- XL RB1/DLEU/
LAMP (Deletion Probe, D-5070-100-TC) - MetaSystems Germany (found in: Contact)
- Carl Zeiss Co., Ltd (カールツァイス株式会社) (found in: Contact)
- Attieh Medico (found in: Contact)
- Carl Zeiss A/S (found in: Contact)
- Werfen S.A.U. (found in: Contact)
- Biosphere Company (found in: Contact)
- Carl Zeiss Sp. z.o.o. (found in: Contact)
- ANNAR Health Technologies (found in: Contact)
- Chaco Internacional SA (found in: Contact)
- Frequent gains of the short arm of chromosome 9 in Multiple Myeloma with normal G-banded karyotype detected by comparative genomic hybridization. (found in: Publications)
- Fluorescence in situ hybridization for the detection of t(X;18)(p11.2;q11.2) in a Synovial Sarcoma tissuemicroarray using a breakapart-style probe. (found in: Publications)
- Automation of manual components and image quantification of direct dual label fluorescence in situ hybridization (FISH) for HER2 gene amplification: A feasibility study. (found in: Publications)
- Early increase of radiation-induced gamma-H2AX foci in a human Ku70/80knockdown cell line characterized by an enhanced radiosensitivity. (found in: Publications)
- An automated scoring procedure for the micronucleus test by image analysis (found in: Publications)
- Telomerase-independent cell survival in Arabidopsis thaliana. (found in: Publications)
- Time-saving in biological dosimetry by using the automatic metaphase finder Metafer2 (found in: Publications)
- New insights into the evolution of chromosome 1. (found in: Publications)
- Are telomeres a specific target for mutagenic attack by cytostatics in neoplastic cells? (found in: Publications)
- Heterogeneity of BCL6 rearrangements in nodular lymphocyte predominant Hodgkin's lymphoma (found in: Publications)
- Prognostic value of structural chromosomal rearrangements and small cell clones with high hyperdiploidy in children with acute lymphoblastic leukemia. (found in: Publications)
- Does a sentinel or a subset of short telomeres determine replicative senescence? (found in: Publications)
- A recurrent translocation breakpoint in breast and pancreatic cancer cell lines targets the Neuregulin/NRG I gene (found in: Publications)
- Disseminated tumour cells in the bone marrow - chances and consequences of microscopical detection methods (found in: Publications)
- Molecular characterizations of derivatives of HCT116 colorectal cancer cells that are resistant to the chemotherapeutic agent 5-fluorouracil. (found in: Publications)
- Secretory carcinoma of the breast containing the ETV6-NTRK3 fusion gene in a male: case report and review of the literature (found in: Publications)
- Fluorescence in situ hybridization analysis of two blastomeres from day 3 frozen-thawed embryos followed by analysis of the remaining embryo on day 5. (found in: Publications)
- Quantitative molecular urinary cytology by fluorescence in situ hybridization: a tool for tailoring surveillance of patients with superficial bladder cancer? (found in: Publications)
- ATM stabilizes DNA double-strand-break complexes during V(D)J recombination. (found in: Publications)
- Systematic genome-wide screens of gene function. (found in: Publications)
- The presence of clonal cell subpopulations in peripheral blood and bone marrow of patients with refractory cytopenia with multilieage dysplasia but not in patients with refractory anemia may reflect a multistep pathogenesis of myelodysplasia. (found in: Publications)
- Fetal cells in maternal blood: a comparison of methods for cell isolation and identification. (found in: Publications)
- mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrations (found in: Publications)
- The chromosomal basis of cancer. (found in: Publications)
