Prader-Willi syndrome and autism spectrum disorders: an evolving story. - Wikidata - wikimedia - TriplyDB

Prader-Willi syndrome and autism spectrum disorders: an evolving story.

Prader-Willi syndrome and autism spectrum disorders: an evolving story.

http://www.wikidata.org/entity/Q35680723

about

Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders.Channelopathy pathogenesis in autism spectrum disorders Dendritic spine dysgenesis in autism related disorders Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders.Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.Incidental memory for faces in children with different genetic subtypes of Prader-Willi syndrome Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.Ontogenesis of oxytocin pathways in the mammalian brain: late maturation and psychosocial disorders Weight control and behavior rehabilitation in a patient suffering from Prader Willi syndrome.Gender Differences in the Behavioral Symptom Severity of Prader-Willi Syndrome Leisure activities in Prader-Wili syndrome: implications for health, cognition and adaptive functioning Social and emotional processing in Prader-Willi syndrome: genetic subtype differences.A Prader-Willi locus lncRNA cloud modulates diurnal genes and energy expenditure Valproic acid silencing of ascl1b/Ascl1 results in the failure of serotonergic differentiation in a zebrafish model of fetal valproate syndrome New Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain.Natural breaking of the maternal silence at the mouse and human imprinted Prader-Willi locus: A whisper with functional consequences.Investigating Autism-Related Symptoms in Children with Prader-Willi Syndrome: A Case Study.Aging in rare intellectual disability syndromes.Integrating the roles of long and small non-coding RNA in brain function and disease.Early Infant Development and Intervention for Autism Spectrum Disorder.Diagnoses and characteristics of autism spectrum disorders in children with Prader-Willi syndrome.Cognitive and adaptive advantages of growth hormone treatment in children with Prader-Willi syndrome.A mindfulness-based intervention for self-management of verbal and physical aggression by adolescents with Prader-Willi syndrome.R Loops and Links to Human Disease.A Comprehensive Guide to the MAGE Family of Ubiquitin Ligases.Cellular and disease functions of the Prader-Willi Syndrome gene MAGEL2.Prader-Willi Syndrome and Schaaf-Yang Syndrome: Neurodevelopmental Diseases Intersecting at the MAGEL2 Gene.The Developmental Trajectory of Self-Injurious Behaviours in Individuals with Prader Willi Syndrome, Autism Spectrum Disorder and Intellectual Disability.Network Diffusion-Based Prioritization of Autism Risk Genes Identifies Significantly Connected Gene Modules.The Locus Preservation Hypothesis: Shared Linguistic Profiles across Developmental Disorders and the Resilient Part of the Human Language Faculty.Epigenetics and cerebral organoids: promising directions in autism spectrum disorders.Oxytocin and Prader-Willi Syndrome.Evaluating the Feasibility of a Play-Based Telehealth Intervention Program for Children with Prader-Willi Syndrome.Dermatologic features of Smith-Magenis syndrome.Loss of Maged1 results in obesity, deficits of social interactions, impaired sexual behavior and severe alteration of mature oxytocin production in the hypothalamus.Assessment of pretend play in Prader-Willi syndrome: a direct comparison to autism spectrum disorder.DSM-5 changes and the prevalence of parent-reported autism spectrum symptoms in Fragile X syndrome.Social responsiveness and competence in Prader-Willi syndrome: direct comparison to autism spectrum disorder.Autism spectrum disorders and hyperactive/impulsive behaviors in Japanese patients with Prader-Willi syndrome: a comparison between maternal uniparental disomy and deletion cases.Reciprocal F1 Hybrids of Two Inbred Mouse Strains Reveal Parent-of-Origin and Perinatal Diet Effects on Behavior and Expression

P2860

Q26748761-CA518266-505D-4B70-94D5-63565ED2E30D Q26864726-5EBF63EC-7470-45D9-9FE6-E96127CE7B37 Q26995242-1C3898DB-05E7-4EAC-9168-757C2EBAFDE1 Q30373162-C28121A0-0E40-457F-9711-519C309F0C7B Q31138426-744D223C-63C1-40CE-9F59-8D0862783528 Q33802818-CE8CE4A6-12F9-4ADF-98F1-C530137075FB Q34314297-27EC669B-213E-4F34-A83C-217326D0154D Q35123962-35BAFAA2-6008-4217-9414-12099A86D41A Q35976911-04F46F51-1F81-45BE-AF43-07F6D0C007C0 Q36304509-A14A1AFB-AFA3-4DE2-8F0D-858C7B37177B Q36322797-5E6295AF-2145-45CB-ADB8-581407F34847 Q36798517-7AE491B5-00B4-40BB-95A7-B998AD4916DA Q37220678-A526ED4F-02A7-40CD-9663-3955B4CD634B Q37438521-78369A67-580A-4BFE-BC60-9A0ACDA7809D Q37445958-093F3AFE-E21D-4346-BCE2-CF48CE8F4399 Q37690666-20DC5208-1B1B-4ADE-A67A-62E19330E808 Q37729060-03CABEF6-E10C-4064-B8FC-7A7C106A160A Q38129326-AB3D06DC-7316-4CF9-82B3-5F2ED1AD66C9 Q38182329-94AAF2ED-02F4-4812-8F4F-E251A0A84FE7 Q38577439-344CD1E4-15D0-42CC-9B88-AED1B213653D Q38673463-22D65317-0763-4764-B1DC-A8F0178888D5 Q38835532-250A91FB-4B53-4406-A66A-370920830400 Q38889569-0BA6876C-FE61-4A33-9DF1-0CAA4F9B26DB Q38947687-7509CC29-AF0E-40C4-8B87-5ECDAE3A3228 Q39181769-0B26E142-A1E6-4D68-8BD8-65C570FA3488 Q39381468-00A519C7-2D6F-480B-87A5-6E6D2792707E Q42058938-D1615F71-74CC-45CB-9B29-30BFDFF17A6C Q42226807-88F13801-E087-4410-9BD2-7740A8D3A20D Q42368125-B5F41FA5-07C2-4972-B6A3-74AE6D775976 Q42682341-C4849E97-3509-45F8-BAE5-60FDC9E259C5 Q47562578-DBF85F1B-8ACA-4840-844F-DBEE1F1B2AF3 Q47675924-01CD8D26-100E-4E08-B5EA-ED14B9F08A55 Q47824011-86F84F3A-9C65-4091-8A83-8594E56DF345 Q48114792-68B2C36D-B826-48C0-91B1-58624A46E22F Q48418722-816C3B48-D327-4CB0-B20D-20BEB2A41D2A Q50304408-79B12798-83CE-4F16-BE2F-4AC00986D50C Q50304432-5F7CCF40-93A5-4FB1-A94F-63194FE9B401 Q50307148-FA525C22-59E9-44C4-B3E5-AD1F501A9985 Q55327238-F34FB48C-BE6C-47F4-A615-3977701028F7 Q58778410-20DCA8BF-66E4-4E69-A384-43B64E07C051

