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]