- Determination of genotoxicity of classical swine fever vaccine in vitro by cytogenetic and comet tests. (found in: Publications)
- Complex chromosome aberrations persist in individuals many years after occupational exposure to densely ionizing radiation: an mFISH study (found in: Publications)
- Breakpoint differentiation in chromosomal aberrations of hematological malignancies: identification of 33 previously unrecorded breakpoints (found in: Publications)
- Low temperature tolerance of human embryonic stem cells. (found in: Publications)
- Chromosomal intrachanges induced by swift iron ions (found in: Publications)
- DNA ploidy and chromosome (FISH) pattern analysis of peripheral nerve sheath tumors (found in: Publications)
- Chromosome intrachanges and interchanges detected by multicolor banding in lymphocytes: searching for clastogen signatures in the human genome (found in: Publications)
- Automated fluorescent in situ hybridization (FISH) analysis of t(9;22)(q34;q11) in interphase nuclei. (found in: Publications)
- Molecular cytogenetic techniques in detecting subtle chromosomal imbalances (found in: Publications)
- Genotoxicity of the volatile anaesthetic desflurane in human lymphocytes in vitro, established by comet assay. (found in: Publications)
- Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping and multicolor banding applying murine probes. (found in: Publications)
- Gains and losses of DNA sequences in malignant mesothelioma by comparative genomic hybridisation (found in: Publications)
- Genomic DNA-chip hybridization in t(11;14)-positive mantle cell lymphomas shows a high frequency of aberrations and allows a refined characterization of consensus regions. (found in: Publications)
- Multicolour-banding fluorescence in situ hybridization (mbanding-FISH) to identify recurrent chromosomal alterations in breast tumour cell lines. (found in: Publications)
- Chromosomal alterations cause the high rates and wide ranges of drug resistance in cancer cells. (found in: Publications)
- Molecular-cytogenetic characterization of the origin and the presence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs) (found in: Publications)
- Evidence for a new microdeletion syndrome in 15q21 (found in: Publications)
- Multicolour FISH probe sets and their applications (found in: Publications)
- Intratumor chromosomal heterogeneity in advanced carcinomas of the uterine cervix. (found in: Publications)
- Sex-specific telomere length profiles and age-dependent erosion dynamics of individual chromosome arms in humans. (found in: Publications)
- Cytogenmetic biomarkers, urinary metabolites and metabolic gene polymorphisms in workers exposed to styrene. (found in: Publications)
- DNA copy number changes in diffuse large B-cell lymphoma - Comparative genomic hybridization study (found in: Publications)
- Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding (found in: Publications)
- Automatic telomere length measurements in interphase nuclei by IQ-FISH. (found in: Publications)
- Karyotyping of human synaptonemal complexes by cenM-FISH (found in: Publications)
- Cytogenetic profile of unknown primary tumors: clues for their pathogenesis and clinical management (found in: Publications)
- Automated analysis of fluorescence in situ hybridization on fixed, paraffin-embedded whole tissue sections in B-cell lymphoma. (found in: Publications)
- Visualization of episomal and integrated Epstein-Barr virus DNA by fiber fluorescence in situ hybridization. (found in: Publications)
- Comparaison de systèmes d'analyse d'images cytologiques en dosimétrie biologique (FRENCH) (found in: Publications)
