- XL MYC amp (Amplification Probe, D-6008-100-OG)
- XL t(8;14) (Translocation/Dual Fusion Probe, D-5008-100-OG)
- Carl Zeiss India (Bangalore) P Ltd. (found in: Contact)
- 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)
- Automated detection of irradiated food with the comet assay. (found in: Publications)
- Lymphocytes of type 2 diabetic women carry a high load of stablechromosomal aberrations: a novel risk factor for disease-relatedearly death. (found in: Publications)
- ESR1 gene amplification in breast cancer: a common phenomenon? (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)
- Use of automated imaging and analysis technology for the detection of aneuploidy in human sperm (found in: Publications)
- The clinical implementation of sperm chromosome aneuploidy testing:pitfalls and promises. (found in: Publications)
- Human ESCs predisposition to karyotypic instability: Is a matterof culture adaptation or differential vulnerability among hESC linesdue to inherent properties? (found in: Publications)
- Creation of monosomic derivatives of human cultured cell lines (found in: Publications)
- Interphase cytogenetic analysis with centromeric probes for chromosomes1, 2, 6, 10, and 17 in 11 tumors from a patient with bilateral renaloncocytosis. (found in: Publications)
- Unusually stable abnormal karyotype in a highly aggressive melanomanegative for telomerase activity. (found in: Publications)
- New cutpoints to identify increased HER2 copy number: analysis of a large, population-based cohort with long-term follow-up (found in: Publications)
- Multiplex genotyping as a biomarker for susceptibility to carcinogenicexposure in the FLEHS biomonitoring study. (found in: Publications)
- Tetrasomy 8 in a patient with acute monoblastic leukemia. (found in: Publications)
- High EVI1 levels predict adverse outcome in acute myeloid leukemia:prevalence of EVI1 overexpression and chromosome 3q26 abnormalitiesunderestimated. (found in: Publications)
- An Evaluation of the Effectiveness of a Semi-automatic MetaphaseLocating and On-screen Karyotyping System. (found in: Publications)
- Increased levels of numerical chromosome aberrations after in vitroexposure of human peripheral blood lymphocytes to radiofrequencyelectromagnetic fields for 72 hours. (found in: Publications)
- Automatic telomere length measurements in interphase nuclei by IQ-FISH. (found in: Publications)
- Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo. (found in: Publications)
- XL Del(20q) (Deletion Probe, D-5020-100-OG)
- XL PDGFRB (Break Apart Probe, D-5031-100-OG)
- XL EVI1 (Break Apart Probe - Triple Color, D-5036-100-TC)
- XL 20q12/20qter (Deletion Probe, D-5040-100-OG)
- XL FGFR1 (Break Apart Probe, D-5041-100-OG)
- XL 5q31/5q33 (Deletion Probe, D-5042-100-OG)
- XL ATM/TP53 (Deletion Probe, D-5046-100-OG)
- XL MDM2 (Enumeration Probe, D-5047-100-OG)
- XL Iso(17q) (Deletion/Isochromosome Probe, D-5048-100-OG)
- XL 1p32/1q21 (Amplification/Deletion Probe, D-5049-100-OG)
- XL DLEU/LAMP (Deletion Probe, D-5054-100-OG)
- XL 5q33 (Deletion Probe, D-5057-100-OG)
- XL MECOM 3q26 (Break Apart Probe, D-5059-100-OG)
- XL MLL plus (Break Apart Probe, D-5060-100-OG)
- XL t(11;14) (Translocation/Dual Fusion Probe, D-5062-100-OG)
- XL t(6;14) (Translocation/Dual Fusion Probe, D-5065-100-OG)
- XL 5q31 (Deletion Probe, D-5066-100-OG)
- XL DLEU/TP53 (Deletion Probe, D-5067-100-OG)
- XL RB1/DLEU/
LAMP (Deletion Probe, D-5070-100-TC) - XL t(14;18) IGH/BCL2 (Translocation/Dual Fusion Probe, D-5080-100-OG)
- XL 5q31/5q33/
5p15 (Deletion Probe, D-5081-100-TC) - XL ALK BA (Break Apart Probe, D-6001-100-OG)
- XL ERBB2 (HER2/NEU) amp (Amplification Probe, D-6010-100-OG)
- XL ROS1-GOPC BA (Break Apart Probe, D-6029-100-OG)
- XL BCR/ABL1/ASS (Translocation/Dual Fusion Probe, D-5082-100-TC)
- XL del(5)(q31) (Deletion Probe, D-5085-100-OG)
- XL KMT2A BA (Break Apart Probe, D-5090-100-OG)
- XL 5p15/9q22/15q22 Hyperdiploidy (Enumeration Probe, D-5095-100-TC)
- XL CDKN2C/
CKS1B (Enumeration Probe, D-5099-100-OG) - XL del(5)(q33) (Deletion Probe, D-5091-100-OG)
- XL TCRA/D (Break Apart Probe, D-5106-100-OG)
- XL TP53/17cen (Deletion Probe, D-5103-100-OG)
- XL 20q12/20qter plus (Deletion/Isochromosome Probe, D-5121-100-OG)
- XL t(14;18) IGH/BCL2 DF (Translocation/Dual Fusion Probe, D-5113-100-OG)
- XL TLX3 BA (Break Apart Probe, D-5129-100-OG)
- XL 22q11 IGL BA (Break Apart Probe, D-5117-100-OG)
- XL 2p11 IGK BA (Break Apart Probe, D-5116-100-OG)
- XL 20q12/20qter/8cen plus (Deletion/Isochromosome/Enumeration Probe, D-5122-100-TC)
- XL DDIT3 BA (Break Apart Probe, D-6032-100-OG)
- XL FOXO1 BA (Break Apart Probe, D-6034-100-OG)
- XL Williams-Beuren (Deletion Probe, D-5418-050-OG)
- XL Smith-Magenis/Miller-Dieker (Deletion Probe, D-5422-050-OG)
- XL t(11;19) KMT2A/ELL DF (Translocation/Dual Fusion Probe, D-5135-100-OG)
- VITCO / Vira Idea Trade Co. (found in: Contact)
- Carl Zeiss Co., Ltd (カールツァイス株式会社) (found in: Contact)
- Carl Zeiss do Brasil (found in: Contact)
- 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)
- A new marker set that identifies fetal cells in maternal circulationwith high specificity. (found in: Publications)
- Mild cognitive impairment identified in older individuals with Downsyndrome by reduced telomere signal numbers and shorter telomeresmeasured in microns. (found in: Publications)
- Positive response to neoadjuvant cyclophosphamide and doxorubicinin topoisomerase II nonamplified/HER2/neu negative/polysomy 17 absentbreast cancer patients. (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)
- Frequency of chromosomal aberrations in Prague mothers and theirnewborns. (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)
Please select your country of residence. Choose International if your country is not listed.
Our internet site may contain information that is not approved in all countries or regions. To ensure accuracy of content, it is required that you select the site which is appropriate for your country of residence.