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Methylation of an intronic region regulates miR-199a in testicular tumor malignancy

Oncogene, 2011-08, Vol.30 (31), p.3404-3415

2011

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Genome-wide DNA methylation profiling reveals novel epigenetically regulated genes and non-coding RNAs in human testicular cancer

British journal of cancer, 2010-01, Vol.102 (2), p.419-427

2010

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Leydig cell hypoplasia due to inactivation of luteinizing hormone receptor by a novel homozygous nonsense truncation mutation in the seventh transmembrane domain

Molecular and cellular endocrinology, 2005-01, Vol.229 (1), p.57-64

2005

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Clinical and genetic studies of Japanese homozygotes for the Gaucher disease L444P mutation

Human genetics, 1999-07, Vol.105 (1-2), p.120-126

1999

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Characteristics of gene mutations among 32 unrelated Japanese Gaucher disease patients : absence of the common Jewish 84GG and 1226G mutations

Human genetics, 1995-06, Vol.95 (6), p.717-720

1995

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Development of a human mitochondria-focused cDNA microarray (hMitChip) and validation in skeletal muscle cells: implications for pharmaco- and mitogenomics

The pharmacogenomics journal, 2006-09, Vol.6 (5), p.333-342

2006

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Mutation screening of 17 Japanese patients with neuropathic Gaucher disease

Human genetics, 1996-08, Vol.98 (2), p.167-171

1996

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Kidney abnormalities in Hajdu-Cheney syndrome

Pediatric nephrology (Berlin, West), 1996-12, Vol.10 (6), p.712-715

1996

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Congenital adrenal hyperplasia : Molecular genetics and alternative approaches to treatment

Advances in pediatrics, 1995, Vol.42 (1), p.113-143

1995

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Pathological and biochemical studies of fetal Krabbe disease

Brain & development (Tokyo. 1979), 1994-11, Vol.16 (6), p.480-484

1994

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Familial congenital diaphragmatic hernia is an autosomal recessive variant

Journal of pediatric surgery, 1989-09, Vol.24 (9), p.860-864

1989

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Case report on SHORT syndrome

Clinical dysmorphology, 1999-07, Vol.8 (3), p.219-222

1999

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Type 1 Gaucher Disease: Phenotypic Expression and Natural History in Japanese Patients

Blood cells, molecules, & diseases, 1998-03, Vol.24 (1), p.73-81

1998

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Genetic Heterogeneity of Adrenocorticotropin (ACTH) Resistance Syndromes: Identification of a Novel Mutation of the ACTH Receptor Gene in Hereditary Glucocorticoid Deficiency

Molecular genetics and metabolism, 1998-08, Vol.64 (4), p.256-265

1998

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Coincidence of seizure susceptibility to caffeine and to the benzodiazepine inverse agonist, DMCM, in SWR and CBA inbred mice

Pharmacology, biochemistry and behavior, 1987-02, Vol.26 (2), p.381-387

1987

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Intestinal transport of manganese from human milk, bovine milk and infant formula in rats

Life sciences (1973), 1984-12, Vol.35 (24), p.2415-2419

1984

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Management and Outcome of Two Pregnancies in a Woman with Craniodiaphyseal Dysplasia

American journal of perinatology, 1991-01, Vol.8 (1), p.56-61

1991

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Interstrain variation in acute toxic response to caffeine among inbred mice

Pharmacology, biochemistry and behavior, 1984-04, Vol.20 (4), p.567-573

1984

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Glucose tolerance and plasma lipid distributions in rats fed a high-sucrose, high-cholesterol, low-chromium diet

Metabolism, clinical and experimental, 1985-12, Vol.34 (12), p.1086-1093

1985

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Different genes specify hyporesponsiveness to seizures induced by caffeine and the benzodiazepine inverse agonist, DMCM

Pharmacology, biochemistry and behavior, 1987-07, Vol.27 (3), p.451-456

1987

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Androgen receptors in ventral prostate glands of zinc deficient rats

Life sciences (1973), 1986-01, Vol.38 (4), p.351-356

1986

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Differential antagonism of the behavioral depressant and hypothermic effects of 5′-(N-ethylcarboxamide) adenosine by theobromine

Pharmacology, biochemistry and behavior, 1986-10, Vol.25 (4), p.769-773

1986

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Comparative biological availability of manganese from extrinsically labelled milk diets using sucking rats as a model

British journal of nutrition, 1986-01, Vol.55 (1), p.49-58

1986

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Inherent hyporesponsiveness to methylxanthine-induced behavioral changes associated with supersensitivity to 5'-N-ethylcarboxamidoadenosine (NECA)

Pharmacology, biochemistry and behavior, 1986-12, Vol.25 (6), p.1271-1277

1986

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Complex genetic determinants of susceptibility to methylxanthine-induced locomotor activity changes

Pharmacology, biochemistry and behavior, 1986-05, Vol.24 (5), p.1333-1341

1986

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Methylation of an intronic region regulates miR-199a in testicular tumor malignancy

Genome-wide DNA methylation profiling reveals novel epigenetically regulated genes and non-coding RNAs in human testicular cancer

Leydig cell hypoplasia due to inactivation of luteinizing hormone receptor by a novel homozygous nonsense truncation mutation in the seventh transmembrane domain

Clinical and genetic studies of Japanese homozygotes for the Gaucher disease L444P mutation

Characteristics of gene mutations among 32 unrelated Japanese Gaucher disease patients : absence of the common Jewish 84GG and 1226G mutations

Development of a human mitochondria-focused cDNA microarray (hMitChip) and validation in skeletal muscle cells: implications for pharmaco- and mitogenomics

Mutation screening of 17 Japanese patients with neuropathic Gaucher disease

Kidney abnormalities in Hajdu-Cheney syndrome

Congenital adrenal hyperplasia : Molecular genetics and alternative approaches to treatment

Pathological and biochemical studies of fetal Krabbe disease

Familial congenital diaphragmatic hernia is an autosomal recessive variant

Case report on SHORT syndrome

Type 1 Gaucher Disease: Phenotypic Expression and Natural History in Japanese Patients

Genetic Heterogeneity of Adrenocorticotropin (ACTH) Resistance Syndromes: Identification of a Novel Mutation of the ACTH Receptor Gene in Hereditary Glucocorticoid Deficiency

Coincidence of seizure susceptibility to caffeine and to the benzodiazepine inverse agonist, DMCM, in SWR and CBA inbred mice

Intestinal transport of manganese from human milk, bovine milk and infant formula in rats

Management and Outcome of Two Pregnancies in a Woman with Craniodiaphyseal Dysplasia

Interstrain variation in acute toxic response to caffeine among inbred mice

Glucose tolerance and plasma lipid distributions in rats fed a high-sucrose, high-cholesterol, low-chromium diet

Different genes specify hyporesponsiveness to seizures induced by caffeine and the benzodiazepine inverse agonist, DMCM

Androgen receptors in ventral prostate glands of zinc deficient rats

Differential antagonism of the behavioral depressant and hypothermic effects of 5′-(N-ethylcarboxamide) adenosine by theobromine

Comparative biological availability of manganese from extrinsically labelled milk diets using sucking rats as a model

Inherent hyporesponsiveness to methylxanthine-induced behavioral changes associated with supersensitivity to 5'-N-ethylcarboxamidoadenosine (NECA)

Complex genetic determinants of susceptibility to methylxanthine-induced locomotor activity changes

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