Published in J Histochem Cytochem on April 01, 1996
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Multicolor fluorescent in situ hybridization to define abutting and overlapping gene expression in the embryonic zebrafish brain. Neural Dev (2011) 1.32
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Mapping ESTs by fiber-FISH. Genome Res (1999) 0.75
Heterogeneity in telomere length of human chromosomes. Hum Mol Genet (1996) 6.55
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Photobleaching kinetics of fluorescein in quantitative fluorescence microscopy. Biophys J (1995) 3.08
Can, a putative oncogene associated with myeloid leukemogenesis, may be activated by fusion of its 3' half to different genes: characterization of the set gene. Mol Cell Biol (1992) 2.99
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Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents. J Med Genet (2005) 2.60
Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization. Cytogenet Cell Genet (1990) 2.60
In situ hybridization as a tool to study numerical chromosome aberrations in solid bladder tumors. Histochemistry (1988) 2.26
Influence of the triplet excited state on the photobleaching kinetics of fluorescein in microscopy. Biophys J (1996) 2.11
Ultra-sensitive FISH using peroxidase-mediated deposition of biotin- or fluorochrome tyramides. Hum Mol Genet (1995) 2.07
Linear 2' O-Methyl RNA probes for the visualization of RNA in living cells. Nucleic Acids Res (2001) 2.03
A new method for fluorescence microscopical localization of specific DNA sequences by in situ hybridization of fluorochromelabelled RNA. Exp Cell Res (1980) 1.91
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Up-converting phosphor reporters for nucleic acid microarrays. Nat Biotechnol (2001) 1.65
Mutational analysis of fibrillarin and its mobility in living human cells. J Cell Biol (2000) 1.57
Detection of the Philadelphia chromosome in interphase nuclei. Cytogenet Cell Genet (1990) 1.52
Correlations between isochores and chromosomal bands in the human genome. Proc Natl Acad Sci U S A (1993) 1.45
Cloning the breakpoint cluster region of the inv(16) in acute nonlymphocytic leukemia M4 Eo. Hum Mol Genet (1993) 1.40
Methods for visualizing RNA processing and transport pathways in living cells. Histochem Cell Biol (2001) 1.38
Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization. Genomics (1991) 1.35
Expression of HLA-DR on T lymphocytes following renal transplantation, and association with graft-rejection episodes and cytomegalovirus infection. Transplantation (1984) 1.32
High-resolution in situ hybridization using DNA halo preparations. Hum Mol Genet (1992) 1.31
Molecular characterization and evolution of the SPRR family of keratinocyte differentiation markers encoding small proline-rich proteins. Genomics (1993) 1.30
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Characterization and chromosomal localization of the human proto-oncogene BMI-1. Hum Mol Genet (1993) 1.28
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Infrared up-converting phosphors for bioassays. IEE Proc Nanobiotechnol (2005) 1.27
A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents. J Med Genet (2009) 1.26
Spreading and staining of human metaphase chromosomes on aminoalkylsilane-treated glass slides. Histochem J (1982) 1.26
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Establishment of a rat cell line inducible for the expression of human cytomegalovirus immediate-early gene products by protein synthesis inhibition. J Virol (1986) 1.23
Multiple fluorescence in situ hybridization. Cytometry (1990) 1.22
Rapid detection of human parvovirus B19 DNA by dot-hybridization and the polymerase chain reaction. J Virol Methods (1989) 1.22
Subnuclear localization of the active variant surface glycoprotein gene expression site in Trypanosoma brucei. Proc Natl Acad Sci U S A (1998) 1.20
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proc Natl Acad Sci U S A (1995) 1.19
New strategy for multi-colour fluorescence in situ hybridisation: COBRA: COmbined Binary RAtio labelling. Eur J Hum Genet (1999) 1.19
Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization. Leukemia (1997) 1.19
Identification of genetic markers for prostatic cancer progression. Lab Invest (2000) 1.19
Comparative genomic hybridization of cancer of the gastroesophageal junction: deletion of 14Q31-32.1 discriminates between esophageal (Barrett's) and gastric cardia adenocarcinomas. Cancer Res (1999) 1.18
The glial and mesenchymal elements of gliosarcomas share similar genetic alterations. J Neuropathol Exp Neurol (1996) 1.17
ULS: a versatile method of labeling nucleic acids for FISH based on a monofunctional reaction of cisplatin derivatives with guanine moieties. Cytogenet Cell Genet (1999) 1.16
