About: Murine embryonic stem cells without pig-a gene activity are competent for hematopoiesis with the PNH phenotype but not for clonal expansion.

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About: Murine embryonic stem cells without pig-a gene activity are competent for hematopoiesis with the PNH phenotype but not for clonal expansion. Goto Sponge NotDistinct Permalink

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scientific article published on September 1997

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 1997 (ast) наукова стаття, опублікована у вересні 1997 (uk) مقالة علمية نشرت في سبتمبر 1997 (ar) scientific article published on September 1997 (en)
publication date	wds:Q37371566-8A8F8EEB-0D56-4AE4-8048-4AEB991DF413
publication date	1997-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37371566-838E8554-25CA-4CDB-B86F-0CA850735BAD
language of work or name	English
cites work	wds:Q37371566-08C3E3D7-79F9-4001-B9B1-F4F95B79477F wds:Q37371566-204FA816-AF54-4563-A842-7297FF48D7CA wds:Q37371566-2C77BA33-6C40-44CA-A34C-0D4A467B17F8 wds:Q37371566-2CAF7D6B-1455-48D9-8FD5-23D02256DA2A wds:Q37371566-3731E470-3710-4479-81A8-0C8CEB8810D2 wds:Q37371566-39F53EE1-66FB-4AC9-8373-2EE4509ABBAB wds:Q37371566-3DFF82F9-06E0-48F0-9E6F-807DBE4F5C66 wds:Q37371566-4041BE1A-CF22-40B3-A529-B305C1DADED2 wds:Q37371566-46CA99A6-8A47-4E0E-9B7C-4243DF095A03 wds:Q37371566-49F4F8A6-2B65-4307-9903-C468C5289E42 wds:Q37371566-4C6D0467-EBD2-47C7-B635-6E7C92597410 wds:Q37371566-4CDA42C0-9E9C-4CD4-BFEC-26C194FA3ACC wds:Q37371566-4F06B1C5-F5B2-45A9-98C7-FDA78EFEBE37 wds:Q37371566-5938EAF6-D968-4841-9946-E9FC4573724A wds:Q37371566-5F4322D3-09B1-4F97-9A80-68B352E201B7 wds:Q37371566-60D99563-5C67-4933-AA36-2CDF09078D51 wds:Q37371566-6DDE8413-695B-4C74-B21A-0A81B46BC99B wds:Q37371566-6E8F9616-6C8A-42A9-9AF3-7667D8FE5CE3 wds:Q37371566-7F7D6572-4C76-4D2D-904C-049E0577FC72 wds:Q37371566-8D7A3AC3-1077-4FBD-9C42-43C967CB8936 wds:Q37371566-A66F4934-E555-4004-8198-D366FBFC1933 wds:Q37371566-B1EACD80-A3D4-4797-9F3A-36C726B78C5F wds:Q37371566-B23E1A61-3BD7-4C47-AC3C-0490316D9898 wds:Q37371566-B3F4EA8E-06D0-4F32-915E-923F921D2DE1 wds:Q37371566-B62FF9DA-A5B2-44D7-8E56-FD174387898C wds:Q37371566-B6F6F8CE-64D0-4739-A612-B1B2EE286B83 wds:Q37371566-C222A31C-0618-4272-8C75-86121B24E0EE wds:Q37371566-CC0B1AF2-3D82-4B5E-89A0-8E2646F1E4C7 wds:Q37371566-D14D3D8B-DB8C-4A9F-8CEB-E4D6406E676B wds:Q37371566-D3DCD159-D327-4E2F-A43C-187A87537DB4 wds:Q37371566-D6D9A284-7773-4302-8FD8-C37C1185CA04 wds:Q37371566-EBD6D867-AAAA-4F49-B620-2E1DDC8AC4F3 wds:Q37371566-EC20168A-858F-460F-962B-ED383B0AA499 wds:Q37371566-F3F98256-4C8E-4371-B8D3-93E90C84252D wds:Q37371566-F60D610F-929D-468B-B8A5-F650B10F5DAA wds:Q37371566-F9E57519-1AB4-4D25-A9EA-FB234895B683
cites work	Glycosylphosphatidylinositol-anchor-deficient mice: implications for clonal dominance of mutant cells in paroxysmal nocturnal hemoglobinuria Embryonic stem cell differentiation in vitro Multiple hematopoietic lineages develop from embryonic stem (ES) cells in culture Development of hematopoietic cells lacking transcription factor GATA-1 Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria Definitive hematopoiesis is autonomously initiated by the AGM region A knock-out model of paroxysmal nocturnal hemoglobinuria: Pig-a(-) hematopoiesis is reconstituted following intercellular transfer of GPI-anchored proteins Stromal cells negatively regulate primitive haemopoietic progenitor cell activation via a phosphatidylinositol-anchored cell adhesion/signalling mechanism Molecular cloning of murine pig-a, a gene for GPI-anchor biosynthesis, and demonstration of interspecies conservation of its structure, function, and genetic locus Compartmentalization of a haematopoietic growth factor (GM-CSF) by glycosaminoglycans in the bone marrow microenvironment Heparan sulphate bound growth factors: a mechanism for stromal cell mediated haemopoiesis Simplified mammalian DNA isolation procedure Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20. The in vitro development of blastocyst-derived embryonic stem cell lines: formation of visceral yolk sac, blood islands and myocardium Natural history of paroxysmal nocturnal hemoglobinuria PIG-A and PIG-H, which participate in glycosylphosphatidylinositol anchor biosynthesis, form a protein complex in the endoplasmic reticulum Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21 Somatic mutations in paroxysmal nocturnal hemoglobinuria: a blessing in disguise? A novel pathway for glycan assembly: biosynthesis of the glycosyl-phosphatidylinositol anchor of the trypanosome variant surface glycoprotein Ontogeny of the Haemopoietic System: Yolk Sac Origin of In Vivo and In Vitro Colony Forming Cells in the Developing Mouse Embryo Erythropoiesis and vasculogenesis in embryoid bodies lacking visceral yolk sac endoderm A spontaneous mutation characterized by chronic proliferative dermatitis in C57BL mice Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. I. The sensitivity of PNH red cells to lysis by complement and specific antibody Paroxysmal nocturnal haemoglobinuria: clinical manifestations, haematology, and nature of the disease The aplastic anaemia--paroxysmal nocturnal haemoglobinuria syndrome Phospholipase C release of basic fibroblast growth factor from human bone marrow cultures as a biologically active complex with a phosphatidylinositol-anchored heparan sulfate proteoglycan Phosphatidylinositol-linked proteins and paroxysmal nocturnal hemoglobinuria Defective glycosyl phosphatidylinositol anchor synthesis and paroxysmal nocturnal hemoglobinuria. Paroxysmal nocturnal haemoglobinuria The molecular basis of paroxysmal nocturnal hemoglobinuria Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria Riddle: what do aplastic anemia, paroxysmal nocturnal hemoglobinuria (PNH) and "hypoplastic" leukemia have in common? The dual pathogenesis of paroxysmal nocturnal hemoglobinuria. A debilitating fatal murine dermatitis. Clonal hematopoiesis in patients with acquired aplastic anemia
author name string	wds:Q37371566-137F6377-B17F-413D-8665-311C3F826D1E wds:Q37371566-862AB9AB-E1AB-450F-84FC-4B36F64A4928 wds:Q37371566-9995587D-D0AA-4306-B784-1607D2DF24DF wds:Q37371566-C352BD4A-D215-41FB-890A-3DD50712A7AA wds:Q37371566-FD30AD2B-2143-4F45-90B1-9FBF9E818216
author name string	P P Pandolfi V Soares

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