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Details on Person Pediatric mastocytosis is a clonal disease associated with D816V and other activating c-KIT mutations
| Class:Id | LiteratureReference:9679981 |
| _displayName | Pediatric mastocytosis is a clonal disease associated with D816V and other activating c-KIT mutations |
| _timestamp | 2020-03-25 20:46:40 |
| author | [Person:5228845] Bodemer, Christine [Person:2077508] Hermine, O [Person:9679971] Palmérini, Fabienne [Person:6789439] Yang, Ying [Person:9679972] Grandpeix-Guyodo, Catherine [Person:2077515] Leventhal, PS [Person:5675668] Hadj-Rabia, Smail [Person:9679982] Nasca, Laurent [Person:9679968] Georgin-Lavialle, Sophie [Person:9679969] Cohen-Akenine, Annick [Person:9679973] Launay, Jean-Marie [Person:9679978] Barete, Stéphane [Person:9679985] Feger, Frédéric [Person:2077488] Arock, M [Person:9679977] Catteau, Benoît [Person:9679984] Sans, Beatrix [Person:9679979] Stalder, Jean François [Person:9679966] Skowron, Francois [Person:9679967] Thomas, Luc [Person:9679974] Lorette, Gérard [Person:9679975] Plantin, Patrice [Person:9679970] Bordigoni, Pierre [Person:9679983] Lortholary, Olivier [Person:5675649] de Prost, Yves [Person:2077525] Moussy, A [Person:9679976] Sobol, Hagay [Person:2077500] Dubreuil, P |
| created | [InstanceEdit:9679980] Rothfels, Karen, 2020-03-25 |
| journal | J. Invest. Dermatol. |
| pages | 804-15 |
| pubMedIdentifier | 19865100 |
| title | Pediatric mastocytosis is a clonal disease associated with D816V and other activating c-KIT mutations |
| volume | 130 |
| year | 2010 |
| (literatureReference) | [Reaction:9680242] Ligand-independent dimerization of KIT extracellular domain mutants [Homo sapiens] [Reaction:9680248] Phosphorylation of extracellular domain KIT mutants [Homo sapiens] [EntityWithAccessionedSequence:9680030] KIT A502_Y503dup [plasma membrane] [Homo sapiens] [EntityWithAccessionedSequence:9680045] KIT C443Y [plasma membrane] [Homo sapiens] [EntityWithAccessionedSequence:9680090] KIT S476I [plasma membrane] [Homo sapiens] [EntityWithAccessionedSequence:9680110] KIT T417_D419delinsY [plasma membrane] [Homo sapiens] [EntityWithAccessionedSequence:9680120] p-7Y-KIT A502_Y503dup [plasma membrane] [Homo sapiens] [EntityWithAccessionedSequence:9680138] p7Y-KIT C443Y [plasma membrane] [Homo sapiens] [EntityWithAccessionedSequence:9680156] p7Y-KIT S476I [plasma membrane] [Homo sapiens] [EntityWithAccessionedSequence:9680165] p-7Y-KIT T417_D419delinsY [plasma membrane] [Homo sapiens] |
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No pathways have been reviewed or authored by Pediatric mastocytosis is a clonal disease associated with D816V and other activating c-KIT mutations (9679981)