FLI1 monoallelic expression combined with its hemizygous loss underlies Paris-Trousseau/Jacobsen thrombopenia

Paris-Trousseau syndrome (PTS; also known as Jacobsen syndrome) is characterized by several congenital anomalies including a dysmegakaryopoiesis with two morphologically distinct populations of megakaryocytes (MKs). PTS patients harbor deletions on the long arm of chromosome 11, including the FLI1 g...

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Bibliografski detalji
Glavni autori: Raslova, Hana, Komura, Emiko, Le Couédic, Jean Pierre, Larbret, Frederic, Debili, Najet, Feunteun, Jean, Danos, Olivier, Albagli, Olivier, Vainchenker, William, Favier, Rémi
Format: Artigo
Jezik:Inglês
Izdano: American Society for Clinical Investigation 2004
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Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC437972/
https://ncbi.nlm.nih.gov/pubmed/15232614
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200421197
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