Cytochemical hybridization with fluorochrome-labeled RNA. I. Development of a method using nucleic acids bound to agarose beads as a model. J Histochem Cytochem (1981) 1.16
Universal linkage system: an improved method for labeling archival DNA for comparative genomic hybridization. Genes Chromosomes Cancer (1999) 1.13
Analysis of antifading reagents for fluorescence microscopy. Cytometry (1995) 1.13
Rapid and high resolution detection of in situ hybridisation to polytene chromosomes using fluorochrome-labeled RNA. Chromosoma (1981) 1.12
Molecular cytogenetic analysis of prostatic adenocarcinomas from screening studies : early cancers may contain aggressive genetic features. Am J Pathol (2001) 1.11
Fluorescence in situ hybridization using horseradish peroxidase-labeled oligodeoxynucleotides and tyramide signal amplification for sensitive DNA and mRNA detection. Histochem Cell Biol (1998) 1.11
Mercurated nucleic acid probes, a new principle for non-radioactive in situ hybridization. Exp Cell Res (1987) 1.11
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome. Int J Cancer (1998) 1.10
New insights in the cellular processing of platinum antitumor compounds, using fluorophore-labeled platinum complexes and digital fluorescence microscopy. J Biol Inorg Chem (2000) 1.10
In situ hybridization with fluoresceinated DNA. Nucleic Acids Res (1991) 1.09
Sensitive mRNA detection by fluorescence in situ hybridization using horseradish peroxidase-labeled oligodeoxynucleotides and tyramide signal amplification. J Histochem Cytochem (1998) 1.09
Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH. Genes Chromosomes Cancer (2001) 1.07
Clonal analysis of a case of multifocal oesophageal (Barrett's) adenocarcinoma by comparative genomic hybridization. J Pathol (1999) 1.07
Somatic pairing of chromosome 1 centromeres in interphase nuclei of human cerebellum. Hum Genet (1989) 1.07
Sensitivity of various visualization methods for peroxidase and alkaline phosphatase activity in immunoenzyme histochemistry. Histochem J (1985) 1.06
Characteristics of A spermatogonia and preleptotene spermatocytes in the vitamin A-deficient rat testis. Biol Reprod (1995) 1.05
Detection of cell and tissue surface antigens using up-converting phosphors: a new reporter technology. Anal Biochem (1999) 1.05
Detection of chromosome aberrations in interphase tumor nuclei by nonradioactive in situ hybridization. Cancer Genet Cytogenet (1989) 1.05
Methodologies for specific intron and exon RNA localization in cultured cells by haptenized and fluorochromized probes. J Cell Sci (1993) 1.05
Specific metaphase and interphase detection of the breakpoint region in 8q24 of Burkitt lymphoma cells by triple-color fluorescence in situ hybridization. Genes Chromosomes Cancer (1992) 1.04
Feasibility of in situ hybridisation with chromosome specific DNA probes on paraffin wax embedded tissue. J Clin Pathol (1991) 1.03
Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres. Br J Cancer (2002) 1.03
Flow cytometric and morphologic studies of HNK1+ (Leu 7+) lymphocytes in relation to cytomegalovirus carrier status. Clin Exp Immunol (1988) 1.03
Double in situ hybridization in combination with digital image analysis: a new approach to study interphase chromosome topography. Exp Cell Res (1989) 1.02
Direct nonradioactive in situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomes. Cytometry (1990) 1.02
Detection of trisomy 8 in hematological disorders by in situ hybridization. Cytogenet Cell Genet (1991) 1.02
Plasmodium species: flow cytometry and microfluorometry assessments of DNA content and synthesis. Exp Parasitol (1987) 1.01
A parameter for the distribution of fluorophores in cells derived from measurements of inner filter effect and reabsorption phenomenon. Cytometry (1982) 1.01
Polymerase chain reaction and viral culture techniques to detect HSV in small volumes of cerebrospinal fluid; an experimental mouse encephalitis study. J Virol Methods (1989) 1.01
Direct visualization of dispersed 11q13 chromosomal translocations in mantle cell lymphoma by multicolor DNA fiber fluorescence in situ hybridization. Blood (1996) 1.01
Fluorescence in situ hybridization on human metaphase chromosomes detected by near-field scanning optical microscopy. J Microsc (1996) 1.00
Three-color fluorescence in situ hybridization for the simultaneous detection of multiple nucleic acid sequences. Cytometry (1989) 1.00
An improved immunocytochemical method for the detection of human cytomegalovirus antigens in peripheral blood leucocytes. Histochemistry (1989) 1.00
On the position of nucleolus organizer regions (NORs) in interphase nuclei. Studies with a new, non-autoradiographic in situ hybridization method. Exp Cell Res (1986) 1.00
Influence of fluorochrome labeling density on the photobleaching kinetics of fluorescein in microscopy. Cytometry (1997) 1.00