Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci. - Wikidata - wikimedia - TriplyDB

Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci.

Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci.

http://www.wikidata.org/entity/Q34329150

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Abnormalities of the DNA methylation mark and its machinery: an emerging cause of neurologic dysfunction Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7.Maternal obesity and fetal metabolic programming: a fertile epigenetic soil.Similar DNA methylation levels in specific imprinting control regions in children conceived with and without assisted reproductive technology: a cross-sectional study.Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction Trophoblasts, invasion, and microRNA.Beckwith Wiedemann imprinting defect found in leucocyte but not buccal DNA in a child born small for gestational age Molecular and clinical studies in 138 Japanese patients with Silver-Russell syndrome An atypical case of hypomethylation at multiple imprinted loci.Altered expression of the imprinted transcription factor PLAGL1 deregulates a network of genes in the human IUGR placenta The role of imprinted genes in fetal growth abnormalities.No evidence for pathogenic variants or maternal effect of ZFP57 as the cause of Beckwith-Wiedemann Syndrome Effects of Maternal Obesity on Fetal Programming: Molecular Approaches.Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes.Genome-wide methylation analysis in Silver-Russell syndrome patients Compromised fertility disrupts Peg1 but not Snrpn and Peg3 imprinted methylation acquisition in mouse oocytes.High Frequency of Imprinted Methylation Errors in Human Preimplantation Embryos The promoter methylomes of monochorionic twin placentas reveal intrauterine growth restriction-specific variations in the methylation patterns.Segmental Maternal UPD6 with Prenatal Growth Restriction.Transient neonatal diabetes, ZFP57, and hypomethylation of multiple imprinted loci: a detailed follow-up The human imprintome: regulatory mechanisms, methods of ascertainment, and roles in disease susceptibility Frequency and characterization of DNA methylation defects in children born SGA.New developments in Silver-Russell syndrome and implications for clinical practice Epigenetic discordance at imprinting control regions in twins.Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith-Wiedemann and Silver-Russell syndromes.Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.Epigenetic deregulation of genomic imprinting in humans: causal mechanisms and clinical implications.Multilocus methylation defects in imprinting disorders.Diagnosis and management of Silver-Russell syndrome: first international consensus statement.An Update on Molecular Diagnostic Testing of Human Imprinting Disorders.Role of DNA methylation in imprinting disorders: an updated review.Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2/H19 in Silver-Russell syndrome.Genome-wide analysis of differential DNA methylation in Silver-Russell syndrome.Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology.Clinical utility gene card for: Silver-Russell syndrome.Comparison of the clinical scoring systems in Silver-Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing.Hepatic IGF1 DNA methylation is influenced by gender but not by intrauterine growth restriction in the young lamb.Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances.

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P2860

Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci.

http://www.wikidata.org/entity/Q34329150

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունվարին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Methylation analysis of 79 pat ...... tion change at imprinted loci.

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Methylation analysis of 79 pat ...... tion change at imprinted loci.

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Methylation analysis of 79 pat ...... tion change at imprinted loci.

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type

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Methylation analysis of 79 pat ...... tion change at imprinted loci.

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Methylation analysis of 79 pat ...... tion change at imprinted loci.

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Methylation analysis of 79 pat ...... tion change at imprinted loci.

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prefLabel

Methylation analysis of 79 pat ...... tion change at imprinted loci.

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Methylation analysis of 79 pat ...... tion change at imprinted loci.

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Methylation analysis of 79 pat ...... tion change at imprinted loci.

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European Journal of Human Genetics

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Methylation analysis of 79 pat ...... tion change at imprinted loci.

@en

P2093

Bruce M Castle

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Claire Louise Susan Turner

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Deborah M Mackay

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Emma C Kivuva

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Emma L Wakeling

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Hilary Bullman

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I Karen Temple

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Jackie Madden

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Jonathan L A Callaway

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Justin H Davies

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P2860

Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57

Genomic imprinting: parental influence on the genome

Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).

Type-2 IGF receptor: a multi-ligand binding protein.

Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling.

Identification of the human homolog of the imprinted mouse Air non-coding RNA.

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

The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria.

Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality.

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648-655

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10.1038/EJHG.2009.246

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6

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18

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41149217

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1034813474

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20104244

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2987339

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