutations.
Baker HA et al.
Journal of Cell Science, 2025
A rare case of complete human erythrocyte AMP deaminase deficiency due to two novel missense mutations in AMPD3.
Yamada Y et al.
Human Mutation, 2001
Erythrocyte amp deaminase deficiency in Japanese: a compound heterozygote responsible for the complete deficiency.
Yamada Y et al.
Advances in Experimental Medicine and Biology, 2000
Gene mutations responsible for human erythrocyte AMP deaminase deficiency in Poles.
Yamada Y et al.
Advances in Experimental Medicine and Biology, 1998
Molecular basis for human erythrocyte AMP deaminase deficiency: screening for the major point mutation and identification of other mutations.
Yamada Y et al.
Human Molecular Genetics, 1994
Gene mutations for human erythrocyte AMP deaminase deficiency.
Yamada Y et al.
Advances in Experimental Medicine and Biology, 1994
Select a paper to view details