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 *

309 related articles for article (PubMed ID: 10464770)

  • 21. The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.
    Rossignol S; Steunou V; Chalas C; Kerjean A; Rigolet M; Viegas-Pequignot E; Jouannet P; Le Bouc Y; Gicquel C
    J Med Genet; 2006 Dec; 43(12):902-7. PubMed ID: 16825435
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.
    Paulsen M; Davies KR; Bowden LM; Villar AJ; Franck O; Fuermann M; Dean WL; Moore TF; Rodrigues N; Davies KE; Hu RJ; Feinberg AP; Maher ER; Reik W; Walter J
    Hum Mol Genet; 1998 Jul; 7(7):1149-59. PubMed ID: 9618174
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Maternal gametic transmission of translocations or inversions of human chromosome 11p15.5 results in regional DNA hypermethylation and downregulation of CDKN1C expression.
    Smith AC; Suzuki M; Thompson R; Choufani S; Higgins MJ; Chiu IW; Squire JA; Greally JM; Weksberg R
    Genomics; 2012 Jan; 99(1):25-35. PubMed ID: 22079941
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutations.
    Li M; Squire J; Shuman C; Fei YL; Atkin J; Pauli R; Smith A; Nishikawa J; Chitayat D; Weksberg R
    Genomics; 2001 Jun; 74(3):370-6. PubMed ID: 11414765
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The two-domain hypothesis in Beckwith-Wiedemann syndrome.
    Feinberg AP
    J Clin Invest; 2000 Sep; 106(6):739-40. PubMed ID: 10995782
    [No Abstract]   [Full Text] [Related]  

  • 27. Genomic imprinting and cancer.
    Tycko B
    Results Probl Cell Differ; 1999; 25():133-69. PubMed ID: 10339745
    [No Abstract]   [Full Text] [Related]  

  • 28. The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster.
    Cerrato F; Sparago A; Di Matteo I; Zou X; Dean W; Sasaki H; Smith P; Genesio R; Bruggemann M; Reik W; Riccio A
    Hum Mol Genet; 2005 Feb; 14(4):503-11. PubMed ID: 15640248
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.
    Sparago A; Cerrato F; Vernucci M; Ferrero GB; Silengo MC; Riccio A
    Nat Genet; 2004 Sep; 36(9):958-60. PubMed ID: 15314640
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders.
    Müller A; Soellner L; Binder G; Begemann M; Eggermann T
    Am J Med Genet A; 2016 Jan; 170A(1):283-4. PubMed ID: 26447000
    [No Abstract]   [Full Text] [Related]  

  • 32. Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences.
    Heide S; Chantot-Bastaraud S; Keren B; Harbison MD; Azzi S; Rossignol S; Michot C; Lackmy-Port Lys M; Demeer B; Heinrichs C; Newfield RS; Sarda P; Van Maldergem L; Trifard V; Giabicani E; Siffroi JP; Le Bouc Y; Netchine I; Brioude F
    J Med Genet; 2018 Mar; 55(3):205-213. PubMed ID: 29223973
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Role of genomic imprinting in Wilms' tumour and overgrowth disorders.
    Reeve AE
    Med Pediatr Oncol; 1996 Nov; 27(5):470-5. PubMed ID: 8827076
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Beckwith-Wiedemann syndrome.
    Weksberg R; Shuman C; Smith AC
    Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):12-23. PubMed ID: 16010676
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domains.
    Eggermann T; Begemann M; Pfeiffer L
    Clin Epigenetics; 2021 Feb; 13(1):30. PubMed ID: 33541417
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Multiple genetic abnormalities of 11p15 in Wilms' tumor.
    Feinberg AP
    Med Pediatr Oncol; 1996 Nov; 27(5):484-9. PubMed ID: 8827078
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome.
    Caspary T; Cleary MA; Perlman EJ; Zhang P; Elledge SJ; Tilghman SM
    Genes Dev; 1999 Dec; 13(23):3115-24. PubMed ID: 10601037
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Wiedemann-Beckwith syndrome: genomic imprinting revisited.
    Weksberg R
    Am J Med Genet; 1994 Aug; 52(2):235-6. PubMed ID: 7802017
    [No Abstract]   [Full Text] [Related]  

  • 40. An 11p15 imprinting centre region 2 deletion in a family with Beckwith Wiedemann syndrome provides insights into imprinting control at CDKN1C.
    Algar E; Dagar V; Sebaj M; Pachter N
    PLoS One; 2011; 6(12):e29034. PubMed ID: 22205991
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.