Pages that link to "Q68488224"
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The following pages link to In situ hybridization as a tool to study numerical chromosome aberrations in solid bladder tumors (Q68488224):
Displaying 50 items.
- Estrogen receptor alpha gene amplification in breast cancer: 25 years of debate (Q24273274) (← links)
- Experimental gastric carcinogenesis in Cebus apella nonhuman primates (Q27332441) (← links)
- Nonradioactive in situ hybridisation of the translocation t(1;7) in myeloid malignancies (Q30814012) (← links)
- Chromosome in situ hybridization on formalin-fixed mammary tissue using non-isotopic, non-fluorescent probes: technical considerations and biological implications (Q31028564) (← links)
- Proteoglycan production in disomic and trisomy 7-carrying human synovial cells. (Q31097295) (← links)
- Specific metaphase and interphase detection of the breakpoint region in 8q24 of Burkitt lymphoma cells by triple-color fluorescence in situ hybridization (Q31170610) (← links)
- Quantification of inter- and intra-nuclear variation of fluorescence in situ hybridization signals (Q33194387) (← links)
- Fluorescence ratio measurements of double-labeled probes for multiple in situ hybridization by digital imaging microscopy (Q33194388) (← links)
- Comparison of effects of zona drilling by non-contact infrared laser or acid Tyrode's on the development of human biopsied embryos as revealed by blastomere viability, cytoskeletal analysis and molecular cytogenetics (Q33231802) (← links)
- Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome-specific libraries and cosmid probes (Q33479671) (← links)
- Interrelationship between TP53 gene deletion, protein expression and chromosome 17 aneusomy in gastric adenocarcinoma (Q33484376) (← links)
- Male and female meiotic behaviour of an intrachromosomal insertion determined by preimplantation genetic diagnosis (Q33695005) (← links)
- Clinical experience with preimplantation diagnosis of sex by dual fluorescent in situ hybridization (Q34316456) (← links)
- Heterogeneity of chromosome 17 and erbB-2 gene copy number in primary and metastatic bladder cancer (Q34367966) (← links)
- Rapid metaphase and interphase detection of radiation-induced chromosome aberrations in human lymphocytes by chromosomal suppression in situ hybridization (Q34446390) (← links)
- Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics (Q34735154) (← links)
- MYC deregulation in gastric cancer and its clinicopathological implications. (Q34745850) (← links)
- Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTRK3 gene fusion: cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma (Q34754714) (← links)
- Molecular biological determinations of meningioma progression and recurrence (Q35145251) (← links)
- Characterization of de novo duplications in eight patients by using fluorescence in situ hybridization with chromosome-specific DNA libraries. (Q35194734) (← links)
- Preimplantation genetic diagnosis for couples at high risk of Down syndrome pregnancy owing to parental translocation or mosaicism (Q35571017) (← links)
- Suppressor of cytokine signalling 2 (SOCS-2) expression in breast carcinoma (Q35588740) (← links)
- Amplification of the c-erbB-2 (HER-2/neu) gene in gastric cancer cells. Detection by fluorescence in situ hybridization (Q35763518) (← links)
- Analysis of chromosome 17p13 (p53 locus) alterations in gastric carcinoma cells by dual-color fluorescence in situ hybridization (Q35782454) (← links)
- Fluorescence in situ hybridization evaluation of chromosome deletion patterns in prostate cancer (Q35782514) (← links)
- Analysis of genetic changes underlying local recurrence of prostate carcinoma during androgen deprivation therapy. (Q35796528) (← links)
- Detection of chromosomal imbalances in transitional cell carcinoma of the bladder by comparative genomic hybridization (Q35798145) (← links)
- Novel fluorescence in situ hybridization approaches in solid tumors. Characterization of frozen specimens, touch preparations, and cytological preparations (Q35798595) (← links)
- Interphase cytogenetics in paraffin sections of lung tumors by non-isotopic in situ hybridization. Mapping genotype/phenotype heterogeneity (Q35832536) (← links)
- Use of FISH to detect chromosomal translocations and deletions. Analysis of chromosome rearrangement in synovial sarcoma cells from paraffin-embedded specimens (Q35832910) (← links)
- Comparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and nonrandom chromosomal gains and losses (Q35834190) (← links)
- Chromosome abnormalities in human arrested preimplantation embryos: a multiple-probe FISH study. (Q35889306) (← links)
- Interphase cytogenetics of lung tumors using in situ hybridization: numerical aberrations (Q35939001) (← links)
- Rapid detection of prognostic genetic factors in neuroblastoma using fluorescence in situ hybridisation on tumour imprints and bone marrow smears. United Kingdom Children's Cancer Study Group (Q35978227) (← links)
- p53 mutations have no additional prognostic value over stage in bladder cancer (Q36079559) (← links)
- Interphase cytogenetics reveals a high incidence of aneuploidy and intra-tumour heterogeneity in breast cancer. (Q36081862) (← links)
- Interphase fluorescence in situ hybridization improves the detection of malignant cells in effusions from breast cancer patients (Q36116296) (← links)
- The relationship of pronuclear stage morphology and chromosome status at cleavage stage (Q36269314) (← links)
- Human embryos derived from in vitro and in vivo matured oocytes: analysis for chromosomal abnormalities and nuclear morphology (Q36269474) (← links)
- Higher degree of chromosome mosaicism in preimplantation embryos from carriers of robertsonian translocation t(13;14) in comparison with embryos from karyotypically normal IVF patients (Q36271831) (← links)
- Chromosome transfer induced aneuploidy results in complex dysregulation of the cellular transcriptome in immortalized and cancer cells (Q36634493) (← links)
- Chromosome painting as a supplement to cytogenetic banding analysis in non‐Hodgkin's lymphoma (Q36697488) (← links)
- Chromosome specific DNA hybridization in suspension for flow cytometric detection of chimerism in bone marrow transplantation and leukemia (Q36709543) (← links)
- Rapid fluorescence in situ hybridization with repetitive DNA probes: quantification by digital image analysis (Q36731014) (← links)
- Chapter 1 DNA Sequence Localization in Metaphase and Interphase Cells by Fluorescence in Situ Hybridization (Q36930425) (← links)
- Speckle-type POZ (pox virus and zinc finger protein) protein gene deletion in ovarian cancer: Fluorescence in situ hybridization analysis of a tissue microarray (Q37002758) (← links)
- In situ hybridisation in perspective (Q37143740) (← links)
- Interphase cytogenetics using biotin and digoxigenin labelled probes: III. Increased sensitivity and flexibility for detecting HPV in cervical biopsy specimens and cell lines (Q37145475) (← links)
- High frequency of genetic alterations in non-small cell lung cancer detected by multi-target fluorescence in situ hybridization (Q37222499) (← links)
- Establishment of a molecular cytogenetic analysis for native tumor tissue of meningiomas-suitable for clinical application (Q37607469) (← links)