P2860

Prader-Willi syndrome and autism spectrum disorders: an evolving story.

http://www.wikidata.org/entity/Q35680723

description

2011 nî lūn-bûn

@nan

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

2011年论文

@zh

2011年论文

@zh-cn

name

Prader-Willi syndrome and autism spectrum disorders: an evolving story.

@ast

Prader-Willi syndrome and autism spectrum disorders: an evolving story.

@en

type

label

Prader-Willi syndrome and autism spectrum disorders: an evolving story.

@ast

Prader-Willi syndrome and autism spectrum disorders: an evolving story.

@en

prefLabel

Prader-Willi syndrome and autism spectrum disorders: an evolving story.

@ast

Prader-Willi syndrome and autism spectrum disorders: an evolving story.

@en

P1433

Q35680723-D8698B50-FE40-44B5-8B99-7FC00EC04F99

P1476

Q35680723-9AA21059-A6DC-4973-8074-8A242E3776A2

P2093

Q35680723-890F8FF1-4A54-4EA5-83FE-905F0A5C0148

Q35680723-9C4E7EA9-32F7-491F-A6E7-717C9FD7C3BB

Q35680723-F33DECAE-C35F-47F9-B079-20E09021524B

P2860

Q35680723-01D39877-68F4-4D9C-BF14-6D0FBF6EEC3A

Q35680723-040DCBA3-4EF8-43ED-B637-E3FED7D3B3DC

Q35680723-04F78AD7-8F34-4586-B76C-AB4620F828DD

Q35680723-0B2D0E4D-C216-489F-A940-2DEE200E509A

Q35680723-0B75B0C8-4A8B-4C55-AE6A-6767E33753FD

Q35680723-11D45ADD-A650-47BF-948E-F8F696F7D1A6

Q35680723-1212F1BF-B17F-4E92-B418-24C78797C389

Q35680723-13DE37AE-A8B6-4A0F-A8C0-A3D2C83154C7

Q35680723-1A312976-8313-4588-96A3-E430E4C1E4FB

Q35680723-1CE7D73D-9E30-48E1-947A-55D86061C1E2

P2888

Q35680723-16D3EC4B-2A5F-40EE-990C-7E87A33F7CEA

P304

Q35680723-3714EA80-423D-4251-BD71-3D2761CF55FC

P31

Q35680723-8A394309-DA4C-437D-9B1B-9C7A1962B574

P356

Q35680723-CF7B931A-0A34-4170-8873-4746BA9A465D

P433

Q35680723-49775459-520F-44C6-A280-38617F85B8CD

P478

Q35680723-7D51C39D-FFA9-42F6-B37A-C279C4625079

P577

Q35680723-7BC506DB-F755-47E3-AEE8-C04391D4EDD4

P5875

Q35680723-3708E127-C74B-4A84-9249-6B105AB02540

P698

Q35680723-E5553F2E-36FB-471F-8658-20E5FE45401A

P921

Q35680723-2BBEC081-340F-478F-A1F3-26629947265B

P932

Q35680723-08583CFA-161F-43B5-85A0-DE3119F2433B

P356

S11689-011-9092-5

P1433

Journal of Neurodevelopmental Disorders

P1476

Prader-Willi syndrome and autism spectrum disorders: an evolving story.

@en

P2093

Elisabeth M Dykens

http://www.w3.org/2001/XMLSchema#string

Elizabeth Roof

http://www.w3.org/2001/XMLSchema#string

Evon Lee

http://www.w3.org/2001/XMLSchema#string

P2860

SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice

Sleep problems in autism spectrum disorders: Prevalence, nature, & possible biopsychosocial aetiologies

The Repetitive Behavior Scale-Revised: Independent Validation in Individuals with Autism Spectrum Disorders

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways

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

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

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

Prader-Willi and Angelman syndromes: sister imprinted disorders

Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions

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

P2888

s11689-011-9092-5

P304

225-237

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1007/S11689-011-9092-5

http://www.w3.org/2001/XMLSchema#string

P433

3

http://www.w3.org/2001/XMLSchema#string

P478

3

http://www.w3.org/2001/XMLSchema#string

P577

2011-08-20T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

51587259

http://www.w3.org/2001/XMLSchema#string

P698

21858456

http://www.w3.org/2001/XMLSchema#string

P921

Autism spectrum

P932

3261277

http://www.w3.org/2001/XMLSchema#string