(Q43937639)

28 November 2017

title

ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis (English)

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28 November 2017

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8

Karen P Steel

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28 November 2017

Amy E Kiernan

1

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28 November 2017

Alexandra Erven

2

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28 November 2017

Stéphanie Voegeling

3

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28 November 2017

Jo Peters

4

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28 November 2017

Pat Nolan

5

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28 November 2017

Jackie Hunter

6

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28 November 2017

Yvonne Bacon

7

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28 November 2017

Steve D M Brown

9

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28 November 2017

Jean-Louis Guénet

10

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28 November 2017

publication date

1 March 2002

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28 November 2017

number of pages

7

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inferred from page(s)

published in

Mammalian Genome

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28 November 2017

volume

13

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28 November 2017

issue

3

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28 November 2017

page(s)

142-148

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A genetic screen for mutations that disrupt an auditory response in Drosophila melanogaster

28 November 2017

cites work

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12 December 2020

Congenital malformations of the inner ear: a classification based on embryogenesis

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12 December 2020

Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development

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12 December 2020

Targeted mutagenesis of the POU-domain gene Brn4/Pou3f4 causes developmental defects in the inner ear.

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12 December 2020

Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5.

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12 December 2020

Pax2 contributes to inner ear patterning and optic nerve trajectory

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12 December 2020

Nkx5-1 controls semicircular canal formation in the mouse inner ear.

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12 December 2020

Heterozygosity mapping of partially congenic lines: mapping of a semidominant neurological mutation, Wheels (Whl), on mouse chromosome 4

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12 December 2020

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

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12 December 2020

Otx1 and Otx2 activities are required for the normal development of the mouse inner ear

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12 December 2020

The Notch ligand Jagged1 is required for inner ear sensory development.

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12 December 2020

Defective myosin VIIA gene responsible for Usher syndrome type 1B

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12 December 2020

Epilepsy and brain abnormalities in mice lacking the Otx1 gene

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12 December 2020

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans

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12 December 2020

The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti

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12 December 2020

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

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12 December 2020

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

1 reference

12 December 2020

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy

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12 December 2020

Comparison of ephrin-A ligand and EphA receptor distribution in the developing inner ear

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12 December 2020

Achondroplasia is defined by recurrent G380R mutations of FGFR3

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12 December 2020

Distribution of the receptor EphA7 and its ligands in development of the mouse nervous system.

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12 December 2020

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

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12 December 2020

Inner ear and maternal reproductive defects in mice lacking the Hmx3 homeobox gene

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12 December 2020

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

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12 December 2020

Congenital anomalies of the inner ear.

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12 December 2020

Epithelial autonomy in the development of the inner ear of a bird embryo.

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12 December 2020

Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1.

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12 December 2020

Descriptive and experimental analysis of the epithelial remodellings that control semicircular canal formation in the developing mouse inner ear

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12 December 2020

The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects.

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12 December 2020

Mutagenesis and behavioral screening for altered circadian activity identifies the mouse mutant, Wheels

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12 December 2020

Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice

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12 December 2020

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

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12 December 2020

Analysis of a mouse alpha-globin gene mutation induced by ethylnitrosourea

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12 December 2020

A type VII myosin encoded by the mouse deafness gene shaker-1

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12 December 2020

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

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12 December 2020

Embryo brain kinase: a novel gene of the eph/elk receptor tyrosine kinase family

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12 December 2020

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

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12 December 2020

Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.

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12 December 2020

Prx1 and Prx2 in skeletogenesis: roles in the craniofacial region, inner ear and limbs

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12 December 2020

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

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12 December 2020

Inductive tissue interactions during inner ear development

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12 December 2020

Netrin 1 is required for semicircular canal formation in the mouse inner ear

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12 December 2020

Standard atlas of the gross anatomy of the developing inner ear of the chicken.

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12 December 2020

The embryonic and postnatal development of the inner ear of the mouse

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12 December 2020

Dlx5 regulates regional development of the branchial arches and sensory capsules

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12 December 2020

A technique for preparation of cochlear specimens for assessment with the scanning electron microscope

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12 December 2020

Congenital lesions of the inner ear, demonstrated by tomography

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12 December 2020

DNA sequence analysis of spontaneous and N-ethyl-N-nitrosourea-induced hprt mutations arising in vivo in cynomolgus monkey T-lymphocytes

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12 December 2020

Requirement for Brn-3c in maturation and survival, but not in fate determination of inner ear hair cells

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12 December 2020

Genetic analysis of vertebrate sensory hair cell mechanosensation: the zebrafish circler mutants

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12 December 2020

Identifiers

DOI

10.1007/BF02684018

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Dimensions Publication ID

28 November 2017

1013535577

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