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 *

141 related articles for article (PubMed ID: 27265324)

  • 1. Imprinted survival genes preclude loss of heterozygosity of chromosome 7 in cancer cells.
    Boot A; Oosting J; de Miranda NF; Zhang Y; Corver WE; van de Water B; Morreau H; van Wezel T
    J Pathol; 2016 Sep; 240(1):72-83. PubMed ID: 27265324
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Methylation and expression analyses of the 7q autism susceptibility locus genes MEST , COPG2, and TSGA14 in human and anthropoid primate cortices.
    Schneider E; Mayer S; El Hajj N; Jensen LR; Kuss AW; Zischler H; Kondova I; Bontrop RE; Navarro B; Fuchs E; Zechner U; Haaf T
    Cytogenet Genome Res; 2012; 136(4):278-87. PubMed ID: 22456293
    [TBL] [Abstract][Full Text] [Related]  

  • 3. High frequency of loss of heterozygosity in imprinted, compared with nonimprinted, genomic regions in follicular thyroid carcinomas and atypical adenomas.
    Sarquis MS; Weber F; Shen L; Broelsch CE; Jhiang SM; Zedenius J; Frilling A; Eng C
    J Clin Endocrinol Metab; 2006 Jan; 91(1):262-9. PubMed ID: 16249278
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Silencing of the maternally imprinted tumor suppressor ARHI contributes to follicular thyroid carcinogenesis.
    Weber F; Aldred MA; Morrison CD; Plass C; Frilling A; Broelsch CE; Waite KA; Eng C
    J Clin Endocrinol Metab; 2005 Feb; 90(2):1149-55. PubMed ID: 15546898
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mit1/Lb9 and Copg2, new members of mouse imprinted genes closely linked to Peg1/Mest(1).
    Lee YJ; Park CW; Hahn Y; Park J; Lee J; Yun JH; Hyun B; Chung JH
    FEBS Lett; 2000 Apr; 472(2-3):230-4. PubMed ID: 10788617
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The novel gene, gamma2-COP (COPG2), in the 7q32 imprinted domain escapes genomic imprinting.
    Yamasaki K; Hayashida S; Miura K; Masuzaki H; Ishimaru T; Niikawa N; Kishino T
    Genomics; 2000 Sep; 68(3):330-5. PubMed ID: 10995575
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32.
    Nakabayashi K; Bentley L; Hitchins MP; Mitsuya K; Meguro M; Minagawa S; Bamforth JS; Stanier P; Preece M; Weksberg R; Oshimura M; Moore GE; Scherer SW
    Hum Mol Genet; 2002 Jul; 11(15):1743-56. PubMed ID: 12095916
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Monoallelic loss of the imprinted gene Grb10 promotes tumor formation in irradiated Nf1+/- mice.
    Mroue R; Huang B; Braunstein S; Firestone AJ; Nakamura JL
    PLoS Genet; 2015 May; 11(5):e1005235. PubMed ID: 26000738
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genome haploidisation with chromosome 7 retention in oncocytic follicular thyroid carcinoma.
    Corver WE; Ruano D; Weijers K; den Hartog WC; van Nieuwenhuizen MP; de Miranda N; van Eijk R; Middeldorp A; Jordanova ES; Oosting J; Kapiteijn E; Hovens G; Smit J; van Wezel T; Morreau H
    PLoS One; 2012; 7(6):e38287. PubMed ID: 22675538
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Aberrant methylation of imprinted genes is associated with negative hormone receptor status in invasive breast cancer.
    Barrow TM; Barault L; Ellsworth RE; Harris HR; Binder AM; Valente AL; Shriver CD; Michels KB
    Int J Cancer; 2015 Aug; 137(3):537-47. PubMed ID: 25560175
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed.
    Hitchins MP; Bentley L; Monk D; Beechey C; Peters J; Kelsey G; Ishino F; Preece MA; Stanier P; Moore GE
    Mamm Genome; 2002 Dec; 13(12):686-91. PubMed ID: 12514746
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Imprinted tumor suppressor genes ARHI and PEG3 are the most frequently down-regulated in human ovarian cancers by loss of heterozygosity and promoter methylation.
    Feng W; Marquez RT; Lu Z; Liu J; Lu KH; Issa JP; Fishman DM; Yu Y; Bast RC
    Cancer; 2008 Apr; 112(7):1489-502. PubMed ID: 18286529
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [From the cytogenetics to the cytogenomics of thyroid tumors].
    Perissel B; Bernheim A; Couturier J; Fouilhoux G; Vago P
    Bull Cancer; 2002 Jun; 89(6):588-92. PubMed ID: 12135859
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Frequent loss of imprinting of PEG1/MEST in invasive breast cancer.
    Pedersen IS; Dervan PA; Broderick D; Harrison M; Miller N; Delany E; O'Shea D; Costello P; McGoldrick A; Keating G; Tobin B; Gorey T; McCann A
    Cancer Res; 1999 Nov; 59(21):5449-51. PubMed ID: 10554015
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis.
    Monk D; Smith R; Arnaud P; Preece MA; Stanier P; Beechey CV; Peters J; Kelsey G; Moore GE
    Mamm Genome; 2003 Dec; 14(12):805-16. PubMed ID: 14724735
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Role of DNA methylation and histone H3 lysine 27 methylation in tissue-specific imprinting of mouse Grb10.
    Yamasaki-Ishizaki Y; Kayashima T; Mapendano CK; Soejima H; Ohta T; Masuzaki H; Kinoshita A; Urano T; Yoshiura K; Matsumoto N; Ishimaru T; Mukai T; Niikawa N; Kishino T
    Mol Cell Biol; 2007 Jan; 27(2):732-42. PubMed ID: 17101788
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Thyroid carcinomas with mixed follicular and C-cell differentiation patterns.
    Papotti M; Volante M; Komminoth P; Sobrinho-Simões M; Bussolati G
    Semin Diagn Pathol; 2000 May; 17(2):109-19. PubMed ID: 10839611
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Frequent loss of heterozygosity on chromosomes 3p and 17p without VHL or p53 mutations suggests involvement of unidentified tumor suppressor genes in follicular thyroid carcinoma.
    Grebe SK; McIver B; Hay ID; Wu PS; Maciel LM; Drabkin HA; Goellner JR; Grant CS; Jenkins RB; Eberhardt NL
    J Clin Endocrinol Metab; 1997 Nov; 82(11):3684-91. PubMed ID: 9360526
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detection of maternal uniparental disomy at the two imprinted genes on chromosome 7, GRB10 and PEG1/MEST, in a Silver-Russell syndrome patient using methylation-specific PCR assays.
    Kim Y; Kim SS; Kim G; Park S; Park IS; Yoo HW
    Clin Genet; 2005 Mar; 67(3):267-9. PubMed ID: 15691366
    [No Abstract]   [Full Text] [Related]  

  • 20. DNA methylation signatures identify biologically distinct thyroid cancer subtypes.
    Rodríguez-Rodero S; Fernández AF; Fernández-Morera JL; Castro-Santos P; Bayon GF; Ferrero C; Urdinguio RG; Gonzalez-Marquez R; Suarez C; Fernández-Vega I; Fresno Forcelledo MF; Martínez-Camblor P; Mancikova V; Castelblanco E; Perez M; Marrón PI; Mendiola M; Hardisson D; Santisteban P; Riesco-Eizaguirre G; Matías-Guiu X; Carnero A; Robledo M; Delgado-Álvarez E; Menéndez-Torre E; Fraga MF
    J Clin Endocrinol Metab; 2013 Jul; 98(7):2811-21. PubMed ID: 23666970
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.