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1. Hereditary leiomyomatosis and renal cell carcinoma

2. Genomic copy number alterations in clear cell renal carcinoma: associations with case characteristics and mechanisms of VHL gene inactivation.

3. A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

4. Combined burden and functional impact tests for cancer driver discovery using DriverPower

5. Integrative pathway enrichment analysis of multivariate omics data

6. Pathway and network analysis of more than 2500 whole cancer genomes

7. Divergent mutational processes distinguish hypoxic and normoxic tumours

8. Genomic footprints of activated telomere maintenance mechanisms in cancer

9. Screening for von Hippel-Lindau disease by DNA polymorphism analysis.

10. Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locus.

12. Genetics of Renal Cell Carcinoma

13. The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma

14. Evaluation of Recipients of Positive and Negative Secondary Findings Evaluations in a Hybrid CLIA-Research Sequencing Pilot

15. Hypoxia-Inducible Factor 2 alpha Mutation-Related Paragangliomas Classify as Discrete Pseudohypoxic Subcluster

16. Unexplained Excess Risk of Bladder Cancer in Men

19. Iodine-131-metaiodobenzylguanidine scintigraphy in preoperative and postoperative evaluation of paragangliomas: comparison with CT and MRI

20. Genotype and Tumor Locus Determine Expression Profile of Pseudohypoxic Pheochromocytomas and Paragangliomas

21. Prostate cancer: where are we going?

23. Genotype and tumor location determine gene expression signatures in pseudohypoxic pheochromocytomas and paragangliomas

25. Identification of a unique epigenetic sub‐microenvironment in prostate cancer

26. Inhibitory effects of gossypol on adrenal function

28. Inhibition of Prostate Cancer Metastasis: a Critical Challenge Ahead

29. Hereditary kidney cancer: unique opportunity for disease-based therapy.

30. Kidney-targeted Birt-Hogg-Dube gene inactivation in a mouse model: Erk1/2 and Akt-mTOR activation, cell hyperproliferation, and polycystic kidneys.

31. Lung cysts, spontaneous pneumothorax, and genetic associations in 89 families with Birt-Hogg-Dubé syndrome.

33. Biochemical diagnosis of pheochromocytoma: which test is best?

34. Cyclophosphamide-induced cystitis and bladder cancer in patients with Wegener granulomatosis.

35. Aids Case for Diagnosis, 1986 Military Medicine

37. Interrelationships between Calcium, Calcemic Hormones and Gastrointestinal Hormones

38. Provocative Agents and the Diagnosis of Medullary Carcinoma of the Thyroid Gland

41. von Hippel-Lindau disease.

42. Imaging finding of renal masses associated with pathogenic variation in succinate dehydrogenase subunit B gene.

43. Oral Hypoxia-Inducible Factor 2α Inhibitor Belzutifan in Ocular von Hippel-Lindau Disease: Subgroup Analysis of the Single-Arm Phase 2 LITESPARK-004 Study.

44. A Prospective Study of the Diagnostic Performance of Photon-Counting CT Compared With MRI in the Characterization of Renal Masses.

45. A novel pathogenic germline chromosome 3 inversion in von Hippel-Lindau disease.

46. Castration Levels of Testosterone Results in Atrophy of Androgen-Sensitive Perineal Muscles: A Potential Biomarker for Male Hypogonadism.

47. Predicting post-surgical complications using renal scoring systems.

48. Toward a CRISPR-based mouse model of Vhl -deficient clear cell kidney cancer: Initial experience and lessons learned.

49. Belzutifan for patients with von Hippel-Lindau disease-associated CNS haemangioblastomas (LITESPARK-004): a multicentre, single-arm, phase 2 study.

50. Exploring the Feasibility of GPT-4 as a Data Extraction Tool for Renal Surgery Operative Notes.

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