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Identification of novel members of the serum amyloid A protein superfamily as constitutive apolipoproteins of high density lipoprotein

The Journal of biological chemistry, 1992-02, Vol.267 (6), p.3862-3867

1992

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A Constitutively Expressed Serum Amyloid A Protein Gene ( SAA4) Is Closely Linked to, and Shares Structural Similarities with, an Acute-Phase Serum Amyloid A Protein Gene ( SAA2)

Genomics (San Diego, Calif.), 1993-05, Vol.16 (2), p.447-454

1993

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Model systems for studies of epithelial ion transport

Steel, D.M

1994

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Characterization, Expression and Evolution of Mouse β 2-Glycoprotein 1 (Apolipoprotein H)

Biochemical and biophysical research communications, 1994, Vol.200 (3), p.1521-1528

1994

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Characterization, Expression and Evolution of Mouse β2-Glycoprotein 1 (Apolipoprotein H)

Biochemical and biophysical research communications, 1994-05, Vol.200 (3), p.1521-1528

1994

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MICROSTRUCTURE AND FRACTURE OF ISOTHERMALLY QUENCHED 40CrMnSiMoV

Mechanical Behaviour of Materials V, 1988, p.341-347

1988

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comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains

Genome Biology, 2013-07, Vol.14 (7), p.R82-R82, Article R82

2013

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Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

Current biology, 2003-07, Vol.13 (13), p.1129-1133

2003

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

Nature genetics, 1997-06, Vol.16 (2), p.188-190

1997

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Prevalence of sexual dimorphism in mammalian phenotypic traits

Nature communications, 2017-06, Vol.8 (1), p.15475-15475, Article 15475

2017

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Myosin VIIa Participates in Opsin Transport through The Photoreceptor Cilium

The Journal of neuroscience, 1999-08, Vol.19 (15), p.6267-6274

1999

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Long term follow-up and risk of breast cancer after a radial scar or complex sclerosing lesion has been identified in a benign open breast biopsy

European journal of surgical oncology, 2011-08, Vol.37 (8), p.709-713

2011

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Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

Nature genetics, 1997-11, Vol.17 (3), p.268-269

1997

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

Nature genetics, 2000-08, Vol.25 (4), p.440-443

2000

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Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

Nature genetics, 2003-08, Vol.34 (4), p.421-428

2003

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Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

Human molecular genetics, 2000, Vol.9 (1), p.63-67

2000

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Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations

Nature neuroscience, 2002-01, Vol.5 (1), p.41-47

2002

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Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells

Development (Cambridge), 1998-02, Vol.125 (4), p.557-566

1998

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The first intramolecular silene Diels-Alder reactions

Chemical communications (Cambridge, England), 2014-01, Vol.50 (22), p.2919-2921

2014

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

Nature (London), 1995-03, Vol.374 (6517), p.62-64

1995

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Defective myosin VIIA gene responsible for Usher syndrome type IB

Nature (London), 1995-03, Vol.374 (6517), p.60-61

1995

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A Mutation (2314delG) in the Usher Syndrome Type IIA Gene: High Prevalence and Phenotypic Variation

American journal of human genetics, 1999-04, Vol.64 (4), p.1221-1225

1999

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Elongation of hair cell stereocilia is defective in the mouse mutant whirler

Journal of comparative neurology (1911), 2002-08, Vol.450 (1), p.94-102

2002

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

Human molecular genetics, 2001-03, Vol.10 (5), p.507-512

2001

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Efficient gene transfer to airway epithelium using recombinant Sendai virus

Nature biotechnology, 2000-09, Vol.18 (9), p.970-973

2000

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Identification of novel members of the serum amyloid A protein superfamily as constitutive apolipoproteins of high density lipoprotein

A Constitutively Expressed Serum Amyloid A Protein Gene ( SAA4) Is Closely Linked to, and Shares Structural Similarities with, an Acute-Phase Serum Amyloid A Protein Gene ( SAA2)

Model systems for studies of epithelial ion transport

Characterization, Expression and Evolution of Mouse β 2-Glycoprotein 1 (Apolipoprotein H)

Characterization, Expression and Evolution of Mouse β2-Glycoprotein 1 (Apolipoprotein H)

MICROSTRUCTURE AND FRACTURE OF ISOTHERMALLY QUENCHED 40CrMnSiMoV

comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains

Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

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

Prevalence of sexual dimorphism in mammalian phenotypic traits

Myosin VIIa Participates in Opsin Transport through The Photoreceptor Cilium

Long term follow-up and risk of breast cancer after a radial scar or complex sclerosing lesion has been identified in a benign open breast biopsy

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

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

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations

Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells

The first intramolecular silene Diels-Alder reactions

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

Defective myosin VIIA gene responsible for Usher syndrome type IB

A Mutation (2314delG) in the Usher Syndrome Type IIA Gene: High Prevalence and Phenotypic Variation

Elongation of hair cell stereocilia is defective in the mouse mutant whirler

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

Efficient gene transfer to airway epithelium using recombinant Sendai virus

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