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Lista de obras de Bin Tean Teh

2011 Young Surgeon's Award Winner: high endothelial venules: a novel prognostic marker in cancer metastasis and the missing link?

artículo científico publicado en 2012

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

artículo científico publicado en 2011

A comparison study reveals important features of agreement and disagreement between summarized DNA and RNA data obtained from renal cell carcinoma

artículo científico publicado en 2008

A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumors

artículo científico publicado en 1998

A genetic mutation panel for differentiating malignant phyllodes tumour from metaplastic breast carcinoma

artículo científico publicado en 2017

A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome

scientific article published on 01 April 2000

A germline mutation in PBRM1 predisposes to renal cell carcinoma

artículo científico publicado en 2015

A kindred with a variant of multiple endocrine neoplasia type 1 demonstrating frequent expression of pituitary tumors but not linked to the multiple endocrine neoplasia type 1 locus at chromosome region 11q13

artículo científico publicado en 1997

A large multiple endocrine neoplasia type 1 family with clinical expression suggestive of anticipation

artículo científico publicado en 1997

A meiotic recombination in a new isolated familial somatotropinoma kindred

artículo científico publicado en 2004

A molecular classification of papillary renal cell carcinoma

artículo científico publicado en 2005

A novel panel of biomarkers predicts radioresistance in patients with squamous cell carcinoma of the head and neck

artículo científico publicado en 2013

A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas. The European Consortium on MEN 1

artículo científico publicado en 1998

A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing

artículo científico publicado en 2005

A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer

artículo científico publicado en 2005

A tribute to George F. Vande Woude, a man of character: 2006 Scientific Symposium Winning the War against Cancer: from Genomics to Bedside and Back.

artículo científico publicado en 2007

A unique case of spontaneous regression of metastatic papillary renal cell carcinoma: a case report

artículo científico publicado en 2009

ADAR-Mediated RNA Editing Predicts Progression and Prognosis of Gastric Cancer.

artículo científico publicado en 2016

Abscisic acid perception and signaling: structural mechanisms and applications

artículo científico publicado en 2014

Accuracy of combined protein gene product 9.5 and parafibromin markers for immunohistochemical diagnosis of parathyroid carcinoma

artículo científico publicado en 2008

Activation of the PI3K/AKT pathway induces urothelial carcinoma of the renal pelvis: identification in human tumors and confirmation in animal models

artículo científico publicado en 2009

Adult cystic nephroma and mixed epithelial and stromal tumor of the kidney are the same disease entity: molecular and histologic evidence

artículo científico publicado en 2009

All the World's a Stage: Facilitating Discovery Science and Improved Cancer Care through the Global Alliance for Genomics and Health

artículo científico publicado en 2015

Allelic loss of the retinoblastoma tumor suppressor gene: a marker for aggressive parathyroid tumors?

artículo científico publicado en 1996

Alterations of the Birt-Hogg-Dubé gene (BHD) in sporadic colorectal tumours

artículo científico publicado en 2003

Alterations of the MEN1 gene in sporadic parathyroid tumors

artículo científico publicado en 1998

Altered expression of members of the IGF-axis in clear cell renal cell carcinoma

artículo científico publicado en 2005

Alternative genetic pathways in parathyroid tumorigenesis

scientific article published on 01 October 1999

An Optimised Protocol Harnessing Laser Capture Microdissection for Transcriptomic Analysis on Matched Primary and Metastatic Colorectal Tumours

scientific article published on 20 January 2020

An antioxidant response phenotype shared between hereditary and sporadic type 2 papillary renal cell carcinoma

artículo científico publicado en 2011

An eleven gene molecular signature for extra-capsular spread in oral squamous cell carcinoma serves as a prognosticator of outcome in patients without nodal metastases

artículo científico publicado en 2015

Anti-cancer drug resistance: understanding the mechanisms through the use of integrative genomics and functional RNA interference.

artículo científico publicado en 2010

Aristolochic acids and their derivatives are widely implicated in liver cancers in Taiwan and throughout Asia

artículo científico publicado en 2017

As an independent unfavorable prognostic factor, IL-8 promotes metastasis of nasopharyngeal carcinoma through induction of epithelial-mesenchymal transition and activation of AKT signaling

artículo científico publicado en 2012

Assessing matched normal and tumor pairs in next-generation sequencing studies

artículo científico publicado en 2011

Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas

artículo científico publicado en 1996

Bilateral multiple renal oncocytomas and cysts associated with a constitutional translocation (8;9)(q24.1;q34.3) and a rare constitutional VHL missense substitution

artículo científico publicado en 1998

Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression

artículo científico publicado en 2010

Birt-Hogg-Dubé syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2.

artículo científico publicado en 2001

C-kit expression in renal oncocytomas and chromophobe renal cell carcinomas

artículo científico publicado en 2005

C306A single nucleotide polymorphism in the human CEBPD gene that maps at 8p11.1-p11.2.

