| P50 | author | Dick Swaab | Q2682716 |
| | Françoise Muscatelli | Q52097093 |
| | Valéry Matarazzo | Q56844964 |
| | Francoise Watrin | Q63436657 |
| | Rachel Wevrick | Q46130607 |
| P2093 | author name string | Laurent Bezin | |
| | Ulrich Zechner | |
| | Unga Unmehopa | |
| | Fabienne Schaller | |
| | François J Michel | |
| | Matthias Linke | |
| | Femke Dijkstra | |
| | Severine Corby | |
| | Keith Dudley | |
| | Anne Rieusset | |
| | Beatrice Georges | |
| | Jocelyn Bischof | |
| | Monique Bloemsma | |
| P2860 | cites work | A modified and improved method for bisulphite based cytosine methylation analysis | Q24544058 |
| | The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene | Q24808766 |
| | Pairing of homologous regions in the mouse genome is associated with transcription but not imprinting status | Q27301083 |
| | The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse | Q28249408 |
| | The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region | Q28253418 |
| | Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice | Q80809786 |
| | Review of 64 cases of death in children with Prader-Willi syndrome (PWS) | Q80832115 |
| | The association between oxytocin receptor gene polymorphism (OXTR) and trait empathy | Q83492124 |
| | Analysis of imprinted genes in subjects with Prader-Willi syndrome and chromosome 15 abnormalities | Q93949736 |
| | Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome. | Q49155367 |
| | Prader-Willi syndrome. | Q51826464 |
| | Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression. | Q52097061 |
| | Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human | Q56982001 |
| | Neuronal histamine production remains unaltered in Parkinson's disease despite the accumulation of Lewy bodies and Lewy neurites in the tuberomamillary nucleus | Q57821060 |
| | Relaxation of imprinting in Prader-Willi syndrome | Q62712526 |
| | Allelic discrimination using fluorogenic probes and the 5' nuclease assay | Q74618454 |
| | Detection of specific polymerase chain reaction product by utilizing the 5'----3' exonuclease activity of Thermus aquaticus DNA polymerase | Q28291219 |
| | Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice | Q28505055 |
| | Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival | Q28508839 |
| | Disruption of the mouse necdin gene results in early post-natal lethality | Q28587922 |
| | Environmental epigenomics and disease susceptibility | Q29547452 |
| | Genomic imprinting: parental influence on the genome | Q29616227 |
| | Highly efficient modification of bacterial artificial chromosomes (BACs) using novel shuttle vectors containing the R6Kgamma origin of replication | Q31120342 |
| | Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death | Q33264123 |
| | Sex-specific expression of the X-linked histone demethylase gene Jarid1c in brain | Q33348587 |
| | Explaining inter-individual variability in phenotype: is epigenetics up to the challenge? | Q33691436 |
| | Variability in gene expression underlies incomplete penetrance | Q33717980 |
| | Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns. | Q33959408 |
| | Necdin protects embryonic motoneurons from programmed cell death | Q34017758 |
| | Prader-Willi Syndrome: Obesity due to Genomic Imprinting | Q34229319 |
| | Prader-Willi syndrome and autism spectrum disorders: an evolving story | Q35680723 |
| | The secret language of destiny: stress imprinting and transgenerational origins of disease | Q36005293 |
| | Loss of imprinting and cancer | Q36687286 |
| | Insights into the regulation of protein abundance from proteomic and transcriptomic analyses | Q36846022 |
| | Genomic imprinting effects in a compromised in utero environment: implications for a healthy pregnancy | Q37625351 |
| | Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13. | Q37715376 |
| | Development of the eating behaviour in Prader-Willi Syndrome: advances in our understanding. | Q37777323 |
| | Regulatory mechanisms and networks couple the different phases of gene expression | Q37901668 |
| | A survey of tissue-specific genomic imprinting in mammals | Q38028387 |
| | Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples | Q38331031 |
| | Establishment and maintenance of DNA methylation patterns in mouse Ndn: implications for maintenance of imprinting in target genes of the imprinting center. | Q39458709 |
| | Transient homologous chromosome pairing marks the onset of X inactivation | Q40327289 |
| | Methylation profiles of DXPas34 during the onset of X-inactivation | Q40834879 |
| | Regulated noise in the epigenetic landscape of development and disease | Q41514448 |
| | Unexpected expression of orexin-B in basal conditions and increased levels in the adult rat hippocampus during pilocarpine-induced epileptogenesis. | Q42499632 |
| | Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome | Q43512902 |
| | Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome | Q46755443 |
| | Selective loss of imprinting in the placenta following preimplantation development in culture | Q47232748 |
| | Evidence for a role of the chemorepellent semaphorin III and its receptor neuropilin-1 in the regeneration of primary olfactory axons. | Q48346569 |
| | Sleep-related breathing disorders in prepubertal children with Prader-Willi syndrome and effects of growth hormone treatment | Q48489602 |
| | The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region | Q48575791 |
| | Increased melanin concentrating hormone receptor type I in the human hypothalamic infundibular nucleus in cachexia | Q49112851 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 9 | |
| P921 | main subject | Prader–Willi syndrome | Q594013 |
| P304 | page(s) | e1003752 | |
| P577 | publication date | 2013-09-05 | |
| P1433 | published in | PLOS Genetics | Q1893441 |
| P1476 | title | Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences | |
| P478 | volume | 9 | |