(Q48434105)

11 February 2018

title

Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism. (English)

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11 February 2018

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Klauck SM

1

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11 February 2018

Felder B

2

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11 February 2018

Kolb-Kokocinski A

3

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11 February 2018

Schuster C

4

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11 February 2018

Chiocchetti A

5

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11 February 2018

Schupp I

6

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11 February 2018

Wellenreuther R

7

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11 February 2018

Schmötzer G

8

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11 February 2018

Poustka F

9

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11 February 2018

Breitenbach-Koller L

10

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11 February 2018

Poustka A

11

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11 February 2018

language of work or name

English

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publication date

29 August 2006

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11 February 2018

published in

Molecular Psychiatry

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11 February 2018

volume

11

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11 February 2018

page(s)

1073-1084

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11 February 2018

issue

12

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11 February 2018

https://scigraph.springernature.com/pub.10.1038/sj.mp.4001883

exact match

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cites work

Genetics of autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Hippocampus in autism: a Golgi analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Epidemiological surveys of autism and other pervasive developmental disorders: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Genetic influences in childhood-onset psychiatric disorders: autism and attention-deficit/hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Genomic screen and follow-up analysis for autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

A genomewide screen of 345 families for autism-susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Genetic linkage analysis of the X chromosome in autism, with emphasis on the fragile X region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

The systematic functional characterisation of Xq28 genes prioritises candidate disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

21 January 2018

Modern Views of Autism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Structure of the 80S ribosome from Saccharomyces cerevisiae--tRNA-ribosome and subunit-subunit interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

60S pre-ribosome formation viewed from assembly in the nucleolus until export to the cytoplasm

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Nuclear export of 60s ribosomal subunits depends on Xpo1p and requires a nuclear export sequence-containing factor, Nmd3p, that associates with the large subunit protein Rpl10p

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Defining the order in which Nmd3p and Rpl10p load onto nascent 60S ribosomal subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Qsr1p, a 60S ribosomal subunit protein, is required for joining of 40S and 60S subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Serotonin transporter (5-HTT) gene variants associated with autism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

The relation between general cognitive level and adaptive behavior domains in individuals with autism with and without co-morbid mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

The yeast growth control gene GRC5 is highly homologous to the mammalian putative tumor suppressor gene QM.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

New yeast-Escherichia coli shuttle vectors constructed with in vitro mutagenized yeast genes lacking six-base pair restriction sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Complex formation by positive and negative translational regulators of GCN4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Translational regulator RpL10p/Grc5p interacts physically and functionally with Sed1p, a dynamic component of the yeast cell surface

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Functional interaction in establishment of ribosomal integrity between small subunit protein rpS6 and translational regulator rpL10/Grc5p.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Heterologous complementation reveals that mutant alleles of QSR1 render 60S ribosomal subunits unstable and translationally inactive

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

SQT1, which encodes an essential WD domain protein of Saccharomyces cerevisiae, suppresses dominant-negative mutations of the ribosomal protein gene QSR1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Neuropathological findings in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Possible mechanisms for atrophy of the human hippocampus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Learning, memory, and transcription factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

RNA and microRNAs in fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

The mGluR theory of fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Autoregulation in the biosynthesis of ribosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Cortical activation and synchronization during sentence comprehension in high-functioning autism: evidence of underconnectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Neurology. Autistic brains out of synch?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

Autism and the serotonin transporter: the long and short of it

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

7 January 2021

Autism as a disorder of neural information processing: directions for research and targets for therapy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

7 January 2021

2-year-old boy who has been diagnosed with autism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

7 January 2021

Ribosomal protein L9 is the product of GRC5, a homolog of the putative tumor suppressor QM in S. cerevisiae

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

7 January 2021

Normal assembly of 60 S ribosomal subunits is required for the signaling in response to a secretory defect in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001883

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001883

1 reference

11 February 2018

PubMed ID

16940977

1 reference

11 February 2018