The molecular defect in a COOH-terminal-modified and shortened mutant of human serum albumin.
about
Point substitutions in albumin genetic variants from Asia.Hypermutability of CpG dinucleotides in the propeptide-encoding sequence of the human albumin gene.Mutations in genetic variants of human serum albumin found in Italy.Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant.A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin.High-affinity binding of laurate to naturally occurring mutants of human serum albumin and proalbumin.Post-translational arginylation of ornithine decarboxylase from rat hepatocytes.
P2860
Q30353686-D61EB292-41A5-46B3-BDF4-D739245C6024Q33592370-C36F84B5-F85C-4E8C-BF07-18BF5A97EF6AQ33887732-74CF162F-95DD-4D0E-ABA1-FF024EA1DBE8Q35576977-18821760-C9B3-42F1-B31E-A8EFEEBB9D80Q37545167-43B7BA7F-C9E0-413D-9CCC-4CD4142D0605Q38350550-17DAA032-B0F0-493A-AAE6-D89B226D1FD2Q42155450-9F5A5E07-4C27-4F18-AB62-313C3A98E5DE
P2860
The molecular defect in a COOH-terminal-modified and shortened mutant of human serum albumin.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年学术文章
@wuu
1989年学术文章
@zh-cn
1989年学术文章
@zh-hans
1989年学术文章
@zh-my
1989年学术文章
@zh-sg
1989年學術文章
@yue
1989年學術文章
@zh
1989年學術文章
@zh-hant
name
The molecular defect in a COOH ...... mutant of human serum albumin.
@en
The molecular defect in a COOH ...... mutant of human serum albumin.
@nl
type
label
The molecular defect in a COOH ...... mutant of human serum albumin.
@en
The molecular defect in a COOH ...... mutant of human serum albumin.
@nl
prefLabel
The molecular defect in a COOH ...... mutant of human serum albumin.
@en
The molecular defect in a COOH ...... mutant of human serum albumin.
@nl
P2093
P1476
The molecular defect in a COOH ...... mutant of human serum albumin
@en
P2093
Castellani AA
Galliano M
Iadarola P
Minchiotti L
P304
P407
P577
1989-02-01T00:00:00Z