Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models - Wikidata - awgldk - TriplyDB

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

http://www.wikidata.org/entity/Q34639776

about

A Dishful of a Troubled Mind: Induced Pluripotent Stem Cells in Psychiatric Research iPSC-derived neurons as a higher-throughput readout for autism: promises and pitfalls RNA Sequencing in Schizophrenia Over-expression of hNGF in adult human olfactory bulb neural stem cells promotes cell growth and oligodendrocytic differentiation.Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression Genetic similarities between tobacco use disorder and related comorbidities: an exploratory study CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment.Reduced CYFIP1 in Human Neural Progenitors Results in Dysregulation of Schizophrenia and Epilepsy Gene Networks.Transcriptomics analysis of iPSC-derived neurons and modeling of neuropsychiatric disorders.Will brain cells derived from induced pluripotent stem cells or directly converted from somatic cells (iNs) be useful for schizophrenia research?Modeling psychiatric disorders: from genomic findings to cellular phenotypes Optimizing neuronal differentiation from induced pluripotent stem cells to model ASD Modeling neurodevelopmental disorders using human pluripotent stem cells.Genetics studies indicate that neural induction and early neuronal maturation are disturbed in autism.The use of stem cells to study autism spectrum disorder Modeling the autistic cell: iPSCs recapitulate developmental principles of syndromic and nonsyndromic ASD.Generation of Cholinergic and Dopaminergic Interneurons from Human Pluripotent Stem Cells as a Relevant Tool for In Vitro Modeling of Neurological Disorders Pathology and Therapy.A molecular model for neurodevelopmental disorders.The functional genetic link of NLGN4X knockdown and neurodevelopment in neural stem cells.Prospects for Modeling Abnormal Neuronal Function in Schizophrenia Using Human Induced Pluripotent Stem Cells.Proteomic and Metabolomic Analyses of Vanishing White Matter Mouse Astrocytes Reveal Deregulation of ER Functions.Enriched expression of genes associated with autism spectrum disorders in human inhibitory neurons.Convergent Pathways in Idiopathic Autism Revealed by Time Course Transcriptomic Analysis of Patient-Derived Neurons.

P2860

Q26770097-793819C8-F12F-446D-8985-8D698AC56297 Q26827249-236F84C3-A4A4-4AD6-BB3B-EC6F6DEB376F Q26996831-15EE8789-E96C-4681-8F7C-6F3A9331AD27 Q35075270-BFD614C0-7455-4F48-85B4-8A0B2BB30E84 Q35109014-7797381A-0D99-4264-94CD-64BDBC1BD665 Q35212842-C855AE99-A840-4B1D-8570-7C14BB51A33D Q36181600-D34E4133-BFEA-4910-B414-E15C162A74AC Q36519585-4194931A-70D2-4D02-994F-4707983AF9DA Q36901962-9C7631F2-594E-4CB8-B495-47954487485E Q37131089-8C02B834-19CF-4FD1-9C53-BEAE87BE8964 Q37199033-A23BFED1-BC75-4F08-9956-FA2646E825EF Q37708281-7A8EECA5-8D52-4F21-A8DA-8D73443C7042 Q38204302-48B65525-641A-4EDE-A1EF-CB4F3CFD2FD2 Q38283524-3A7F8137-C3B2-4DA7-BC76-A3A383161901 Q38368547-07C80109-B4B0-4F82-B376-26098AE6426B Q38816786-31FA00ED-8446-435F-ADEB-9BC10234CFB2 Q39095805-8C50985C-A448-4CF6-AE5F-E88E22FF91CC Q42426166-C247EC99-C3A4-4783-A0D3-C6E337BA8839 Q42563240-6D958B60-92F1-4FBA-8263-E422A521BC8C Q47104449-AF4F7CD7-756C-4D77-B74E-84C9ACB0290C Q47836573-CB23A5EE-1B43-4BD6-B88A-B2C464ADC439 Q48276910-AF50EDAD-5268-4866-BF89-57ECE87C8869 Q54983701-3017D1B9-EFDD-4486-8828-F9B1CDD8E6E5

