NPC1 defect results in abnormal platelet formation and function: studies in Niemann-Pick disease type C1 patients and zebrafish.
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Genetic dissection of a cell-autonomous neurodegenerative disorder: lessons learned from mouse models of Niemann-Pick disease type CBiomarkers for disease progression and AAV therapeutic efficacy in feline Sandhoff diseaseA dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies.Modeling Niemann-Pick disease type C1 in zebrafish: a robust platform for screening of candidate therapeutic compounds
P2860
NPC1 defect results in abnormal platelet formation and function: studies in Niemann-Pick disease type C1 patients and zebrafish.
description
2012 nî lūn-bûn
@nan
2012 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
NPC1 defect results in abnorma ...... ype C1 patients and zebrafish.
@ast
NPC1 defect results in abnorma ...... ype C1 patients and zebrafish.
@en
type
label
NPC1 defect results in abnorma ...... ype C1 patients and zebrafish.
@ast
NPC1 defect results in abnorma ...... ype C1 patients and zebrafish.
@en
prefLabel
NPC1 defect results in abnorma ...... ype C1 patients and zebrafish.
@ast
NPC1 defect results in abnorma ...... ype C1 patients and zebrafish.
@en
P2093
P2860
P356
P1476
NPC1 defect results in abnorma ...... ype C1 patients and zebrafish.
@en
P2093
Chantal Thys
Chris Van Geet
Christine Wittevrongel
Elisa Decuyper
Gwenny Vandeweeghde
Jaak Jaeken
Peter Leemans
Rita De Vos
Sophie Louwette
P2860
P356
10.1093/HMG/DDS401
P577
2012-09-24T00:00:00Z