artículo científico publicado en 2001

CD1d expression in renal cell carcinoma is associated with higher relapse rates, poorer cancer-specific and overall survival

artículo científico publicado en 2014

CDC73/HRPT2 CpG island hypermethylation and mutation of 5'-untranslated sequence are uncommon mechanisms of silencing parafibromin in parathyroid tumors.

artículo científico publicado en 2010

CUL3 and NRF2 mutations confer an NRF2 activation phenotype in a sporadic form of papillary renal cell carcinoma

artículo científico publicado en 2013

Cancer: biology and therapeutics--a tribute to George Vande Woude

artículo científico publicado en 2007

Cause of death in multiple endocrine neoplasia type 1

artículo científico publicado en 1993

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy

artículo científico publicado en 1997

Characterization of a new SNP c767A/T (Arg222Trp) in the candidate TSG FUS2 on human chromosome 3p21.3: prevalence in Asian populations and analysis of association with nasopharyngeal cancer

artículo científico publicado en 2004

Characterization of the mouse Men1 gene and its expression during development

scientific journal article

Chromosomal amplification of leucine-rich repeat kinase-2 (LRRK2) is required for oncogenic MET signaling in papillary renal and thyroid carcinomas

artículo científico publicado en 2011

Chronic kidney disease and upper tract urothelial carcinomas.

artículo científico publicado en 2014

Classification of renal neoplasms based on molecular signatures

scientific article published on 01 June 2006

Clear cell sarcomas of the kidney are characterised by BCOR gene abnormalities, including exon 15 internal tandem duplications and BCOR-CCNB3 gene fusion

artículo científico publicado en 2017

Clinical and genetic studies of Van der Woude syndrome in Sweden

artículo científico publicado en 1999

Clinicopathologic studies of thymic carcinoids in multiple endocrine neoplasia type 1

scientific article published on 01 January 1997

Clonal loss of INT-2 alleles in sporadic and familial pancreatic endocrine tumours

artículo científico publicado en 1990

Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains

artículo científico publicado en 1996

Combined gene expression profiling and RNAi screening in clear cell renal cell carcinoma identify PLK1 and other therapeutic kinase targets

artículo científico publicado en 2011

Combining differential expression, chromosomal and pathway analyses for the molecular characterization of renal cell carcinoma

artículo científico publicado en 2007

Comparative gene expression profiling analysis of urothelial carcinoma of the renal pelvis and bladder

artículo científico publicado en 2010

Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology

artículo científico publicado en 2000

Comparative genomic hybridization studies in tumours from a patient with multiple endocrine neoplasia type 1.

artículo científico publicado en 1998

Comparison of the UCLA Integrated Staging System and the Leibovich score in survival prediction for patients with nonmetastatic clear cell renal cell carcinoma

artículo científico publicado en 2010

Complexity of tumor vasculature in clear cell renal cell carcinoma

scientific article published on May 2009

Confirmation of a susceptibility locus on chromosome 13 in Australian breast cancer families

article

Correction: Deficiency of FLCN in Mouse Kidney Led to Development of Polycystic Kidneys and Renal Neoplasia.

artículo científico publicado en 2008

Correction: Deficiency of FLCN in Mouse Kidney Led to Development of Polycystic Kidneys and Renal Neoplasia.

artículo científico publicado en 2008

Correction: Methylation Profiles Reveal Distinct Subgroup of Hepatocellular Carcinoma Patients with Poor Prognosis

artículo científico publicado en 2016

Correction: Somatic Pairing of Chromosome 19 in Renal Oncocytoma Is Associated with Deregulated EGLN2-Mediated Oxygen-Sensing Response.

artículo científico publicado en 2008

Corrigendum re “Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma” [Eur Urol 2017;72:747–54]

scholarly article published in European Urology

Corrigendum: Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

artículo científico publicado en 2012

Cystic renal neoplasia following conditional inactivation of apc in mouse renal tubular epithelium

scientific journal article

DOK4/IRS-5 expression is altered in clear cell renal cell carcinoma

artículo científico publicado en 2007

Deficiency of FLCN in mouse kidney led to development of polycystic kidneys and renal neoplasia

scientific journal article

Defining the Molecular Alterations of Ampullary Carcinoma.

artículo científico publicado en 2016

Definition of the MinimalMEN1Candidate Area Based on a 5-Mb Integrated Map of Proximal 11q13

artículo científico publicado en 1996

Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1)

artículo científico publicado en 1996

Deregulation of E2-EPF ubiquitin carrier protein in papillary renal cell carcinoma

artículo científico publicado en 2011

Detection of DNA copy number changes and oncogenic signaling abnormalities from gene expression data reveals MYC activation in high-grade papillary renal cell carcinoma

artículo científico publicado en 2007

Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism

scientific article published on 01 March 1997

Digital phenotyping by consumer wearables identifies sleep-associated markers of cardiovascular disease risk and biological aging

scientific article published on 04 October 2019

Disruption of tubular Flcn expression as a mouse model for renal tumor induction.

