(Q27325479)

12

0 references

Gerton Lunter

16

0 references

Katherine R Bull

1

0 references

Anselm Enders

6

0 references

Paul K Potter

10

0 references

Owen M Siggs

object named as

Owen M Siggs

3

0 references

author name string

Andrew J Rimmer

2

0 references

Lisa A Miosge

4

0 references

Carla M Roots

5

0 references

Edward M Bertram

7

0 references

Tanya L Crockford

8

0 references

Belinda Whittle

9

0 references

Michelle M Simon

11

0 references

Steve D M Brown

13

0 references

Christopher C Goodnow

15

0 references

Richard J Cornall

Creative Commons Attribution 4.0 International

17

0 references

language of work or name

English

0 references

publication date

2013

0 references

published in

PLOS Genetics

0 references

volume

9

0 references

page(s)

e1003219

0 references

issue

1

0 references

copyright license

start time

31 January 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Initial sequencing and comparative analysis of the mouse genome

21 March 2017

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A method and server for predicting damaging missense mutations

21 March 2017

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The Sequence Alignment/Map format and SAMtools

21 March 2017

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Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

21 March 2017

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Cutting edge: Toll-like receptor 4 (TLR4)-deficient mice are hyporesponsive to lipopolysaccharide: evidence for TLR4 as the Lps gene product

21 March 2017

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Stampy: a statistical algorithm for sensitive and fast mapping of Illumina sequence reads

21 March 2017

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Specific-locus test shows ethylnitrosourea to be the most potent mutagen in the mouse

21 March 2017

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ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

21 March 2017

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BEDTools: a flexible suite of utilities for comparing genomic features

7 April 2017

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Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1.

7 April 2017

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Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models.

28 September 2017

1 reference

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Fine-scale maps of recombination rates and hotspots in the mouse genome

28 September 2017

1 reference

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Mutation mapping and identification by whole-genome sequencing

28 September 2017

1 reference

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Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism

28 September 2017

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Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse.

28 September 2017

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Imputation of single-nucleotide polymorphisms in inbred mice using local phylogeny.

28 September 2017

1 reference

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Mutation discovery in mice by whole exome sequencing

28 September 2017

1 reference

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Integration of SNP genotyping confidence scores in IBD inference

28 September 2017

1 reference

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An ENU-mutagenesis screen in the mouse: identification of novel developmental gene functions.

28 September 2017

1 reference

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Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders

28 September 2017

1 reference

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Rapid identification of a disease allele in mouse through whole genome sequencing and bulk segregation analysis

28 September 2017

1 reference

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A new standard genetic map for the laboratory mouse

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

ENU mutagenesis, a way forward to understand gene function

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

A series of ENU-induced single-base substitutions in a long-range cis-element altering Sonic hedgehog expression in the developing mouse limb bud.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

Molecular characterization of ENU mouse mutagenesis and archives

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

Connecting mammalian genome with phenome by ENU mouse mutagenesis: gene combinations specifying the immune system.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

Unraveling innate immunity using large scale N-ethyl-N-nitrosourea mutagenesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

Mutation rate and predicted phenotypic target sizes in ethylnitrosourea-treated mice

28 September 2017

1 reference

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A gene-driven ENU-based approach to generating an allelic series in any gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

ENU mutagenesis in the mouse: application to human genetic disease

28 September 2017

1 reference

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A gene-driven approach to the identification of ENU mutants in the mouse

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

Genome-wide ENU mutagenesis to reveal immune regulators

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

Sequence-based analysis of mutagenized mice

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

28 September 2017

Mouse ENU mutagenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

Construction of multilocus genetic linkage maps in humans

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

Use of shuttle vectors to study the molecular processing of defined carcinogen-induced DNA damage: mutagenicity of single O4-ethylthymine adducts in HeLa cells

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

In vitroDNA replication implicates O2-ethyldeoxythymidine in transversion mutagenesis by ethylating agents

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

Reducing the exome search space for mendelian diseases using genetic linkage analysis of exome genotypes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

Mutational pattern and frequency of induced nucleotide changes in mouse ENU mutagenesis

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3561070

A kinase-dead allele of Lyn attenuates autoimmune disease normally associated with Lyn deficiency

2 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003219

Spectrum of ENU-induced mutations in phenotype-driven and gene-driven screens in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003219

A tutorial on hidden Markov models and selected applications in speech recognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003219

Effects of ENU dosage on mouse strains

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003219

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003219

ENU mutagenesis in the mouse electrophoretic specific-locus test, 1. Dose-response relationship of electrophoretically-detected mutations arising from mouse spermatogonia treated with ethylnitrosourea

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23382690

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A dose-response analysis of ethylnitrosourea-induced recessive specific-locus mutations in treated spermatogonia of the mouse

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23382690

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1003219

1 reference

4030728

4030728

1 reference

1 reference

1 reference