- Two novel in vitro human hepatoblastoma models, HepU1 and HepU2, are highly characteristic of fetal-embryonal differentiation in hepatoblastoma (found in: Publications)
- AML with 11q23/MLL abnormalities as defined by the WHO classification: incidence, partner chromosomes, FAB subtype, age distribution, and prognostic impact in an unselected series of 1897 cytogenetically analyzed AMl cases. (found in: Publications)
- New developments in automated cytogenetic imaging: unattended scoring of dicentric chromosomes, micronuclei, single cell electrophoresis, and fluorescence signals. (found in: Publications)
- A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature. (found in: Publications)
- The breakage-fusion-bridge (BFB) cycle as a mechanism for generating genetic heterogeneity in osteosarcoma. (found in: Publications)
- Dynamics of telomere erosion and its association with genome instability in myelodysplastic syndromes (MDS) and acute myelogenous leukemia arising from MDS: a marker of disease prognosis? (found in: Publications)
- First Patient with trisomy 21 accompanied by an aditional der(4)(:p11->q11:) plus partial uniparental disomy 4p15-16 (found in: Publications)
- XL CUX1/EZH2/
7cen (Deletion Probe, D-5144-100-TC) - 24XCyte (Human Multicolor FISH Probe, D-0125-060-DI)
- XL PML/RARA (Translocation/Dual Fusion Probe, D-5023-100-OG)
- XL AML1/ETO (Translocation/Dual Fusion Probe, D-5026-100-OG)
- XL AML1 (Break Apart Probe, D-5027-100-OG)
- XL PDGFRB (Break Apart Probe, D-5031-100-OG)
- XL IGL (Break Apart Probe, D-5033-100-OG)
- XL IGK (Break Apart Probe, D-5034-100-OG)
- XL FGFR1 (Break Apart Probe, D-5041-100-OG)
- XL 7q22/7q36 (Deletion Probe, D-5043-100-TC)
- XL ATM/TP53 (Deletion Probe, D-5046-100-OG)
- XL DLEU/LAMP (Deletion Probe, D-5054-100-OG)
- XL t(11;14) (Translocation/Dual Fusion Probe, D-5062-100-OG)
- XL DLEU/TP53 (Deletion Probe, D-5067-100-OG)
- XL del(7)(q22q31) (Deletion Probe, D-5068-100-TC)
- XL t(12;21) (Translocation/Dual Fusion Probe, D-5069-100-OG)
- XL CCND1 (Break Apart Probe, D-5071-100-OG)
- XL t(14;18) IGH/BCL2 (Translocation/Dual Fusion Probe, D-5080-100-OG)
- XL ALK BA (Break Apart Probe, D-6001-100-OG)
- XL ROS1-GOPC BA (Break Apart Probe, D-6029-100-OG)
- TissueFISH Pretreatment Kit (General Reagents, D-0905-025-TF)
- XL CBFB (Break Apart Probe, D-5092-100-OG)
- XL t(15;17) DF (Translocation/Dual Fusion Probe, D-5086-100-OG)
- XL RARA BA (Break Apart Probe, D-5087-100-OG)
- XL KMT2A BA (Break Apart Probe, D-5090-100-OG)
- XL RUNX1 (Break Apart Probe, D-5096-100-OG)
- XL BCL6 BA (Break Apart Probe, D-6016-100-OG)
- XL del(5)(q33) (Deletion Probe, D-5091-100-OG)
- 24XCyte (Human Multicolor FISH Probe, D-0125-120-DI)
- 24XCyte (Human Multicolor FISH Probe, D-0125-600-DI)
- XL t(8;21) plus (Translocation/Dual Fusion Probe, D-5114-100-OG)
- XL NUP98 (Break Apart Probe, D-5077-100-OG)
- XL ATM/11cen (Deletion Probe, D-5102-100-OG)
- XL 5q32 PDGFRB BA (Break Apart Probe, D-5104-100-OG)
- XL TP53/17cen (Deletion Probe, D-5103-100-OG)
- XL t(4;14) FGFR3/IGH DF (Translocation/Dual Fusion Probe, D-5108-100-OG)
- XL t(11;14) MYEOV/IGH DF (Translocation/Dual Fusion Probe, D-5111-100-OG)
- XL t(12;21) ETV6/RUNX1 DF (Translocation/Dual Fusion Probe, D-5115-100-OG)
- XL 22q11 IGL BA (Break Apart Probe, D-5117-100-OG)
- XL 2p11 IGK BA (Break Apart Probe, D-5116-100-OG)
- XL CBFB/MYH11 (Translocation/Dual Fusion Probe, D-5022-100-OG)
- XL CRLF2 BA (Break Apart Probe, D-5130-100-OG)
- XL t(8;9) PCM1/JAK2 DF (Translocation/Dual Fusion Probe, D-5120-100-OG)
- XL t(11;14) CCND1/IGH DF (Translocation/Dual Fusion Probe, D-5140-100-OG)
- XL PAX5 BA (Break Apart Probe, D-5143-100-OG)
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