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Niemann-Pick type C proteins promote microautophagy by expanding raft-like membrane domains in the yeast vacuole

eLife, 2017-06, Vol.6

2017

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The replication foci targeting sequence (RFTS) of DNMT1 functions as a potent histone H3 binding domain regulated by autoinhibition

Biochemical and biophysical research communications, 2016-02, Vol.470 (3), p.741-747

2016

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PP1-Dependent Formin Bnr1 Dephosphorylation and Delocalization from a Cell Division Site

PloS one, 2016-01, Vol.11 (1), p.e0146941-e0146941

2016

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Methylation analysis of circadian clock gene promoters in forensic autopsy specimens

Legal medicine (Tokyo, Japan), 2011-07, Vol.13 (4), p.205-209

2011

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Calreticulin-2 is localized in the lumen of the endoplasmic reticulum but is not a Ca2+-binding protein

Histochemistry and cell biology, 2011-06, Vol.135 (6), p.531-538

2011

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Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection

Clinical genetics, 1991-06, Vol.39 (6), p.419-424

1991

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Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophy

Jinrui idengaku zasshi. Japanese journal of human genetics, 1990-06, Vol.35 (2), p.159-168

1990

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Hurler's syndromes without alpha-L-iduronidase deficiency

Pediatrics (Evanston), 1977-11, Vol.60 (5), p.764-765

1977

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Lysosomal acid hydrolases in established lymphoblastoid cell lines, transformed by Epstein-Barr virus, from patients with genetic lysosomal storage diseases

Human genetics, 1978-01, Vol.44 (1), p.79-87

1978

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Decrease of Urinary Acid Mucopolysaccharides in Hurler's Syndrome after Plasma Infusion

The Tohoku Journal of Experimental Medicine, 1974, Vol.112(4), pp.385-387

1974

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Pattern of Urinary Acid Mucopolysaccharide Excretion in Five Patients with Genetic Mucopolysaccharidoses

The Tohoku Journal of Experimental Medicine, 1973, Vol.110(1), pp.41-48

1973

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Activities of sulfatases for the degradation of acidic glycosaminoglycans in cultured skin fibroblasts from two siblings with multiple sulfatase deficiency

Clinica chimica acta, 1983-04, Vol.129 (2), p.175-180

1983

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Hyperglycopeptiduria in Genetic Mucolipidoses

The Tohoku Journal of Experimental Medicine, 1974, Vol.112(4), pp.373-380

1974

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Influence of Fresh Plasma Infusions on Patients with Genetic Mucopolysaccharidosis

The Tohoku Journal of Experimental Medicine, 1974, Vol.114(4), pp.385-392

1974

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Atypical Hurler Syndrome without α-L-Iduronidase Deficiency

The Tohoku Journal of Experimental Medicine, 1976, Vol.120(2), pp.113-123

1976

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Sphingomyelinase activities in cultured skin fibroblasts from patients with Niemann-Pick Disease

Human genetics, 1979-01, Vol.47 (2), p.159-167

1979

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Pattern of urinary acid mucopolysaccharide excretion in normale male children

Tohoku journal of experimental medicine, 1972-12, Vol.108 (4), p.369-375

1972

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Pattern of β-Galactosidase Deficiency in GM1-Gangliosidosis Type 1 and Type 2

The Tohoku Journal of Experimental Medicine, 1973, Vol.110(3), pp.309-310

1973

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Urinary acid mucopolysaccharides in patients with Hurler's syndrome

Saishin igaku, 1970-10, Vol.25 (10), p.2156

1970

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Urinary acidic mucopolysaccharides in normal individuals and patients with Hurler's syndrome

Nihon Shonika Gakkai zasshi. Acta paediatrica Japonica, 1969-06, Vol.73 (6), p.715

1969

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α-L-Iduronidase Activity in Established Lymphoblastoid Cells from Patients with Hurler and Scheie Syndromes Transformed by Epstein-Barr Virus

The Tohoku Journal of Experimental Medicine, 1977, Vol.122(4), pp.393-396

1977

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A new type of mucolipidosis with -galactosidase deficiency and glycopeptiduria

Tohoku journal of experimental medicine, 1972-08, Vol.107 (4), p.303-315

1972

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Niemann-Pick type C proteins promote microautophagy by expanding raft-like membrane domains in the yeast vacuole

The replication foci targeting sequence (RFTS) of DNMT1 functions as a potent histone H3 binding domain regulated by autoinhibition

PP1-Dependent Formin Bnr1 Dephosphorylation and Delocalization from a Cell Division Site

Methylation analysis of circadian clock gene promoters in forensic autopsy specimens

Calreticulin-2 is localized in the lumen of the endoplasmic reticulum but is not a Ca2+-binding protein

Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection

Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophy

Hurler's syndromes without alpha-L-iduronidase deficiency

Lysosomal acid hydrolases in established lymphoblastoid cell lines, transformed by Epstein-Barr virus, from patients with genetic lysosomal storage diseases

Decrease of Urinary Acid Mucopolysaccharides in Hurler's Syndrome after Plasma Infusion

Pattern of Urinary Acid Mucopolysaccharide Excretion in Five Patients with Genetic Mucopolysaccharidoses

Activities of sulfatases for the degradation of acidic glycosaminoglycans in cultured skin fibroblasts from two siblings with multiple sulfatase deficiency

Hyperglycopeptiduria in Genetic Mucolipidoses

Influence of Fresh Plasma Infusions on Patients with Genetic Mucopolysaccharidosis

Atypical Hurler Syndrome without α-L-Iduronidase Deficiency

Sphingomyelinase activities in cultured skin fibroblasts from patients with Niemann-Pick Disease

Pattern of urinary acid mucopolysaccharide excretion in normale male children

Pattern of β-Galactosidase Deficiency in GM1-Gangliosidosis Type 1 and Type 2

Urinary acid mucopolysaccharides in patients with Hurler's syndrome

Urinary acidic mucopolysaccharides in normal individuals and patients with Hurler's syndrome

α-L-Iduronidase Activity in Established Lymphoblastoid Cells from Patients with Hurler and Scheie Syndromes Transformed by Epstein-Barr Virus

A new type of mucolipidosis with -galactosidase deficiency and glycopeptiduria

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