Inherited human complement C3 deficiency. An amino acid substitution in the beta-chain (ASP549 to ASN) impairs C3 secretion.
about
Screening for C3 deficiency in newborns using microarrays.Urinary proteome analysis of irritable bowel syndrome (IBS) symptom subgroups.Intracellular complement activation sustains T cell homeostasis and mediates effector differentiation.A C3(H20) recycling pathway is a component of the intracellular complement system.New functional and structural insights from updated mutational databases for complement factor H, Factor I, membrane cofactor protein and C3.
P2860
Inherited human complement C3 deficiency. An amino acid substitution in the beta-chain (ASP549 to ASN) impairs C3 secretion.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Inherited human complement C3 ...... to ASN) impairs C3 secretion.
@ast
Inherited human complement C3 ...... to ASN) impairs C3 secretion.
@en
type
label
Inherited human complement C3 ...... to ASN) impairs C3 secretion.
@ast
Inherited human complement C3 ...... to ASN) impairs C3 secretion.
@en
prefLabel
Inherited human complement C3 ...... to ASN) impairs C3 secretion.
@ast
Inherited human complement C3 ...... to ASN) impairs C3 secretion.
@en
P2093
P1476
Inherited human complement C3 ...... to ASN) impairs C3 secretion.
@en
P2093
P304
28494-28499
P407
P577
1994-11-01T00:00:00Z