Titlebook: Epithelial Tumors of the Thymus; Pathology, Biology, Alexander Marx,Hans Konrad Müller-Hermelink Book 1997 Springer Science+Business Media

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書目名稱Epithelial Tumors of the Thymus影響因子(影響力)




書目名稱Epithelial Tumors of the Thymus影響因子(影響力)學(xué)科排名




書目名稱Epithelial Tumors of the Thymus網(wǎng)絡(luò)公開度




書目名稱Epithelial Tumors of the Thymus網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Epithelial Tumors of the Thymus被引頻次




書目名稱Epithelial Tumors of the Thymus被引頻次學(xué)科排名




書目名稱Epithelial Tumors of the Thymus年度引用




書目名稱Epithelial Tumors of the Thymus年度引用學(xué)科排名




書目名稱Epithelial Tumors of the Thymus讀者反饋




書目名稱Epithelial Tumors of the Thymus讀者反饋學(xué)科排名

ARBOR

-Alterations in Thymic Epithelial Tumorsas detected with both the monoclonal and the polyclonal antibodies. The integration of morphological, clinical and .-analysis data identified three major groups of thymic epithelial tumors: (1) benign thymomas with a low incidence of .-protein alterations; (2) malignant thymomas (including well-diff

ALLEY

p53 Overexpression and Thymoma Prognosisining and AgNOR counts: p53 positive cases had higher AgNOR counts (6.34) than p53 negative thymomas (5.36, p=0.012). In univariate analysis, the 10 year survival rates were significantly higher (83%) for p53 negative than for p53 positive patients (52%, p=0.019). AgNOR counts, tumour DNA content, h

傻

Cerumen

Histiocytosis -X of the Thymusng function is ascribed to interdigitating cells (IDC) which constitute a cellular substrate for intrathymic negative selection process.. Both LC and IDC are believed to develop from common ancestral cells based within the bone marrow monocytic precursor compartment.

責(zé)問

T Cell Epitopes of the Acetylcholine Receptor and the Pathogenesis of Myasthenia Gravisand prevent EAMG in vivo (Waldor et al., 1983). MHC class II molecules bind peptides in a preformed binding groove and allelic products differ in their binding requirements which have been described as allele-specific ligand or binding motifs (Rammensee et al., 1995). For example, the bm-12 mutation

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seroma

Eosinophils

metropolitan

Discussion of Papers by Suomi and Bowlbyeing fluid, allowed the definition of several quite distinct CK phenotypes. All thymomas co-expressed simple-epithelial (CKs 8, 18, 19) and stratified-epithelial (mainly CKs 5, 14, 15 and 17) CKs. Half of the cortical thymomas revealed a phenotype with predominance of CKs 5 and 15 while 5/9 medullar