artículo científico publicado en 2015

Does 'granular cell' renal cell carcinoma exist? Molecular and histological reclassification

artículo científico publicado en 2007

Downregulation of CASR expression and global loss of parafibromin staining are strong negative determinants of prognosis in parathyroid carcinoma

Dual KS: Defining Gene Sets with Tissue Set Enrichment Analysis

artículo científico publicado en 2010

Dual modulation of MCL-1 and mTOR determines the response to sunitinib

artículo científico publicado en 2016

Effect of Ang-2-VEGF-A Bispecific Antibody in Renal Cell Carcinoma

artículo científico publicado en 2015

Effect of sildenafil citrate on an orthotopic prostate cancer growth and metastasis model

artículo científico publicado en 2003

Elucidation of the molecular signatures of renal cell carcinoma by gene expression profiling

artículo científico publicado en 2006

Epigenomic Consequences of Coding and Noncoding Driver Mutations

artículo científico publicado en 2016

Epigenomic Promoter Alterations Amplify Gene Isoform and Immunogenic Diversity in Gastric Adenocarcinoma

artículo científico publicado en 2017

Epigenomic profiling of primary gastric adenocarcinoma reveals super-enhancer heterogeneity

artículo científico publicado en 2016

Erratum: Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

artículo científico publicado en 2015

Evaluation of retinoblastoma and Ki-67 immunostaining as diagnostic markers of benign and malignant parathyroid disease

scientific article published on 01 January 1999

Excessive fatty acid oxidation induces muscle atrophy in cancer cachexia

artículo científico publicado en 2016

Exclusion of the 13-kDa rapamycin binding protein gene (FKBP2) as a candidate gene for multiple endocrine neoplasia type 1

Exome sequencing identifies distinct mutational patterns in liver fluke-related and non-infection-related bile duct cancers

artículo científico publicado en 2013

Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

artículo científico publicado en 2011

Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma.

artículo científico publicado en 2014

Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes

scientific article published on 01 May 2012

Exome sequencing of liver fluke-associated cholangiocarcinoma

artículo científico publicado en 2012

Exome sequencing reveals recurrent REV3L mutations in cisplatin-resistant squamous cell carcinoma of head and neck

artículo científico publicado en 2016

Exome-wide Sequencing Shows Low Mutation Rates and Identifies Novel Mutated Genes in Seminomas

artículo científico publicado en 2015

Expression and chromosomal localization of the Requiem gene

scientific journal article

Expression of RON Proto-oncogene in Renal Oncocytoma and Chromophobe Renal Cell Carcinoma

artículo científico publicado en 2004

Expression of S-100 protein in renal cell neoplasms

scientific article published on 01 April 2006

Expression of alpha-methylacyl-CoA racemase in papillary renal cell carcinoma

scientific article published on 01 January 2004

Expression of kidney-specific cadherin in chromophobe renal cell carcinoma and renal oncocytoma

scientific article published on 01 July 2006

Expression of the PTTG1 oncogene is associated with aggressive clear cell renal cell carcinoma

artículo científico publicado en 2012

FXYD3: A Promising Biomarker for Urothelial Carcinoma

artículo científico publicado el 15 de febrero de 2011

Facilitating a culture of responsible and effective sharing of cancer genome data

artículo científico publicado en 2016

Familial adult renal neoplasia

artículo científico publicado en 2002

Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations.

artículo científico publicado en 2008

Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree

artículo científico publicado en 2000

Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14

artículo científico publicado en 2006

Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families

scientific article published on 01 June 1998

Familial non-VHL non-papillary clear-cell renal cancer

scientific article published on 01 March 1997

Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19p13

artículo científico publicado en 1995

Familial testicular cancer: lack of evidence for trinucleotide repeat expansions and association with PKD1 in one family

artículo científico publicado en 1999

Familial testicular carcinoma: in search of genetic triggers

scientific article published on 01 June 1994

Fanconi's anemia in adulthood: chemoradiation-induced bone marrow failure and a novel FANCA mutation identified by targeted deep sequencing

scientific article published on 25 April 2011

Fine mapping of the MLK-3 gene within 11q13 and its exclusion as the MEN1 susceptibility gene

artículo científico publicado en 1997

First somatic mutation of E2F1 in a critical DNA binding residue discovered in well-differentiated papillary mesothelioma of the peritoneum.

