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Regulation of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) by bone resorptive factors in osteoblastic cells

Journal of cellular physiology, 2000-11, Vol.185 (2), p.207-214

2000

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Hypophosphatemic rickets accompanying McCune-Albright syndrome : evidence that a humoral factor causes hypophosphatemia

Journal of bone and mineral metabolism, 2001-01, Vol.19 (5), p.287-295

2001

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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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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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Alendronate and pharmacological doses of 1α OHD3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia

Journal of bone and mineral metabolism, 2002-01, Vol.20 (3), p.170-173

2002

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Hypophosphatemic Rickets Accompanying Congenital Microvillous Atrophy

Journal of bone and mineral research, 1998-12, Vol.13 (12), p.1946-1952

1998

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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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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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Role of advanced glycation end products in adynamic bone disease in patients with diabetic nephropathy

American journal of kidney diseases, 2001-10, Vol.38 (4), p.S161-S164

2001

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Intrarenal localization of degradation of atrial natriuretic peptide in isolated glomeruli and cortical nephron segments

Life sciences (1973), 1988, Vol.43 (4), p.357-363

1988

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Treatment with recombinant IL-2 for recurrent respiratory infection in a case of cartilage-hair hypoplasia with autoimmune hemolytic anemia

Journal of bone and mineral metabolism, 2000, Vol.18 (1), p.36-40

2000

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A patient with Shiga toxin-associated hemolytic uremic syndrome who developed hyperkalemia in the recovery period

Clinical and experimental nephrology, 2001-03, Vol.5 (1), p.44-46

2001

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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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Transcriptional Induction of Matrix Metalloproteinase‐13 (Collagenase‐3) by 1α,25‐Dihydroxyvitamin D3 in Mouse Osteoblastic MC3T3‐E1 Cells

Journal of bone and mineral research, 2001-02, Vol.16 (2), p.221-230

2001

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No Enzyme Activity of 25-Hydroxyvitamin D3 1α-Hydroxylase Gene Product in Pseudovitamin D Deficiency Rickets, Including That with Mild Clinical Manifestation

The journal of clinical endocrinology and metabolism, 1999-11, Vol.84 (11), p.4111-4117

1999

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The role of IGF-I in phosphate therapy for the short stature of patients with hypophosphatemic vitamin D-resistant rickets

Journal of bone and mineral metabolism, 1996, Vol.14 (4), p.222-228

1996

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Treatment with Cytochrome c and Evaluation of Insulin Secretion in a Patient with Kearns-Sayre Syndrome

Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 1998, Vol.7 (2), p.81-85

1998

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Treatment with Cytochrome c and Evaluation of Insulin Secretion in a Patient with Kearns-Sayre Syndrome

Clinical Pediatric Endocrinology, 1998, Vol.7 (2), p.81-85

1998

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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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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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Synergistic effect of 1,25-dihydroxyvitamin D3 and retinoic acid in inducing U937 cell differentiation

Journal of Nutritional Science and Vitaminology, 1992, Vol.38(5), pp.415-426

1992

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A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia

Journal of human genetics, 2001-01, Vol.46 (1), p.41-44

2001

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Alendronate and pharmacological doses of 1[alpha] OHD3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia

Journal of bone and mineral metabolism, 2002-05, Vol.20 (3), p.170

2002

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Alendronate and pharmacological doses of 1à OHD 3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia

Journal of bone and mineral metabolism, 2002-05, Vol.20 (3), p.170-173

2002

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24R,25-dihydroxyvitamin D3 increases cyclic GMP contents, leading to an enhancement of osteocalcin synthesis by 1,25-dihydroxyvitamin D3 in cultured human osteoblastic cells

Experimental cell research, 1998-10, Vol.244 (1), p.71

1998

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Regulation of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) by bone resorptive factors in osteoblastic cells

Hypophosphatemic rickets accompanying McCune-Albright syndrome : evidence that a humoral factor causes hypophosphatemia

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

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

Alendronate and pharmacological doses of 1α OHD3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia

Hypophosphatemic Rickets Accompanying Congenital Microvillous Atrophy

Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome

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

Role of advanced glycation end products in adynamic bone disease in patients with diabetic nephropathy

Intrarenal localization of degradation of atrial natriuretic peptide in isolated glomeruli and cortical nephron segments

Treatment with recombinant IL-2 for recurrent respiratory infection in a case of cartilage-hair hypoplasia with autoimmune hemolytic anemia

A patient with Shiga toxin-associated hemolytic uremic syndrome who developed hyperkalemia in the recovery period

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

Transcriptional Induction of Matrix Metalloproteinase‐13 (Collagenase‐3) by 1α,25‐Dihydroxyvitamin D3 in Mouse Osteoblastic MC3T3‐E1 Cells

No Enzyme Activity of 25-Hydroxyvitamin D3 1α-Hydroxylase Gene Product in Pseudovitamin D Deficiency Rickets, Including That with Mild Clinical Manifestation

The role of IGF-I in phosphate therapy for the short stature of patients with hypophosphatemic vitamin D-resistant rickets

Treatment with Cytochrome c and Evaluation of Insulin Secretion in a Patient with Kearns-Sayre Syndrome

Treatment with Cytochrome c and Evaluation of Insulin Secretion in a Patient with Kearns-Sayre Syndrome

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

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

Synergistic effect of 1,25-dihydroxyvitamin D3 and retinoic acid in inducing U937 cell differentiation

A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia

Alendronate and pharmacological doses of 1[alpha] OHD3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia

Alendronate and pharmacological doses of 1à OHD 3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia

24R,25-dihydroxyvitamin D3 increases cyclic GMP contents, leading to an enhancement of osteocalcin synthesis by 1,25-dihydroxyvitamin D3 in cultured human osteoblastic cells

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