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Image Fusion Processing for IKONOS 1-m Color Imagery

IEEE transactions on geoscience and remote sensing, 2007-10, Vol.45 (10), p.3075-3086

2007

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The complete type of pachydermoperiostosis: A novel nonsense mutation p.E141 of the SLCO2A1 gene

Journal of dermatological science, 2014-09, Vol.75 (3), p.193-195

2014

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Characterization of the human ABCG1 gene: liver X receptor activates an internal promoter that produces a novel transcript encoding an alternative form of the protein

The Journal of biological chemistry, 2001-10, Vol.276 (42), p.39438-39447

2001

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Cholesterol 25-hydroxylase is a metabolic switch to constrain T cell-mediated inflammation in the skin

Science immunology, 2021-10, Vol.6 (64), p.eabb6444

2021

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The novel SLCO2A1 heterozygous missense mutation p.E427K and nonsense mutation p.R603 in a female patient with pachydermoperiostosis with an atypical phenotype

British journal of dermatology (1951), 2014-05, Vol.170 (5), p.1187-1189

2014

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The DNA sequence of human chromosome 21

Nature (London), 2000-05, Vol.405 (6784), p.311-319

2000

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Simulation model of an eyeball based on finite element analysis on a supercomputer

British journal of ophthalmology, 1999-10, Vol.83 (10), p.1106-1111

1999

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A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients

Human genetics, 1998-10, Vol.103 (4), p.428-434

1998

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Recurrent herpes simplex virus infection in a patient with autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy associated with L29P and IVS9‐1G>C compound heterozygous autoimmune regulator gene mutations

Journal of internal medicine, 2007-06, Vol.261 (6), p.605-610

2007

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LTRPC2 Ca2+-permeable channel activated by changes in redox status confers susceptibility to cell death

Molecular cell, 2002-01, Vol.9 (1), p.163-173

2002

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Detailed mapping of the ERG– ETS2 interval of human chromosome 21 and comparison with the region of conserved synteny on mouse chromosome 16

Gene, 2004-01, Vol.324, p.65-77

2004

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A-HIGHERS-The system to produce the High spatial Resolution sea surface temperature maps of the Western North Pacific using the AVHRR/NOAA

Journal of oceanography, 2000-12, Vol.56 (6), p.707-716

2000

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Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

Journal of medical genetics, 2001-06, Vol.38 (6), p.396-400

2001

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Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I

Neurology, 2003-04, Vol.60 (8), p.1341-1344

2003

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Theoretical study of polarons and self-trapped excited states in one-dimensional C60 crystal

Computational materials science, 2006-05, Vol.36 (1-2), p.17-25

2006

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Cloud detection for the Far East region using NOAA AVHRR images

International journal of remote sensing, 2001-05, Vol.22 (7), p.1349-1360

2001

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Safety and efficacy of silodosin for the treatment of benign prostatic hyperplasia

Clinical interventions in aging, 2011-01, Vol.6, p.161-172

2011

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Theoretical study of polarons and self-trapped excited states in one-dimensional C 60 crystal

Computational materials science, 2006-05, Vol.36 (1), p.17-25

2006

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Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains

Human genetics, 2001-03, Vol.108 (2), p.140-147

2001

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Thermodynamic properties of hydrate phases immersed in ice phase

Journal of physics. Conference series, 2006-01, Vol.29 (1), p.198-205

2006

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Cloning of two human homologs of the Drosophila single-minded gene SIM1 on chromosome 6q and SIM2 on 21q within the Down syndrome chromosomal region

Genome research, 1997-06, Vol.7 (6), p.615-624

1997

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Severe form of juvenile corneal stromal dystrophy with homozygous R124H mutation in the keratoepithelin gene in five Japanese patients

British journal of ophthalmology, 1998-11, Vol.82 (11), p.1280-1284

1998

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Structure of human holocarboxylase synthetase gene and mutation spectrum of holocarboxylase synthetase deficiency

Human genetics, 2001-11, Vol.109 (5), p.526-534

2001

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A study of a three-dimensional histogram using the NOAA AVHRR images

IEEE transactions on geoscience and remote sensing, 1991-09, Vol.29 (5), p.736-741

1991

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Homogeneity of Kerato-Epithelin Codon 124 Mutations in Japanese Patients with Either of Two Types of Corneal Stromal Dystrophy

American journal of human genetics, 1997-12, Vol.61 (6), p.1448-1450

1997

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Image Fusion Processing for IKONOS 1-m Color Imagery

The complete type of pachydermoperiostosis: A novel nonsense mutation p.E141 of the SLCO2A1 gene

Characterization of the human ABCG1 gene: liver X receptor activates an internal promoter that produces a novel transcript encoding an alternative form of the protein

Cholesterol 25-hydroxylase is a metabolic switch to constrain T cell-mediated inflammation in the skin

The novel SLCO2A1 heterozygous missense mutation p.E427K and nonsense mutation p.R603 in a female patient with pachydermoperiostosis with an atypical phenotype

The DNA sequence of human chromosome 21

Simulation model of an eyeball based on finite element analysis on a supercomputer

A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients

Recurrent herpes simplex virus infection in a patient with autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy associated with L29P and IVS9‐1G>C compound heterozygous autoimmune regulator gene mutations

LTRPC2 Ca2+-permeable channel activated by changes in redox status confers susceptibility to cell death

Detailed mapping of the ERG– ETS2 interval of human chromosome 21 and comparison with the region of conserved synteny on mouse chromosome 16

A-HIGHERS-The system to produce the High spatial Resolution sea surface temperature maps of the Western North Pacific using the AVHRR/NOAA

Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I

Theoretical study of polarons and self-trapped excited states in one-dimensional C60 crystal

Cloud detection for the Far East region using NOAA AVHRR images

Safety and efficacy of silodosin for the treatment of benign prostatic hyperplasia

Theoretical study of polarons and self-trapped excited states in one-dimensional C 60 crystal

Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains

Thermodynamic properties of hydrate phases immersed in ice phase

Cloning of two human homologs of the Drosophila single-minded gene SIM1 on chromosome 6q and SIM2 on 21q within the Down syndrome chromosomal region

Severe form of juvenile corneal stromal dystrophy with homozygous R124H mutation in the keratoepithelin gene in five Japanese patients

Structure of human holocarboxylase synthetase gene and mutation spectrum of holocarboxylase synthetase deficiency

A study of a three-dimensional histogram using the NOAA AVHRR images

Homogeneity of Kerato-Epithelin Codon 124 Mutations in Japanese Patients with Either of Two Types of Corneal Stromal Dystrophy

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