Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype. - Wikidata - wikimedia - TriplyDB

Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype.

Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype.

http://www.wikidata.org/entity/Q35787720

about

Review of renal cell carcinoma and its common subtypes in radiology Understanding and Targeting MET Signaling in Solid Tumors - Are We There Yet?Biomarker development in MET-targeted therapy Genetic and Chromosomal Aberrations and Their Clinical Significance in Renal Neoplasms Renal cell carcinoma: histological classification and correlation with imaging findings Met in urological cancers The metabolic basis of kidney cancer Mechanisms of disease: the role of heat-shock protein 90 in genitourinary malignancy Percutaneous radio frequency ablation of small renal tumors: initial results The Nephrologist's Tumor: Basic Biology and Management of Renal Cell Carcinoma.The genetic basis of kidney cancer: a metabolic disease Targeted therapies for non-clear renal cell carcinoma.Inherited susceptibility to uterine leiomyomas and renal cell cancer Incidence of end-stage renal disease in the Turkish-Cypriot population of Northern Cyprus: a population based study Kidney pathology: current classification of renal cell carcinoma.Evolving classification of renal cell neoplasia.Repeat partial nephrectomy: surgical, functional and oncological outcomes.Nephron-sparing surgery for multifocal and hereditary renal tumors.Sarcomatoid renal cell carcinoma: a comprehensive review of the biology and current treatment strategies.Unique patterns of allelic imbalance distinguish type 1 from type 2 sporadic papillary renal cell carcinoma Inherited forms of renal cell carcinoma.Renal cancer: oxygen meets metabolism The genetic basis of cancer of kidney cancer: implications for gene-specific clinical management.Molecular pathogenetics of renal cancer.Role of carbonic anhydrases in the progression of renal cell carcinoma subtypes: proposal of a unified hypothesis.New strategies in renal cell carcinoma: targeting the genetic and metabolic basis of disease.Current understanding of the molecular mechanisms of kidney cancer: a primer for urologists.Genetic basis of kidney cancer: a model for developing molecular-targeted therapies.Initial clinical sensitivity and acquired resistance to MET inhibition in MET-mutated papillary renal cell carcinoma Tyrosine kinase inhibitors and anti-angiogenic therapies in kidney cancer.Oncocytic papillary renal cell carcinoma: a clinicopathological study emphasizing distinct morphology, extended immunohistochemical profile and cytogenetic features.MicroRNA profiles classify papillary renal cell carcinoma subtypes.Hereditary kidney cancer: unique opportunity for disease-based therapy.Recent developments in the treatment of renal cell carcinoma.Targeting the Met signaling pathway in renal cancer.Hereditary kidney cancer syndromes.Defining early-onset kidney cancer: implications for germline and somatic mutation testing and clinical management.Meta-analysis of gene expression and integrin-associated signaling pathways in papillary renal cell carcinoma subtypes.Epidermal growth factor receptor mutation and diverse tumors: case report and concise literature review.Understanding the molecular genetics of renal cell neoplasia: implications for diagnosis, prognosis and therapy.

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P2860

Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype.

http://www.wikidata.org/entity/Q35787720

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Hereditary and sporadic papill ...... tinct morphological phenotype.

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Hereditary and sporadic papill ...... tinct morphological phenotype.

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The American Journal of Pathology

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Sequence of MET protooncogene cDNA has features characteristic of the tyrosine kinase family of growth-factor receptors

The t(X;1)(p11.2;q21.2) translocation in papillary renal cell carcinoma fuses a novel gene PRCC to the TFE3 transcription factor gene

Identification of the von Hippel-Lindau disease tumor suppressor gene

Papillary renal cell carcinoma: a clinical, radiologic, and pathologic study of 34 cases.

Hereditary papillary renal cell carcinoma: clinical studies in 10 families.

Papillary and metanephric adenomas of the kidney.

Chromosomal imbalances in papillary renal cell carcinoma: genetic differences between histological subtypes.

Allelic deletions of the VHL gene detected in multiple microscopic clear cell renal lesions in von Hippel-Lindau disease patients.

Papillary renal cell carcinoma. A morphologic and cytogenetic study of 11 cases.

Hepatocyte growth factor/scatter factor induces a variety of tissue-specific morphogenic programs in epithelial cells

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