These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

105 related articles for article (PubMed ID: 9111994)

  • 1. Centromeric alphoid DNA heteromorphisms of chromosome 21 revealed by FISH-technique.
    Verma RS; Batish SD; Gogineni SK; Kleyman SM; Stetka DG
    Clin Genet; 1997 Feb; 51(2):91-3. PubMed ID: 9111994
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pericentromeric heteromorphism of human chromosome 18 as revealed by FISH-technique.
    Verma RS; Ishwar L; Gogineni SK; Kleyman SM
    Ann Genet; 1998; 41(3):154-6. PubMed ID: 9833069
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Variations in alphoid DNA sequences escape detection of aneuploidy at interphase by FISH technique.
    Verma RS; Luke S
    Genomics; 1992 Sep; 14(1):113-6. PubMed ID: 1427817
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Structural rearrangements and insertions of dispersed elements in pericentromeric alpha satellites occur preferably at kinkable DNA sites.
    Mashkova TD; Oparina NY; Lacroix MH; Fedorova LI; G Tumeneva I; Zinovieva OL; Kisselev LL
    J Mol Biol; 2001 Jan; 305(1):33-48. PubMed ID: 11114245
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of pericentromeric chromosome 21 specific YAC clones by FISH: identification of new markers for molecular-cytogenetic application.
    Yurov YB; Laurent AM; Marcais B; Vorsanova SG; Roizes G
    Hum Genet; 1995 Mar; 95(3):287-92. PubMed ID: 7868120
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of alphoid DNA variation and kinetochore size in human chromosome 21: evidence against pathological significance of alphoid satellite DNA diminutions.
    Marzais B; Vorsanova SG; Roizes G; Yurov YB
    Tsitol Genet; 1999; 33(1):25-31. PubMed ID: 10330695
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Centromeric alphoid DNA heteromorphisms of chromosome 22 revealed by FISH-technique.
    Liehr T; Pfeiffer RA; Trautmann U; Gebhart E
    Clin Genet; 1998 Mar; 53(3):231-2. PubMed ID: 9630084
    [No Abstract]   [Full Text] [Related]  

  • 8. Extreme reduction of chromosome-specific alpha-satellite array is unusually common in human chromosome 21.
    Lo AW; Liao GC; Rocchi M; Choo KH
    Genome Res; 1999 Oct; 9(10):895-908. PubMed ID: 10523519
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization].
    Solov'ev IV; Iurov IuB; Vorsanova SG; Marcais B; Rogaev EI; Kapanadze BI; Brodianskiĭ VM; Iankovskiĭ NK; Roizes G
    Genetika; 1998 Nov; 34(11):1470-9. PubMed ID: 10096024
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Centromeric inactivation in a dicentric human Y;21 translocation chromosome.
    Fisher AM; Al-Gazali L; Pramathan T; Quaife R; Cockwell AE; Barber JC; Earnshaw WC; Axelman J; Migeon BR; Tyler-Smith C
    Chromosoma; 1997 Sep; 106(4):199-206. PubMed ID: 9254721
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Characterization of an alphoid subfamily located near p-arm sequences on human chromosome 22.
    Eisenbarth I; König-Greger D; Wöhr G; Kehrer-Sawatzki H; Assum G
    Chromosome Res; 1999; 7(1):65-9. PubMed ID: 10219734
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Application of fluorescence in situ hybridization techniques in clinical genetics: use of two alphoid repeat probes detecting the centromeres of chromosomes 13 and 21 or chromosomes 14 and 22, respectively.
    Kølvraa S; Koch J; Gregersen N; Jensen PK; Jørgensen AL; Petersen KB; Rasmussen K; Bolund L
    Clin Genet; 1991 Apr; 39(4):278-86. PubMed ID: 1829987
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of the monomeric alphoid sequences in the pericentromeric region of human chromosome 7.
    de la Puente A; Velasco E; Pérez Jurado LA; Hernández-Chico C; van de Rijke FM; Scherer SW; Raap AK; Cruces J
    Cytogenet Cell Genet; 1998; 83(3-4):176-81. PubMed ID: 10072574
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human chromosome 9 pericentric homologies: implications for chromosome 9 heteromorphisms.
    Park JP; Wojiski SA; Spellman RA; Rhodes CH; Mohandas TK
    Cytogenet Cell Genet; 1998; 82(3-4):192-4. PubMed ID: 9858814
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.
    Iourov IY; Soloviev IV; Vorsanova SG; Monakhov VV; Yurov YB
    J Histochem Cytochem; 2005 Mar; 53(3):401-8. PubMed ID: 15750029
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Human (Homo sapiens) and chimpanzee (Pan troglodytes) share similar ancestral centromeric alpha satellite DNA sequences but other fractions of heterochromatin differ considerably.
    Luke S; Verma RS
    Am J Phys Anthropol; 1995 Jan; 96(1):63-71. PubMed ID: 7726296
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A degenerate alpha satellite probe, detecting a centromeric deletion on chromosome 21 in an apparently normal human male, shows limitations of the use of satellite DNA probes for interphase ploidy analysis.
    Weier HU; Gray JW
    Anal Cell Pathol; 1992 Mar; 4(2):81-6. PubMed ID: 1550797
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome.
    Bartsch O; König U; Petersen MB; Poulsen H; Mikkelsen M; Palau F; Prieto F; Schwinger E
    Hum Genet; 1993 Sep; 92(2):127-32. PubMed ID: 8370577
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A study of cryptic terminal chromosome rearrangements in recurrent miscarriage couples detects unsuspected acrocentric pericentromeric abnormalities.
    Cockwell AE; Jacobs PA; Beal SJ; Crolla JA
    Hum Genet; 2003 Mar; 112(3):298-302. PubMed ID: 12596054
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Centromeric alphoid sequences are breakage prone resulting in pericentromeric inversion heteromorphism of qh region of chromosome 1.
    Verma RS; Ramesh KH; Mathews T; Kleyman SM; Conte RA
    Ann Genet; 1996; 39(4):205-8. PubMed ID: 9037348
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.