Transient neonatal diabetes, ZFP57, and hypomethylation of multiple imprinted loci: a detailed follow-up - Wikidata - wikimedia - TriplyDB

Transient neonatal diabetes, ZFP57, and hypomethylation of multiple imprinted loci: a detailed follow-up

Transient neonatal diabetes, ZFP57, and hypomethylation of multiple imprinted loci: a detailed follow-up

http://www.wikidata.org/entity/Q36629581

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The specification of imprints in mammals Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes Erythrocyte folate concentrations, CpG methylation at genomically imprinted domains, and birth weight in a multiethnic newborn cohort Hyperhomocysteinemia potentiates hyperglycemia-induced inflammatory monocyte differentiation and atherosclerosis.Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57 The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome.Mechanisms and Disease Associations of Haplotype-Dependent Allele-Specific DNA Methylation Chromosome 6q24 methylation defects are uncommon in childhood-onset non-autoimmune diabetes mellitus patients born appropriate- or large-for-gestational age.Multilocus methylation defects in imprinting disorders.ZFP57 and the Targeted Maintenance of Postfertilization Genomic Imprints.Human and mouse ZFP57 proteins are functionally interchangeable in maintaining genomic imprinting at multiple imprinted regions in mouse ES cells.An Update on Molecular Diagnostic Testing of Human Imprinting Disorders.Role of DNA methylation in imprinting disorders: an updated review.Abnormalities in chromosome 6q24 as a cause of early-onset, non-obese, non-autoimmune diabetes mellitus without history of neonatal diabetes.Potential Roles of Intrinsic Disorder in Maternal-Effect Proteins Involved in the Maintenance of DNA Methylation.Transient neonatal diabetes mellitus in a Turkish patient with three novel homozygous variants in the ZFP57 gene.Clinical utility gene card for: Transient Neonatal Diabetes Mellitus, 6q24-related Is ZFP57 binding to H19/IGF2:IG-DMR affected in Silver-Russell syndrome?Neonatal diabetes with intractable epilepsy: DEND syndrome.Chromosome 6q24-related diabetes mellitus.

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Transient neonatal diabetes, ZFP57, and hypomethylation of multiple imprinted loci: a detailed follow-up

http://www.wikidata.org/entity/Q36629581

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Transient neonatal diabetes, Z ...... ted loci: a detailed follow-up

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Transient neonatal diabetes, Z ...... ted loci: a detailed follow-up

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Transient neonatal diabetes, Z ...... ted loci: a detailed follow-up

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Transient neonatal diabetes, Z ...... ted loci: a detailed follow-up

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Transient neonatal diabetes, Z ...... ted loci: a detailed follow-up

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Transient neonatal diabetes, Z ...... ted loci: a detailed follow-up

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Ahmed F Massoud

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Andreas P Haemers

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Anna Lehmann

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C T Bich Ngoc

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Dung Chí Vu

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Frida Sundberg

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Johanne M D Hahnemann

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Lise G Larsen

http://www.w3.org/2001/XMLSchema#string

Louise Docherty

http://www.w3.org/2001/XMLSchema#string

Lutgarde Dooms

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P2860

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

A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints

A novel nuclear protein with zinc fingers down-regulated during early mammalian cell differentiation

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

Identifying genes preferentially expressed in undifferentiated embryonic stem cells

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

Fortuitous detection of uniparental isodisomy of chromosome 6.

Neonatal diabetes: new insights into aetiology and implications.

Transient neonatal diabetes mellitus type 1.

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.

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Carlo L Acerini

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Isabel Karen Temple

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2012-11-12T00:00:00Z

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