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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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Genetic association of a polymorphism of the cAMP-responsive element binding protein-binding protein with steroid-induced osteonecrosis after kidney transplantation

Journal of bone and mineral metabolism, 2007-09, Vol.25 (5), p.320-325

2007

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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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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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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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Examination of megalin in renal tubular epithelium from patients with Dent disease

Pediatric nephrology (Berlin, West), 2004-06, Vol.19 (6), p.612-615

2004

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Megalin and proximal renal tubular dysfunction in Dent disease

Pediatric nephrology (Berlin, West), 2004-11, Vol.19 (11), p.1305; author reply 1306-1305

Watanabe, Toru

2004

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Retinoid X receptors stimulate and 9-cis retinoic acid inhibits 1,25-dihydroxyvitamin D3-activated expression of the rat osteocalcin gene

Molecular and Cellular Biology, 1993-09, Vol.13 (9), p.5907-5917

1993

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Genetic analysis for prevention of steroid-induced osteonecrosis of the femoral head

Clinical calcium, 2007-06, Vol.17 (6), p.894

2007

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Successful stenting for renal artery stenosis in a patient with Alagille syndrome

Pediatric nephrology (Berlin, West), 2005-06, Vol.20 (6), p.831-833

2005

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Familial hypoparathyroidism

Nihon rinshō, 2005-10, Vol.63 Suppl 10, p.330

2005

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Isolation of baculovirus-expressed human vitamin D receptor: DNA responsive element interactions and phosphorylation of the purified receptor

Journal of cellular biochemistry, 2002, Vol.85 (2), p.435-457

2002

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Human vitamin D receptor phosphorylation by casein kinase II at Ser-208 potentiates transcriptional activation

Proceedings of the National Academy of Sciences - PNAS, 1996-04, Vol.93 (8), p.3519-3524

1996

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Analysis of localization of mutated tissue-nonspecific alkaline phosphatase proteins associated with neonatal hypophosphatasia using green fluorescent protein chimeras

The journal of clinical endocrinology and metabolism, 1998-11, Vol.83 (11), p.3936-3942

1998

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Rapid deterioration of renal artery dysplasia in tuberous sclerosis

The Journal of pediatrics, 2003-09, Vol.143 (3), p.406-406

2003

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Shift of serum osteocalcin components between cord blood and blood at day 5 of life

Pediatric research, 2002-11, Vol.52 (5), p.656-659

2002

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Identification of novel missense mutations (Phe310Leu and Gly439Arg) in a neonatal case of hypophosphatasia

The journal of clinical endocrinology and metabolism, 1996-12, Vol.81 (12), p.4458-4461

1996

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A highly conserved region in the hormone-binding domain of the human vitamin D receptor contains residues vital for heterodimerization with retinoid X receptor and for transcriptional activation

Molecular endocrinology (Baltimore, Md.), 1995-09, Vol.9 (9), p.1166-1179

1995

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Effect of cyclic adenosine 3′,5′-monophosphate and protein kinase A on ligand-dependent transactivation via the vitamin D receptor

Molecular and cellular endocrinology, 2000-01, Vol.159 (1), p.45-51

2000

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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

Genetic association of a polymorphism of the cAMP-responsive element binding protein-binding protein with steroid-induced osteonecrosis after kidney transplantation

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

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

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

Examination of megalin in renal tubular epithelium from patients with Dent disease

Megalin and proximal renal tubular dysfunction in Dent disease

Retinoid X receptors stimulate and 9-cis retinoic acid inhibits 1,25-dihydroxyvitamin D3-activated expression of the rat osteocalcin gene

Genetic analysis for prevention of steroid-induced osteonecrosis of the femoral head

Successful stenting for renal artery stenosis in a patient with Alagille syndrome

Familial hypoparathyroidism

Isolation of baculovirus-expressed human vitamin D receptor: DNA responsive element interactions and phosphorylation of the purified receptor

Human vitamin D receptor phosphorylation by casein kinase II at Ser-208 potentiates transcriptional activation

Analysis of localization of mutated tissue-nonspecific alkaline phosphatase proteins associated with neonatal hypophosphatasia using green fluorescent protein chimeras

Rapid deterioration of renal artery dysplasia in tuberous sclerosis

Shift of serum osteocalcin components between cord blood and blood at day 5 of life

Identification of novel missense mutations (Phe310Leu and Gly439Arg) in a neonatal case of hypophosphatasia

A highly conserved region in the hormone-binding domain of the human vitamin D receptor contains residues vital for heterodimerization with retinoid X receptor and for transcriptional activation

Effect of cyclic adenosine 3′,5′-monophosphate and protein kinase A on ligand-dependent transactivation via the vitamin D receptor

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