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GenomicsA Prader-Willi locus lncRNA cloud modulates diurnal genes and energy expenditure.
Prader-Willi syndrome (PWS), a genetic cause of childhood obesity, is characterized by intellectual disabilities and sleep abnormalities. PWS-causing deletions include a neuronal long, non-coding RNA (lncRNA) processed into small nucleolar RNAs and a spliced lncRNA,116HG. We show that 116HG forms a ...
ORGANISM(S): Mus musculus 
2013-06-20 | E-GEOD-43575 | biostudies-arrayexpress
GenomicsHypothalamic transcriptome in Prader-Willi syndrome
Transcriptional analysis of brain tissue from people with molecularly defined causes of obesity may highlight novel disease mechanisms and therapeutic targets. Prader-Willi syndrome (PWS) is a genetic obesity syndrome characterised by severe hyperphagia. We performed RNA sequencing of the hypothalam...
EGAS00001002901 | EGA
UnknownPharmacogenomic testing for Prader-Willi syndrome: a mixed methods analysis of caregiver experiences and utilization.
Not available
S-EPMC12915763 | biostudies-literature
TranscriptomicsThe noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome
Parental imprinting is a form of epigenetic regulation that results in parent-of-origin differential gene expression. To study Prader-Willi syndrome (PWS), a developmental imprinting disorder, we generated patient-derived induced pluripotent stem cells (iPSCs) harboring distinct deletions in the aff...
ORGANISM(S): Homo sapiens 
2014-04-03 | E-GEOD-56136 | biostudies-arrayexpress
UnknownCauses of death in Prader-Willi syndrome: Prader-Willi Syndrome Association (USA) 40-year mortality survey.
Not available
S-EPMC5435554 | biostudies-literature
TranscriptomicsDifferential Gene Expression and Mitochondrial Dysfunction in Imprinting center deletion (PWS- IC del) Mouse model of Prader-Willi Syndrome
Prader-Willi syndrome (PWS) is a genetic disorder caused by deficiency of imprinted gene expression from the paternal chromosome 15q11-15q13 and clinically characterized by neonatal hypotonia, short stature, cognitive impairment, hypogonadism, hyperphagia, morbid obesity and diabetes. Previous clini...
ORGANISM(S): Mus musculus 
2013-04-19 | E-GEOD-41759 | biostudies-arrayexpress
UnknownEarly oxytocin treatment in infants with Prader-Willi syndrome is safe and is associated with better endocrine, metabolic and behavioral outcomes.
Not available
S-EPMC11872305 | biostudies-literature
UnknownContributing factors of mortality in Prader-Willi syndrome.
Not available
S-EPMC6349475 | biostudies-literature
UnknownFood socialization of children with Prader-Willi syndrome: an interdisciplinary problematization.
Not available
S-EPMC10280295 | biostudies-literature
UnknownIrisin and the Metabolic Phenotype of Adults with Prader-Willi Syndrome.
Not available
S-EPMC4559418 | biostudies-literature
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