Fluorescence in situ hybridization (FISH): Overview and medical applications

Journal of Clinical Ligand Assay

Volumn 23, Issue 1, 2000, Pages 33-42

  Anguiano, A ^a  

^a QUEST DIAGNOSTICS NICHOLS INSTITUTE   (United States)

Author keywords

FISH; Fluorescence in situ hybridization; Medical applications; New methods; Trends

Indexed keywords

ARTICLE; CHROMOSOME ABERRATION; CHROMOSOME PAINTING; COMPARATIVE GENOMIC HYBRIDIZATION; DIAGNOSTIC VALUE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; PRENATAL DIAGNOSIS; PRIMED IN SITU LABELING;

EID: 0033678442     PISSN: 10811672     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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15. Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using chromosome specific library probes
16. Molecular cloning and screening
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21. Molecular cytogenetics and prenatal diagnosis
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23. Prenatal detection of chromosome aneuploidies by fluorescence in situ hybridization: Experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trial
24. Prenatal interphase: Fluorescence in situ hybridization (FISH) policy statement
25. Prenatal interphase detection by FISH of a sex chromosome mosaicism when cytogenetics reports a pseudomosaicism
26. Prenatal diagnosis through the analysis of fetal cells in the maternal circulation
27. Preimplantation genetic diagnosis
28. Fluorescent in-situ hybridization on human embryos showing cleavage arrest after freezing and thawing
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31. Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres
32. Diagnosis and monitoring of chromosome aberrations in hematological malignancies by fluorescence in situ hybridization
33. Highly sensitive fluorescence in situ hybridization method to detect double BCR/ABL fusion and monitor response to therapy in chronic myeloid leukemia
34. Combined cytogenetic, FISH and molecular analysis in acute promyelocytic leukaemia at diagnosis and in complete remission
35. A subtle deletion of 12p by routine cytogenetics is found to be a translocation to 21q by fluorescence in situ hybridization: t(12;21)(p13;q22)
36. Detection of 11q23/MLL rearrangements in infant leukemias with fluorescence in situ hybridization and molecular analysis
37. FISH identifies inv(16)(p13q22) masked by translocations in three cases of acute myeloid leukemia
38. Interphase FISH analysis of sex-mismatched BMT utilizing dual color XY probes
39. Chromosomal translocations in human soft tissue sarcomas by interphase fluorescence in situ hybridization
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41. Fluorescence in situ hybridization analysis of chromosome 1p36 deletions in human MYCN amplified neuroblastoma
42. The HER-2/neu oncogene in breast cancer: Prognostic factor, predictive factor, and target for therapy
43. Fluorescence in situ hybridization mapping of the cystic fibrosis transmembrane conductance regulator (CFTR) gene to 7q31.3
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45. High-resolution DNA Fiber-FISH for genomic DNA mapping and colour bar-coding of large genes
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48. Visualization of single RNA transcripts in situ
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52. Validation of primed in situ labeling (PRINS) for interphase analysis: Comparative studies with conventional fluorescence in situ hybridization and chromosome analyses
53. Multiple colors by fluorescence in situ hybridization using ratio-labelled DNA probes create a molecular karyotype
54. Karyotyping human chromosomes by combinatorial multi-fluor FISH
55. Multicolor spectral karyotyping of human chromosomes
56. Cross-species colour segmenting: A novel tool in human karyotype analysis
57. High resolution multicolor-banding: A new technique for refined FISH analysis of human chromosomes
58. Padlock probes reveal single-nucleotide differences, parent of origin and in situ distribution of centromeric sequences in human chromosomes 13 and 21
59. Mutation detection and single-molecule counting using isothermal rolling-circle amplification
60. Peptide nucleic acids (PNA) and PNA-DNA chimeras: From high binding affinity towards biological function
61. Mapping ESTs by fiber-FISH
62. Amplification methods to increase the sensitivity of in situ hybridization. Play card
63. Visible integration of the adenosine deaminase (ADA) gene into the recipient genome after gene therapy
64. High-resolution FISH of the entire integrated Epstein-Barr virus genome on extended human DNA
65. Fast-FISH technique for rapid, simultaneous labeling of all human centromeres
66. Triplex DNA: Fundamentals, advances, and potential applications for gene therapy
67. Peptide nucleic acid (PNA) binding-mediated induction of human [gamma]-globin gene expression