(Q43590746)

English

Identification of single nucleotide polymorphisms (SNPs) and other sequence changes and estimation of nucleotide diversity in coding and flanking regions of the NMDAR1 receptor gene in schizophrenic patients

scientific article published in May 2001

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scholarly article

1 reference

Europe PubMed Central

25 November 2017

Identification of single nucleotide polymorphisms (SNPs) and other sequence changes and estimation of nucleotide diversity in coding and flanking regions of the NMDAR1 receptor gene in schizophrenic patients (English)

1 reference

Europe PubMed Central

25 November 2017

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single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

author name string

Rice SR

1

1 reference

Europe PubMed Central

25 November 2017

Niu N

2

1 reference

Europe PubMed Central

25 November 2017

Berman DB

3

1 reference

Europe PubMed Central

25 November 2017

Heston LL

4

1 reference

Europe PubMed Central

25 November 2017

Sobell JL

5

1 reference

Europe PubMed Central

25 November 2017

language of work or name

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publication date

1 May 2001

1 reference

Europe PubMed Central

25 November 2017

Molecular Psychiatry

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Europe PubMed Central

25 November 2017

6

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Europe PubMed Central

25 November 2017

3

1 reference

Europe PubMed Central

25 November 2017

274-284

1 reference

Europe PubMed Central

25 November 2017

https://scigraph.springernature.com/pub.10.1038/sj.mp.4000838

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Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

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Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

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Accurate selection of a 5' splice site requires sequences within fibronectin alternative exon B.

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Genetic regulation of glutamate receptor ion channels

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Characterization of single-nucleotide polymorphisms in coding regions of human genes

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DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene.

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Evidence for a tetrameric structure of recombinant NMDA receptors.

1 reference

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Schizophrenia and glutamatergic transmission

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Bi-directional dideoxy fingerprinting (Bi-ddF): a rapid method for quantitative detection of mutations in genomic regions of 300-600 bp

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Dideoxy fingerprinting (ddF): A rapid and efficient screen for the presence of mutations

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Silent mutation induces exon skipping of fibrillin-1 gene in Marfan syndrome

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Identifiers

10.1038/SJ.MP.4000838

1 reference

Europe PubMed Central

25 November 2017

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1 reference

Europe PubMed Central

25 November 2017

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