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Aberrant serine protease activities in atopic dermatitis

Journal of dermatological science, 2022-07, Vol.107 (1), p.2-7

2022

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Uncovering Direct Targets of MiR-19a Involved in Lung Cancer Progression

PloS one, 2015-09, Vol.10 (9), p.e0137887-e0137887

2015

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Thioredoxin deficiency increases oxidative stress and causes bilateral symmetrical degeneration in rat midbrain

Neurobiology of disease, 2022-12, Vol.175, p.105921-105921, Article 105921

2022

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VLX1570 induces apoptosis through the generation of ROS and induction of ER stress on leukemia cell lines

Cancer science, 2021-08, Vol.112 (8), p.3302-3313

2021

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“Input/output cytokines” in epidermal keratinocytes and the involvement in inflammatory skin diseases

Frontiers in immunology, 2023-10, Vol.14, p.1239598-1239598

2023

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Multifaceted Analysis of IL-23A- and/or EBI3-Including Cytokines Produced by Psoriatic Keratinocytes

International journal of molecular sciences, 2021-11, Vol.22 (23), p.12659

2021

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Novel direct targets of miR-19a identified in breast cancer cells by a quantitative proteomic approach

PloS one, 2012-08, Vol.7 (8), p.e44095

2012

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REPAIR FROM NEURONAL DEATH OCCURS SPONTANEOUSLY WITHIN 4 WEEKS IN TXN1 MUTANT RATS

IBRO neuroscience reports, 2023-10, Vol.15, p.S191-S191

2023

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CACNA1A variants may modify the epileptic phenotype of Dravet syndrome

Neurobiology of disease, 2013-02, Vol.50, p.209-217

2013

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Detection of EGFR Gene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay

Clinical cancer research, 2006-01, Vol.12 (1), p.43-48

2006

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A Screening test for the prediction of Dravet syndrome before one year of age

Epilepsia (Copenhagen), 2008-04, Vol.49 (4), p.626-633

2008

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Five-aza-2'-deoxycytidine-induced hypomethylation of cholesterol 25-hydroxylase gene is responsible for cell death of myelodysplasia/leukemia cells

Scientific reports, 2015-11, Vol.5 (1), p.16709, Article 16709

2015

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Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy

Biochemical and biophysical research communications, 2002-07, Vol.295 (1), p.17-23

2002

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Analysis of All 34 Exons of the SPINK5 Gene in Japanese Atopic Dermatitis Patients

Acta medica Okayama, 2018-06, Vol.72 (3), p.275-282

2018

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A missense mutation of the gene encoding voltage-dependent sodium channel (Nav1.1) confers susceptibility to febrile seizures in rats

The Journal of neuroscience, 2010-04, Vol.30 (16), p.5744-5753

2010

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Identification of direct targets for the miR-17-92 cluster by proteomic analysis

Proteomics (Weinheim), 2011-09, Vol.11 (17), p.3531-3539

2011

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A case of Dravet syndrome with cortical myoclonus indicated by jerk-locked back-averaging of electroencephalogram data

Brain & development (Tokyo. 1979), 2017-01, Vol.39 (1), p.75-79

2017

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Methylphenidate improves learning impairments and hyperthermia‐induced seizures caused by an Scn1a mutation

Epilepsia (Copenhagen), 2014-10, Vol.55 (10), p.1558-1567

2014

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Human RAD 17 Polymorphism at Codon 546 Is Associated with the Risk of Colorectal Cancer

Acta medica Okayama, 2017-02, Vol.71 (1), p.59-68

2017

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Allelic loss and reduced expression of the ING3, a candidate tumor suppressor gene at 7q31, in human head and neck cancers

Oncogene, 2002-06, Vol.21 (28), p.4462-4470

2002

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Truncated SSX protein suppresses synovial sarcoma cell proliferation by inhibiting the localization of SS18-SSX fusion protein

PloS one, 2013-10, Vol.8 (10), p.e77564-e77564

2013

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Therapy for hyperthermia‐induced seizures in Scn1a mutant rats

Epilepsia (Copenhagen), 2011-05, Vol.52 (5), p.1010-1017

2011

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Frequent deletion and down-regulation of ING4, a candidate tumor suppressor gene at 12p13, in head and neck squamous cell carcinomas

Gene, 2005-08, Vol.356, p.109-117

2005

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Loss or down‐regulation of HLA class I expression at the allelic level in freshly isolated leukemic blasts

Cancer science, 2007-01, Vol.98 (1), p.102-108

2007

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Missense polymorphisms of PTPRJ and PTPN13 genes affect susceptibility to a variety of human cancers

Journal of cancer research and clinical oncology, 2010-02, Vol.136 (2), p.249-259

2010

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Aberrant serine protease activities in atopic dermatitis

Uncovering Direct Targets of MiR-19a Involved in Lung Cancer Progression

Thioredoxin deficiency increases oxidative stress and causes bilateral symmetrical degeneration in rat midbrain

VLX1570 induces apoptosis through the generation of ROS and induction of ER stress on leukemia cell lines

“Input/output cytokines” in epidermal keratinocytes and the involvement in inflammatory skin diseases

Multifaceted Analysis of IL-23A- and/or EBI3-Including Cytokines Produced by Psoriatic Keratinocytes

Novel direct targets of miR-19a identified in breast cancer cells by a quantitative proteomic approach

REPAIR FROM NEURONAL DEATH OCCURS SPONTANEOUSLY WITHIN 4 WEEKS IN TXN1 MUTANT RATS

CACNA1A variants may modify the epileptic phenotype of Dravet syndrome

Detection of EGFR Gene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay

A Screening test for the prediction of Dravet syndrome before one year of age

Five-aza-2'-deoxycytidine-induced hypomethylation of cholesterol 25-hydroxylase gene is responsible for cell death of myelodysplasia/leukemia cells

Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy

Analysis of All 34 Exons of the SPINK5 Gene in Japanese Atopic Dermatitis Patients

A missense mutation of the gene encoding voltage-dependent sodium channel (Nav1.1) confers susceptibility to febrile seizures in rats

Identification of direct targets for the miR-17-92 cluster by proteomic analysis

A case of Dravet syndrome with cortical myoclonus indicated by jerk-locked back-averaging of electroencephalogram data

Methylphenidate improves learning impairments and hyperthermia‐induced seizures caused by an Scn1a mutation

Human RAD 17 Polymorphism at Codon 546 Is Associated with the Risk of Colorectal Cancer

Allelic loss and reduced expression of the ING3, a candidate tumor suppressor gene at 7q31, in human head and neck cancers

Truncated SSX protein suppresses synovial sarcoma cell proliferation by inhibiting the localization of SS18-SSX fusion protein

Therapy for hyperthermia‐induced seizures in Scn1a mutant rats

Frequent deletion and down-regulation of ING4, a candidate tumor suppressor gene at 12p13, in head and neck squamous cell carcinomas

Loss or down‐regulation of HLA class I expression at the allelic level in freshly isolated leukemic blasts

Missense polymorphisms of PTPRJ and PTPN13 genes affect susceptibility to a variety of human cancers

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