Hereditary kidney cancer: unique opportunity for disease-based therapy.
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Renal cell carcinoma: Evolving and emerging subtypesGenome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3Common variation at 2q22.3 (ZEB2) influences the risk of renal cancerThe Nephrologist's Tumor: Basic Biology and Management of Renal Cell Carcinoma.Non-clear cell renal cancer: disease-based management and opportunities for targeted therapeutic approaches.The changing face of renal-cell carcinoma.Management of metastatic renal cell carcinoma patients with poor-risk features: current status and future perspectives.Subtyping of renal cortical neoplasms in fine needle aspiration biopsies using a decision tree based on genomic alterations detected by fluorescence in situ hybridizationExploring a glycolytic inhibitor for the treatment of an FH-deficient type-2 papillary RCCFnip1 regulates skeletal muscle fiber type specification, fatigue resistance, and susceptibility to muscular dystrophy.Familial testicular germ cell tumors in adults: 2010 summary of genetic risk factors and clinical phenotype.Biology of metastatic renal cell carcinoma.Common variation at 1q24.1 (ALDH9A1) is a potential risk factor for renal cancerMetastatic non-clear cell renal cell carcinoma: an evidence based review of current treatment strategiesWhole-exome sequencing of neoplastic cysts of the pancreas reveals recurrent mutations in components of ubiquitin-dependent pathways.A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma.Dysfunctional miRNA-Mediated Regulation in Chromophobe Renal Cell CarcinomaDecreasing the indications for radical nephrectomy: a study of multifocal renal cell carcinoma.MET as a possible target for non-small-cell lung cancer.Canadian guideline on genetic screening for hereditary renal cell cancersHereditary kidney cancer syndromes.Novel germline mutations in FLCN gene identified in two Chinese patients with Birt-Hogg-Dubé syndromeGenetic profiles in renal tumors.Understanding the molecular genetics of renal cell neoplasia: implications for diagnosis, prognosis and therapy.Misdiagnosis of clear cell renal cell carcinoma.Sequential therapy in metastatic clear cell renal carcinoma: TKI-TKI vs TKI-mTOR.Foretinib (XL880): c-MET inhibitor with activity in papillary renal cell cancer.PBRM1 and BAP1 as novel targets for renal cell carcinomaMolecular aberrations, targeted therapy, and renal cell carcinoma: current state-of-the-art.Pathology, therapy and prognosis of papillary renal carcinoma.Renal cell carcinoma: new insights and challenges for a clinician scientist.Mutations of the von Hippel-Lindau gene confer increased susceptibility to natural killer cells of clear-cell renal cell carcinoma.A common variant at 8q24.21 is associated with renal cell cancer.
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P2860
Hereditary kidney cancer: unique opportunity for disease-based therapy.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on May 2009
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vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Hereditary kidney cancer: unique opportunity for disease-based therapy.
@en
Hereditary kidney cancer: unique opportunity for disease-based therapy.
@nl
type
label
Hereditary kidney cancer: unique opportunity for disease-based therapy.
@en
Hereditary kidney cancer: unique opportunity for disease-based therapy.
@nl
prefLabel
Hereditary kidney cancer: unique opportunity for disease-based therapy.
@en
Hereditary kidney cancer: unique opportunity for disease-based therapy.
@nl
P2093
P2860
P356
P1433
P1476
Hereditary kidney cancer: unique opportunity for disease-based therapy
@en
P2093
Cathy D Vocke
Elizabeth Pfaffenroth
Gennady Bratslavsky
Jorge R Toro
Laura S Schmidt
Len Neckers
Maria Merino
Peter A Pinto
Ramaprasad Srinivasan
W Marston Linehan
P2860
P304
P356
10.1002/CNCR.24230
P407
P433
P577
2009-05-01T00:00:00Z