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 *

85 related articles for article (PubMed ID: 8952381)

  • 21. [Epimutations of imprinting genes in the human genome: classification, causes, association with hereditary pathology].
    Lebedev IN; Sazhenova EA
    Genetika; 2008 Oct; 44(10):1356-73. PubMed ID: 19062532
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [The structure of a conserved region of porcine genome, represented in human genome by chromosome 17].
    Larkin DM; Astakhova IM; Kozhin AIu; Karamysheva TV; Rubtsov NB; Kuznetsov SB; Zhdanova NS
    Genetika; 2004 Jul; 40(7):961-7. PubMed ID: 15458207
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Isochores and replication time zones: a perfect match.
    Schmegner C; Hameister H; Vogel W; Assum G
    Cytogenet Genome Res; 2007; 116(3):167-72. PubMed ID: 17317955
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Spatial preservation of nuclear chromatin architecture during three-dimensional fluorescence in situ hybridization (3D-FISH).
    Solovei I; Cavallo A; Schermelleh L; Jaunin F; Scasselati C; Cmarko D; Cremer C; Fakan S; Cremer T
    Exp Cell Res; 2002 May; 276(1):10-23. PubMed ID: 11978004
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region.
    Watrin F; Roëckel N; Lacroix L; Mignon C; Mattei MG; Disteche C; Muscatelli F
    Eur J Hum Genet; 1997; 5(5):324-32. PubMed ID: 9412790
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Genomic imprinting].
    Kato R; Niikawa N
    Tanpakushitsu Kakusan Koso; 1996 Nov; 41(15 Suppl):2325-34. PubMed ID: 8952395
    [No Abstract]   [Full Text] [Related]  

  • 27. Asynchronous replication of imprinted genes is established in the gametes and maintained during development.
    Simon I; Tenzen T; Reubinoff BE; Hillman D; McCarrey JR; Cedar H
    Nature; 1999 Oct; 401(6756):929-32. PubMed ID: 10553911
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Regulatory mechanisms of mammalian imprinting].
    Patkin EL; Suchkova IO
    Tsitologiia; 2006; 48(7):578-94. PubMed ID: 17087149
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Chromosome 11 genomic changes in parathyroid adenoma and hyperplasia: array CGH, FISH, and tissue microarrays.
    Yi Y; Nowak NJ; Pacchia AL; Morrison C
    Genes Chromosomes Cancer; 2008 Aug; 47(8):639-48. PubMed ID: 18398822
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mapping of the human DNA primase 1 (PRIM1) to chromosome 12q13.
    Cloutier S; Hamel H; Champagne M; Yotov WV
    Genomics; 1997 Aug; 43(3):398-401. PubMed ID: 9268648
    [No Abstract]   [Full Text] [Related]  

  • 31. Physical mapping of the IGF2 locus in the South American opossum Monodelphis domestica.
    Lawton BR; Obergfell C; O'Neill RJ; O'Neill MJ
    Cytogenet Genome Res; 2007; 116(1-2):130-1. PubMed ID: 17268191
    [TBL] [Abstract][Full Text] [Related]  

  • 32. High-density genome array is superior to fluorescence in-situ hybridization analysis of monosomy 3 in choroidal melanoma fine needle aspiration biopsy.
    Young TA; Burgess BL; Rao NP; Gorin MB; Straatsma BR
    Mol Vis; 2007 Dec; 13():2328-33. PubMed ID: 18199974
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Utilization of the human genome sequence localizes human papillomavirus type 16 DNA integrated into the TNFAIP2 gene in a fatal cervical cancer from a 39-year-old woman.
    Einstein MH; Cruz Y; El-Awady MK; Popescu NC; DiPaolo JA; van Ranst M; Kadish AS; Romney S; Runowicz CD; Burk RD
    Clin Cancer Res; 2002 Feb; 8(2):549-54. PubMed ID: 11839676
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Fluorescent in situ hybridization].
    Zheng WL; Wu M
    Zhonghua Yi Xue Za Zhi; 1994 Aug; 74(8):511-3. PubMed ID: 7994664
    [No Abstract]   [Full Text] [Related]  

  • 35. Use of microgenomic technology for analysis of alterations in DNA copy number and gene expression in malignant melanoma.
    Trent JM; Bittner M; Zhang J; Wiltshire R; Ray M; Su Y; Gracia E; Meltzer P; De Risi J; Penland L; Brown P
    Clin Exp Immunol; 1997 Jan; 107 Suppl 1():33-40. PubMed ID: 9020934
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.
    Tamiya G; Shinya M; Imanishi T; Ikuta T; Makino S; Okamoto K; Furugaki K; Matsumoto T; Mano S; Ando S; Nozaki Y; Yukawa W; Nakashige R; Yamaguchi D; Ishibashi H; Yonekura M; Nakami Y; Takayama S; Endo T; Saruwatari T; Yagura M; Yoshikawa Y; Fujimoto K; Oka A; Chiku S; Linsen SE; Giphart MJ; Kulski JK; Fukazawa T; Hashimoto H; Kimura M; Hoshina Y; Suzuki Y; Hotta T; Mochida J; Minezaki T; Komai K; Shiozawa S; Taniguchi A; Yamanaka H; Kamatani N; Gojobori T; Bahram S; Inoko H
    Hum Mol Genet; 2005 Aug; 14(16):2305-21. PubMed ID: 16000323
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Absence of genomic imprinting at the DiGeorge locus.
    Theophile D; Bérubé D; Augé J; Vekemans M
    Acta Genet Med Gemellol (Roma); 1996; 45(1-2):277-80. PubMed ID: 8872046
    [No Abstract]   [Full Text] [Related]  

  • 38. [The high fork of genome programs].
    Weissenbach J
    C R Acad Sci III; 1996 Apr; 319(4):247-8. PubMed ID: 8762972
    [No Abstract]   [Full Text] [Related]  

  • 39. [Relationship between the DNA-replication pattern, fluorescence pattern, and band structure of human chromosomes].
    Wittwer B
    Dtsch Gesundheitsw; 1973 Jan; 28(4):149-53. PubMed ID: 4720010
    [No Abstract]   [Full Text] [Related]  

  • 40. Genome-wide analysis of the replication program in mammals.
    Farkash-Amar S; Simon I
    Chromosome Res; 2010 Jan; 18(1):115-25. PubMed ID: 20205353
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.