Pages that link to "Q81362541"
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The following pages link to Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias (Q81362541):
Displaying 50 items.
- Structural and functional alterations of FLT3 in acute myeloid leukemia (Q24338964) (← links)
- Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML (Q24645177) (← links)
- The application of single nucleotide polymorphism microarrays in cancer research (Q24653582) (← links)
- Allelic imbalances and microdeletions affecting the PTPRD gene in cutaneous squamous cell carcinomas detected using single nucleotide polymorphism microarray analysis (Q24657188) (← links)
- Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays (Q24676798) (← links)
- Molecular landscape of acute myeloid leukemia in younger adults and its clinical relevance (Q26776393) (← links)
- Genetic and molecular pathogenesis of mantle cell lymphoma: perspectives for new targeted therapeutics (Q27851412) (← links)
- Use of single nucleotide polymorphism array technology to improve the identification of chromosomal lesions in leukemia (Q28390558) (← links)
- Mll partial tandem duplication and Flt3 internal tandem duplication in a double knock-in mouse recapitulates features of counterpart human acute myeloid leukemias (Q28594733) (← links)
- Quantification of normal cell fraction and copy number neutral LOH in clinical lung cancer samples using SNP array data (Q28752458) (← links)
- SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levels (Q33316565) (← links)
- Prevalence of copy-number neutral LOH in glioblastomas revealed by genomewide analysis of laser-microdissected tissues (Q33359490) (← links)
- Association between polymorphisms in RMI1, TOP3A, and BLM and risk of cancer, a case-control study (Q33443484) (← links)
- Leukemia associated antigens: their dual role as biomarkers and immunotherapeutic targets for acute myeloid leukemia (Q33491557) (← links)
- Oncogene mutations, copy number gains and mutant allele specific imbalance (MASI) frequently occur together in tumor cells (Q33510334) (← links)
- Genome wide analysis of DNA copy number neutral loss of heterozygosity (CNNLOH) and its relation to gene expression in esophageal squamous cell carcinoma (Q33721447) (← links)
- Association between Acquired Uniparental Disomy and Homozygous Mutations and HER2/ER/PR Status in Breast Cancer (Q33770092) (← links)
- Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies (Q33788643) (← links)
- Homozygous inv(11)(q21q23) and MLL gene rearrangement in two patients with myeloid neoplasms (Q33898504) (← links)
- Prevalence and prognostic implications of WT1 mutations in pediatric acute myeloid leukemia (AML): a report from the Children's Oncology Group. (Q34052581) (← links)
- NF1 inactivation in adult acute myelogenous leukemia (Q34065032) (← links)
- Submicroscopic deletion of 5q involving tumor suppressor genes (CTNNA1, HSPA9) and copy neutral loss of heterozygosity associated with TET2 and EZH2 mutations in a case of MDS with normal chromosome and FISH results (Q34109454) (← links)
- Genomic aberrations in myeloid sarcoma without blood or bone marrow involvement: characterization of formalin-fixed paraffin-embedded samples by chromosomal microarrays (Q34146721) (← links)
- Accurate detection of uniparental disomy and microdeletions by SNP array analysis in myelodysplastic syndromes with normal cytogenetics (Q34179367) (← links)
- The Biology and Targeting of FLT3 in Pediatric Leukemia (Q34229555) (← links)
- Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia (Q34411660) (← links)
- Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia (Q34450715) (← links)
- Rapid Identification of Therapeutic Targets in Hematologic Malignancies via Functional Genomics (Q34654334) (← links)
- Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies (Q34997720) (← links)
- High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping (Q35012994) (← links)
- Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2. (Q35023429) (← links)
- Loss of the wild-type allele contributes to myeloid expansion and disease aggressiveness in FLT3/ITD knockin mice (Q35525611) (← links)
- Clinical relevance of mutations and gene-expression changes in adult acute myeloid leukemia with normal cytogenetics: are we ready for a prognostically prioritized molecular classification? (Q35615901) (← links)
- JAK2 V617F in myeloid disorders: molecular diagnostic techniques and their clinical utility: a paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology (Q35790260) (← links)
- Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies (Q35849015) (← links)
- High-resolution genomic profiling of adult and pediatric core-binding factor acute myeloid leukemia reveals new recurrent genomic alterations (Q35849281) (← links)
- Interchromosomal crossover in human cells is associated with long gene conversion tracts (Q35950053) (← links)
- Application of oligonucleotide arrays to high-content genetic analysis (Q36481133) (← links)
- Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays (Q36802303) (← links)
- Whole genome scanning as a cytogenetic tool in hematologic malignancies (Q36835203) (← links)
- A decade of genome-wide gene expression profiling in acute myeloid leukemia: flashback and prospects (Q37041909) (← links)
- Cooperating gene mutations in acute myeloid leukemia: a review of the literature. (Q37089717) (← links)
- Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity (Q37090402) (← links)
- Dysregulation of the C/EBPalpha differentiation pathway in human cancer (Q37104787) (← links)
- Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations (Q37109353) (← links)
- Genome-wide loss of heterozygosity and uniparental disomy in BRCA1/2-associated ovarian carcinomas (Q37180251) (← links)
- Genetic complexity of myeloproliferative neoplasms. (Q37255024) (← links)
- Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms (Q37262428) (← links)
- Acquired copy number alterations in adult acute myeloid leukemia genomes (Q37276767) (← links)
- Chromosomal abnormalities and novel disease-related regions in progression from Barrett's esophagus to esophageal adenocarcinoma (Q37398079) (← links)