BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

639 related articles for article (PubMed ID: 12410230)

  • 1. Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1.
    Fitzpatrick GV; Soloway PD; Higgins MJ
    Nat Genet; 2002 Nov; 32(3):426-31. PubMed ID: 12410230
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.
    Gaston V; Le Bouc Y; Soupre V; Burglen L; Donadieu J; Oro H; Audry G; Vazquez MP; Gicquel C
    Eur J Hum Genet; 2001 Jun; 9(6):409-18. PubMed ID: 11436121
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome.
    Diaz-Meyer N; Day CD; Khatod K; Maher ER; Cooper W; Reik W; Junien C; Graham G; Algar E; Der Kaloustian VM; Higgins MJ
    J Med Genet; 2003 Nov; 40(11):797-801. PubMed ID: 14627666
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice.
    Cleary MA; van Raamsdonk CD; Levorse J; Zheng B; Bradley A; Tilghman SM
    Nat Genet; 2001 Sep; 29(1):78-82. PubMed ID: 11528397
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Aberrant CpG methylation of the imprinting control region KvDMR1 detected in assisted reproductive technology-produced calves and pathogenesis of large offspring syndrome.
    Hori N; Nagai M; Hirayama M; Hirai T; Matsuda K; Hayashi M; Tanaka T; Ozawa T; Horike S
    Anim Reprod Sci; 2010 Dec; 122(3-4):303-12. PubMed ID: 21035970
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.
    Cooper WN; Luharia A; Evans GA; Raza H; Haire AC; Grundy R; Bowdin SC; Riccio A; Sebastio G; Bliek J; Schofield PN; Reik W; Macdonald F; Maher ER
    Eur J Hum Genet; 2005 Sep; 13(9):1025-32. PubMed ID: 15999116
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
    Engel JR; Smallwood A; Harper A; Higgins MJ; Oshimura M; Reik W; Schofield PN; Maher ER
    J Med Genet; 2000 Dec; 37(12):921-6. PubMed ID: 11106355
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CDKN1C expression in Beckwith-Wiedemann syndrome patients with allele imbalance.
    Algar EM; Deeble GJ; Smith PJ
    J Med Genet; 1999 Jul; 36(7):524-31. PubMed ID: 10424812
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.
    Soejima H; Higashimoto K
    J Hum Genet; 2013 Jul; 58(7):402-9. PubMed ID: 23719190
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Alternative mechanisms associated with silencing of CDKN1C in Beckwith-Wiedemann syndrome.
    Diaz-Meyer N; Yang Y; Sait SN; Maher ER; Higgins MJ
    J Med Genet; 2005 Aug; 42(8):648-55. PubMed ID: 16061564
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes.
    Sperandeo MP; Ungaro P; Vernucci M; Pedone PV; Cerrato F; Perone L; Casola S; Cubellis MV; Bruni CB; Andria G; Sebastio G; Riccio A
    Am J Hum Genet; 2000 Mar; 66(3):841-7. PubMed ID: 10712200
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular biology of Beckwith-Wiedemann syndrome.
    Weksberg R; Squire JA
    Med Pediatr Oncol; 1996 Nov; 27(5):462-9. PubMed ID: 8827075
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype.
    Murrell A; Heeson S; Cooper WN; Douglas E; Apostolidou S; Moore GE; Maher ER; Reik W
    Hum Mol Genet; 2004 Jan; 13(2):247-55. PubMed ID: 14645199
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of CDKN1C in Beckwith Wiedemann syndrome.
    Algar E; Brickell S; Deeble G; Amor D; Smith P
    Hum Mutat; 2000; 15(6):497-508. PubMed ID: 10862080
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Methylation at mouse Cdkn1c is acquired during postimplantation development and functions to maintain imprinted expression.
    Bhogal B; Arnaudo A; Dymkowski A; Best A; Davis TL
    Genomics; 2004 Dec; 84(6):961-70. PubMed ID: 15533713
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome.
    Hatada I; Ohashi H; Fukushima Y; Kaneko Y; Inoue M; Komoto Y; Okada A; Ohishi S; Nabetani A; Morisaki H; Nakayama M; Niikawa N; Mukai T
    Nat Genet; 1996 Oct; 14(2):171-3. PubMed ID: 8841187
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Epigenetics, genomic imprinting and developmental disorders].
    Le Bouc Y; Rossignol S; Azzi S; Brioude F; Cabrol S; Gicquel C; Netchine I
    Bull Acad Natl Med; 2010 Feb; 194(2):287-97; discussion 297-300. PubMed ID: 21166119
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain.
    Cooper PR; Smilinich NJ; Day CD; Nowak NJ; Reid LH; Pearsall RS; Reece M; Prawitt D; Landers J; Housman DE; Winterpacht A; Zabel BU; Pelletier J; Weissman BE; Shows TB; Higgins MJ
    Genomics; 1998 Apr; 49(1):38-51. PubMed ID: 9570947
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New insights into the pathogenesis of Beckwith-Wiedemann and Silver-Russell syndromes: contribution of small copy number variations to 11p15 imprinting defects.
    Demars J; Rossignol S; Netchine I; Lee KS; Shmela M; Faivre L; Weill J; Odent S; Azzi S; Callier P; Lucas J; Dubourg C; Andrieux J; Le Bouc Y; El-Osta A; Gicquel C
    Hum Mutat; 2011 Oct; 32(10):1171-82. PubMed ID: 21780245
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.
    Kubota T; Saitoh S; Matsumoto T; Narahara K; Fukushima Y; Jinno Y; Niikawa N
    Am J Med Genet; 1994 Feb; 49(4):378-83. PubMed ID: 7909196
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 32.