artículo científico publicado en 2011

Flcn-deficient renal cells are tumorigenic and sensitive to mTOR suppression

artículo científico publicado en 2015

Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis

artículo científico publicado en 2012

Founder effect in multiple endocrine neoplasia type 1 (MEN 1) in Finland

artículo científico publicado en 2001

Functional characterisation guides classification of novel BAP1 germline variants

scientific article published on 19 November 2020

Functional characterization of JMJD2A, a histone deacetylase- and retinoblastoma-binding protein

scientific journal article

Functional epigenomics approach to identify methylated candidate tumour suppressor genes in renal cell carcinoma

artículo científico publicado en 2008

Functional genomics identifies specific vulnerabilities in PTEN-deficient breast cancer.

artículo científico publicado en 2018

Functional importance of Dicer protein in the adaptive cellular response to hypoxia

artículo científico publicado en 2012

Functional studies of the MEN1 gene

artículo científico publicado en 2003

Gene expression of parathyroid tumors: molecular subclassification and identification of the potential malignant phenotype

artículo científico publicado en 2004

Gene expression profiling in kidney cancer: combining differential expression and chromosomal and pathway analyses

artículo científico publicado en 2006

Gene expression profiling of early- and late-relapse nonseminomatous germ cell tumor and primitive neuroectodermal tumor of the testis

scientific article published on 01 April 2004

Gene expression profiling of mesoblastic nephroma and Wilms tumors--comparison and clinical implications

artículo científico publicado en 2004

Gene expression profiling of renal cell carcinoma

artículo científico publicado en 2004

Gene expression profiling of renal cell carcinoma and clinical implications

artículo científico publicado en 2005

Gene expression profiling of renal cell carcinoma and its implications in diagnosis, prognosis, and therapeutics

artículo científico publicado en 2003

Gene expression profiling of renal medullary carcinoma: potential clinical relevance

artículo científico publicado en 2004

Gene expression signatures delineate biological and prognostic subgroups in peripheral T-cell lymphoma

artículo científico publicado en 2014

Gene identification in autosomal dominant disorders

scientific article published on 01 May 1997

Gene profiling suggests a common evolution of bladder cancer subtypes

artículo científico publicado en 2013

Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma

artículo científico publicado en 2017

Genetic and clinical characterization of sporadic cystic parathyroid tumours

artículo científico publicado en 2002

Genetic and expression profiles of squamous cell carcinoma of the head and neck correlate with cisplatin sensitivity and resistance in cell lines and patients.

artículo científico publicado en 2004

Genetic and structural variation in the gastric cancer kinome revealed through targeted deep sequencing

artículo científico publicado en 2010

Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome

artículo científico publicado en 2001

Genetic mapping of the multiple endocrine neoplasia type 1 locus at 11q13

artículo científico publicado el 1 de septiembre de 1995

Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study.

artículo científico publicado en 2016

Genetic screening for MEN1 mutations in families presenting with familial primary hyperparathyroidism

artículo científico publicado en 2002

Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndrome

artículo científico publicado en 1999

Genetic studies of thymic carcinoids in multiple endocrine neoplasia type 1

artículo científico publicado en 1994

Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications

artículo científico publicado en 2004

Genetics and genomics of breast fibroadenomas

artículo científico publicado en 2017

Genetics of Opisthorchis viverrini-related cholangiocarcinoma

artículo científico publicado en 2015

Genetics of multiple endocrine neoplasia type 1.

artículo científico publicado en 1994

Genome assembly and chemogenomic profiling of National Flower of Singapore Papilionanthe Miss Joaquim ‘Agnes’ reveals metabolic pathways regulating floral traits

scientific article published in 2022

Genome-scale mutational signatures of aflatoxin in cells, mice, and human tumors

artículo científico publicado en 2017

Genome-wide association study identifies multiple risk loci for renal cell carcinoma

artículo científico publicado en 2017

Genome-wide mutational signatures of aristolochic acid and its application as a screening tool

artículo científico publicado en 2013

Genome-wide scan identifies novel modifier loci of acromegalic phenotypes for isolated familial somatotropinoma

artículo científico publicado en 2009

Genome-wide screening using array-CGH does not reveal microdeletions/microduplications in children with Kabuki syndrome.

artículo científico publicado en 2005

Genomic and proteomic characterization of ARID1A chromatin remodeller in ampullary tumors

artículo científico publicado en 2017

Genomic expression and single-nucleotide polymorphism profiling discriminates chromophobe renal cell carcinoma and oncocytoma

artículo científico publicado en 2010

Genomic landscapes of breast fibroepithelial tumors

artículo científico publicado en 2015

Genomic profiling reveals mutational landscape in parathyroid carcinomas

artículo científico publicado en 2017

Genomics of worms, with an emphasis on Opisthorchis viverrini - opportunities for fundamental discovery and biomedical outcomes

artículo científico publicado en 2016

Germline Mutations in Cancer Predisposition Genes are Frequent in Sporadic Sarcomas

artículo científico publicado en 2017

Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP)

