BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

331 related articles for article (PubMed ID: 11468278)

  • 41. CDKN1C mutations: two sides of the same coin.
    Eggermann T; Binder G; Brioude F; Maher ER; Lapunzina P; Cubellis MV; Bergadá I; Prawitt D; Begemann M
    Trends Mol Med; 2014 Nov; 20(11):614-22. PubMed ID: 25262539
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.
    Catchpoole D; Lam WW; Valler D; Temple IK; Joyce JA; Reik W; Schofield PN; Maher ER
    J Med Genet; 1997 May; 34(5):353-9. PubMed ID: 9152830
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome.
    Lin HY; Chuang CK; Tu RY; Fang YY; Su YN; Chen CP; Chang CY; Liu HC; Chu TH; Niu DM; Lin SP
    Mol Genet Metab; 2016 Sep; 119(1-2):8-13. PubMed ID: 27436784
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Beckwith-Wiedemann syndrome: multiple molecular mechanisms.
    Enklaar T; Zabel BU; Prawitt D
    Expert Rev Mol Med; 2006 Jul; 8(17):1-19. PubMed ID: 16842655
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients.
    Rovina D; La Vecchia M; Cortesi A; Fontana L; Pesant M; Maitz S; Tabano S; Bodega B; Miozzo M; Sirchia SM
    Sci Rep; 2020 May; 10(1):8275. PubMed ID: 32427849
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Lsh controls silencing of the imprinted Cdkn1c gene.
    Fan T; Hagan JP; Kozlov SV; Stewart CL; Muegge K
    Development; 2005 Feb; 132(4):635-44. PubMed ID: 15647320
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Age-dependent changes of p57(Kip2) and p21(Cip1/Waf1) expression in skeletal muscle and lung of mice.
    Park CW; Chung JH
    Biochim Biophys Acta; 2001 Aug; 1520(2):163-8. PubMed ID: 11513958
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 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]  

  • 50. Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer.
    Soejima H; Nakagawachi T; Zhao W; Higashimoto K; Urano T; Matsukura S; Kitajima Y; Takeuchi M; Nakayama M; Oshimura M; Miyazaki K; Joh K; Mukai T
    Oncogene; 2004 May; 23(25):4380-8. PubMed ID: 15007390
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Variable Expressivity of the Beckwith-Wiedemann Syndrome in Four Pedigrees Segregating Loss-of-Function Variants of
    Sparago A; Cerrato F; Pignata L; Cammarata-Scalisi F; Garavelli L; Piscopo C; Vancini A; Riccio A
    Genes (Basel); 2021 May; 12(5):. PubMed ID: 34065128
    [TBL] [Abstract][Full Text] [Related]  

  • 52. (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome.
    Mussa A; Russo S; De Crescenzo A; Freschi A; Calzari L; Maitz S; Macchiaiolo M; Molinatto C; Baldassarre G; Mariani M; Tarani L; Bedeschi MF; Milani D; Melis D; Bartuli A; Cubellis MV; Selicorni A; Cirillo Silengo M; Larizza L; Riccio A; Ferrero GB
    Eur J Hum Genet; 2016 Feb; 24(2):183-90. PubMed ID: 25898929
    [TBL] [Abstract][Full Text] [Related]  

  • 53. The long non-coding RNA Kcnq1ot1 controls maternal p57 expression in muscle cells by promoting H3K27me3 accumulation to an intragenic MyoD-binding region.
    Andresini O; Rossi MN; Matteini F; Petrai S; Santini T; Maione R
    Epigenetics Chromatin; 2019 Jan; 12(1):8. PubMed ID: 30651140
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Genetic and Epigenetic Control of CDKN1C Expression: Importance in Cell Commitment and Differentiation, Tissue Homeostasis and Human Diseases.
    Stampone E; Caldarelli I; Zullo A; Bencivenga D; Mancini FP; Della Ragione F; Borriello A
    Int J Mol Sci; 2018 Apr; 19(4):. PubMed ID: 29614816
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report.
    Lekszas C; Nanda I; Vona B; Böck J; Ashrafzadeh F; Donyadideh N; Ebrahimzadeh F; Ahangari N; Maroofian R; Karimiani EG; Haaf T
    BMC Med Genomics; 2019 Jun; 12(1):83. PubMed ID: 31174542
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Mechanism of imprinting on mouse distal chromosome 7.
    Ainscough JF; John RM; Surani MA
    Genet Res; 1998 Dec; 72(3):237-45. PubMed ID: 10036981
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Brain abnormalities in patients with Beckwith-Wiedemann syndrome.
    Gardiner K; Chitayat D; Choufani S; Shuman C; Blaser S; Terespolsky D; Farrell S; Reiss R; Wodak S; Pu S; Ray PN; Baskin B; Weksberg R
    Am J Med Genet A; 2012 Jun; 158A(6):1388-94. PubMed ID: 22585446
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The placenta in Beckwith-Wiedemann syndrome: genotype-phenotype associations, excessive extravillous trophoblast and placental mesenchymal dysplasia.
    Armes JE; McGown I; Williams M; Broomfield A; Gough K; Lehane F; Lourie R
    Pathology; 2012 Oct; 44(6):519-27. PubMed ID: 22772341
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 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]  

  • 60. Large offspring syndrome: a bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann.
    Chen Z; Robbins KM; Wells KD; Rivera RM
    Epigenetics; 2013 Jun; 8(6):591-601. PubMed ID: 23751783
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.