An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions (Q30457871)

15 August 2017

An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions (English)

1 reference

15 August 2017

Fred A Pereira

8

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author name string

Bum Jun Kim

1

1 reference

15 August 2017

Hitisha P Zaveri

2

1 reference

15 August 2017

Oleg A Shchelochkov

3

1 reference

15 August 2017

Zhiyin Yu

4

1 reference

15 August 2017

Andrés Hernández-García

5

1 reference

15 August 2017

Michelle L Seymour

6

1 reference

15 August 2017

John S Oghalai

7

1 reference

15 August 2017

David W Stockton

9

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15 August 2017

Monica J Justice

10

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15 August 2017

Brendan Lee

11

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15 August 2017

Daryl A Scott

12

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15 August 2017

language of work or name

English

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publication date

25 February 2013

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15 August 2017

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15 August 2017

8

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15 August 2017

2

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15 August 2017

e57460

1 reference

Creative Commons Attribution 4.0 International

15 August 2017

start time

25 February 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3581587/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

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Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome

20 June 2018

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Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6

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Cardiac outflow tract: a review of some embryogenetic aspects of the conotruncal region of the heart

20 June 2018

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Mutation of the atrophin2 gene in the zebrafish disrupts signaling by fibroblast growth factor during development of the inner ear.

20 June 2018

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Genetic variables that influence phenotype

20 June 2018

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Histone deacetylase-associating Atrophin proteins are nuclear receptor corepressors

20 June 2018

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Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure

20 June 2018

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Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)

20 June 2018

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20 June 2018

The medial temporal lobe

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Atrophin 2 recruits histone deacetylase and is required for the function of multiple signaling centers during mouse embryogenesis

20 June 2018

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20 June 2018

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Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome

20 June 2018

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20 June 2018

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Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice

20 June 2018

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20 June 2018

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Embryonic retinoic acid synthesis is essential for heart morphogenesis in the mouse

20 June 2018

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20 June 2018

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Effect of the genetic background on the phenotype of mouse mutations

20 June 2018

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Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine

20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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Embryonic retinoic acid synthesis is essential for early mouse post-implantation development

20 June 2018

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Neuronal nuclear antigen (NeuN): a marker of neuronal maturation in early human fetal nervous system

20 June 2018

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Defective limbic system in mice lacking the tailless gene

20 June 2018

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Mice lacking the ski proto-oncogene have defects in neurulation, craniofacial, patterning, and skeletal muscle development

20 June 2018

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Retinoid-dependent pathways suppress myocardial cell hypertrophy.

20 June 2018

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Why there are complementary learning systems in the hippocampus and neocortex: insights from the successes and failures of connectionist models of learning and memory

20 June 2018

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Function of the retinoic acid receptors (RARs) during development: (II) Multiple abnormalities at various stages of organogenesis in RAR double mutants

20 June 2018

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CNS stem cells express a new class of intermediate filament protein

20 June 2018

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Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.

20 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0057460

Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation

21 January 2018

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Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions

21 January 2018

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Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletions.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0057460

Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome.

21 January 2018

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Neural tube defects and impaired neural progenitor cell proliferation in Gbeta1-deficient mice

21 January 2018

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Novel lethal mouse mutants produced in balancer chromosome screens.

21 January 2018

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Mouse mutagenesis with the chemical supermutagen ENU.

21 January 2018

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The use of behavioral test batteries: effects of training history.

21 January 2018

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REREa/Atrophin-2 interacts with histone deacetylase and Fgf8 signaling to regulate multiple processes of zebrafish development

21 January 2018

1 reference

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Genetic analysis of RXR alpha developmental function: convergence of RXR and RAR signaling pathways in heart and eye morphogenesis.

21 January 2018

1 reference

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All-trans retinoic acid prevents development of cardiac remodeling in aortic banded rats by inhibiting the renin-angiotensin system

21 January 2018

1 reference

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Jaw and branchial arch mutants in zebrafish I: branchial arches.

21 January 2018

1 reference

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Distribution of calretinin immunoreactivity in the mouse dentate gyrus. I. General description.

26 November 2018

1 reference

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Contiguous ∼16 Mb 1p36 deletion: Dominant features of classical distal 1p36 monosomy with haplo-lethality

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23451234

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A new case of proximal monosomy 1p36, extending the phenotype

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23451234

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0057460

1 reference

15 August 2017

0 references

1 reference

15 August 2017

1 reference