Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays (Q28144479)

22 June 2017

title

Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays (English)

1 reference

22 June 2017

R Mei

1

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22 June 2017

P C Galipeau

2

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22 June 2017

C Prass

3

1 reference

22 June 2017

A Berno

4

1 reference

22 June 2017

G Ghandour

5

1 reference

22 June 2017

N Patil

6

1 reference

22 June 2017

R K Wolff

7

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22 June 2017

M S Chee

8

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22 June 2017

B J Reid

9

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22 June 2017

D J Lockhart

10

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22 June 2017

publication date

1 August 2000

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22 June 2017

language of work or name

0 references

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22 June 2017

volume

10

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22 June 2017

issue

8

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22 June 2017

page(s)

1126-1137

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Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

22 June 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Characterization of single-nucleotide polymorphisms in coding regions of human genes

20 March 2017

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Evolution of neoplastic cell lineages in Barrett oesophagus

20 March 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Expression monitoring by hybridization to high-density oligonucleotide arrays

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Light-generated oligonucleotide arrays for rapid DNA sequence analysis

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Genome-wide analysis of DNA copy-number changes using cDNA microarrays

20 March 2017

1 reference

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Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Loss of heterozygosity analysis using whole genome amplification, cell sorting, and fluorescence-based PCR.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Allelotype of gastric adenocarcinoma.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Mitotic recombination map of 13cen-13q14 derived from an investigation of loss of heterozygosity in retinoblastomas

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Allelotype analysis of oesophageal adenocarcinoma: loss of heterozygosity occurs at multiple sites

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Genome screening by comparative genomic hybridization

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

PCR-based microsatellite polymorphisms in the detection of loss of heterozygosity in fresh and archival tumour tissue

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Comprehensive allelotyping of human renal cell carcinomas using microsatellite DNA probes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Multiplexed biochemical assays with biological chips

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Genetics of cancer predisposition.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Allelotype of colorectal carcinomas

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Human tumor suppressor genes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Light-directed, spatially addressable parallel chemical synthesis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumors

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

High-resolution allelotype analysis of childhood B-lineage acute lymphoblastic leukemia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Allelotype analysis of adenocarcinoma of the gastric cardia

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Allelotype and replication error phenotype of small cell lung carcinoma

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Tumor Suppressor Genes and Human Cancer

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Allelotype analysis of childhood acute lymphoblastic leukemia

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Allelotype of squamous cell carcinoma of the head and neck: fractional allele loss correlates with survival.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Hereditary cancer, oncogenes, and antioncogenes.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Allelotype of human malignant astrocytoma

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Allelotype analysis in osteosarcomas: frequent allele loss on 3q, 13q, 17p, and 18q.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Mutation detection by ligation to complete n-mer DNA arrays

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Concerted nonsyntenic allelic losses in hyperploid hepatocellular carcinoma as determined by a high-resolution allelotype

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Accessing genetic information with high-density DNA arrays

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2235196

Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer

27 November 2018

1 reference

12 December 2020

Allelotype of non-small cell lung carcinoma--comparison between loss of heterozygosity in squamous cell carcinoma and adenocarcinoma

1 reference

12 December 2020

Determination of the frequency of loss of heterozygosity in esophageal adenocarcinoma by cell sorting, whole genome amplification and microsatellite polymorphisms

1 reference

12 December 2020

Allelotype of salivary gland tumors

1 reference

12 December 2020

Allelotype analysis of esophageal adenocarcinomas: evidence for the involvement of sequences on the long arm of chromosome 4

1 reference

12 December 2020

An allelotype of papillary thyroid cancer

1 reference

12 December 2020

Allelotype of adenoma and differentiated adenocarcinoma of the stomach

1 reference

12 December 2020

Barrett's esophagus: ordering the events that lead to cancer

1 reference

12 December 2020

High frequency in vivo loss of heterozygosity is primarily a consequence of mitotic recombination

1 reference

12 December 2020

The use of a genetic map of biallelic markers in linkage studies

1 reference

12 December 2020

Allelotype analysis in the evolution of chronic myelocytic leukemia

1 reference

12 December 2020

Allelic loss in childhood acute lymphoblastic leukemia

1 reference

12 December 2020

Genome-wide expression monitoring in Saccharomyces cerevisiae

1 reference

12 December 2020

Allelotype analysis of hepatocellular carcinoma

1 reference

12 December 2020

No evidence for microsatellite instability from allelotype analysis of benign and low malignant potential ovarian neoplasms

1 reference

12 December 2020

Allelotype analysis of adult T-cell leukemia

1 reference

12 December 2020

Allelotype of pancreatic adenocarcinoma using xenograft enrichment

1 reference

12 December 2020

Allelotype of uterine leiomyomas

1 reference

12 December 2020

Identifiers

DOI

10.1101/GR.10.8.1126

1 reference

22 June 2017

0 references

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