artículo científico publicado en 2004

Glypican 3 overexpression in primary and metastatic Wilms tumors

artículo científico publicado en 2014

Glypican 3: a novel marker in testicular germ cell tumors

artículo científico publicado en 2006

HRPT2 and parathyroid cancer

scientific article published on 01 February 2004

HRPT2 gene alterations in ossifying fibroma of the jaws

artículo científico publicado en 2006

HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours

artículo científico publicado en 2003

HRPT2, a tumor suppressor gene for hyperparathyroidism-jaw tumor syndrome

artículo científico publicado en 2005

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome

artículo científico publicado en 2002

Haem oxygenase 1 expression is associated with prognosis in cholangiocarcinoma patients and with drug sensitivity in xenografted mice

artículo científico publicado en 2016

High-depth sequencing of over 750 genes supports linear progression of primary tumors and metastases in most patients with liver-limited metastatic colorectal cancer

artículo científico publicado en 2015

Human folliculin delays cell cycle progression through late S and G2/M-phases: effect of phosphorylation and tumor associated mutations

artículo científico publicado en 2013

Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.

artículo científico publicado en 2004

Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome

artículo científico publicado en 2004

Human kidney injury molecule-1 (hKIM-1): a useful immunohistochemical marker for diagnosing renal cell carcinoma and ovarian clear cell carcinoma

artículo científico publicado en 2007

Hyperparathyroidism with normal albumin-corrected total calcium in patients with multiple endocrine neoplasia type 1.

artículo científico publicado en 1992

Hyperparathyroidism-jaw tumour syndrome

artículo científico publicado en 2003

Hypoxia promotes ligand-independent EGF receptor signaling via hypoxia-inducible factor-mediated upregulation of caveolin-1

artículo científico publicado en 2012

Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas

scientific article published on 06 June 2007

Identification of MEN1 gene mutations in families with MEN 1 and related disorders

artículo científico publicado en 2000

Identification of copy number alterations and its association with pathological features in clear cell and papillary RCC

scientific article published on 03 August 2008

Identification of deregulated oncogenic pathways in renal cell carcinoma: an integrated oncogenomic approach based on gene expression profiling

artículo científico publicado en 2007

Identification of molecular subtypes of gastric cancer with different responses to PI3-kinase inhibitors and 5-fluorouracil

artículo científico

Identification of somatic mutations of the MEN1 gene in sporadic endocrine tumours

artículo científico publicado en 2000

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1

artículo científico publicado en 1997

Implementation of genomics in medical practice to deliver precision medicine for an Asian population.

artículo científico publicado en 2019

In-depth characterization of the cisplatin mutational signature in human cell lines and in esophageal and liver tumors.

artículo científico publicado en 2018

Inactivation of BHD in sporadic renal tumors.

artículo científico publicado en 2003

Independent genetic events associated with the development of multiple parathyroid tumors in patients with primary hyperparathyroidism

artículo científico publicado en 2002

Inhibition of MAPK kinase signaling pathways suppressed renal cell carcinoma growth and angiogenesis in vivo.

artículo científico publicado en 2008

Inhibition of placental growth factor in renal cell carcinoma

artículo científico publicado en 2015

Innovations and challenges in renal cancer: consensus statement from the first international conference

artículo científico publicado en 2004

Innovations and challenges in renal cancer: summary statement from the Third Cambridge Conference

artículo científico publicado en 2009

Integrated epigenomics identifies BMP4 as a modulator of cisplatin sensitivity in gastric cancer

artículo científico publicado en 2012

Integration of high-risk human papillomavirus into cellular cancer-related genes in head and neck cancer cell lines.

artículo científico publicado en 2017

Interleukin-8 mediates resistance to antiangiogenic agent sunitinib in renal cell carcinoma

artículo científico publicado en 2010

JAK-STAT and G-protein-coupled receptor signaling pathways are frequently altered in epitheliotropic intestinal T-cell lymphoma

artículo científico publicado en 2016

Janus kinase 3-activating mutations identified in natural killer/T-cell lymphoma

artículo científico publicado en 2012

Keratin 15, transcobalamin I and homeobox gene Hox-B13 expression in breast phyllodes tumors: novel markers in biological classification

artículo científico publicado en 2011

Kinase targets in renal-cell carcinomas: reassessing the old and discovering the new.

artículo científico publicado en 2010

Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families

artículo científico publicado en 2000

Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1)

artículo científico publicado el 1 de octubre de 1997

Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13

artículo científico publicado en 2000

Loss of parafibromin immunoreactivity is a distinguishing feature of parathyroid carcinoma

artículo científico publicado en 2004

Loss of tumor suppressor KDM6A amplifies PRC2-regulated transcriptional repression in bladder cancer and can be targeted through inhibition of EZH2.

artículo científico publicado en 2017

Lung cancer: intragenic ERBB2 kinase mutations in tumours

artículo científico publicado en 2004

Lymphoblastoid cell line with B1 cell characteristics established from a chronic lymphocytic leukemia clone by in vitro EBV infection

artículo científico publicado en 2012

MED12 is frequently mutated in breast phyllodes tumours: a study of 112 cases

artículo científico publicado en 2015

MED12 protein expression in breast fibroepithelial lesions: correlation with mutation status and oestrogen receptor expression.

