Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays - Wikidata - thesis-toulmin - TriplyDB

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

http://www.wikidata.org/entity/Q24676798

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Virtual karyotyping with SNP microarrays reduces uncertainty in the diagnosis of renal epithelial tumors Microcephaly with simplified gyration, epilepsy, and infantile diabetes linked to inappropriate apoptosis of neural progenitors TMEM165 deficiency causes a congenital disorder of glycosylation Prevalence and prognostic impact of allelic imbalances associated with leukemic transformation of Philadelphia chromosome-negative myeloproliferative neoplasms Array-based karyotyping for prognostic assessment in chronic lymphocytic leukemia: performance comparison of Affymetrix 10K2.0, 250K Nsp, and SNP6.0 arrays Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray Integrated molecular analysis of clear-cell renal cell carcinoma.Genomic and molecular characterization of esophageal squamous cell carcinoma Quantification of normal cell fraction and copy number neutral LOH in clinical lung cancer samples using SNP array data Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders The CRKL gene encoding an adaptor protein is amplified, overexpressed, and a possible therapeutic target in gastric cancer.Comprehensive SNP array study of frequently used neuroblastoma cell lines; copy neutral loss of heterozygosity is common in the cell lines but uncommon in primary tumors High-resolution whole-genome analysis of skull base chordomas implicates FHIT loss in chordoma pathogenesis SNP array karyotyping allows for the detection of uniparental disomy and cryptic chromosomal abnormalities in MDS/MPD-U and MPD.Major copy proportion analysis of tumor samples using SNP arrays.High-resolution array copy number analyses for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors: four cases of homozygous deletions of the CDKN2A gene.Molecular allelokaryotyping of T-cell prolymphocytic leukemia cells with high density single nucleotide polymorphism arrays identifies novel common genomic lesions and acquired uniparental disomy Oncogene mutations, copy number gains and mutant allele specific imbalance (MASI) frequently occur together in tumor cells.SNP array analysis of tyrosine kinase inhibitor-resistant chronic myeloid leukemia identifies heterogeneous secondary genomic alterations.TumorBoost: normalization of allele-specific tumor copy numbers from a single pair of tumor-normal genotyping microarrays A statistical approach for detecting genomic aberrations in heterogeneous tumor samples from single nucleotide polymorphism genotyping data High-risk neuroblastoma tumors with 11q-deletion display a poor prognostic, chromosome instability phenotype with later onset.Association between acquired uniparental disomy and homozygous mutations and HER2/ER/PR status in breast cancer Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies A novel SNP analysis method to detect copy number alterations with an unbiased reference signal directly from tumor samples.miR-34a functions as a tumor suppressor modulating EGFR in glioblastoma multiforme BACOM: in silico detection of genomic deletion types and correction of normal cell contamination in copy number data.Renal cell carcinoma primary cultures maintain genomic and phenotypic profile of parental tumor tissues.Genomic profiling of adult acute lymphoblastic leukemia by single nucleotide polymorphism oligonucleotide microarray and comparison to pediatric acute lymphoblastic leukemia Genome-wide Mapping of Copy Number Variations Using SNP Arrays.SNP array analysis of acute promyelocytic leukemia may be of prognostic relevance and identifies a potential high risk group with recurrent deletions on chromosomal subband 1q31.3.A genome-wide homozygosity association study identifies runs of homozygosity associated with rheumatoid arthritis in the human major histocompatibility complex.Copy number alteration and uniparental disomy analysis categorizes Japanese papillary thyroid carcinomas into distinct groups.Single nucleotide polymorphism (SNP)-based loss of heterozygosity (LOH) testing by real time PCR in patients suspect of myeloproliferative disease Allelotypes of lung adenocarcinomas featuring ALK fusion demonstrate fewer onco- and suppressor gene changes.Genetic instability and intratumoral heterogeneity in neuroblastoma with MYCN amplification plus 11q deletion.Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms.Common somatic alterations identified in maffucci syndrome by molecular karyotyping Identifying the similarities and differences between single nucleotide polymorphism array (SNPa) analysis and karyotyping in acute myeloid leukemia and myelodysplastic syndromes.Establishment and characterization of novel human primary and metastatic anaplastic thyroid cancer cell lines and their genomic evolution over a year as a primagraft.

P2860

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P2860

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

http://www.wikidata.org/entity/Q24676798

description

2007 nî lūn-bûn

@nan

2007 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի հուլիսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Highly sensitive method for ge ...... orphism genotyping microarrays

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Highly sensitive method for ge ...... orphism genotyping microarrays

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Highly sensitive method for ge ...... orphism genotyping microarrays

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type

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Highly sensitive method for ge ...... orphism genotyping microarrays

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Highly sensitive method for ge ...... orphism genotyping microarrays

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Highly sensitive method for ge ...... orphism genotyping microarrays

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Highly sensitive method for ge ...... orphism genotyping microarrays

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P1433

American Journal of Human Genetics

P1476

Highly sensitive method for ge ...... orphism genotyping microarrays

@en

P2093

Akira Hangaishi

http://www.w3.org/2001/XMLSchema#string

D Gary Gilliland

http://www.w3.org/2001/XMLSchema#string

Go Yamamoto

http://www.w3.org/2001/XMLSchema#string

H Phillip Koeffler

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Masashi Sanada

http://www.w3.org/2001/XMLSchema#string

Mineo Kurokawa

http://www.w3.org/2001/XMLSchema#string

Norihiko Kawamata

http://www.w3.org/2001/XMLSchema#string

Ross L Levine

http://www.w3.org/2001/XMLSchema#string

Seishi Ogawa

http://www.w3.org/2001/XMLSchema#string

Shigeru Chiba

http://www.w3.org/2001/XMLSchema#string

P2860

Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arrays

Two genetic hits (more or less) to cancer

CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.

Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays.

A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera

A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia

Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis

A gain-of-function mutation of JAK2 in myeloproliferative disorders

Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array data.

P304

114-26

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scholarly article

P356

10.1086/518809

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P407

P433

1

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P478

81

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P577

2007-07-01T00:00:00Z

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P5875

6272032

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P698

17564968

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P921

single-nucleotide polymorphism

P932

1950910

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