(Q35840678)

10 August 2017

Mutation discovery in mice by whole exome sequencing (English)

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10 August 2017

33

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10 August 2017

24

Kerstin Lindblad-Toh

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Snaevar Sigurdsson

object named as

Snaevar Sigurdsson

21

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Benjamin T. Kile

object named as

Benjamin T Kile

18

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Carol J Bult

16

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Carol Bult

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10 August 2017

22

Evan Mauceli

1 reference

10 August 2017

Heather Fairfield

1

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10 August 2017

Griffith J Gilbert

2

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10 August 2017

Mary Barter

3

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10 August 2017

Rebecca R Corrigan

4

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10 August 2017

Michelle Curtain

5

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10 August 2017

Yueming Ding

6

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10 August 2017

Mark D'Ascenzo

7

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10 August 2017

Daniel J Gerhardt

8

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10 August 2017

Chao He

9

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10 August 2017

Wenhui Huang

10

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10 August 2017

Todd Richmond

11

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10 August 2017

Lucy Rowe

12

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10 August 2017

Frank J Probst

13

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10 August 2017

David E Bergstrom

14

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10 August 2017

Stephen A Murray

15

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10 August 2017

Joel Richardson

17

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10 August 2017

Ivo Gut

19

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10 August 2017

Jorg Hager

20

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10 August 2017

Federica Di Palma

23

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10 August 2017

Michael L Cunningham

25

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10 August 2017

Timothy C Cox

26

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10 August 2017

Monica J Justice

27

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10 August 2017

Mona S Spector

28

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10 August 2017

Scott W Lowe

29

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10 August 2017

Thomas Albert

30

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10 August 2017

Leah Rae Donahue

31

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10 August 2017

Jeffrey Jeddeloh

32

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10 August 2017

Laura G Reinholdt

34

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10 August 2017

14 September 2011

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10 August 2017

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10 August 2017

12

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10 August 2017

9

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10 August 2017

R86

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Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

The Mouse Genome Database (MGD): premier model organism resource for mammalian genomics and genetics

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Whole exome capture in solution with 3 Gbp of data

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Exome sequencing identifies the cause of a mendelian disorder

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Mutation discovery in the mouse using genetically guided array capture and resequencing

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Next-generation DNA sequencing

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Role of MLK3 in the regulation of mitogen-activated protein kinase signaling cascades

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Functional genetic analysis of mouse chromosome 11

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Dose-repetition increases the mutagenic effectiveness of N-ethyl-N-nitrosourea in mouse spermatogonia

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3308049

Loss of procollagen IIA from the anterior mesendoderm disrupts the development of mouse embryonic forebrain.

11 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FGB-2011-12-9-R86

Novel lethal mouse mutants produced in balancer chromosome screens.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FGB-2011-12-9-R86

Engineering a mouse balancer chromosome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21917142

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/GB-2011-12-9-R86

1 reference

Dimensions Publication ID

10 August 2017

0 references

1 reference

10 August 2017

PubMed publication ID

21917142

1 reference