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A critical review of measures of childhood vaccine confidence

Current opinion in immunology, 2021-08, Vol.71, p.34-45

2021

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Pitpnm1 is expressed in hair cells during development but is not required for hearing

Neuroscience, 2013-09, Vol.248, p.620-625

2013

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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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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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PL.06.01 Deafness: on the road from genes to therapy

European neuropsychopharmacology, 2013-10, Vol.23, p.S109-S109

2013

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Presence of interstereocilial links in waltzer mutants suggests Cdh23 is not essential for tip Link formation

Neuroscience, 2009-01, Vol.158 (2), p.365-368

2009

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Mutation of the Na-K-Cl Co-Transporter Gene Slc12a2 Results in Deafness in Mice

Human molecular genetics, 1999-08, Vol.8 (8), p.1579-1584

1999

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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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Older adults’ views on sports and physical activity complexity: The match and mismatch to the professional's taxonomy

Journal of science and medicine in sport, 2014-12, Vol.18, p.e70-e71

2014

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Experimental Demonstration of Reservoir Computing with Self‐Assembled Percolating Networks of Nanoparticles

Advanced materials (Weinheim), 2024-07, Vol.36 (29), p.e2402319-n/a

2024

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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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THU0456 Psoriatic Arthritis Locus Correlates with Cell-Specific Gene Expression

Annals of the rheumatic diseases, 2014-06, Vol.73 (Suppl 2), p.341-341

2014

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A genetic approach to understanding auditory function

Nature genetics, 2001-02, Vol.27 (2), p.143-149

2001

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Mutations in Cdh23 , encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

Nature genetics, 2001-01, Vol.27 (1), p.103-107

2001

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Computation via Neuron-like Spiking in Percolating Networks of Nanoparticles

Nano letters, 2023-11, Vol.23 (22), p.10594-10599

2023

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Myosin VIIA Is Required for Aminoglycoside Accumulation in Cochlear Hair Cells

The Journal of neuroscience, 1997-12, Vol.17 (24), p.9506-9519

1997

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Combustion behaviour of ultra clean coal obtained by chemical demineralisation

Fuel (Guildford), 2003-10, Vol.82 (15), p.2145-2151

2003

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The Stability of Thioglycollate Solutions: Part II. Miscellaneous Factors Associated with the Oxidation and Stability

Journal of pharmacy and pharmacology, 2011-04, Vol.11 (1), p.434-441

2011

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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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OP0050 Fine Mapping and Expression of a Locus Overlapping 3 Types of Inflammatory Arthritis

Annals of the rheumatic diseases, 2013-06, Vol.72 (Suppl 3), p.A66-A67

2013

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Coal structure and reactivity changes induced by chemical demineralisation

Fuel processing technology, 2002-12, Vol.79 (3), p.273-279

2002

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Nursing Homes in 10 Nations: A Comparison Between Countries and Settings

Age and ageing, 1997-09, Vol.26 (suppl-2), p.3-12

1997

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Electroretinographic Anomalies in Mice with Mutations in Myo7a, the Gene Involved in Human Usher Syndrome Type 1B

Investigative ophthalmology & visual science, 2001-03, Vol.42 (3), p.770-778

2001

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Beethoven, a mouse model for dominant, progressive hearing loss DFNA36

Nature genetics, 2002-03, Vol.30 (3), p.257-258

2002

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Analysis of the frequency and spectrum of mutations recognised to cause familial hypercholesterolaemia in routine clinical practice in a UK specialist hospital lipid clinic

Atherosclerosis, 2013-07, Vol.229 (1), p.161-168

2013

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A critical review of measures of childhood vaccine confidence

Pitpnm1 is expressed in hair cells during development but is not required for hearing

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

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

PL.06.01 Deafness: on the road from genes to therapy

Presence of interstereocilial links in waltzer mutants suggests Cdh23 is not essential for tip Link formation

Mutation of the Na-K-Cl Co-Transporter Gene Slc12a2 Results in Deafness in Mice

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

Older adults’ views on sports and physical activity complexity: The match and mismatch to the professional's taxonomy

Experimental Demonstration of Reservoir Computing with Self‐Assembled Percolating Networks of Nanoparticles

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

THU0456 Psoriatic Arthritis Locus Correlates with Cell-Specific Gene Expression

A genetic approach to understanding auditory function

Mutations in Cdh23 , encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

Computation via Neuron-like Spiking in Percolating Networks of Nanoparticles

Myosin VIIA Is Required for Aminoglycoside Accumulation in Cochlear Hair Cells

Combustion behaviour of ultra clean coal obtained by chemical demineralisation

The Stability of Thioglycollate Solutions: Part II. Miscellaneous Factors Associated with the Oxidation and Stability

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

OP0050 Fine Mapping and Expression of a Locus Overlapping 3 Types of Inflammatory Arthritis

Coal structure and reactivity changes induced by chemical demineralisation

Nursing Homes in 10 Nations: A Comparison Between Countries and Settings

Electroretinographic Anomalies in Mice with Mutations in Myo7a, the Gene Involved in Human Usher Syndrome Type 1B

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36

Analysis of the frequency and spectrum of mutations recognised to cause familial hypercholesterolaemia in routine clinical practice in a UK specialist hospital lipid clinic

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