- KAIKA S.A.S (found in: Contact)
- Research Instruments Sdn Bhd (found in: Contact)
- Scientific Technical Corporation (found in: Contact)
- ALOGO, s.r.o. (found in: Contact)
- Defining the steps that lead to cancer: Replicative telomere erosion, aneuploidy and an epigenetic maturation arrest of tissue stem cells. (found in: Publications)
- Distinct classes of chromosomal rearrangements create oncogenic ETS gene fusions in prostate cancer. (found in: Publications)
- Strategy for population triage based on dicentric analysis. (found in: Publications)
- Elevated chromosome translocation frequencies in New Zealand nuclear test veterans. (found in: Publications)
- Human telomere length correlates to the size of the associated chromosome arm. (found in: Publications)
- Automated FISH analysis using dual-fusion and break-apart probes on paraffin-embedded tissue sections. (found in: Publications)
- Chromosomal 20q gain in the DNA diploid component of aneuploid colorectal carcinomas. (found in: Publications)
- Analysis of complex chromosomal rearrangements in adult patients with MDS and AML by multicolor FISH. (found in: Publications)
- Automated four-color interphase fluorescence in situ hybridization approach for the simultaneous detection of specific aneuploidies of diagnostic and prognostic significance in high hyperdiploid acute lymphoblastic leukemia. (found in: Publications)
- Nuclear FISH. Automation, analysis, and interpretation. (found in: Publications)
- Cytosine arabinoside, vinblastine, 5-fluorouracil and 2-aminoanthracenetesting in the in vitro micronucleus assay with L5178Y mouse lymphomacells at Sanofi Aventis, with different cytotoxicity measurements,in support of the draft OECD Test Guidel (found in: Publications)
- Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cells. (found in: Publications)
- Detailed characterization of 7q deletions by multicolor banding (mBAND) in marginal zone cell lymphoma. (found in: Publications)
- A new platform linking chromosomal and sequence information. (found in: Publications)
- Sequence based high resolution chromosomal CGH. (found in: Publications)
- Cancer-causing karyotypes: chromosomal equilibria between destabilizing aneuploidy and stabilizing selection for oncogenic function. (found in: Publications)
- Automated image analysis of micronuclei in binucleated human lymphocytes. (found in: Publications)
- Entamoeba histolytica encodes unique formins, a subset of which regulates DNA content and cell division. (found in: Publications)
- Comprehensive assessment of TMPRSS2 and ETS family gene aberrations in clinically localized prostate cancer. (found in: Publications)
- Automatic telomere length measurements in interphase nuclei by IQ-FISH. (found in: Publications)
- Development of automated brightfield double In Situ hybridization (BDISH) application for HER2 gene and chromosome 17 centromere (CEN 17) for breast carcinomas and an assay performance comparison to manual dual color HER2 fluorescence In Situ hybridizatio (found in: Publications)
- Detection of Malignant Cells in Cerebrospinal Fluid Using Fluorescence In Situ Hybridization (found in: Publications)
- Chromosome inter- and intrachanges detected by arm-specific DNA probes in the progeny of human lymphocytes exposed to energetic heavy ions. (found in: Publications)
- Mutations in the pericentrin (PCNT) gene cause primordial dwarfism (found in: Publications)
- Gene amplification in myeloid leukemias elucidated by fluorescence in situ hybridization. (found in: Publications)
- The impact of air pollution on the levels of micronuclei measured by automated image analysis. (found in: Publications)
- Assessment of potential cancer risk in children exposed to urban air pollution in Bangkok, Thailand. (found in: Publications)
