about
A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical regionAn imprinted, mammalian bicistronic transcript encodes two independent proteinsBehavioural phenotypes and special educational needs: is aetiology important in the classroom?Neuroendocrine secretory protein 7B2: structure, expression and functionsSeparate necdin domains bind ARNT2 and HIF1alpha and repress transcriptionDBS for ObesityPrader-Willi and Angelman syndromes: sister imprinted disordersDecreased bone mineral density in Prader-Willi syndrome: comparison with obese subjectsRapid birth-and-death evolution of imprinted snoRNAs in the Prader-Willi syndrome locus: implications for neural development in EuarchontogliresChild health, developmental plasticity, and epigenetic programmingDoes the brain shrink as the waist expands?Sleep, plasticity and the pathophysiology of neurodevelopmental disorders: the potential roles of protein synthesis and other cellular processes.The association between primary tooth emergence and anthropometric measures in young adults: findings from a large prospective cohort study.Nutritient intake of young children with Prader-Willi syndrome.Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndromeFamilial Prader-Willi syndrome: case report and a literature review.Imprinted genes and mental dysfunction.Different distribution of the genetic subtypes of the Prader-Willi syndrome in the elderly.Imprinting-mutation mechanisms in Prader-Willi syndromeChromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints.Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders.The MAGE proteins: emerging roles in cell cycle progression, apoptosis, and neurogenetic disease.Systematic review of the clinical and genetic aspects of Prader-Willi syndrome.Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients with Prader-Willi syndrome: a randomised placebo-controlled trial in 24 patients.From genotype to phenotype: genetics and medical practice in the new millennium.Clinical implications of gait analysis in the rehabilitation of adult patients with "Prader-Willi" Syndrome: a cross-sectional comparative study ("Prader-Willi" Syndrome vs matched obese patients and healthy subjects)Prader-Willi Critical Region, a Non-Translated, Imprinted Central Regulator of Bone Mass: Possible Role in Skeletal Abnormalities in Prader-Willi Syndrome.Do the interactions between glucocorticoids and sex hormones regulate the development of the metabolic syndrome?Death during GH therapy in children with Prader-Willi syndrome: description of two new cases.A very large protein with diverse functional motifs is deficient in rjs (runty, jerky, sterile) mice.Molecular basis of genetic neuropsychiatric disordersAltered functional brain networks in Prader-Willi syndrome.The interstitial duplication 15q11.2-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature.Plasma peptide YY and ghrelin levels in infants and children with Prader-Willi syndrome.Self-injurious behavior and Prader-Willi syndrome: behavioral forms and body locations.The imprinted NPAP1 gene in the Prader-Willi syndrome region belongs to a POM121-related family of retrogenes.Axial and appendicular body proportions for evaluation of limb and trunk asymmetry.Development of the eating behaviour in Prader-Willi Syndrome: advances in our understanding.Multidisciplinary assessment and treatment of self-injurious behavior in autism spectrum disorder and intellectual disability: integration of psychological and biological theory and approach.A short clinical overview of Prader-Willi syndrome.
P2860
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P2860
description
1997 nî lūn-bûn
@nan
1997 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Prader-Willi syndrome
@ast
Prader-Willi syndrome
@en
Prader-Willi syndrome
@en-gb
Prader-Willi syndrome
@nl
type
label
Prader-Willi syndrome
@ast
Prader-Willi syndrome
@en
Prader-Willi syndrome
@en-gb
Prader-Willi syndrome
@nl
prefLabel
Prader-Willi syndrome
@ast
Prader-Willi syndrome
@en
Prader-Willi syndrome
@en-gb
Prader-Willi syndrome
@nl
P2860
P3181
P356
P1476
Prader-Willi syndrome
@en
P2093
Cassidy SB
P2860
P304
P3181
P356
10.1136/JMG.34.11.917
P407
P577
1997-11-01T00:00:00Z