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| 28005/34347 | US=47 / Clín/Medica Labbozzetta M, Notarbartolo M, Poma P, Giannitrapani L, Cervello M, Montalto G, D'Alessandro N. Significance of autologous interleukin-6 production in the HA22T/VGH cell model of hepatocellular carcinoma. In: Bradlow KL, Carruba G. Estrogens and human diseases. Boston: Blackwell, 2006. p. 268-75. ISBN 978-1-57331-699-5. CARCINOMA HEPATOCELULAR; INTERLEUCINA-6; CIRCUITO ESTIMULANTE DO CRESCIMENTO CELULAR AUTOCRINE; NF-KB |
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| 28012/34347 | US=47 / Clín/Medica Cavalieri E, Rogan E. Catechol quinones of estrogens in the initiation of breast, prostate, and other human cancers. In: Bradlow KL, Carruba G. Estrogens and human diseases. Boston: Blackwell, 2006. p. 286-301. ISBN 978-1-57331-699-5. METABOLISMO DOS ESTROGENIOS; CATECOL QUINOSES; GENOTOXICIDADE DE ESTROGENOS; DEPURINATING ADUTOS DE DNA; MUTAGENICIDADE DE ESTROGENOS; BIOMARCADORES DE RISCO DE CANCER |
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| 28017/34347 | US=47 / Clín/Medica Ragonese P, D'Amélio M, Savettieri G. Implications for estrogens in Parkinson's disease: an epidemiological approach. In: Bradlow KL, Carruba G. Estrogens and human diseases. Boston: Blackwell, 2006. p. 373-82. ISBN 978-1-57331-699-5. DOENCA DE PARKINSON; EPIDEMIOLOGIA; FATORES DE RISCO; VIDA FERTIL; IDADE DA MENOPAUSA; MULHERES |
| 28018/34347 | US=47 / Clín/Medica Pagnucco G, Giambanco C, Gervasi F. The role of flow cytometric immunophenotyping in myelodysplastic syndromes. In: Bradlow KL, Carruba G. Estrogens and human diseases. Boston: Blackwell, 2006. p. 383-94. ISBN 978-1-57331-699-5. SINDROME MIELODISPLASICA; CITOMETRIA DE FLUXO; IMUNOFENOTIPAGEM; IMUNOFENOTIPAGEM POR CITOMETRIA DE FLUXO; SINDROMES MIELODISPLASICAS |
| 28019/34347 | US=47 / Clín/Medica Bernasconi P, Boni M, Cavigliano PM, Calatroni S, Giardini I, Rocca B, Zappatore R, Dambruoso I, Caresana M. Clinical relevance of cytogenetics in myelodysplastic syndromes. In: Bradlow KL, Carruba G. Estrogens and human diseases. Boston: Blackwell, 2006. p. 395-410. ISBN 978-1-57331-699-5. SINDROMES MIELODISPLASICAS; SUBTIPO FAB; ANORMALIDADES CROMOSSOMICAS; HIBRIDACAO IN SITU FLUORESCENTE |
| 28020/34347 | US=47 / Clín/Medica Cilloni D, Messa E, Messa F, Carturan S, Defilippi I, Arruga F, Rosso V, Catalano R, Bracco E, Nicoli P, Saglio G. Genetics abnormalities as targets for molecular therapies in myelodysplastic syndromes. In: Bradlow KL, Carruba G. Estrogens and human diseases. Boston: Blackwell, 2006. p. 411-23. ISBN 978-1-57331-699-5. DEFEITOS GENETICOS; SINDROMES MIELODISPLASICAS; TERAPIA MOLECULAR; WT1; EV11; TIROSINA CINASE |