(Q31039073)

28 June 2017

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

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28 June 2017

Roger D Cox

8

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author name string

Emma L Coghill

1

1 reference

28 June 2017

Alison Hugill

2

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28 June 2017

Nick Parkinson

3

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28 June 2017

Claire Davison

4

1 reference

28 June 2017

Peter Glenister

5

1 reference

28 June 2017

Sian Clements

6

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28 June 2017

Jackie Hunter

7

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28 June 2017

Steve D M Brown

9

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28 June 2017

language of work or name

English

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publication date

19 February 2002

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28 June 2017

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28 June 2017

30

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28 June 2017

255-256

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28 June 2017

3

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Sequence interpretation. Functional annotation of mouse genome sequences

28 June 2017

1 reference

7 January 2021

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

1 reference

7 January 2021

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

1 reference

7 January 2021

Genotype-based screen for ENU-induced mutations in mouse embryonic stem cells

1 reference

7 January 2021

Mouse mutants from chemically mutagenized embryonic stem cells

1 reference

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

7 January 2021

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

1 reference

7 January 2021

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

1 reference

7 January 2021

Connexin-26 mutations in sporadic and inherited sensorineural deafness

1 reference

7 January 2021

Connexin 26 gene linked to a dominant deafness.

1 reference

7 January 2021

Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice

1 reference

7 January 2021

Large numbers of mice established by in vitro fertilization with cryopreserved spermatozoa: implications and applications for genetic resource banks, mutagenesis screens, and mouse backcrosses

1 reference

7 January 2021

Sequence-based analysis of mutagenized mice

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7 January 2021

Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG847

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Dimensions Publication ID

28 June 2017

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1 reference