Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy. - Wikidata - awgldk - TriplyDB

Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy.

Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy.

http://www.wikidata.org/entity/Q33281355

about

Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans Clustered organization of homologous KRAB zinc-finger genes with enhanced expression in human T lymphoid cells Mammalian ubiquitin-conjugating enzyme Ubc9 interacts with Rad51 recombination protein and localizes in synaptonemal complexes Concerted evolution of the tandem array encoding primate U2 snRNA occurs in situ, without changing the cytological context of the RNU2 locus A GLRA1 null mutation in recessive hyperekplexia challenges the functional role of glycine receptors A high-resolution map of human chromosome 12 Comprehensive characterization of evolutionary conserved breakpoints in four New World Monkey karyotypes compared to Chlorocebus aethiops and Homo sapiens Evolutionary analysis of the highly dynamic CHEK2 duplicon in anthropoids Intrachromosomal triplication of 15q11-q13.Y chromosomal variation tracks the evolution of mating systems in chimpanzee and bonobo.ZOO-FISH analysis with 7 human chromosome specific libraries detects conserved regions between human and camel (Camelus dromedarius).Molecular structure of a functional Drosophila centromere.Y-Chromosome variation in hominids: intraspecific variation is limited to the polygamous chimpanzee.Basal body-associated DNA: in situ studies in Chlamydomonas reinhardtii.Metaphase and interphase fluorescence in situ hybridization mapping of the rice genome with bacterial artificial chromosomes Spatial distribution of Escherichia coli in the mouse large intestine inferred from rRNA in situ hybridization Distribution of crossing over on mouse synaptonemal complexes using immunofluorescent localization of MLH1 protein.Optical mapping of site-directed cleavages on single DNA molecules by the RecA-assisted restriction endonuclease technique.Detection of nondisjunction and recombination in meiotic and postmeiotic cells from XYSxr [XY,Tp(Y)1Ct] mice using multicolor fluorescence in situ hybridization.Differentially painting human chromosome arms with combined binary ratio-labeling fluorescence in situ hybridization.Characterization of three de novo derivative chromosomes 16 by "reverse chromosome painting" and molecular analysis Minireview: cryptic translocations and telomere integrity FISH deletion mapping defines a single location for the Y chromosome stature gene, GCY.The tumor-suppressor gene FHIT is involved in the regulation of apoptosis and in cell cycle control A novel murine model of myeloproliferative disorders generated by overexpression of the transcription factor NF-E2.'Chromosomal Rainbows' Detect Oncogenic Rearrangements of Signaling Molecules in Thyroid Tumors.Interphase cytogenetics in paraffin sections of lung tumors by non-isotopic in situ hybridization. Mapping genotype/phenotype heterogeneity.Evidence for a role for DNA polymerase beta in mammalian meiosis.Detection of TP53 mutation, loss of heterozygosity and DNA content in fine-needle aspirates of breast carcinoma Bloom's syndrome protein, BLM, colocalizes with replication protein A in meiotic prophase nuclei of mammalian spermatocytes.Small-cell lung cancer is characterized by a high incidence of deletions on chromosomes 3p, 4q, 5q, 10q, 13q and 17p A hybrid approach of using wavelets and fuzzy clustering for classifying multispectral florescence in situ hybridization images Multiplex-FISH (M-FISH): technique, developments and applications.Combined multicolor-FISH and immunostaining.Multicolor chromosome bar codes.Esthesioneuroblastoma is not a member of the primitive peripheral neuroectodermal tumour-Ewing's group.Microscopy and image analysis Pre- and Postnatal Analysis of Chromosome 15q26.1 and 8p23.1 Deletions in Congenital Diaphragmatic Hernia.Fluorescence in situ hybridisation of multiple probes on a single microscope slide.Directly labeled DNA probes using fluorescent nucleotides with different length linkers.

P2860

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P2860

Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy.

http://www.wikidata.org/entity/Q33281355

description

1992 nî lūn-bûn

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1992 թվականի փետրվարին հրատարակված գիտական հոդված

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1992年の論文

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P2093

A Baldini

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P2860

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

Cyanine dye labeling reagents for sulfhydryl groups

Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8

Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes.

A human chromosome 9-specific alphoid DNA repeat spatially resolvable from satellite 3 DNA by fluorescent in situ hybridization.

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

Detection of the Philadelphia chromosome in interphase nuclei.

A human alpha satellite DNA subset specific for chromosome 12

Analysis of genes and chromosomes by nonisotopic in situ hybridization.

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