BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

300 related articles for article (PubMed ID: 22771538)

  • 41. Hypomethylation along with increased H19 expression in placentas from pregnancies complicated with fetal growth restriction.
    Koukoura O; Sifakis S; Zaravinos A; Apostolidou S; Jones A; Hajiioannou J; Widschwendter M; Spandidos DA
    Placenta; 2011 Jan; 32(1):51-7. PubMed ID: 21129773
    [TBL] [Abstract][Full Text] [Related]  

  • 42. A review of known imprinting syndromes and their association with assisted reproduction technologies.
    Amor DJ; Halliday J
    Hum Reprod; 2008 Dec; 23(12):2826-34. PubMed ID: 18703582
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith-Wiedemann or Silver-Russell syndrome in a single family.
    Jurkiewicz D; Kugaudo M; Skórka A; Śmigiel R; Smyk M; Ciara E; Chrzanowska K; Krajewska-Walasek M
    Am J Med Genet A; 2017 Jan; 173(1):72-78. PubMed ID: 27612309
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Genomic imprinting syndromes and cancer.
    Lim DH; Maher ER
    Adv Genet; 2010; 70():145-75. PubMed ID: 20920748
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Imprinting in human disease with special reference to transient neonatal diabetes and Beckwith-Wiedemann syndrome.
    Temple IK
    Endocr Dev; 2007; 12():113-123. PubMed ID: 17923774
    [TBL] [Abstract][Full Text] [Related]  

  • 46. A retrospective analysis of the prevalence of imprinting disorders in Estonia from 1998 to 2016.
    Yakoreva M; Kahre T; Žordania R; Reinson K; Teek R; Tillmann V; Peet A; Õiglane-Shlik E; Pajusalu S; Murumets Ü; Vals MA; Mee P; Wojcik MH; Õunap K
    Eur J Hum Genet; 2019 Nov; 27(11):1649-1658. PubMed ID: 31186545
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Genome-wide allelic methylation analysis reveals disease-specific susceptibility to multiple methylation defects in imprinting syndromes.
    Court F; Martin-Trujillo A; Romanelli V; Garin I; Iglesias-Platas I; Salafsky I; Guitart M; Perez de Nanclares G; Lapunzina P; Monk D
    Hum Mutat; 2013 Apr; 34(4):595-602. PubMed ID: 23335487
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases.
    Chiesa N; De Crescenzo A; Mishra K; Perone L; Carella M; Palumbo O; Mussa A; Sparago A; Cerrato F; Russo S; Lapi E; Cubellis MV; Kanduri C; Cirillo Silengo M; Riccio A; Ferrero GB
    Hum Mol Genet; 2012 Jan; 21(1):10-25. PubMed ID: 21920939
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Genomic imprinting: the influence of differential methylation in the two sexes.
    Biliya S; Bulla LA
    Exp Biol Med (Maywood); 2010 Feb; 235(2):139-47. PubMed ID: 20404028
    [TBL] [Abstract][Full Text] [Related]  

  • 50. DNA methylation in genomic imprinting, development, and disease.
    Paulsen M; Ferguson-Smith AC
    J Pathol; 2001 Sep; 195(1):97-110. PubMed ID: 11568896
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Genomic imprinting].
    Tachdjian G; Baumann C
    Presse Med; 1998 Feb; 27(8):365-9. PubMed ID: 9768006
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Genes, assisted reproductive technology and trans-illumination.
    Dias RP; Maher ER
    Epigenomics; 2013 Jun; 5(3):331-40. PubMed ID: 23750647
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A survey of assisted reproductive technology births and imprinting disorders.
    Bowdin S; Allen C; Kirby G; Brueton L; Afnan M; Barratt C; Kirkman-Brown J; Harrison R; Maher ER; Reardon W
    Hum Reprod; 2007 Dec; 22(12):3237-40. PubMed ID: 17921133
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders.
    Fontana L; Bedeschi MF; Maitz S; Cereda A; Faré C; Motta S; Seresini A; D'Ursi P; Orro A; Pecile V; Calvello M; Selicorni A; Lalatta F; Milani D; Sirchia SM; Miozzo M; Tabano S
    Epigenetics; 2018; 13(9):897-909. PubMed ID: 30221575
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Silver-Russell and Beckwith-Wiedemann syndromes: opposite (epi)mutations in 11p15 result in opposite clinical pictures.
    Eggermann T
    Horm Res; 2009 Apr; 71 Suppl 2():30-5. PubMed ID: 19407494
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Genomic imprinting and human disease--toward the elucidation of the imprinting mechanism].
    Hatada I; Mukai T
    Seikagaku; 1997 Dec; 69(12):1378-84. PubMed ID: 9483983
    [No Abstract]   [Full Text] [Related]  

  • 57. Imprinting and disease.
    Walter J; Paulsen M
    Semin Cell Dev Biol; 2003 Feb; 14(1):101-10. PubMed ID: 12524013
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Multi-locus imprinting disturbances of Beckwith-Wiedemann and Large offspring syndrome/Abnormal offspring syndrome: A brief review.
    Mangiavacchi PM; Caldas-Bussiere MC; Mendonça MDS; Dias AJB; Rios ÁFL
    Theriogenology; 2021 Oct; 173():193-201. PubMed ID: 34399383
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Prader-Willi and Angelman syndromes. Disorders of genomic imprinting.
    Cassidy SB; Schwartz S
    Medicine (Baltimore); 1998 Mar; 77(2):140-51. PubMed ID: 9556704
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Parental genomic imprinting.
    Deal CL
    Curr Opin Pediatr; 1995 Aug; 7(4):445-58. PubMed ID: 7581651
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.