Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia. (Q47231098)

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scientific article published on 4 January 2018

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English	Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia.	scientific article published on 4 January 2018

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12 January 2018

http://europepmc.org/abstract/MED/29302076

Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia (English)

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12 May 2020

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oligodendrocyte

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4 January 2018

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7 January 2021

based on heuristic

inferred from DOI database lookup

Linking the SWI/SNF complex to prostate cancer.

1 reference

https://api.crossref.org/works/10.1038%2FS41380-017-0004-2

7 January 2021

based on heuristic

inferred from DOI database lookup

CSPG4-Specific Immunity and Survival Prolongation in Dogs with Oral Malignant Melanoma Immunized with Human CSPG4 DNA

1 reference

https://api.crossref.org/works/10.1038%2FS41380-017-0004-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Interneurons and oligodendrocyte progenitors form a structured synaptic network in the developing neocortex

1 reference

https://api.crossref.org/works/10.1038%2FS41380-017-0004-2

7 January 2021

based on heuristic

inferred from DOI database lookup

Chondroitin sulfate and cytoplasmic domain-dependent membrane targeting of the NG2 proteoglycan promotes retraction fiber formation and cell polarization.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29302076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Numbers and patterns in compulsory admissions in 3 Dutch cities; problems in urban areas and regional differences in the implementation of the law on special admissions to psychiatric hospitals]

1 reference

https://pubmed.ncbi.nlm.nih.gov/29302076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of protein-coding genetic variation in 60,706 humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/29302076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/29302076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/S41380-017-0004-2

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6755981&resulttype=core&format=json

12 May 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6755981&resulttype=core&format=json

12 May 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6755981&resulttype=core&format=json

12 May 2020

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