Prader-Willi Syndrome: Obesity due to Genomic Imprinting. - Wikidata - awgldk - TriplyDB

Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

http://www.wikidata.org/entity/Q34229319

about

Adenosine-to-inosine RNA editing and human disease A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men The neurobiology of the Prader-Willi phenotype of fragile X syndrome Transcript diversification in the nervous system: a to I RNA editing in CNS function and disease development Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.Adult-onset deletion of the Prader-Willi syndrome susceptibility gene Snord116 in mice results in reduced feeding and increased fat mass.Causes of death in Prader-Willi syndrome: Prader-Willi Syndrome Association (USA) 40-year mortality survey Growth hormone treatment in non-growth hormone-deficient children Early diagnosis and care is achieved but should be improved in infants with Prader-Willi syndrome Prader-Willi syndrome and growth hormone deficiency Effects of growth hormone treatment in adults with Prader-Willi syndrome Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology.Identification of differentially expressed non-coding RNAs in embryonic stem cell neural differentiation Differential regulation of non-protein coding RNAs from Prader-Willi Syndrome locus.Insulin and insulin-like growth factor 1 receptors are required for normal expression of imprinted genes.Clinical Presentation and Microarray Analysis of Peruvian Children with Atypical Development and/or Aberrant Behavior Polymorphisms in the SNRPN gene are associated with obesity susceptibility in a Spanish population.Growth charts for non-growth hormone treated Prader-Willi syndrome Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes.Clinically relevant known and candidate genes for obesity and their overlap with human infertility and reproduction.High-resolution chromosome ideogram representation of currently recognized genes for autism spectrum disorders Dietary Modulation of Gut Microbiota Contributes to Alleviation of Both Genetic and Simple Obesity in Children.Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.Weight control and behavior rehabilitation in a patient suffering from Prader Willi syndrome.Metabolic profiling in Prader-Willi syndrome and nonsyndromic obesity: sex differences and the role of growth hormone A clinical follow-up of 35 Brazilian patients with Prader-Willi syndrome.Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.A compendium of human genes regulating feeding behavior and body weight, its functional characterization and identification of GWAS genes involved in brain-specific PPI network Maternal transcription of non-protein coding RNAs from the PWS-critical region rescues growth retardation in mice.Molecular characterization of a patient presumed to have prader-willi syndrome.A twin sibling with Prader-Willi syndrome caused by type 2 microdeletion following assisted reproductive technology: A case report.GrowthHormone Research Society workshop summary: consensus guidelines for recombinant human growth hormone therapy in Prader-Willi syndrome.Obesity in adults with 22q11.2 deletion syndrome.Congenital Arthrogryposis: An Extension of the 15q11.2 BP1-BP2 Microdeletion Syndrome?Natural breaking of the maternal silence at the mouse and human imprinted Prader-Willi locus: A whisper with functional consequences.Prader-Willi Syndrome: A spectrum of anatomical and clinical features.Clinical and Molecular Characterization of Prader-Willi Syndrome.Benefits and limitations of prenatal screening for Prader-Willi syndrome.Model mice for 15q11-13 duplication syndrome exhibit late-onset obesity and altered lipid metabolism.Cellular and disease functions of the Prader-Willi Syndrome gene MAGEL2.

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P2860

Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

http://www.wikidata.org/entity/Q34229319

description

2011 nî lūn-bûn

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2011 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2011 թվականի մայիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

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type

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

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Current Genomics

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

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Merlin G Butler

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P2860

Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons

Genomic imprinting disorders in humans: a mini-review

Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism

Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD

Neural mechanisms underlying hyperphagia in Prader-Willi syndrome

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology

The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C

Are jigsaw puzzle skills 'spared' in persons with Prader-Willi syndrome?

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10.2174/138920211795677877

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