- 21XMouse (Multicolor FISH Probe for Mouse Chromosomes, D-0425-060-DI)
- XL PDGFRB (Break Apart Probe, D-5031-100-OG)
- XL CLL Probe Kit (XL DLEU/LAMP/12cen + XL ATM/TP53) (Deletion/Enumeration Probe, D-5044-100-TC)
- XL BCR/ABL1 plus (Translocation/Dual Fusion Probe, D-5052-100-OG)
- XL DLEU/LAMP/12cen (Deletion/Enumeration Probe, D-5055-100-TC)
- XL MLL plus (Break Apart Probe, D-5060-100-OG)
- XL t(14;16) (Translocation/Dual Fusion Probe, D-5072-100-OG)
- XL EGFR amp (Amplification Probe, D-6005-100-OG)
- XL MYC amp (Amplification Probe, D-6008-100-OG)
- XL ERBB2 (HER2/NEU) amp (Amplification Probe, D-6010-100-OG)
- XL BCL2 BA (Break Apart Probe, D-6018-100-OG)
- XL ROS1-GOPC BA (Break Apart Probe, D-6029-100-OG)
- TissueFISH Pretreatment Kit (General Reagents, D-0905-025-TF)
- XL 4q12 (Translocation/Deletion Probe, D-5063-100-TC)
- XL MALT1 BA (Break Apart Probe, D-6015-100-OG)
- XL 5p15/9q22/15q22 Hyperdiploidy (Enumeration Probe, D-5095-100-TC)
- 21XMouse (Multicolor FISH Probe for Mouse Chromosomes, D-0425-120-DI)
- XL t(8;21) plus (Translocation/Dual Fusion Probe, D-5114-100-OG)
- XL TCRA/D (Break Apart Probe, D-5106-100-OG)
- XL 5q32 PDGFRB BA (Break Apart Probe, D-5104-100-OG)
- XL t(4;14) FGFR3/IGH DF (Translocation/Dual Fusion Probe, D-5108-100-OG)
- XL 4q12 DC (Translocation/Deletion Probe, D-5123-100-OG)
- XL TLX3 BA (Break Apart Probe, D-5129-100-OG)
- XL 20q12/20qter/8cen plus (Deletion/Isochromosome/Enumeration Probe, D-5122-100-TC)
- XL FOXO1 BA (Break Apart Probe, D-6034-100-OG)
- XL PDGFRA BA (Break Apart Probe, D-5137-100-OG)
- XL Wolf-Hirschhorn (Deletion Probe, D-5416-050-OG)
- XL Williams-Beuren (Deletion Probe, D-5418-050-OG)
- XL t(14;18) IGH/MALT1 DF (Translocation/Dual Fusion Probe, D-6020-100-OG)
- XL TCL1 BA (Break Apart Probe, D-5142-100-OG)
- MetaSystems India (found in: Contact)
- Carl Zeiss Pty Ltd South Africa (found in: Contact)
- VITCO / Vira Idea Trade Co. (found in: Contact)
- Carl Zeiss do Brasil (found in: Contact)
- The micronucleus assay in radiation accidents (found in: Publications)
- A rapid, semi-automated method for scoring micronuclei in mononucleatedmouse lymphoma cells. (found in: Publications)
- Validation of automatic scanning of microscope slides in recoveringrare cellular events: application for detection of fetal cells inmaternal blood. (found in: Publications)
- Impact of additional cytogenetic aberrations at diagnosis on prognosisof CML: long-term observation of 1151 patients from the randomizedCML Study IV. (found in: Publications)
- A new marker set that identifies fetal cells in maternal circulationwith high specificity. (found in: Publications)
- Telomere shortening and chromosomal instability in myelodysplasticsyndromes. (found in: Publications)
- FISH and tips: a large scale analysis of automated versus manual scoring for sperm aneuploidy detection (found in: Publications)
- Validation of a fully automated COMET assay: 1.75 million singlecells measured over a 5 year period. (found in: Publications)
- Persisting ring chromosomes detected by mFISH in lymphocytes of acancer patient-A case report. (found in: Publications)
- Multiple mechanisms limit meiotic crossovers: TOP3alpha and two BLM homologs antagonize crossovers in parallel to FANCM. (found in: Publications)
- Analysis of chromosome translocation frequency after a single CT scan in adults. (found in: Publications)
- Evaluation of ETV6/RUNX1 Fusion and Additional Abnormalities Involving ETV6 and/or RUNX1 Genes Using FISH Technique in Patients with Childhood Acute Lymphoblastic Leukemia. (found in: Publications)
- Genotoxic risk of ethyl-paraben could be related to telomere shortening. (found in: Publications)
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