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Journal of Neurological Surgery. Part B, Skull Base|May 31, 2019
High p16 Expression Is Associated with Malignancy and Shorter Disease-Free Survival Time in Solitary Fibrous Tumor/HemangiopericytomaYuanxin Liang, Robert S Heller, Julian K Wu, et al.
Histopathology|December 15, 2017
Pathology and genetics of phaeochromocytoma and paragangliomaJohn Turchini, Veronica K Y Cheung, Arthur S Tischler, et al.
Endocrine Pathology|May 15, 2003
A comparative immunohistochemical study of spontaneous and chemically induced pheochromocytomas in B6C3F1 miceGeorgette D Hill, Virgilio Pace, Elke Persohn, et al.
Molecular and Cellular Neurosciences|July 26, 2002
High-level expression of receptor tyrosine kinase Ret and responsiveness to Ret-activating ligands in pheochromocytoma cell lines from neurofibromatosis knockout miceJames F Powers, Kimberley Schelling, Jaime M Brachold, et al.
Endocrine-Related Cancer|May 1, 2025
Oxygen regulates proliferation and phenotype in the RS0 SDH-deficient pheochromocytoma cell lineJames F Powers, Brent Cochran, James D Baleja, et al.
Cancer Letters|December 14, 2011
Characterization of two mouse models of metastatic pheochromocytoma using bioluminescence imagingAlessio Giubellino, Girma M Woldemichael, Carole Sourbier, et al.
The American Journal of Surgical Pathology|January 16, 2009
Observer variation in the application of the Pheochromocytoma of the Adrenal Gland Scaled ScoreDavid Wu, Arthur S Tischler, Ricardo V Lloyd, et al.
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