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 *

118 related articles for article (PubMed ID: 2905880)

  • 1. Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndrome.
    Henry I; Jeanpierre M; Barichard F; Serre JL; Mallet J; Turleau C; de Grouchy J; Junien C
    Ann Genet; 1988; 31(4):216-20. PubMed ID: 2905880
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome.
    Spritz RA; Mager D; Pauli RM; Laxova R
    Am J Hum Genet; 1986 Aug; 39(2):265-73. PubMed ID: 3529947
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome.
    Weksberg R; Shen DR; Fei YL; Song QL; Squire J
    Nat Genet; 1993 Oct; 5(2):143-50. PubMed ID: 8252039
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Uniparental paternal disomy in a genetic cancer-predisposing syndrome.
    Henry I; Bonaiti-Pellié C; Chehensse V; Beldjord C; Schwartz C; Utermann G; Junien C
    Nature; 1991 Jun; 351(6328):665-7. PubMed ID: 1675767
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locus.
    Nordenskjöld A; Hedborg F; Luthman H; Nordenskjöld M
    Hum Genet; 1993 Oct; 92(3):296-8. PubMed ID: 8104862
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor.
    Prawitt D; Enklaar T; Gärtner-Rupprecht B; Spangenberg C; Oswald M; Lausch E; Schmidtke P; Reutzel D; Fees S; Lucito R; Korzon M; Brozek I; Limon J; Housman DE; Pelletier J; Zabel B
    Proc Natl Acad Sci U S A; 2005 Mar; 102(11):4085-90. PubMed ID: 15743916
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Insulin-like growth factor 2 cannot be linked to a familial form of Beckwith-Wiedemann syndrome.
    Nyström A; Hedborg F; Ohlsson R
    Eur J Pediatr; 1994 Aug; 153(8):574-80. PubMed ID: 7957404
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.
    Mannens M; Hoovers JM; Redeker E; Verjaal M; Feinberg AP; Little P; Boavida M; Coad N; Steenman M; Bliek J
    Eur J Hum Genet; 1994; 2(1):3-23. PubMed ID: 7913866
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular analysis of a patient with Beckwith-Wiedemann syndrome, rhabdomyosarcoma and renal cell carcinoma.
    Matsumoto T; Kinoshita E; Maeda H; Niikawa N; Kurosaki N; Harada N; Yun K; Sawai T; Aoki S; Kondoh T
    Jpn J Hum Genet; 1994 Jun; 39(2):225-34. PubMed ID: 8086640
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Paternally inherited submicroscopic duplication at 11p15.5 implicates insulin-like growth factor II in overgrowth and Wilms' tumorigenesis.
    Algar EM; St Heaps L; Darmanian A; Dagar V; Prawitt D; Peters GB; Collins F
    Cancer Res; 2007 Mar; 67(5):2360-5. PubMed ID: 17325026
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evidence of multiple causal sites affecting weight in the IGF2-INS-TH region of human chromosome 11.
    Gu D; O'Dell SD; Chen XH; Miller GJ; Day IN
    Hum Genet; 2002 Feb; 110(2):173-81. PubMed ID: 11935324
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Wiedemann-Beckwith syndrome, imprinting, IGF2, and H19: implications for hemihyperplasia, associated neoplasms, and overgrowth.
    Cohen MM
    Am J Med Genet; 1994 Aug; 52(2):233-4. PubMed ID: 7802016
    [No Abstract]   [Full Text] [Related]  

  • 17. Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.
    Sun FL; Dean WL; Kelsey G; Allen ND; Reik W
    Nature; 1997 Oct; 389(6653):809-15. PubMed ID: 9349812
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.
    Riccio A; Sparago A; Verde G; De Crescenzo A; Citro V; Cubellis MV; Ferrero GB; Silengo MC; Russo S; Larizza L; Cerrato F
    Endocr Dev; 2009; 14():1-9. PubMed ID: 19293570
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted.
    Weksberg R; Teshima I; Williams BR; Greenberg CR; Pueschel SM; Chernos JE; Fowlow SB; Hoyme E; Anderson IJ; Whiteman DA
    Hum Mol Genet; 1993 May; 2(5):549-56. PubMed ID: 8518793
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Loss of heterozygosity in non-tumoral tissue in two children with Beckwith-Wiedemann syndrome.
    Schneid H; Vazquez MP; Seurin D; le Bouc Y
    Growth Regul; 1991 Dec; 1(4):168-70. PubMed ID: 1688177
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.