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Growth-related skeletal changes and alterations in phosphate metabolism

Bone (New York, N.Y.), 2022-08, Vol.161, p.116430-116430, Article 116430

2022

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Hypophosphatasia in Japan: ALPL Mutation Analysis in 98 Unrelated Patients

Calcified tissue international, 2020-03, Vol.106 (3), p.221-231

2020

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A unique case of childhood hypophosphatasia caused by a novel heterozygous 51-bp in-frame deletion in the ALPL gene

Clinical Pediatric Endocrinology, 2023, Vol.32(3), pp.180-187

2023

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Extracellular Phosphate Induces the Expression of Dentin Matrix Protein 1 Through the FGF Receptor in Osteoblasts

Journal of cellular biochemistry, 2017-05, Vol.118 (5), p.1151-1163

2017

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Novel mutation in the ALPL gene with a dominant negative effect in a Japanese family

Journal of bone and mineral metabolism, 2021-09, Vol.39 (5), p.804-809

2021

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CREB activation in hypertrophic chondrocytes is involved in the skeletal overgrowth in epiphyseal chondrodysplasia Miura type caused by activating mutations of natriuretic peptide receptor B

Human molecular genetics, 2019-04, Vol.28 (7), p.1183-1198

2019

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Findings of amplitude-integrated electroencephalogram recordings and serum vitamin B6 metabolites in perinatal lethal hypophosphatasia during enzyme replacement therapy

Brain & development (Tokyo. 1979), 2019-09, Vol.41 (8), p.721-725

2019

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Elevated Fibroblast Growth Factor 23 Exerts Its Effects on Placenta and Regulates Vitamin D Metabolism in Pregnancy of Hyp Mice

Journal of bone and mineral research, 2014-07, Vol.29 (7), p.1627-1638

2014

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Dysregulated gene expression in the primary osteoblasts and osteocytes isolated from hypophosphatemic Hyp mice

PloS one, 2014-04, Vol.9 (4), p.e93840-e93840

2014

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Both FGF23 and extracellular phosphate activate Raf/MEK/ERK pathway via FGF receptors in HEK293 cells

Journal of cellular biochemistry, 2010-12, Vol.111 (5), p.1210-1221

2010

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Signaling of extracellular inorganic phosphate up-regulates cyclin D1 expression in proliferating chondrocytes via the Na+ /Pi cotransporter Pit-1 and Raf/MEK/ERK pathway

Bone (New York, N.Y.), 2010-11, Vol.47 (5), p.938-947

2010

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Interleukin-1-induced acute bone resorption facilitates the secretion of fibroblast growth factor 23 into the circulation

Journal of bone and mineral metabolism, 2015-05, Vol.33 (3), p.342-354

2015

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The Effect of Asfotase Alfa on Plasma and Urine Pyrophosphate Levels and Pseudofractures in a Patient With Adult‐Onset Hypophosphatasia

JBMR plus, 2023-12, Vol.7 (12), p.e10842-n/a

2023

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Discordant fetal phenotype of hypophosphatasia in two siblings

American journal of medical genetics. Part A, 2018-01, Vol.176 (1), p.171-174

2018

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Sodium-coupled neutral amino acid transporter 4 functions as a regulator of protein synthesis during liver development

Hepatology research, 2013-11, Vol.43 (11), p.1211-1223

2013

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Cover Image, Volume 176A, Number 1, January 2018

American journal of medical genetics. Part A, 2018-01, Vol.176 (1), p.i-i

2018

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Complex intrinsic abnormalities in osteoblast lineage cells of X-linked hypophosphatemia: Analysis of human iPS cell models generated by CRISPR/Cas9-mediated gene ablation

Bone (New York, N.Y.), 2024-04, Vol.181, p.117044-117044, Article 117044

2024

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A unique case of childhood hypophosphatasia caused by a novel heterozygous 51-bp in-frame deletion in the ALPL gene

Clinical Pediatric Endocrinology, 2023, pp.2023-0019

2023

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Clinical Characteristics of Perinatal Lethal Hypophosphatasia: A Report of 6 Cases

Clinical Pediatric Endocrinology, 2010, Vol.19(1), pp.7-13

2010

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Clonal osteoblastic cell lines with CRISPR/Cas9-mediated ablation of Pit1 or Pit2 show enhanced mineralization despite reduced osteogenic gene expression

