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Anonymization of Sensitive Quasi-Identifiers for l-Diversity and t-Closeness

IEEE transactions on dependable and secure computing, 2019-07, Vol.16 (4), p.580-593

2019

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Distributed Data Federation without Disclosure of User Existence

Data and Applications Security and Privacy XXVI, p.282-297

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More Accurate and Robust PRNU-Based Source Camera Identification with 3-Step 3-Class Approach

Digital Forensics and Watermarking, p.87-101

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A Fair Anonymous Auction Scheme Utilizing Trusted Hardware and Blockchain

2019 17th International Conference on Privacy, Security and Trust (PST), 2019, p.1-5

2019

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Behavioral Tendency Obfuscation Framework for Personalization Services

Database and Expert Systems Applications, p.289-303

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(l1, ..., lq)-diversity for Anonymizing Sensitive Quasi-Identifiers

2015 IEEE Trustcom/BigDataSE/ISPA, 2015, Vol.1, p.596-603

2015

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Development of knowledge-filtering agent along with user context in ubiquitous environment

Systems and computers in Japan, 2007-07, Vol.38 (8), p.11-19

2007

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Development of Knowledge-Filtering Agent Along with User Context in Ubiquitous Environment

Embedded and Ubiquitous Computing – EUC 2005 Workshops, 2005, Vol.3823, p.71-80

2005

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Hiding of User Presence for Privacy Preserving Data Mining

2012 IIAI International Conference on Advanced Applied Informatics, 2012, p.133-138

2012

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Top-down itemset recoding for releasing private complex data

2013 Eleventh Annual Conference on Privacy, Security and Trust, 2013, p.373-376

2013

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Hypoxic regulation of the cerebral microcirculation is mediated by a carbon monoxide-sensitive hydrogen sulfide pathway

Proceedings of the National Academy of Sciences - PNAS, 2012-01, Vol.109 (4), p.1293-1298

2012

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Predictive performance of the human Cell Line Activation Test (h-CLAT) for lipophilic chemicals with high octanol-water partition coefficients

The Journal of Toxicological Sciences, 2013/08/01, Vol.38(4), pp.599-609

2013

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Decisive evidence of direct effect of ACTH treatment in West syndrome: A case report

Seizure (London, England), 2021-10, Vol.91, p.49-51

2021

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Neuropsychiatric systemic lupus erythematosus in a girl with neurocutaneous melanosis caused by a somatic mutation in NRAS

Rheumatology (Oxford, England), 2022-08, Vol.61 (8), p.e224-e226

2022

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Poly(2-methoxyethyl acrylate) (PMEA) improves the thromboresistance of FRED flow diverters: a thrombogenic evaluation of flow diverters with human blood under flow conditions

Journal of neurointerventional surgery, 2023-10, Vol.15 (10), p.1001-1006

2023

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Biallelic mutations in NALCN: Expanding the genotypic and phenotypic spectra of IHPRF1

American journal of medical genetics. Part A, 2018-02, Vol.176 (2), p.431-437

2018

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Further evidence of a causal association between AGO1, a critical regulator of microRNA formation, and intellectual disability/autism spectrum disorder

European journal of medical genetics, 2019-06, Vol.62 (6), p.103537-103537, Article 103537

2019

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Severe congenital lipodystrophy and a progeroid appearance: Mutation in the penultimate exon of FBN1 causing a recognizable phenotype

American journal of medical genetics. Part A, 2013-12, Vol.161A (12), p.3057-3062

2013

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Respiratory arrest at the onset of idiopathic childhood occipital epilepsy of Gastaut

Brain & development (Tokyo. 1979), 2018-01, Vol.40 (1), p.74-76

2018

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Evaluation of combinations of in vitro sensitization test descriptors for the artificial neural network-based risk assessment model of skin sensitization

Journal of applied toxicology, 2015-11, Vol.35 (11), p.1333-1347

2015

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Noninvasive diagnosis of TRIT1‐related mitochondrial disorder by measuring i6A37 and ms2i6A37 modifications in tRNAs from blood and urine samples

American journal of medical genetics. Part A, 2019-08, Vol.179 (8), p.1609-1614

2019

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Porencephaly in a fetus and HANAC in her father: Variable expression of COL4A1 mutation

American journal of medical genetics. Part A, 2015-01, Vol.167A (1), p.156-158

2015

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Therapeutic Hypothermia Achieves Neuroprotection via a Decrease in Acetylcholine with a Concurrent Increase in Carnitine in the Neonatal Hypoxia-Ischemia

Journal of cerebral blood flow and metabolism, 2015-05, Vol.35 (5), p.794-805

2015

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Test battery with the human cell line activation test, direct peptide reactivity assay and DEREK based on a 139 chemical data set for predicting skin sensitizing potential and potency of chemicals

Journal of applied toxicology, 2015-11, Vol.35 (11), p.1318-1332

2015

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Hirschsprung disease as a yet undescribed phenotype in a patient with ARID1B mutation

American journal of medical genetics. Part A, 2016-12, Vol.170A (12), p.3249-3252

2016

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Anonymization of Sensitive Quasi-Identifiers for l-Diversity and t-Closeness

Distributed Data Federation without Disclosure of User Existence

More Accurate and Robust PRNU-Based Source Camera Identification with 3-Step 3-Class Approach

A Fair Anonymous Auction Scheme Utilizing Trusted Hardware and Blockchain

Behavioral Tendency Obfuscation Framework for Personalization Services

(l1, ..., lq)-diversity for Anonymizing Sensitive Quasi-Identifiers

Development of knowledge-filtering agent along with user context in ubiquitous environment

Development of Knowledge-Filtering Agent Along with User Context in Ubiquitous Environment

Hiding of User Presence for Privacy Preserving Data Mining

Top-down itemset recoding for releasing private complex data

Hypoxic regulation of the cerebral microcirculation is mediated by a carbon monoxide-sensitive hydrogen sulfide pathway

Predictive performance of the human Cell Line Activation Test (h-CLAT) for lipophilic chemicals with high octanol-water partition coefficients

Decisive evidence of direct effect of ACTH treatment in West syndrome: A case report

Neuropsychiatric systemic lupus erythematosus in a girl with neurocutaneous melanosis caused by a somatic mutation in NRAS

Poly(2-methoxyethyl acrylate) (PMEA) improves the thromboresistance of FRED flow diverters: a thrombogenic evaluation of flow diverters with human blood under flow conditions

Biallelic mutations in NALCN: Expanding the genotypic and phenotypic spectra of IHPRF1

Further evidence of a causal association between AGO1, a critical regulator of microRNA formation, and intellectual disability/autism spectrum disorder

Severe congenital lipodystrophy and a progeroid appearance: Mutation in the penultimate exon of FBN1 causing a recognizable phenotype

Respiratory arrest at the onset of idiopathic childhood occipital epilepsy of Gastaut

Evaluation of combinations of in vitro sensitization test descriptors for the artificial neural network-based risk assessment model of skin sensitization

Noninvasive diagnosis of TRIT1‐related mitochondrial disorder by measuring i6A37 and ms2i6A37 modifications in tRNAs from blood and urine samples

Porencephaly in a fetus and HANAC in her father: Variable expression of COL4A1 mutation

Therapeutic Hypothermia Achieves Neuroprotection via a Decrease in Acetylcholine with a Concurrent Increase in Carnitine in the Neonatal Hypoxia-Ischemia

Test battery with the human cell line activation test, direct peptide reactivity assay and DEREK based on a 139 chemical data set for predicting skin sensitizing potential and potency of chemicals

Hirschsprung disease as a yet undescribed phenotype in a patient with ARID1B mutation

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