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Lipopolysaccharide induces adipose differentiation-related protein expression and lipid accumulation in the liver through inhibition of fatty acid oxidation in mice

Journal of gastroenterology, 2007-12, Vol.42 (12), p.969-978

2007

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Identification and Characterization of a Novel Human Collectin CL-K1

Microbiology and immunology, 2006-01, Vol.50 (12), p.1001-1013

2006

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Scavenger Receptor Collectin Placenta 1 (CL-P1) Predominantly Mediates Zymosan Phagocytosis by Human Vascular Endothelial Cells

The Journal of biological chemistry, 2009-02, Vol.284 (6), p.3956-3965

2009

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Molecular cloning and functional analysis of scavenger receptor zebrafish CL-P1

Biochimica et biophysica acta, 2011-12, Vol.1810 (12), p.1150-1159

2011

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The induction of human CL-P1 expression in hypoxia/reoxygenation culture condition and rat CL-P1 after ischemic/reperfusion treatment

Biochimica et biophysica acta, 2011-09, Vol.1810 (9), p.836-842

2011

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Involvement of MEK–ERK signaling pathway in the inhibition of cell growth by troglitazone in human pancreatic cancer cells

Biochemical and biophysical research communications, 2005-06, Vol.332 (1), p.89-94

2005

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Octreotide-Treated Diabetes Accompanied by Endogenous Hyperinsulinemic Hypoglycemia and Protein-Losing Gastroenteropathy

Case Reports in Medicine, 2011-01, Vol.2011 (2011), p.336-343-084

2011

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Timing Verification System for Relay Circuit Behaviors

Journal of nuclear science and technology, 1996-06, Vol.33 (6), p.455-463

1996

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A system for the calculation and visualisation of radiation field for maintenance support in nuclear power plants

Radiation protection dosimetry, 2005-12, Vol.116 (1-4), p.592-596

2005

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Loss probability characteristics of two-dimensional traffic

Electronics & communications in Japan. Part 1, Communications, 1990-02, Vol.73 (2), p.64-74

1990

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Logic Verification System for Power Plant Sequence Diagrams

Journal of nuclear science and technology, 1994-02, Vol.31 (2), p.102-112

1994

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Plant Operator Performance Evaluation System

Journal of nuclear science and technology, 1989-06, Vol.26 (6), p.591-606

1989

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Development of a Connectivity Verification System for Sequence Diagrams of Power Plants

Nuclear technology, 1993-04, Vol.102 (1), p.90-99

1993

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Octreotide-treated diabetes accompanied by endogenous hyperinsulinemic hypoglycemia and protein-losing gastroenteropathy

Case reports in medicine, 2011, Vol.2011, p.381203-381203

2011

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Leukocoria in a child due to endophthalmitis caused by an intraocular eyelash

American journal of ophthalmology, 2022-05, Vol.237, p.e6-e6

2022

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Identification of de novo CSNK2A1 and CSNK2B variants in cases of global developmental delay with seizures

Journal of human genetics, 2019-04, Vol.64 (4), p.313-322

2019

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ATP6V0A1 encoding the a1-subunit of the V0 domain of vacuolar H+-ATPases is essential for brain development in humans and mice

Nature communications, 2021-04, Vol.12 (1), p.2107-2107, Article 2107

2021

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Utilization and Issues Related to Discharge Medication Summaries from Hospital Pharmacies to Community Pharmacies

YAKUGAKU ZASSHI, 2024/07/01, Vol.144(7), pp.741-748

2024

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Global developmental delay, systemic dysmorphism and epilepsy in a patient with a de novo U2AF2 variant

Journal of human genetics, 2021-12, Vol.66 (12), p.1185-1187

2021

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Retrotransposition disrupting EBP in a girl and her mother with X-linked dominant chondrodysplasia punctata

Journal of human genetics, 2022-05, Vol.67 (5), p.303-306

2022

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Atypical conjunctival hyaline deposition in a case of granular corneal dystrophy type 2

American journal of ophthalmology, 2022-08, Vol.240, p.e1-e2

2022

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Impaired neuronal KCC2 function by biallelic SLC12A5 mutations in migrating focal seizures and severe developmental delay

Scientific reports, 2016-07, Vol.6 (1), p.30072-30072, Article 30072

2016

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De novo KCNB1 mutations in infantile epilepsy inhibit repetitive neuronal firing

Scientific reports, 2015-10, Vol.5 (1), p.15199-15199, Article 15199

2015

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A novel de novo KCNB1 variant altering channel characteristics in a patient with periventricular heterotopia, abnormal corpus callosum, and mild seizure outcome

Journal of human genetics, 2023-01, Vol.68 (1), p.25-31

2023

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A novel partner of TFE3 in the Xp11 translocation renal cell carcinoma: clinicopathological analyses and detection of EWSR1-TFE3 fusion

Virchows Archiv : an international journal of pathology, 2019-03, Vol.474 (3), p.389-393

2019

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Lipopolysaccharide induces adipose differentiation-related protein expression and lipid accumulation in the liver through inhibition of fatty acid oxidation in mice

Identification and Characterization of a Novel Human Collectin CL-K1

Scavenger Receptor Collectin Placenta 1 (CL-P1) Predominantly Mediates Zymosan Phagocytosis by Human Vascular Endothelial Cells

Molecular cloning and functional analysis of scavenger receptor zebrafish CL-P1

The induction of human CL-P1 expression in hypoxia/reoxygenation culture condition and rat CL-P1 after ischemic/reperfusion treatment

Involvement of MEK–ERK signaling pathway in the inhibition of cell growth by troglitazone in human pancreatic cancer cells

Octreotide-Treated Diabetes Accompanied by Endogenous Hyperinsulinemic Hypoglycemia and Protein-Losing Gastroenteropathy

Timing Verification System for Relay Circuit Behaviors

A system for the calculation and visualisation of radiation field for maintenance support in nuclear power plants

Loss probability characteristics of two-dimensional traffic

Logic Verification System for Power Plant Sequence Diagrams

Plant Operator Performance Evaluation System

Development of a Connectivity Verification System for Sequence Diagrams of Power Plants

Octreotide-treated diabetes accompanied by endogenous hyperinsulinemic hypoglycemia and protein-losing gastroenteropathy

Leukocoria in a child due to endophthalmitis caused by an intraocular eyelash

Identification of de novo CSNK2A1 and CSNK2B variants in cases of global developmental delay with seizures

ATP6V0A1 encoding the a1-subunit of the V0 domain of vacuolar H+-ATPases is essential for brain development in humans and mice

Utilization and Issues Related to Discharge Medication Summaries from Hospital Pharmacies to Community Pharmacies

Global developmental delay, systemic dysmorphism and epilepsy in a patient with a de novo U2AF2 variant

Retrotransposition disrupting EBP in a girl and her mother with X-linked dominant chondrodysplasia punctata

Atypical conjunctival hyaline deposition in a case of granular corneal dystrophy type 2

Impaired neuronal KCC2 function by biallelic SLC12A5 mutations in migrating focal seizures and severe developmental delay

De novo KCNB1 mutations in infantile epilepsy inhibit repetitive neuronal firing

A novel de novo KCNB1 variant altering channel characteristics in a patient with periventricular heterotopia, abnormal corpus callosum, and mild seizure outcome

A novel partner of TFE3 in the Xp11 translocation renal cell carcinoma: clinicopathological analyses and detection of EWSR1-TFE3 fusion

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