| scholarly article | Q13442814 |
| P50 | author | Janine M. LaSalle | Q52280008 |
| P2093 | author name string | James L Resnick | |
| Amanda J DuBose | |||
| Karen N Leung | |||
| Roxanne O Vallero | |||
| P2860 | cites work | Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation | Q21092489 |
| SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice | Q21562297 | ||
| The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression | Q24291232 | ||
| Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain | Q24534447 | ||
| Characterization of cis- and trans-acting elements in the imprinted human SNURF-SNRPN locus | Q24535658 | ||
| Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism | Q24599984 | ||
| Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster | Q24653893 | ||
| Large recurrent microdeletions associated with schizophrenia | Q24654741 | ||
| A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism | Q24655126 | ||
| Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization | Q24673252 | ||
| A well-connected and conserved nucleoplasmic helicase is required for production of box C/D and H/ACA snoRNAs and localization of snoRNP proteins. | Q27935012 | ||
| Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region | Q28202378 | ||
| The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A | Q28207947 | ||
| Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region | Q28242397 | ||
| The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C | Q28287199 | ||
| Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain | Q28511651 | ||
| The multifunctional nucleolus | Q29615151 | ||
| Recent segmental duplications in the human genome | Q29616016 | ||
| Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13). | Q30630998 | ||
| A novel brain-specific box C/D small nucleolar RNA processed from tandemly repeated introns of a noncoding RNA gene in rats | Q30667377 | ||
| Generic features of tertiary chromatin structure as detected in natural chromosomes | Q33207927 | ||
| The impact of genomic neighborhood on the evolution of human and chimpanzee transcriptome | Q33411222 | ||
| Three probands with autistic disorder and isodicentric chromosome 15. | Q33970872 | ||
| The molecular genetics of autism | Q34108364 | ||
| A view of interphase chromosomes | Q34285078 | ||
| Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder | Q34325671 | ||
| A 15q13.3 microdeletion segregating with autism | Q34326191 | ||
| A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome | Q34326210 | ||
| A census of mammalian imprinting. | Q34430259 | ||
| Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region. | Q34446311 | ||
| Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion | Q34461093 | ||
| 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy | Q34519312 | ||
| Genomic imprinting effects on brain development and function | Q34699894 | ||
| Non-coding RNAs in imprinted gene clusters | Q34749691 | ||
| The callipyge locus: evidence for the trans interaction of reciprocally imprinted genes | Q35113377 | ||
| Dynamic changes in Histone H3 lysine 9 acetylation localization patterns during neuronal maturation require MeCP2. | Q35762162 | ||
| A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures | Q36627230 | ||
| Noncoding RNAs and RNA editing in brain development, functional diversification, and neurological disease | Q36872209 | ||
| Noncoding RNAs in Long-Term Memory Formation | Q37321828 | ||
| Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders. | Q37419604 | ||
| Eukaryotic snoRNAs: a paradigm for gene expression flexibility. | Q37484412 | ||
| Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples | Q38331031 | ||
| A computational screen for C/D box snoRNAs in the human genomic region associated with Prader-Willi and Angelman syndromes | Q46459796 | ||
| Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb | Q47933557 | ||
| Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain | Q48045492 | ||
| Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes | Q48075617 | ||
| The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain. | Q48630943 | ||
| A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects. | Q50654332 | ||
| Nuclear re-organisation of the Hoxb complex during mouse embryonic development. | Q52052528 | ||
| Nuclear topology of murine, cerebellar Purkinje neurons: changes as a function of development. | Q52169648 | ||
| An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript | Q60035843 | ||
| Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprintedDLK1/GTL2gene cluster | Q61312142 | ||
| Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression | Q67510275 | ||
| Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13 | Q67993243 | ||
| Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination | Q74527989 | ||
| Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice | Q80809786 | ||
| P433 | issue | 22 | |
| P304 | page(s) | 4227-4238 | |
| P577 | publication date | 2009-08-05 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size | |
| P478 | volume | 18 |
| Q35389369 | 15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain. |
| Q37220678 | A Prader-Willi locus lncRNA cloud modulates diurnal genes and energy expenditure |
| Q37699565 | Allelic specificity of Ube3a expression in the mouse brain during postnatal development |
| Q24612484 | Angelman syndrome: insights into genomic imprinting and neurodevelopmental phenotypes |
| Q39179848 | Box C/D small nucleolar RNA genes and the Prader-Willi syndrome: a complex interplay |
| Q42693517 | Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy |
| Q35622570 | DNA methylation differences in monozygotic twin pairs discordant for schizophrenia identifies psychosis related genes and networks |
| Q42646979 | Diagnosing and Treating Nervous System Disorders by Targeting Novel Classes of Non-coding RNAs |
| Q26863209 | Emerging roles of the neuronal nucleolus |
| Q37076219 | Epigenetic layers and players underlying neurodevelopment. |
| Q39970087 | Expression of non-coding RNA AB063319 derived from Rian gene during mouse development |
| Q39428484 | Gene amplification of ESR1 in breast cancers--fact or fiction? A fluorescence in situ hybridization and multiplex ligation-dependent probe amplification study |
| Q37961799 | Genetic and epigenetic dysregulation of imprinted genes in the brain |
| Q36223316 | Hypothalamic expression of snoRNA Snord116 is consistent with a link to the hyperphagia and obesity symptoms of Prader-Willi syndrome |
| Q47548397 | Hypothalamic loss of Snord116 recapitulates the hyperphagia of Prader-Willi syndrome. |
| Q36114041 | Imprinted DLK1-DIO3 region of 14q32 defines a schizophrenia-associated miRNA signature in peripheral blood mononuclear cells |
| Q37615120 | Imprinting evolution and human health |
| Q34401155 | Induced pluripotent stem cells can be used to model the genomic imprinting disorder Prader-Willi syndrome |
| Q91666170 | Lithium alters expression of RNAs in a type-specific manner in differentiated human neuroblastoma neuronal cultures, including specific genes involved in Alzheimer's disease |
| Q24603933 | Long-lasting alterations to DNA methylation and ncRNAs could underlie the effects of fetal alcohol exposure in mice |
| Q48035493 | Loss of the imprinted, non-coding Snord116 gene cluster in the interval deleted in the Prader Willi syndrome results in murine neuronal and endocrine pancreatic developmental phenotypes |
| Q38051910 | Neurodegeneration as an RNA disorder |
| Q35200175 | Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome |
| Q34956275 | Neuronal chromatin dynamics of imprinting in development and disease |
| Q41733066 | Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome |
| Q64094464 | Preclinical Testing in Translational Animal Models of Prader-Willi Syndrome: Overview and Gap Analysis |
| Q36675332 | Protein Delivery of an Artificial Transcription Factor Restores Widespread Ube3a Expression in an Angelman Syndrome Mouse Brain |
| Q37117728 | R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensation. |
| Q31134674 | RGS2 expression predicts amyloid-β sensitivity, MCI and Alzheimer's disease: genome-wide transcriptomic profiling and bioinformatics data mining. |
| Q44803556 | Recommendations for the investigation of animal models of Prader-Willi syndrome |
| Q36674660 | Requirement of Neuronal Ribosome Synthesis for Growth and Maintenance of the Dendritic Tree |
| Q56337423 | Ribosomal biogenesis as an emerging target of neurodevelopmental pathologies |
| Q35111712 | Small nucleolar RNAs U32a, U33, and U35a are critical mediators of metabolic stress |
| Q55363384 | Snord116-dependent diurnal rhythm of DNA methylation in mouse cortex. |
| Q37284354 | Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism |
| Q100750446 | What can we learn from PWS and SNORD116 genes about the pathophysiology of addictive disorders? |
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