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Revealing the thermal oxidation stability and its mechanism of rice bran oil

Scientific reports, 2020-08, Vol.10 (1), p.14091-14091, Article 14091

2020

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Linolenic Acid as the Main Source of Acrolein Formed During Heating of Vegetable Oils

Journal of the American Oil Chemists' Society, 2013-07, Vol.90 (7), p.959-964

2013

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Autoxidation of Fish Oil Blended with Rice Bran Oil

Journal of Oleo Science, 2017, Vol.66(6), pp.573-577

2017

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Combination analysis of three polymorphisms for predicting the risk for steroid-induced osteonecrosis of the femoral head

Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association, 2008-07, Vol.13 (4), p.297-303

2008

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Hereditary hypophosphatemic rickets with hypercalciuria: a study for the phosphate transporter gene type IIc and osteoblastic function

Journal of bone and mineral metabolism, 2007-11, Vol.25 (6), p.407-413

2007

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ApoB C7623T polymorphism predicts risk for steroid-induced osteonecrosis of the femoral head after renal transplantation

Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association, 2007-05, Vol.12 (3), p.199-206

2007

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Genetic analysis of steroid-induced osteonecrosis of the femoral head

Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association, 2003-05, Vol.8 (3), p.329-333

2003

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A Male Patient with Humoral Hypercalcemia of Malignancy (HHM) with Leukocytosis Caused by Cutaneous Squamous Cell Carcinoma Resulting from Recessive Dystrophic Epidermolysis Bullosa

Clinical Pediatric Endocrinology, 2011, Vol.20(3), pp.65-71

2011

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Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome

Endocrine Journal, 2006, Vol.53(3), pp.371-376

2006

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Low molecular weight phenotype of Apo(a) is a risk factor of corticosteroid-induced osteonecrosis of the femoral head after renal transplant

Journal of rheumatology, 2007-03, Vol.34 (3), p.516

2007

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Molecular Bases of Diseases Characterized by Hypophosphatemia and Phosphaturia: New Understanding

Clinical Pediatric Endocrinology, 2006, Vol.15(4), pp.129-135

2006

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Autoxidation of Fish Oil Blended with Rice Bran Oil

Journal of Oleo Science, 2017-06, Vol.66 (6), p.573-577

2017

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Lrp6 Hypomorphic Mutation Affects Bone Mass Through Bone Resorption in Mice and Impairs Interaction With Mesd

Journal of bone and mineral research, 2008-10, Vol.23 (10), p.1661-1671

2008

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Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss

Clinical Pediatric Endocrinology, 2006, Vol.15(3), pp.101-107

2006

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A Male Patient with Humoral Hypercalcemia of Malignancy (HHM) with Leukocytosis Caused by Cutaneous Squamous Cell Carcinoma Resulting from Recessive Dystrophic Epidermolysis Bullosa

Clinical Pediatric Endocrinology, 2011, Vol.20 (3), p.65-71

2011

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Effect of transmit multi-port amplifiers used in base stations for wireless cellular systems

2016 Wireless Telecommunications Symposium (WTS), 2016, p.1-3

2016

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A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency

Clinical Pediatric Endocrinology, 2006, Vol.15(1), pp.23-28

2006

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Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome

ENDOCRINE JOURNAL, 2006, Vol.53 (3), p.371-376

2006

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Long-term hospitalization during pregnancy is a risk factor for vitamin D deficiency in neonates

Journal of bone and mineral metabolism, 2003-01, Vol.21 (2), p.103-108

2003

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A Case with Marshall-Smith Syndrome without Life-threatening Complications

Clinical Pediatric Endocrinology, 2005, Vol.14(Supplement24), pp.S24_63-S24_67

2005

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Common mutations F310L and T1559del in the tissue-nonspecific alkaline phosphatase gene are related to distinct phenotypes in Japanese patients with hypophosphatasia

European journal of pediatrics, 2005-05, Vol.164 (5), p.277-282

2005

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Analysis of the stable levels of messenger RNA derived from different polymorphic alleles in the vitamin D receptor gene

Journal of bone and mineral metabolism, 1999-01, Vol.17 (3), p.164-170

1999

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Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome

Journal of human genetics, 2000-01, Vol.45 (1), p.60-62

2000

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Reply to the letter from T. Watanabe

Pediatric nephrology (Berlin, West), 2004-11, Vol.19 (11), p.1306-1306

2004

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A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency

Clinical Pediatric Endocrinology, 2006, Vol.15 (1), p.23-28

2006

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Revealing the thermal oxidation stability and its mechanism of rice bran oil

Linolenic Acid as the Main Source of Acrolein Formed During Heating of Vegetable Oils

Autoxidation of Fish Oil Blended with Rice Bran Oil

Combination analysis of three polymorphisms for predicting the risk for steroid-induced osteonecrosis of the femoral head

Hereditary hypophosphatemic rickets with hypercalciuria: a study for the phosphate transporter gene type IIc and osteoblastic function

ApoB C7623T polymorphism predicts risk for steroid-induced osteonecrosis of the femoral head after renal transplantation

Genetic analysis of steroid-induced osteonecrosis of the femoral head

A Male Patient with Humoral Hypercalcemia of Malignancy (HHM) with Leukocytosis Caused by Cutaneous Squamous Cell Carcinoma Resulting from Recessive Dystrophic Epidermolysis Bullosa

Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome

Low molecular weight phenotype of Apo(a) is a risk factor of corticosteroid-induced osteonecrosis of the femoral head after renal transplant

Molecular Bases of Diseases Characterized by Hypophosphatemia and Phosphaturia: New Understanding

Autoxidation of Fish Oil Blended with Rice Bran Oil

Lrp6 Hypomorphic Mutation Affects Bone Mass Through Bone Resorption in Mice and Impairs Interaction With Mesd

Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss

A Male Patient with Humoral Hypercalcemia of Malignancy (HHM) with Leukocytosis Caused by Cutaneous Squamous Cell Carcinoma Resulting from Recessive Dystrophic Epidermolysis Bullosa

Effect of transmit multi-port amplifiers used in base stations for wireless cellular systems

A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency

Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome

Long-term hospitalization during pregnancy is a risk factor for vitamin D deficiency in neonates

A Case with Marshall-Smith Syndrome without Life-threatening Complications

Common mutations F310L and T1559del in the tissue-nonspecific alkaline phosphatase gene are related to distinct phenotypes in Japanese patients with hypophosphatasia

Analysis of the stable levels of messenger RNA derived from different polymorphic alleles in the vitamin D receptor gene

Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome

Reply to the letter from T. Watanabe

A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency

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