626 results on '"Krausz, Thomas"'
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2. Atypical Vascular Lesions
3. The concept of mesothelioma in situ, with consideration of its potential impact on cytology diagnosis
4. Malignant peritoneal mesothelioma: prognostic significance of clinical and pathologic parameters and validation of a nuclear-grading system in a multi-institutional series of 225 cases
5. Female adnexal tumors of probable Wolffian origin: morphological, immunohistochemical, and molecular analysis of 15 cases
6. MTAP immunohistochemistry is an accurate and reproducible surrogate for CDKN2A fluorescence in situ hybridization in diagnosis of malignant pleural mesothelioma
7. Mesothelioma in situ of the peritoneum: report of three cases and review of the literature
8. Epigenetic Dysregulation of 5-hydroxymethylcytosine in Well-Differentiated Pancreatic Neuroendocrine Tumors
9. Loss of microfibril-associated protein 5 (MFAP5) expression in colon cancer stroma
10. Skin, Melanocytic Neoplasms
11. Immunohistochemical evaluation of nuclear 5-hydroxymethylcytosine (5-hmC) accurately distinguishes malignant pleural mesothelioma from benign mesothelial proliferations
12. Mesothelioma in situ of the peritoneum: report of three cases and review of the literature.
13. Nuclear grade and necrosis predict prognosis in malignant epithelioid pleural mesothelioma: a multi-institutional study
14. Ubiquitin Immunostaining in Thyroid Neoplasms Marks True Intranuclear Cytoplasmic Pseudoinclusions and May Help Differentiate Papillary Carcinoma from NIFTP
15. Uterine Tumor Resembling Ovarian Sex Cord Stromal Tumor (UTROSCT): A Series of 3 Cases With Extensive Rhabdoid Differentiation, Malignant Behavior, and ESR1-NCOA2 Fusions
16. BAP1 immunohistochemistry has limited prognostic utility as a complement of CDKN2A (p16) fluorescence in situ hybridization in malignant pleural mesothelioma
17. Melanocytic Tumors
18. Atypical Vascular Lesions
19. Guidelines for Pathologic Diagnosis of Malignant Mesothelioma: 2017 Update of the Consensus Statement From the International Mesothelioma Interest Group
20. Table S6 from Integrative Molecular Characterization of Malignant Pleural Mesothelioma
21. Perspective on this Article from A Model of Gene-Environment Interaction Reveals Altered Mammary Gland Gene Expression and Increased Tumor Growth following Social Isolation
22. Supplementary Figure 1 from A Model of Gene-Environment Interaction Reveals Altered Mammary Gland Gene Expression and Increased Tumor Growth following Social Isolation
23. Perspective on this Article from Effects of Oral Contraceptives or a Gonadotropin-Releasing Hormone Agonist on Ovarian Carcinogenesis in Genetically Engineered Mice
24. Data from Effects of Oral Contraceptives or a Gonadotropin-Releasing Hormone Agonist on Ovarian Carcinogenesis in Genetically Engineered Mice
25. Supplementary Figure 2 from A Model of Gene-Environment Interaction Reveals Altered Mammary Gland Gene Expression and Increased Tumor Growth following Social Isolation
26. Data from Integrative Molecular Characterization of Malignant Pleural Mesothelioma
27. Data from A Model of Gene-Environment Interaction Reveals Altered Mammary Gland Gene Expression and Increased Tumor Growth following Social Isolation
28. Supplementary Data from Integrative Molecular Characterization of Malignant Pleural Mesothelioma
29. Supplementary Tables 1-6 from A Model of Gene-Environment Interaction Reveals Altered Mammary Gland Gene Expression and Increased Tumor Growth following Social Isolation
30. Supplementary Figure 1 from Effects of Oral Contraceptives or a Gonadotropin-Releasing Hormone Agonist on Ovarian Carcinogenesis in Genetically Engineered Mice
31. Supplementary Figure S1 from c-Met Is a Potentially New Therapeutic Target for Treatment of Human Melanoma
32. Data from Metastasis Suppressors Regulate the Tumor Microenvironment by Blocking Recruitment of Prometastatic Tumor-Associated Macrophages
33. Supplementary Table 2 from Paxillin Is a Target for Somatic Mutations in Lung Cancer: Implications for Cell Growth and Invasion
34. Supplementary Figure 2 from Paxillin Is a Target for Somatic Mutations in Lung Cancer: Implications for Cell Growth and Invasion
35. Supplementary Figure 6 from Densely Granulated Murine NK Cells Eradicate Large Solid Tumors
36. Supplementary Figure 3 from Densely Granulated Murine NK Cells Eradicate Large Solid Tumors
37. Data from Densely Granulated Murine NK Cells Eradicate Large Solid Tumors
38. Supplementary Figure 3 from Paxillin Is a Target for Somatic Mutations in Lung Cancer: Implications for Cell Growth and Invasion
39. Supplementary Figure 4 from Paxillin Is a Target for Somatic Mutations in Lung Cancer: Implications for Cell Growth and Invasion
40. Data from Paxillin Is a Target for Somatic Mutations in Lung Cancer: Implications for Cell Growth and Invasion
41. Supplementary Figure 1 from Paxillin Is a Target for Somatic Mutations in Lung Cancer: Implications for Cell Growth and Invasion
42. Supplementary Methods, Figure Legends 1-6 from Densely Granulated Murine NK Cells Eradicate Large Solid Tumors
43. Supplementary Figure 4 from Densely Granulated Murine NK Cells Eradicate Large Solid Tumors
44. Supplementary Table 4 from Paxillin Is a Target for Somatic Mutations in Lung Cancer: Implications for Cell Growth and Invasion
45. Supplementary Figure 2 from Densely Granulated Murine NK Cells Eradicate Large Solid Tumors
46. Supplementary Figure 5 from Paxillin Is a Target for Somatic Mutations in Lung Cancer: Implications for Cell Growth and Invasion
47. Supplementary Methods from Metastasis Suppressors Regulate the Tumor Microenvironment by Blocking Recruitment of Prometastatic Tumor-Associated Macrophages
48. Supplementary Table 1 from Paxillin Is a Target for Somatic Mutations in Lung Cancer: Implications for Cell Growth and Invasion
49. Supplementary Figure 5 from Densely Granulated Murine NK Cells Eradicate Large Solid Tumors
50. Supplementary Tables 1 and 2, Figures S1-16 from Metastasis Suppressors Regulate the Tumor Microenvironment by Blocking Recruitment of Prometastatic Tumor-Associated Macrophages
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