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Identification of a gain-of-function STAT3 mutation (p.Y640F) in lymphocytic variant hypereosinophilic syndrome.
Walker, Sarah; Wang, Chen; Walradt, Trent; Hong, Bok Sil; Tanner, Justin R; Levinsohn, Jonathan L; Goh, Gerald; Subtil, Antonio; Lessin, Stuart R; Heymann, Warren R; Vonderheid, Eric C; King, Brett A; Lifton, Richard P; Choi, Jaehyuk.
Afiliación
  • Walker S; Dana-Farber Cancer Institute, Boston, MA;
  • Wang C; Department of Dermatology, Yale School of Medicine, New Haven, CT;
  • Walradt T; Department of Dermatology, Yale School of Medicine, New Haven, CT;
  • Hong BS; Department of Dermatology, Yale School of Medicine, New Haven, CT;
  • Tanner JR; Department of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, IL;
  • Levinsohn JL; Department of Dermatology, Yale School of Medicine, New Haven, CT;
  • Goh G; University College London Cancer Institute, London, United Kingdom;
  • Subtil A; Department of Dermatology, Yale School of Medicine, New Haven, CT;
  • Lessin SR; Division of Dermatology, Fox Chase Cancer Center, University of Pennsylvania, Philadelphia, PA;
  • Heymann WR; Division of Dermatology, Cooper Medical School of Rowan University, Camden, NJ; Department of Dermatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA;
  • Vonderheid EC; Sidney Kimmel Cancer Center, Johns Hopkins Medical Institutes, Baltimore, MD;
  • King BA; Department of Dermatology, Yale School of Medicine, New Haven, CT;
  • Lifton RP; Department of Genetics, Howard Hughes Medical Institute, and Yale Center for Mendelian Genomics, Yale School of Medicine, New Haven, CT;
  • Choi J; Department of Dermatology, Yale School of Medicine, New Haven, CT; Department of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, IL; Department of Dermatology, Department of Veterans Affairs Connecticut Healthcare, West Haven, CT; and Department of Biochemistry and Molecu
Blood ; 127(7): 948-51, 2016 Feb 18.
Article en En | MEDLINE | ID: mdl-26702067
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome Hipereosinofílico / Mutación Missense / Factor de Transcripción STAT3 Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans Idioma: En Revista: Blood Año: 2016 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome Hipereosinofílico / Mutación Missense / Factor de Transcripción STAT3 Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans Idioma: En Revista: Blood Año: 2016 Tipo del documento: Article