Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients.
about
Molecular mechanisms of disease-causing missense mutationsWhole-Exome Sequencing Reveals Mutations in Genes Linked to Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome in Fatal Cases of H1N1 Influenza.Modulatory effects of perforin gene dosage on pathogen-associated blood-brain barrier (BBB) disruption.Familial hemophagocytic lymphohistiocytosis: when rare diseases shed light on immune system functioning.Finding a Balance between Protection and Pathology: The Dual Role of Perforin in Human Disease.Human perforin gene variation is geographically distributed.HAX1 mutation positive children presenting with haemophagocytic lymphohistiocytosis.
P2860
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P2860
Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients.
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Structural and functional anal ...... ytosis type 2 (FHL2) patients.
@ast
Structural and functional anal ...... ytosis type 2 (FHL2) patients.
@en
type
label
Structural and functional anal ...... ytosis type 2 (FHL2) patients.
@ast
Structural and functional anal ...... ytosis type 2 (FHL2) patients.
@en
prefLabel
Structural and functional anal ...... ytosis type 2 (FHL2) patients.
@ast
Structural and functional anal ...... ytosis type 2 (FHL2) patients.
@en
P2860
P356
P1433
P1476
Structural and functional anal ...... cytosis type 2 (FHL2) patients
@en
P2093
Aytemiz Gurgey
Ozlem Keskin
P2860
P304
P356
10.1002/PRO.2265
P577
2013-06-01T00:00:00Z