artículo científico publicado en 2016

MET mutation and familial gastric cancer

artículo científico publicado en 2001

MSIseq: Software for Assessing Microsatellite Instability from Catalogs of Somatic Mutations

artículo científico publicado en 2015

Malignant melanoma in patients with multiple endocrine neoplasia type 1 and involvement of the MEN1 gene in sporadic melanoma.

artículo científico publicado en 2000

Management of kidney cancer in Asia: resource-stratified guidelines from the Asian Oncology Summit 2012.

artículo científico publicado en 2012

Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.

artículo científico publicado en 2001

Met protein expression level correlates with survival in patients with late-stage nasopharyngeal carcinoma

artículo científico publicado en 2002

Methylation profiles reveal distinct subgroup of hepatocellular carcinoma patients with poor prognosis

artículo científico publicado en 2014

Methylation subtypes and large-scale epigenetic alterations in gastric cancer

artículo científico publicado en 2012

Mice deleted for cell division cycle 73 gene develop parathyroid and uterine tumours: model for the hyperparathyroidism-jaw tumour syndrome

artículo científico publicado en 2017

MicroRNA profiling of human kidney cancer subtypes

artículo científico publicado en 2009

Microarray gene expression profiling using core biopsies of renal neoplasia.

scientific article published on January 2009

Molecular Classification of Patients With Unexplained Hamartomatous and Hyperplastic Polyposis

artículo científico publicado en 2005

Molecular characterization of human telomerase reverse transcriptase-immortalized human fibroblasts by gene expression profiling: activation of the epiregulin gene

artículo científico publicado en 2003

Molecular classification of breast phyllodes tumors: validation of the histologic grading scheme and insights into malignant progression

artículo científico publicado en 2010

Molecular genetics of primary and secondary hyperparathyroidism

artículo científico publicado en 1996

Molecular subclassification of kidney tumors and the discovery of new diagnostic markers

artículo científico publicado en 2003

Molecular targets on the horizon for kidney and urothelial cancer

artículo científico

Molecular tools for presymptomatic testing in multiple endocrine neoplasia type 1

scientific article published on 01 September 1995

Morphologic and genetic heterogeneity in breast fibroepithelial lesions-a comprehensive mapping study

artículo científico publicado en 2020

Multiple endocrine neoplasia

artículo científico publicado en 2003

Multiple endocrine neoplasia type 1 (MEN1) in two Asian families

article

Multiple endocrine neoplasia type 1 (MEN1): genetic and clinical analysis in the Southern Chinese.

artículo científico publicado en 2003

Multiple endocrine neoplasia type 1 and the search for the genetic trigger.

artículo científico publicado en 1997

Multiple endocrine neoplasia type I: clinical syndrome to molecular genetics

artículo científico publicado en 1995

Multiple endocrine neoplasm, type 1. Gastrinomas, pancreatic neoplasms, microcarcinoids, the Zollinger-Ellison syndrome, lymph nodes, and hepatic metastases

scientific article published on 01 October 1993

Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism

article

Mutation signatures implicate aristolochic acid in bladder cancer development

artículo científico publicado en 2015

Mutation signatures of carcinogen exposure: genome-wide detection and new opportunities for cancer prevention

artículo científico publicado en 2014

Mutational Signatures in Mandibular Ameloblastoma Correlate with Smoking

scientific article published on 27 March 2019

Mutational landscapes of tongue carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance.

artículo científico publicado en 2015

Mutations in BHD and TP53 genes, but not in HNF1beta gene, in a large series of sporadic chromophobe renal cell carcinoma

artículo científico publicado en 2006

NanoString expression profiling identifies candidate biomarkers of RAD001 response in metastatic gastric cancer.

artículo científico publicado en 2016

Nanoscale chromatin profiling of gastric adenocarcinoma reveals cancer-associated cryptic promoters and somatically acquired regulatory elements

artículo científico publicado en 2014

Negative regulation of EGFR signalling by the human folliculin tumour suppressor protein

artículo científico publicado en 2017

Next-generation sequencing of translocation renal cell carcinoma reveals novel RNA splicing partners and frequent mutations of chromatin-remodeling genes

artículo científico publicado en 2014

Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma

artículo científico publicado en 2011

Nuclear expression of MATK is a novel marker of type II enteropathy-associated T-cell lymphoma

scientific article published on 14 January 2011

Nuclear imaging of Met-expressing human and canine cancer xenografts with radiolabeled monoclonal antibodies (MetSeek).