P2860

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

http://www.wikidata.org/entity/Q34639776

description

2013 nî lūn-bûn

@nan

2013 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի մարտին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

@ast

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

@en

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

@nl

type

label

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

@ast

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

@en

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

@nl

prefLabel

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

@ast

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

@en

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

@nl

P1433

Q34639776-2C1B7C19-F227-4E3F-BBF4-CBAC2C8AEB5C

P1476

Q34639776-1E5C1CBA-7C60-4713-8A47-D11EA9B86E4F

P2093

Q34639776-4573E674-66CE-473B-8215-2CE58D8559D1

Q34639776-5084EE48-B8EC-4305-B867-6EAAFD3BC16A

Q34639776-9100CE3E-FA40-4ECA-9BFB-40BFDA84A608

Q34639776-A8E2EF46-4D14-4B9E-BCC0-CB76DE7E974D

Q34639776-B542FE9C-511C-4EA5-88B2-92C54C8AAF81

Q34639776-F7B62320-ABB0-4637-9AAC-B24288714937

P2860

Q34639776-00132F96-F60B-4D08-9D2E-6F837BDD502A

Q34639776-0D0FF44F-BF16-4781-8BE7-5782A95BAA91

Q34639776-0DDB7AFE-6224-469A-997F-9F048221C002

Q34639776-0E29F232-6B20-40CA-8B8C-D50E3A879E40

Q34639776-139A1CEA-D013-4A66-A58B-B89CF39D20F5

Q34639776-18B45FB9-5903-4463-BCD1-6268F33EEFAA

Q34639776-198605C6-9D22-40C3-B740-CB2037C2496B

Q34639776-1A4BEC0C-DDD5-47AF-A8FF-5F3D52CAD31E

Q34639776-1BF554DB-5F6E-4A3C-8C0C-1EA9D443DB13

Q34639776-1FF5F7AC-4FCD-4040-A123-C9AC7AC9535D

P304

Q34639776-BCE8D626-7EE0-4CC2-B6A5-BC33B399C6ED

P31

Q34639776-F3DF40C5-086E-46B1-BA29-A74946C89E9D

P356

Q34639776-E2FE52CD-E549-4C8D-9CB5-37DCA62DB32E

P407

Q34639776-DCE9CF74-59F5-47B1-8776-B1FD9599A7B3

P433

Q34639776-E7BFF4FD-5BC1-4830-BAD5-6EE029F09BA4

P478

Q34639776-504CC9F9-2353-4A5C-9CEA-E0263FD1576D

P577

Q34639776-5B59A7B8-DB89-4227-AA3D-B773C4EABB44

P5875

Q34639776-6CEDCD14-170E-4B02-9FA9-0C4F44C34AB8

P698

Q34639776-C6F54B7B-7D21-4451-83BD-3C11A35D08FB

P921

Q34639776-7A05CD43-8170-49AA-A4B6-9C9A0B444BAB

P932

Q34639776-A9A39948-1BF3-440A-84B4-5CD18615A25D

P356

JOURNAL.PONE.0059685

P1433

P1476

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

@en

P2093

Kai Wang

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

Lingling Shi

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

Liyun Zeng

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

Peilin Zhang

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

Vicky Yamamoto

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

Wange Lu

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

P2860

Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

Towards a proteome-scale map of the human protein–protein interaction network

Copy-number variations associated with neuropsychiatric conditions

Neuroligins and neurexins link synaptic function to cognitive disease

Rare chromosomal deletions and duplications increase risk of schizophrenia

Tripartite synapses: astrocytes process and control synaptic information

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

High frequency of neurexin 1beta signal peptide structural variants in patients with autism

Neurexophilins form a conserved family of neuropeptide-like glycoproteins

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

P304

e59685

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

P31

scholarly article

P356

10.1371/JOURNAL.PONE.0059685

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

P407

P433

3

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

P478

8

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

P577

2013-03-25T00:00:00Z

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

P5875

236088345

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

P698

23536886

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

P921

P932

3607566

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