The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region. - Test2 - elhamkhani - TriplyDB

The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.

The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.

http://www.wikidata.org/entity/Q36927144

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Silver-Russell syndrome: genetic basis and molecular genetic testing Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57 Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology Environmental epigenomics and disease susceptibility Child health, developmental plasticity, and epigenetic programming Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).The impact of assisted reproductive technologies on genomic imprinting and imprinting disorders.Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield.Neonatal risks from in vitro fertilization and delayed motherhood.Similar DNA methylation levels in specific imprinting control regions in children conceived with and without assisted reproductive technology: a cross-sectional study.Computational Epigenetics: the new scientific paradigm.Imprinting methylation errors in ART.Culture of oocytes and risk of imprinting defects.Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci.A systematic review and meta-analysis of DNA methylation levels and imprinting disorders in children conceived by IVF/ICSI compared with children conceived spontaneously.A review of known imprinting syndromes and their association with assisted reproduction technologies.Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations A survey of assisted reproductive technology births and imprinting disorders.An atypical case of hypomethylation at multiple imprinted loci.The periconceptional environment and cardiovascular disease: does in vitro embryo culture and transfer influence cardiovascular development and health?No evidence for pathogenic variants or maternal effect of ZFP57 as the cause of Beckwith-Wiedemann Syndrome Loss of genomic imprinting in mouse embryos with fast rates of preimplantation development in culture.Parental infertility, infertility treatment and hepatoblastoma: a report from the Children's Oncology Group.Methylation levels at imprinting control regions are not altered with ovulation induction or in vitro fertilization in a birth cohort Compromised fertility disrupts Peg1 but not Snrpn and Peg3 imprinted methylation acquisition in mouse oocytes.Study of DNA methylation patterns of imprinted genes in children born after assisted reproductive technologies reveals no imprinting errors: A pilot study.High Frequency of Imprinted Methylation Errors in Human Preimplantation Embryos Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine.Duplication of 17q11.2 and Features of Albright Hereditary Osteodystrophy Secondary to Methylation Defects within the GNAS Cluster: Coincidence or Causal?Transient neonatal diabetes, ZFP57, and hypomethylation of multiple imprinted loci: a detailed follow-up Male fertility: Is spermiogenesis the critical step for answering biomedical issues?Epigenetic consequences of assisted reproduction and infertility on the human preimplantation embryo.Role of ART in imprinting disorders Large offspring syndrome: a bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann.Intersections of epigenetics, twinning and developmental asymmetries: insights into monogenic and complex diseases and a role for 3D facial analysis.DNA methylation profiling highlights the unique nature of the human placental epigenome.Epigenetic discordance at imprinting control regions in twins.Human imprinting syndromes.

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The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.

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ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.

In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene

Beckwith-Wiedemann syndrome and IVF: a case-control study

Bisulfite genomic sequencing: systematic investigation of critical experimental parameters

Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis

Genomic imprinting: parental influence on the genome

Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome

Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor.

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