artículo científico publicado en 2005

Oculopharyngeal muscular dystrophy (OPMD)--report and genetic studies of an Australian kindred

scientific article published on 01 January 1997

Oncogenic activation of JAK3-STAT signaling confers clinical sensitivity to PRN371, a novel selective and potent JAK3 inhibitor, in natural killer/T-cell lymphoma

artículo científico publicado en 2018

Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer

artículo científico publicado en 2014

Osteoblast-specific deletion of Hrpt2/Cdc73 results in high bone mass and increased bone turnover

artículo científico publicado en 2017

Over expression of insulin-like growth factor binding protein 3 in clear cell renal cell carcinoma

artículo científico publicado en 2008

Overexpression of asparagine synthetase and matrix metalloproteinase 19 confers cisplatin sensitivity in nasopharyngeal carcinoma cells

artículo científico publicado en 2013

Overexpression of glutathione s-transferase alpha in clear cell renal cell carcinoma

artículo científico publicado en 2005

Overexpression of microRNA-21 regulating PDCD4 during tumorigenesis of liver fluke-associated cholangiocarcinoma contributes to tumor growth and metastasis

artículo científico publicado en 2013

Parafibromin inhibits cancer cell growth and causes G1 phase arrest

artículo científico publicado en 2006

Pathogenesis of cholangiocarcinoma: From genetics to signalling pathways

artículo científico

Patterns of somatic mutation in human cancer genomes

artículo científico publicado en 2007

Pericyte coverage of differentiated vessels inside tumor vasculature is an independent unfavorable prognostic factor for patients with clear cell renal cell carcinoma

artículo científico publicado en 2012

Phenotype and phenocopy: the relationship between genotype and clinical phenotype in a single large family with multiple endocrine neoplasia type 1 (MEN 1)

artículo científico publicado en 2000

Predictive diagnosis of multiple endocrine neoplasia (MEN 1) in four Australian kindreds

article

Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms

artículo científico publicado el 1 de abril de 1992

Preparing the "soil": the primary tumor induces vasculature reorganization in the sentinel lymph node before the arrival of metastatic cancer cells

artículo científico publicado en 2006

Prognostic value of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) and TRAIL receptors in renal cell cancer

artículo científico publicado en 2009

Prospective clinical trial of preoperative sunitinib in patients with renal cell carcinoma

artículo científico publicado en 2010

Prospects for vasculature reorganization in sentinel lymph nodes

artículo científico publicado en 2007

Radiosensitization by inhibiting STAT1 in renal cell carcinoma

artículo científico publicado en 2009

Recognizing the Continuous Nature of Expression Heterogeneity and Clinical Outcomes in Clear Cell Renal Cell Carcinoma.

artículo científico publicado en 2017

Regulation of endocytosis via the oxygen-sensing pathway

artículo científico publicado en 2009

Renal cell carcinoma deep sequencing: recent developments

artículo científico

Renal medullary carcinoma: molecular, pathological and clinical evidence for treatment with topoisomerase-inhibiting therapy

artículo científico

Renal neoplasia in the hyperparathyroidism-jaw tumor syndrome

artículo científico publicado en 2004

Renal papillary adenoma--a putative precursor of papillary renal cell carcinoma

artículo científico publicado en 2006

Renal translocation carcinomas: clinicopathologic, immunohistochemical, and gene expression profiling analysis of 31 cases with a review of the literature.

artículo científico publicado en 2008

Reversible epithelial to mesenchymal transition and acquired resistance to sunitinib in patients with renal cell carcinoma: evidence from a xenograft study

artículo científico publicado en 2010

Robust classification of renal cell carcinoma based on gene expression data and predicted cytogenetic profiles

artículo científico publicado en 2004

Role of eIF3a in regulating cisplatin sensitivity and in translational control of nucleotide excision repair of nasopharyngeal carcinoma

artículo científico publicado en 2011

SETD2 histone modifier loss in aggressive GI stromal tumours

artículo científico publicado en 2015

Serglycin expression: An independent marker of distant metastases in nasopharyngeal carcinoma.

artículo científico publicado en 2015

Serglycin is a theranostic target in nasopharyngeal carcinoma that promotes metastasis

artículo científico publicado en 2011

Sex specific associations in genome wide association analysis of renal cell carcinoma

scientific article published on 23 June 2019

Signatures of mutation and selection in the cancer genome

artículo científico publicado en 2010

Single base mutation in the hormone binding domain of the thyroid hormone receptor beta gene in generalised thyroid hormone resistance demonstrated by single stranded conformation polymorphism analysis.

