Literature DB >> 10366452

An in situ study of variant telomeric repeats in human chromosomes.

K Krejcí1, J Koch.   

Abstract

Variant telomeric repeats are selectively detected in human telomeres in situ by the novel approach of dideoxy-PRINS, displaying their organization in a format where all the individual chromosome ends can be viewed individually and simultaneously. All human chromosome ends are found to contain variant repeats, though not all types of repeats can be detected on all chromosome ends. Although the staining frequency at particular chromosome ends seems polymorphic among individuals, some chromosome ends are more commonly stained with a given probe than others. A few chromosome ends also appear with particularly strong signals. With a probe for one type of variant repeat ((AGGGTG)n), peculiar patterns with more than two signals per chromosome end are observed. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10366452     DOI: 10.1006/geno.1999.5809

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  3 in total

1.  Molecular cytogenetics investigation of the telomeres in a case of Philadelphia positive B-ALL with a single telomere expansion.

Authors:  K Krejcí; J Stentoft; J Koch
Journal:  Neoplasia       Date:  1999-12       Impact factor: 5.715

2.  Telomere length assessment in human archival tissues: combined telomere fluorescence in situ hybridization and immunostaining.

Authors:  Alan K Meeker; Wesley R Gage; Jessica L Hicks; Inpakala Simon; Jonathan R Coffman; Elizabeth A Platz; Gerrun E March; Angelo M De Marzo
Journal:  Am J Pathol       Date:  2002-04       Impact factor: 4.307

3.  Mouse telomere analysis using an optimized primed in situ (PRINS) labeling technique.

Authors:  Josée Lavoie; Marc Bronsard; Michel Lebel; Régen Drouin
Journal:  Chromosoma       Date:  2003-03-11       Impact factor: 4.316

  3 in total

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