Bone (New York, N.Y.), 2021-10, Vol.151, p.116036-116036, Article 116036

2021

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Involvement of nuclear factor I transcription/replication factor in the early stage of chondrocytic differentiation

Bone (New York, N.Y.), 2007-12, Vol.41 (6), p.1025-1035

2007

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A case of osteopathia striata with cranial sclerosis with facial nerve palsies

Pediatrics international, 2023-01, Vol.65 (1), p.e15648-n/a

2023

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Reversible Deterioration in Hypophosphatasia Caused by Renal Failure With Bisphosphonate Treatment

Journal of bone and mineral research, 2015-09, Vol.30 (9), p.1726-1737

2015

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PTH/cAMP/PKA signaling facilitates canonical Wnt signaling via inactivation of glycogen synthase kinase-3β in osteoblastic Saos-2 cells

Journal of cellular biochemistry, 2008-05, Vol.104 (1), p.304-317

2008

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Vinculin Functions as Regulator of Chondrogenesis

The Journal of biological chemistry, 2012-05, Vol.287 (19), p.15760-15775

2012

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Growth-related skeletal changes and alterations in phosphate metabolism

Hypophosphatasia in Japan: ALPL Mutation Analysis in 98 Unrelated Patients

A unique case of childhood hypophosphatasia caused by a novel heterozygous 51-bp in-frame deletion in the ALPL gene

Extracellular Phosphate Induces the Expression of Dentin Matrix Protein 1 Through the FGF Receptor in Osteoblasts

Novel mutation in the ALPL gene with a dominant negative effect in a Japanese family

CREB activation in hypertrophic chondrocytes is involved in the skeletal overgrowth in epiphyseal chondrodysplasia Miura type caused by activating mutations of natriuretic peptide receptor B

Findings of amplitude-integrated electroencephalogram recordings and serum vitamin B6 metabolites in perinatal lethal hypophosphatasia during enzyme replacement therapy

Elevated Fibroblast Growth Factor 23 Exerts Its Effects on Placenta and Regulates Vitamin D Metabolism in Pregnancy of Hyp Mice

Dysregulated gene expression in the primary osteoblasts and osteocytes isolated from hypophosphatemic Hyp mice

Both FGF23 and extracellular phosphate activate Raf/MEK/ERK pathway via FGF receptors in HEK293 cells

Signaling of extracellular inorganic phosphate up-regulates cyclin D1 expression in proliferating chondrocytes via the Na+ /Pi cotransporter Pit-1 and Raf/MEK/ERK pathway

Interleukin-1-induced acute bone resorption facilitates the secretion of fibroblast growth factor 23 into the circulation

The Effect of Asfotase Alfa on Plasma and Urine Pyrophosphate Levels and Pseudofractures in a Patient With Adult‐Onset Hypophosphatasia

Discordant fetal phenotype of hypophosphatasia in two siblings

Sodium-coupled neutral amino acid transporter 4 functions as a regulator of protein synthesis during liver development

Cover Image, Volume 176A, Number 1, January 2018

Complex intrinsic abnormalities in osteoblast lineage cells of X-linked hypophosphatemia: Analysis of human iPS cell models generated by CRISPR/Cas9-mediated gene ablation

A unique case of childhood hypophosphatasia caused by a novel heterozygous 51-bp in-frame deletion in the ALPL gene

Clinical Characteristics of Perinatal Lethal Hypophosphatasia: A Report of 6 Cases

Clonal osteoblastic cell lines with CRISPR/Cas9-mediated ablation of Pit1 or Pit2 show enhanced mineralization despite reduced osteogenic gene expression

Involvement of nuclear factor I transcription/replication factor in the early stage of chondrocytic differentiation

A case of osteopathia striata with cranial sclerosis with facial nerve palsies

Reversible Deterioration in Hypophosphatasia Caused by Renal Failure With Bisphosphonate Treatment

PTH/cAMP/PKA signaling facilitates canonical Wnt signaling via inactivation of glycogen synthase kinase-3β in osteoblastic Saos-2 cells

Vinculin Functions as Regulator of Chondrogenesis

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