artículo científico publicado en 1991

Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer

artículo científico publicado en 2009

Somatic mutations of the protein kinase gene family in human lung cancer

artículo científico publicado en 2005

Somatic pairing of chromosome 19 in renal oncocytoma is associated with deregulated EGLN2-mediated [corrected] oxygen-sensing response

artículo científico publicado en 2008

Sporadic primary hyperparathyroidism in the setting of multiple endocrine neoplasia type 1

scientific article published on 01 November 1996

Sunitinib acts primarily on tumor endothelium rather than tumor cells to inhibit the growth of renal cell carcinoma

artículo científico publicado en 2010

Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes

artículo científico publicado en 2010

The E2F3-Oncomir-1 axis is activated in Wilms' tumor

artículo científico publicado en 2008

The Opisthorchis viverrini genome provides insights into life in the bile duct

artículo científico publicado en 2014

The draft genome of tropical fruit durian (Durio zibethinus).

artículo científico publicado en 2017

The effect of Aurora kinases on cell proliferation, cell cycle regulation and metastasis in renal cell carcinoma

artículo científico publicado en 2012

The importance of including diverse populations in cancer genomic and epigenomic studies

scientific article published on 01 July 2019

The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study

scientific article published on 03 January 2019

The investigational Aurora kinase A inhibitor MLN8237 induces defects in cell viability and cell-cycle progression in malignant bladder cancer cells in vitro and in vivo.

artículo científico publicado en 2013

The management of familial breast cancer.

artículo científico publicado en 2000

The performance of CGH array for the detection of cryptic constitutional chromosome imbalances

artículo científico publicado en 2004

The phospholipase C beta 3 gene located in the MEN1 region shows loss of expression in endocrine tumours

artículo científico publicado en 1994

The t(1;3) breakpoint-spanning genes LSAMP and NORE1 are involved in clear cell renal cell carcinomas

artículo científico publicado en 2003

The tumor suppressor parafibromin is required for posttranscriptional processing of histone mRNA.

artículo científico publicado en 2010

Therapeutic and immunomodulatory potential of pazopanib in malignant phyllodes tumor

artículo científico publicado en 2022

Thymic carcinoid in multiple endocrine neoplasia 1: genotype-phenotype correlation and prevention

artículo científico publicado en 2006

Thymic carcinoids in multiple endocrine neoplasia type 1

scientific article published on 01 July 1998

Thymic carcinoids in multiple endocrine neoplasia type 1

artículo científico publicado en 1998

Tissue Microbiome Profiling Identifies an Enrichment of Specific Enteric Bacteria in Opisthorchis viverrini Associated Cholangiocarcinoma

artículo científico publicado en 2016

Topoisomerase IIalpha in Wilms' tumour: gene alterations and immunoexpression.

artículo científico publicado en 2006

Transient bilateral abducens neuropathy with post-tetanic facilitation and acute hypokalemia associated with oxaliplatin: a case report

artículo científico publicado en 2010

Tubulocystic carcinoma of the kidney: clinicopathologic and molecular characterization

scientific article published on 01 February 2008

Tumor suppressor activity and epigenetic inactivation of hepatocyte growth factor activator inhibitor type 2/SPINT2 in papillary and clear cell renal cell carcinoma

artículo científico publicado en 2005

Tumor suppressor genes (TSG).

artículo científico publicado en 1999

Two distinct types of blood vessels in clear cell renal cell carcinoma have contrasting prognostic implications

artículo científico publicado en 2007

Type II EATL (epitheliotropic intestinal T-cell lymphoma): a neoplasm of intra-epithelial T-cells with predominant CD8αα phenotype.

artículo científico

Upper tract urothelial carcinomas in patients with chronic kidney disease: relationship with diagnostic challenge

artículo científico publicado en 2014

VHL promotes E2 box-dependent E-cadherin transcription by HIF-mediated regulation of SIP1 and snail

artículo científico publicado en 2006

VHL substrate transcription factor ZHX2 as an oncogenic driver in clear cell renal cell carcinoma

artículo científico publicado en 2018

VX680/MK-0457, a potent and selective Aurora kinase inhibitor, targets both tumor and endothelial cells in clear cell renal cell carcinoma.

artículo científico publicado en 2010

Vascular endothelial growth factor expression is increased in renal cell carcinoma

artículo científico publicado en 1997

Whole-exome sequencing of breast cancer, malignant peripheral nerve sheath tumor and neurofibroma from a patient with neurofibromatosis type 1.

artículo científico publicado en 2015

Whole-exome sequencing studies of parathyroid carcinomas reveal novel PRUNE2 mutations, distinctive mutational spectra related to APOBEC-catalyzed DNA mutagenesis and mutational enrichment in kinases associated with cell migration and invasion.

artículo científico publicado en 2014

Whole-genome reconstruction and mutational signatures in gastric cancer.

artículo científico publicado en 2012

[Prophylactic parathyroidectomy for familial parathyroid carcinoma]

artículo científico publicado en 2006

cDNA microarray analysis assists in diagnosis of malignant intrarenal pheochromocytoma originally masquerading as a renal cell carcinoma

artículo científico publicado en 2005

p38delta/MAPK13 as a diagnostic marker for cholangiocarcinoma and its involvement in cell motility and invasion

artículo científico publicado en 2010