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Nerve growth factor regulation and production by macrophages in osteoarthritic synovium

Clinical and experimental immunology, 2017-11, Vol.190 (2), p.235-243

2017

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Synovial macrophage‐derived IL‐1β regulates the calcitonin receptor in osteoarthritic mice

Clinical and experimental immunology, 2016-01, Vol.183 (1), p.143-149

2016

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Multiple isozymes of heparan sulfate/heparin GlcNAc N-deacetylase/GlcN N-sulfotransferase. Structure and activity of the fourth member, NDST4

The Journal of biological chemistry, 2001-02, Vol.276 (8), p.5876

2001

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Functional roles of GlcNAc N-deacetylase/GlcN N-sulfotransferases in the biosynthesis of heparan sulfate/heparin

Seikagaku. The Journal of Japanese Biochemical Society, 2001-06, Vol.73 (6), p.479

Aikawa, J

2001

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Molecular cloning and expression of a third member of the heparan sulfate/heparin GlcNAc N-deacetylase/ N-sulfotransferase family

The Journal of biological chemistry, 1999-01, Vol.274 (5), p.2690-2695

1999

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Angioedema for the Epiglottis Associated With Enalapril

The Laryngoscope, 2000-12, Vol.110 (12), p.2147-2148

2000

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The prepro-peptide of Mucor rennin directs the secretion of human growth hormone by Saccharomyces cerevisiae

Applied and Environmental Microbiology, 1990-07, Vol.56 (7), p.2125-2132

1990

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Primary Cutaneous T-Cell Lymphoma Involving the Cheek: An Infant Case with a Unique Clinicopathologic Feature

Leukemia & lymphoma, 1998, Vol.31 (1-2), p.225-229

1998

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A novel inborn error of metabolism detected by elevated methionine and/or galactose in newborn screening: neonatal intrahepatic cholestasis caused by citrin deficiency

European journal of pediatrics, 2003-05, Vol.162 (5), p.317-322

2003

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Low-Density Particles (W-Particles) Containing Catalase in Zellweger Syndrome and Normal Fibroblasts

Proceedings of the National Academy of Sciences - PNAS, 1991-11, Vol.88 (22), p.10084-10088

1991

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Bent (Head-Down) Posture and Aberrant Common Carotid Arteries of the Neck: Another New Risk Factor for Stroke?

The Laryngoscope, 2005-11, Vol.115 (11), p.2074-2075

2005

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Prenatal diagnosis in a new peroxisomal disease by the W‐particle separation method

Journal of inherited metabolic disease, 1994-09, Vol.17 (5), p.621-625

1994

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Treatment of heart failure in the aged and problems

Nihon Naika Gakkai zasshi, 1994-01, Vol.83 (1), p.88

1994

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Import of human bifunctional enzyme into peroxisomes of human hepatoma cells in vitro

Biochemical and biophysical research communications, 1991-08, Vol.178 (3), p.1084-1091

1991

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Bent (head-down) posture and aberrant internal carotid artery in the mouth: a new risk factor for stroke?

Annals of internal medicine, 2003-07, Vol.139 (1), p.W

2003

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Liquid-chromatographic determination of urinary glycosaminoglycans for differential diagnosis of genetic mucopolysaccharidoses

Clinical chemistry (Baltimore, Md.), 1986-01, Vol.32 (1 Pt 1), p.30-34

1986

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Biochemistry and physiology of magnesium

World review of nutrition and dietetics, 1978, Vol.28, p.112

Aikawa, J K

1978

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Biosynthesis of peroxisomal membrane polypeptides in infants with Zellweger syndrome

Journal of inherited metabolic disease, 1987-09, Vol.10 (3), p.297-300

1987

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Type 4 renal tubular acidosis (subtype 2) in a patient with methylmalonic acidaemia

European journal of pediatrics, 1990-12, Vol.150 (2), p.115-118

1990

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The Heterogeneity of Leber's Congenital Amaurosis

Journal of inherited metabolic disease, 1989-01, Vol.12 (S2), p.361-364

1989

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Magnesium

The Western journal of medicine, 1980-10, Vol.133 (4), p.333

Aikawa, J K

1980

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Enzymatic analysis in lymphocytes and erythrocytes from six patients with different phenotypes of phosphorylase kinase deficiency

Journal of inherited metabolic disease, 1988-09, Vol.11 (3), p.315-318

1988

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A Survey on Prenatal Diagnosis of Inherited Metabolic Diseases in Japan

Journal of inherited metabolic disease, 1989-01, Vol.12 (S2), p.260-262

1989

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The nature of myxedema: alterations in the serum electrolyte concentrations and radiosodium space and in the exchangeable sodium and potassium contents

Annals of internal medicine, 1956-01, Vol.44 (1), p.30

AIKAWA, J K

1956

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Hypomagnesemia

The Western journal of medicine, 1987-07, Vol.147 (1), p.86

1987

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Nerve growth factor regulation and production by macrophages in osteoarthritic synovium

Synovial macrophage‐derived IL‐1β regulates the calcitonin receptor in osteoarthritic mice

Multiple isozymes of heparan sulfate/heparin GlcNAc N-deacetylase/GlcN N-sulfotransferase. Structure and activity of the fourth member, NDST4

Functional roles of GlcNAc N-deacetylase/GlcN N-sulfotransferases in the biosynthesis of heparan sulfate/heparin

Molecular cloning and expression of a third member of the heparan sulfate/heparin GlcNAc N-deacetylase/ N-sulfotransferase family

Angioedema for the Epiglottis Associated With Enalapril

The prepro-peptide of Mucor rennin directs the secretion of human growth hormone by Saccharomyces cerevisiae

Primary Cutaneous T-Cell Lymphoma Involving the Cheek: An Infant Case with a Unique Clinicopathologic Feature

A novel inborn error of metabolism detected by elevated methionine and/or galactose in newborn screening: neonatal intrahepatic cholestasis caused by citrin deficiency

Low-Density Particles (W-Particles) Containing Catalase in Zellweger Syndrome and Normal Fibroblasts

Bent (Head-Down) Posture and Aberrant Common Carotid Arteries of the Neck: Another New Risk Factor for Stroke?

Prenatal diagnosis in a new peroxisomal disease by the W‐particle separation method

Treatment of heart failure in the aged and problems

Import of human bifunctional enzyme into peroxisomes of human hepatoma cells in vitro

Bent (head-down) posture and aberrant internal carotid artery in the mouth: a new risk factor for stroke?

Liquid-chromatographic determination of urinary glycosaminoglycans for differential diagnosis of genetic mucopolysaccharidoses

Biochemistry and physiology of magnesium

Biosynthesis of peroxisomal membrane polypeptides in infants with Zellweger syndrome

Type 4 renal tubular acidosis (subtype 2) in a patient with methylmalonic acidaemia

The Heterogeneity of Leber's Congenital Amaurosis

Magnesium

Enzymatic analysis in lymphocytes and erythrocytes from six patients with different phenotypes of phosphorylase kinase deficiency

A Survey on Prenatal Diagnosis of Inherited Metabolic Diseases in Japan

The nature of myxedema: alterations in the serum electrolyte concentrations and radiosodium space and in the exchangeable sodium and potassium contents

Hypomagnesemia

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