Functional characterization of missense mutations in severe methylenetetrahydrofolate reductase deficiency using a human expression system.
about
Clinical or ATPase domain mutations in ABCD4 disrupt the interaction between the vitamin B12-trafficking proteins ABCD4 and LMBD1.The methylenetetrahydrofolate reductase c.c.677 C>T and c.c.1298 A>C polymorphisms in reproductive failures: Experience from an RSA and RIF study on a Polish population.Structural basis for the regulation of human 5,10-methylenetetrahydrofolate reductase by phosphorylation and S-adenosylmethionine inhibition.
P2860
Functional characterization of missense mutations in severe methylenetetrahydrofolate reductase deficiency using a human expression system.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
@wuu
2016年学术文章
@zh
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh-hant
name
Functional characterization of ...... ing a human expression system.
@en
Functional characterization of ...... ing a human expression system.
@nl
type
label
Functional characterization of ...... ing a human expression system.
@en
Functional characterization of ...... ing a human expression system.
@nl
prefLabel
Functional characterization of ...... ing a human expression system.
@en
Functional characterization of ...... ing a human expression system.
@nl
P2093
P2860
P1476
Functional characterization of ...... sing a human expression system
@en
P2093
Alexandra Schäfer
Brian Fowler
Dorothea Heuberger
Patricie Burda
Terttu Suormala
P2860
P2888
P304
P356
10.1007/S10545-016-9987-0
P577
2016-10-14T00:00:00Z