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scopus(7)
Concurrent Mutations in SF3B1 and PHF6 in Myeloid Neoplasms
ArticleAbstract: It has been reported that gene mutations in SF3B1 and PHF6 are mutually exclusive. However, this obsPalabras claves:myeloid neoplasms, PHF6, SF3B1Autores:Chien K.S., Garcia-Manero G., Jelloul F.Z., Kanagal-Shamanna R., Loghavi S., Luthra R., Medeiros L.J., Ok C.Y., Patel K.P., Routbort M.J., Sofía A. Garcés, Yin C.C., Zuo Z.Fuentes:scopusCyclin D1 expression in Rosai-Dorfman disease: a near-constant finding that is not invariably associated with mitogen-activated protein kinase/extracellular signal–regulated kinase pathway activation
ArticleAbstract: Activating mutations in the mitogen-activated protein kinase/extracellular signal–regulated kinase (Palabras claves:BCL-2, Cyclin D1, Ki-67, MAPK/ERK, p-ERK, pathogenesis, Rosai-dorfman diseaseAutores:Bhattacharjee M.B., Coelho Siqueira S.A., Cuglievan B., Garces J.C., Jelloul F.Z., Khoury J.D., Li S., Marques-Piubelli M.L., Medeiros L.J., Medina A.M., Miranda R.N., Saluja K., Sofía A. Garcés, Sriganeshan V., Thakral B., Xu J., Yin C.C.Fuentes:scopusETNK1 mutation occurs in a wide spectrum of myeloid neoplasms and is not specific for atypical chronic myeloid leukemia
ArticleAbstract: Background: ETNK1 mutation has been suggested as a useful tool to support the diagnosis of atypicalPalabras claves:acute myeloid leukemia (AML), ethanolamine kinase 1 (ETNK1), myelodysplastic syndrome (MDS), myelodysplastic/myeloproliferative neoplasm (MDS/MPN), myeloproliferative neoplasm (MPN)Autores:Jabbour E.J., Jelloul F.Z., Li N., Li S., Medeiros L.J., Ok C.Y., Patel K.P., Rehder C., Shuai W., Sofía A. Garcés, Wang W., Xu J., Yin C.C., You M.J., Zuo Z.Fuentes:scopusNon-coding NOTCH1 mutations in chronic lymphocytic leukemia negatively impact prognosis
OtherAbstract:Palabras claves:Autores:Bassett R.L., Floyd K., Jain N., Jelloul F.Z., Kanagal-Shamanna R., Loghavi S., Luthra R., Medeiros L.J., Ok C.Y., Patel K.P., Routbort M.J., Sofía A. Garcés, Thompson P.A., Wang P., Wierda W.G., Yang R.K., Yin C.C., Zuo Z.Fuentes:scopusLandscape of NOTCH1 mutations and co-occurring biomarker alterations in chronic lymphocytic leukemia
ArticleAbstract: NOTCH1 is one of the most frequently mutated genes in chronic lymphocytic leukemia and has emerged aPalabras claves:Chronic lymphocytic leukemia, Coding, Non-coding, NOTCH1 mutationsAutores:Bassett R.L., Floyd K., Jain N., Jelloul F.Z., Kanagal-Shamanna R., Loghavi S., Luthra R., Medeiros L.J., Ok C.Y., Patel K.P., Routbort M.J., Sofía A. Garcés, Thompson P.A., Wierda W.G., Yang R.K., Yin C.C., Zuo Z.Fuentes:scopusMUM1/IRF4 is Highly Expressed in Dermatopathic Lymphadenopathy: Potential Utility in Diagnosis and Differential Diagnosis
ArticleAbstract: Dermatopathic lymphadenopathy (DL) is a distinctive type of lymph node hyperplasia that typically ocPalabras claves:Dendritic cells, dermatopathic lymphadenopathy, Langerhans cell histiocytosis, MUM1/IRF4Autores:Cuglievan B., Garces J.C., Jelloul F.Z., Khoury J.D., Li S., Medeiros L.J., Medina A.M., Miranda R.N., Rudzki Z., Sofía A. Garcés, Sriganeshan V., Tang G., Thakral B., Xu J., Yin C.C.Fuentes:scopusWell-differentiated systemic mastocytosis with associated myeloid sarcoma and myelodysplastic syndrome: Diagnostic challenges of an underrecognized entity
OtherAbstract:Palabras claves:Autores:Bueso-Ramos C., El Hussein S., Fang H., Hu S., Jelloul F.Z., Medeiros L.J., Muzzafar T., Sofía A. Garcés, Wang S.A.Fuentes:scopus