Paroxysmal nocturnal hemoglobinuria: An acquired genetic disease.
about
GPI-anchor synthesis is indispensable for the germline development of the nematode Caenorhabditis elegans.The management of Cesarean delivery in a parturient with paroxysmal nocturnal hemoglobinuria complicated by severe preeclampsia.Glycation of the complement regulatory protein CD59 is a novel biomarker for glucose handling in humansParoxysmal nocturnal haemoglobinuria: nature's gene therapy?Pig-a mutation: kinetics in rat erythrocytes following exposure to five prototypical mutagens.Detection of PIGO-deficient cells using proaerolysin: a valuable tool to investigate mechanisms of mutagenesis in the DT40 cell systemPIG-A mutations in normal hematopoiesisParoxysmal nocturnal haemoglobinuria in pregnancy--not to be confused with pre-eclampsia or HELLP syndrome. Case report and literature review.Simultaneous measurement of benzo[a]pyrene-induced Pig-a and lacZ mutations, micronuclei and DNA adducts in Muta™ Mouse.Both PIGA and PIGL mutations cause GPI-a deficient isolates in the Tk6 cell line.Molecular basis for a link between complement and the vascular complications of diabetesErythrocyte-based Pig-a gene mutation assay: demonstration of cross-species potential.Sensitivity of the Pig-a assay for detecting gene mutation in rats exposed acutely to strong clastogens.Mutation analysis with random DNA identifiers (MARDI) catalogs Pig-a mutations in heterogeneous pools of CD48-deficient T cells derived from DMBA-treated rats.Development of an in vitro PIG-A gene mutation assay in human cells.The Pig-a Gene Mutation Assay in Mice and Human Cells: A Review.A population study using the human erythrocyte PIG-A assay.Report on stage III Pig-a mutation assays using benzo[a]pyrene.Monitoring humans for somatic mutation in the endogenous PIG-a gene using red blood cells.Nuclear envelope localization of PIG-B is essential for GPI-anchor synthesis in
P2860
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P2860
Paroxysmal nocturnal hemoglobinuria: An acquired genetic disease.
description
1999 nî lūn-bûn
@nan
1999 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Paroxysmal nocturnal hemoglobinuria: An acquired genetic disease.
@ast
Paroxysmal nocturnal hemoglobinuria: An acquired genetic disease.
@en
type
label
Paroxysmal nocturnal hemoglobinuria: An acquired genetic disease.
@ast
Paroxysmal nocturnal hemoglobinuria: An acquired genetic disease.
@en
prefLabel
Paroxysmal nocturnal hemoglobinuria: An acquired genetic disease.
@ast
Paroxysmal nocturnal hemoglobinuria: An acquired genetic disease.
@en
P2093
P1476
Paroxysmal nocturnal hemoglobinuria: An acquired genetic disease.
@en
P2093
Kinoshita T
Murakami Y
Nishimura J
P2860
P304
P356
10.1002/(SICI)1096-8652(199911)62:3<175::AID-AJH7>3.0.CO;2-8
P577
1999-11-01T00:00:00Z