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Focused Fluid Flow Along the Nootka Fault Zone and Continental Slope, Explorer‐Juan de Fuca Plate Boundary

Geochemistry, geophysics, geosystems : G3, 2020-08, Vol.21 (8), p.n/a

2020

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Mutational screening of VSX1 in keratoconus patients from the European population

Eye (London), 2010-06, Vol.24 (6), p.1085-1092

2010

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Phenotypic heterogeneity and mutational spectrum in a cohort of 45 Italian males subjects with X-linked ectodermal dysplasia

Clinical genetics, 2015-04, Vol.87 (4), p.338-342

2015

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A mutation in the Norrie disease gene ( ) associated with familial exudative vitreoretinopathy

Eye (London), 2011-12, Vol.25 (12), p.1658-1658

2011

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Collagen Corneal Shields

Survey of Ophthalmology, 2002-03, Vol.47 (2), p.174-182

2002

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Seafloor compliance imaging of marine gas hydrate deposits and cold vent structures

Journal of Geophysical Research - Solid Earth, 2008-07, Vol.113 (B7), p.B07107-n/a

2008

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Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43)

Eye (London), 2009-03, Vol.23 (3), p.549-555

2009

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A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract

Journal of medical genetics, 2003-11, Vol.40 (11), p.e124-124

2003

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Earthquake rate, slip rate, and the effective seismic thickness for oceanic transform faults of the Juan de Fuca plate system

Geophysical journal international, 2005-03, Vol.160 (3), p.855-868

2005

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Temporal fluctuations of microseismic noise in Yellowstone's Upper Geyser Basin from a continuous gravity observation

Geophysical research letters, 2006-06, Vol.33 (11), p.L11306-n/a

2006

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Osmotic tolerance limits and properties of murine spermatozoa

Biology of reproduction, 1996-09, Vol.55 (3), p.715-727

1996

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Epstein-Barr virus (types 1 and 2) in the tear film in Sjogren's syndrome and HIV infection

Journal of medical virology, 2002-11, Vol.68 (3), p.378-383

2002

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The ocular phenotype of stiff-skin syndrome

Eye (London), 2016-01, Vol.30 (1), p.156-159

2016

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A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family

Journal of the European Academy of Dermatology and Venereology, 2016-02, Vol.30 (2), p.341-343

2016

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Effects of Percoll separation, cryoprotective agents, and temperature on plasma membrane permeability characteristics of murine spermatozoa and their relevance to cryopreservation

Biology of reproduction, 1999-10, Vol.61 (4), p.1031-1041

1999

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Identification of a novel frameshift mutation in the EDAR gene causing autosomal dominant hypohidrotic ectodermal dysplasia

Journal of the European Academy of Dermatology and Venereology, 2015-05, Vol.29 (5), p.1032-1034

2015

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Shear velocities in Cascadia from seafloor compliance measurements

Geophysical research letters, 2000-04, Vol.27 (7), p.1021-1024

2000

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Oral manifestations in a boy with X-linked reticulate pigmentary disorder

Head & face medicine, 2012-05, Vol.8 (S1), p.P9-P9, Article P9

2012

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The preparation of laminated ceramic composites using paint technology

Journal of materials science, 1996, Vol.31 (9), p.2333-2337

1996

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Molecular diagnosis for heterogeneous genetic diseases with targeted high-throughput DNA sequencing applied to retinitis pigmentosa

Journal of medical genetics, 2011-03, Vol.48 (3), p.145-151

2011

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Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

Nature communications, 2018-05, Vol.9 (1), p.1864-11, Article 1864

2018

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Targeting the NLRP3 Inflammasome in Glaucoma

Biomolecules (Basel, Switzerland), 2021-08, Vol.11 (8), p.1239

2021

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Assessment of the value of congenital hypertrophy of the retinal pigment epithelium as an ocular marker for familial adenomatous polyposis coli

Eye (London), 1993-01, Vol.7 (4), p.562-564

1993

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The presence of congenital hypertrophy of the retinal pigment epithelium in a subgroup of patients with adenomatous polyposis coli mutations

Eye (London), 1998, Vol.12 ( Pt 3a), p.488-489

Willoughby, C E

1998

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Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome

American journal of human genetics, 2002-05, Vol.70 (5), p.1341-1348

2002

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Focused Fluid Flow Along the Nootka Fault Zone and Continental Slope, Explorer‐Juan de Fuca Plate Boundary

Mutational screening of VSX1 in keratoconus patients from the European population

Phenotypic heterogeneity and mutational spectrum in a cohort of 45 Italian males subjects with X-linked ectodermal dysplasia

A mutation in the Norrie disease gene ( ) associated with familial exudative vitreoretinopathy

Collagen Corneal Shields

Seafloor compliance imaging of marine gas hydrate deposits and cold vent structures

Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43)

A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract

Earthquake rate, slip rate, and the effective seismic thickness for oceanic transform faults of the Juan de Fuca plate system

Temporal fluctuations of microseismic noise in Yellowstone's Upper Geyser Basin from a continuous gravity observation

Osmotic tolerance limits and properties of murine spermatozoa

Epstein-Barr virus (types 1 and 2) in the tear film in Sjogren's syndrome and HIV infection

The ocular phenotype of stiff-skin syndrome

A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family

Effects of Percoll separation, cryoprotective agents, and temperature on plasma membrane permeability characteristics of murine spermatozoa and their relevance to cryopreservation

Identification of a novel frameshift mutation in the EDAR gene causing autosomal dominant hypohidrotic ectodermal dysplasia

Shear velocities in Cascadia from seafloor compliance measurements

Oral manifestations in a boy with X-linked reticulate pigmentary disorder

The preparation of laminated ceramic composites using paint technology

Molecular diagnosis for heterogeneous genetic diseases with targeted high-throughput DNA sequencing applied to retinitis pigmentosa

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

Targeting the NLRP3 Inflammasome in Glaucoma

Assessment of the value of congenital hypertrophy of the retinal pigment epithelium as an ocular marker for familial adenomatous polyposis coli

The presence of congenital hypertrophy of the retinal pigment epithelium in a subgroup of patients with adenomatous polyposis coli mutations

Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome

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