(Q41614673)

English

Zebrafish homologs of genes within 16p11.2, a genomic region associated with brain disorders, are active during brain development, and include two deletion dosage sensor genes.

scientific article published on May 2012

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22566537%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

Zebrafish homologs of genes within 16p11.2, a genomic region associated with brain disorders, are active during brain development, and include two deletion dosage sensor genes (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22566537%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

0 references

PAXIP1 associated glutamate-rich protein 1

1 reference

GOA release 2020-03-11

Aspartate beta-hydroxylase domain containing 1

1 reference

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Protein phosphatase 4, catalytic subunit a

1 reference

GOA release 2020-03-11

Glycerophosphodiester phosphodiesterase domain containing 3a

1 reference

GOA release 2020-03-11

Kinesin family member 22

1 reference

GOA release 2020-03-11

Potassium channel tetramerization domain containing 13

1 reference

GOA release 2020-03-11

Major vault protein

1 reference

GOA release 2020-03-11

Coronin, actin binding protein, 1A

1 reference

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Uncharacterized LOC107988037

1 reference

GOA release 2020-03-11

Aldolase a, fructose-bisphosphate, a

1 reference

GOA release 2020-03-11

T-box transcription factor 6

1 reference

GOA release 2020-03-11

Mitogen-activated protein kinase 3

1 reference

GOA release 2020-03-11

5

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Europe PubMed Central

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31 January 2020

author name string

Alicia Blaker-Lee

1

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31 January 2020

Sunny Gupta

2

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31 January 2020

Jasmine M McCammon

3

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31 January 2020

Gianluca De Rienzo

4

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31 January 2020

publication date

1 May 2012

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31 January 2020

Disease Models & Mechanisms

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31 January 2020

5

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31 January 2020

6

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31 January 2020

834-851

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31 January 2020

copyright license

Creative Commons Attribution 2.0 Generic

18 May 2021

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April 2022 Public Data File from Crossref

copyright status

0 references

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Identification of de novo copy number variants associated with human disorders of sexual development

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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

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Two cases of red cell aldolase deficiency associated with hereditary hemolytic anemia in a japanese family

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Red cell aldolase deficiency and hemolytic anemia: a new syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

6 June 2018

Retinal pathology in autistic children--a possible biological marker for a subtype?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

6 June 2018

Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

6 June 2018

Reduced midbrain and pons size in children with autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

6 June 2018

Abnormal neuronal differentiation (functional maturation) in mental retardation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

6 June 2018

Alternative startle motor patterns and behaviors in the larval zebrafish (Danio rerio).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Mental retardation and autism associated with recurrent 16p11.2 microdeletion: incomplete penetrance and variable expressivity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Developmental transition of touch response from slow muscle-mediated coilings to fast muscle-mediated burst swimming in zebrafish

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Migration and homeostasis of naive T cells depends on coronin 1-mediated prosurvival signals and not on coronin 1-dependent filamentous actin modulation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Narrowing the critical deletion region for autism spectrum disorders on 16p11.2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Gait patterns in children with autism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

A familial 593-kb microdeletion of 16p11.2 associated with mental retardation and hemivertebrae.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Zebrafish brain ventricle injection.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Distinct functions for ERK1 and ERK2 in cell migration processes during zebrafish gastrulation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Kid-mediated chromosome compaction ensures proper nuclear envelope formation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Epilepsia, epileptiform abnormalities, non-right-handedness, hypotonia and severe decreased IQ are associated with language impairment in autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Expression characteristics and stimulatory functions of CD43 in human CD4+ memory T cells: analysis using a monoclonal antibody to CD43 that has a novel lineage specificity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Tbx24, encoding a T-box protein, is mutated in the zebrafish somite-segmentation mutant fused somites.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Differentiation and maturation of zebrafish dorsal root and sympathetic ganglion neurons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Doc2alpha is an activity-dependent modulator of excitatory synaptic transmission.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Time course of the development of motor behaviors in the zebrafish embryo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Segment and cell type lineage restrictions during pharyngeal arch development in the zebrafish embryo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3484866

19 August 2018

Microdeletion of 16p11.2 associated with endocardial fibroelastosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22566537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel microdeletion at 16p11.2 harbors candidate genes for aortic valve development, seizure disorder, and mild mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22566537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of ERK1 and ERK2 in the CNS causes cortical abnormalities and neonatal lethality: Erk1 deficiency enhances the impairment of neurogenesis in Erk2-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/22566537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical report of microphthalmia and optic nerve coloboma associated with a de novo microdeletion of chromosome 16p11.2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22566537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1242/DMM.009944

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22566537%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22566537%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22566537%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

ResearchGate publication ID

0 references

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