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1. Author Correction: Single-nuclei and bulk-tissue gene-expression analysis of pheochromocytoma and paraganglioma links disease subtypes with tumor microenvironment

2. TMEM127 suppresses tumor development by promoting RET ubiquitination, positioning, and degradation

3. A membrane-associated MHC-I inhibitory axis for cancer immune evasion

4. Author response: Loss of tumor suppressor TMEM127 drives RET-mediated transformation through disrupted membrane dynamics

5. Single-nuclei and bulk-tissue gene-expression analysis of pheochromocytoma and paraganglioma links disease subtypes with tumor microenvironment

6. International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriers

9. IRF8-mutant B cell lymphoma evades immunity through a CD74-dependent deregulation of antigen processing and presentation in MHC CII complexes

10. Loss of Tumour Suppressor TMEM127 Drives RET-mediated Transformation Through Disrupted Membrane Dynamics

12. A membrane-associated inhibitory axis of MHC-I presentation for cancer immune evasion

13. Abstract A10: Targeting MHC-I antigen presentation for cancer immune evasion in acute myeloid leukemia

14. Abstract 195: Establishment and validation of pheochromocytoma organoids for high-throughput drug screening

15. Supplementary Figure 1 from A Novel Germline Mutation in BAP1 Predisposes to Familial Clear-Cell Renal Cell Carcinoma

16. Supplementary Methods from A Novel Germline Mutation in BAP1 Predisposes to Familial Clear-Cell Renal Cell Carcinoma

17. Supplementary Figure 2 from A Novel Germline Mutation in BAP1 Predisposes to Familial Clear-Cell Renal Cell Carcinoma

18. Supplementary Figure Legend from A Novel Germline Mutation in BAP1 Predisposes to Familial Clear-Cell Renal Cell Carcinoma

19. Data from A Novel Germline Mutation in BAP1 Predisposes to Familial Clear-Cell Renal Cell Carcinoma

20. The tumor suppressor TMEM127 regulates insulin sensitivity in a tissue-specific manner

21. A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas.

22. Supplemental Figures 1-6 from Recurrent Mutations of Chromatin-Remodeling Genes and Kinase Receptors in Pheochromocytomas and Paragangliomas

23. Supplemental Tables 1-5 from Recurrent Mutations of Chromatin-Remodeling Genes and Kinase Receptors in Pheochromocytomas and Paragangliomas

24. Supplementary Figures 1 - 3 from MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

25. Supplementary Appendix List and Supplemental Methods from Recurrent Mutations of Chromatin-Remodeling Genes and Kinase Receptors in Pheochromocytomas and Paragangliomas

26. Supplementary Data and Table 1 from Novel Pheochromocytoma Susceptibility Loci Identified by Integrative Genomics

29. Case report: Two sisters with a germline CHEK2 variant and distinct endocrine neoplasias

31. A RET::GRB2 fusion in pheochromocytoma defies the classic paradigm of RET oncogenic fusions

33. Hypoxia-Inducible Factor 2 Alpha (HIF2α) Inhibitors: Targeting Genetically Driven Tumor Hypoxia.

34. Consensus on molecular imaging and theranostics in neuroendocrine neoplasms

39. Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations

44. International initiative for a curated SDHB variant database improving the diagnosis of hereditary paraganglioma and pheochromocytoma

46. International initiative for a curated SDHB variant database improving the diagnosis of hereditary paraganglioma and pheochromocytoma.

47. The North American Neuroendocrine Tumor Society Consensus Guidelines for Surveillance and Management of Metastatic and/or Unresectable Pheochromocytoma and Paraganglioma

49. Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas

50. Targeting of SMAD5 links microRNA-155 to the TGF-[beta] pathway and lymphomagenesis

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