(Q36730935)

English

Loss of heterozygosity and copy number abnormality in clear cell renal cell carcinoma discovered by high-density affymetrix 10K single nucleotide polymorphism mapping array

scientific article published on July 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Loss of heterozygosity and copy number abnormality in clear cell renal cell carcinoma discovered by high-density affymetrix 10K single nucleotide polymorphism mapping array (English)

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

renal cell carcinoma

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Marieta I Toma

1

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Marianne Grosser

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Alexander Herr

3

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Daniela E Aust

4

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Axel Meye

5

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Christian Hoefling

6

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Susanne Fuessel

7

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Daniela Wuttig

8

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Manfred P Wirth

9

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Gustavo B Baretton

10

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

publication date

1 July 2008

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

10

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

7

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

634-642

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Mechanisms of disease: hereditary leiomyomatosis and renal cell cancer--a distinct form of hereditary kidney cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

The major 8p22 tumor suppressor DLC1 is frequently silenced by methylation in both endemic and sporadic nasopharyngeal, esophageal, and cervical carcinomas, and inhibits tumor cell colony formation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

Loss of heterozygosity analyzed by single nucleotide polymorphism array in cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

Abnormal methylation of the common PARK2 and PACRG promoter is associated with downregulation of gene expression in acute lymphoblastic leukemia and chronic myeloid leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

Loss of expression and nuclear/cytoplasmic localization of the FOXP1 forkhead transcription factor are common events in early endometrial cancer: relationship with estrogen receptors and HIF-1alpha expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

Expression of the forkhead transcription factor FOXP1 is associated with estrogen receptor alpha and improved survival in primary human breast carcinomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

Gene expression patterns in renal cell carcinoma assessed by complementary DNA microarray.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

Identification of a novel gene linked to parkin via a bi-directional promoter

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

The FOXP1 winged helix transcription factor is a novel candidate tumor suppressor gene on chromosome 3p.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

Expression profiling of renal epithelial neoplasms: a method for tumor classification and discovery of diagnostic molecular markers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

A new mathematical model for relative quantification in real-time RT-PCR

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

CDKNA2A mutation analysis, protein expression, and deletion mapping of chromosome 9p in conventional clear-cell renal carcinomas: evidence for a second tumor suppressor gene proximal to CDKN2A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

Role of chromosome 3p12-p21 tumour suppressor genes in clear cell renal cell carcinoma: analysis of VHL dependent and VHL independent pathways of tumorigenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

Association between early-onset Parkinson's disease and mutations in the parkin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

30 September 2017

Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL-independent pathway in clear cell renal tumourigenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

28 June 2018

Mutations of the VHL tumour suppressor gene in renal carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

28 June 2018

Gene array studies in renal neoplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

5 September 2018

High-resolution analysis of chromosomal imbalances using the Affymetrix 10K SNP genotyping chip.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

5 September 2018

Positive correlation between allelic loss at chromosome 14q24-31 and poor prognosis of patients with renal cell carcinoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

5 September 2018

Array-based comparative genomic hybridization for the differential diagnosis of renal cell cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

5 September 2018

Genetic aberrations detected by comparative genomic hybridization are associated with clinical outcome in renal cell carcinoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

5 September 2018

A combination of molecular cytogenetic analyses reveals complex genetic alterations in conventional renal cell carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435001

4 December 2018

Cytogenetic and molecular findings in 75 clear cell renal cell carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/18592004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sporadic human renal tumors display frequent allelic imbalances and novel mutations of the HRPT2 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18592004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic loss of 3p25 associated with alterations of 5q22.3 approximately q23.2 may affect the prognosis of conventional renal cell carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/18592004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays

1 reference

https://pubmed.ncbi.nlm.nih.gov/18592004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic imbalances in human bladder cancer: genome-wide detection with high-density single-nucleotide polymorphism arrays

1 reference

https://pubmed.ncbi.nlm.nih.gov/18592004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ALLELIC LOSS ON CHROMOSOMES 8 AND 9 CORRELATES WITH CLINICAL OUTCOME IN LOCALLY ADVANCED CLEAR CELL CARCINOMA OF THE KIDNEY

1 reference

https://pubmed.ncbi.nlm.nih.gov/18592004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comprehensive mutational analysis of the VHL gene in sporadic renal cell carcinoma: relationship to clinicopathological parameters

1 reference

https://pubmed.ncbi.nlm.nih.gov/18592004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 14q LOH in localized clear cell renal cell carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/18592004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide genetic characterization of bladder cancer: a comparison of high-density single-nucleotide polymorphism arrays and PCR-based microsatellite analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18592004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of 14q31-q32.2 in renal cell carcinoma is associated with high malignancy grade and poor survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/18592004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic alterations and instabilities in renal cell carcinomas and their relationship to tumor pathology

1 reference

https://pubmed.ncbi.nlm.nih.gov/18592004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide detection of allelic imbalance in renal cell carcinoma using high-density single-nucleotide polymorphism microarrays.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18592004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1593/NEO.08160

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

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