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A review of the effectiveness of motivational interviewing interventions (MI) in the field of occupational health

Safety and health at work, 2022-01, Vol.13, p.S110-S110

2022

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RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: a study of the Japanese Childhood AML Cooperative Study Group

International journal of hematology, 2012-05, Vol.95 (5), p.509-515

2012

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Preferential release of newly synthesized insulin assessed by a multi-label reporter system using pancreatic β-cell line MIN6

PloS one, 2012-10, Vol.7 (10), p.e47921-e47921

2012

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WT1 mutation in pediatric patients with acute myeloid leukemia: a report from the Japanese Childhood AML Cooperative Study Group

International journal of hematology, 2013-10, Vol.98 (4), p.437-445

2013

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Immunohistochemical Analysis of IA-2 Family of Protein Tyrosine Phosphatases in Rat Gastrointestinal Endocrine Cells

The journal of histochemistry and cytochemistry, 2013-02, Vol.61 (2), p.156-168

2013

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Dynamic behavior and alkyne insertion reactions of alkenyl- and thiolate-bridged diiron carbonyl complexes

Journal of organometallic chemistry, 2023-09, Vol.997, p.122766, Article 122766

2023

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CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML)

Blood, 2012-03, Vol.119 (11), p.2612-2614

2012

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THE METABOLIC SYNDROME FROM THE VIEW POINT OF PUBLIC HEALTH: WITH SPECIAL REFERENCE TO NONALCOHOLIC FATTY LIVER DISEASE

Nihon Koshu Eisei Zasshi(JAPANESE JOURNAL OF PUBLIC HEALTH), 2005, Vol.52(11), pp.934-942

2005

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Preferential Release of Newly Synthesized Insulin Assessed by a Multi-Label Reporter System Using Pancreatic [beta]-Cell Line MIN6

PloS one, 2012-10, Vol.7 (10), p.e47921

2012

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Down-regulation of endogenous Wt1 expression by sry transgene in the murine embryonic mesonephros-derived M15 cell line

Journal of Reproduction and Development, 2006, Vol.52(3), pp.415-427

2006

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ASSOCIATION OF CHANGE IN THE TYPE OF JOB WITH PREVALENCE OF COMPONENTS OF THE METABOLIC SYNDROME—SPECIAL REFERENCE TO JOB STRESS

Nihon Koshu Eisei Zasshi(JAPANESE JOURNAL OF PUBLIC HEALTH), 2005, Vol.52(11), pp.987-993

2005

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Design of Hammerhead Ribozymes that Cleave Murine Sry mRNA In Vitro and In Vivo

Journal of Reproduction and Development, 2006, Vol.52(1), pp.73-80

2006

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CHANGE OF COMPONENTS OF THE METABOLIC SYNDROME IN A WORKERS’ HEALTH CHECKUP AFTER FIVE YEARS —RELATION WITH ELEVATED LIVER ENZYMES, GENE POLYMORPHISMS FOR ALDH 2, β3-AR AND LIFESTYLE

Nihon Koshu Eisei Zasshi(JAPANESE JOURNAL OF PUBLIC HEALTH), 2005, Vol.52(11), pp.979-986

2005

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NUP98-NSD1 Fusion Gene Is Strongly Associated with a Poor Prognosis in Pediatric Acute Myeloid Leukemia: A Study of the Japanese Childhood AML99 Cooperative Study Group

Blood, 2011-11, Vol.118 (21), p.1475-1475

2011

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A case of diabetic amyotrophy associated with 3243 mitochondrial tRNA(leu; UUR) mutation and successful therapy with coenzyme Q10

Endocrine journal, 1995-04, Vol.42 (2), p.141-145

1995

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Aldehyde dehydrogenase 2 and β3-Adrenergic receptor gene polymorphisms: Their association with elevated liver enzymes and metabolic syndrome

Metabolism, clinical and experimental, 2003-09, Vol.52 (9), p.1096-1101

2003

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Diet therapy and physical exercise for diabetes

Nihon rinshō, 2002-09, Vol.60 Suppl 9, p.199

2002

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ALDH 2 Gene Mutation and Glycemic Control in Type-2 Diabetes

Journal of the Japan Diabetes Society, 2000/07/30, Vol.43(7), pp.567-569

2000

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Mitochondrial tRNALeu(UUR) Mutation at Position 3243 and Symptomatic Polyneuropathy in Type 2 Diabetes

Diabetes care, 2003-04, Vol.26 (4), p.1315-1316

2003

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Clinical Effects of Metformin in Patients with Nonobese Type 2 Diabetes

Journal of the Japan Diabetes Society, 2009/01/30, Vol.52(1), pp.1-6

2009

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Mitochondrial tRNA(Leu(UUR)) mutation at position 3243 and symptomatic polyneuropathy in type 2 diabetes

Diabetes care, 2003-04, Vol.26 (4), p.1315-1316

2003

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A mitochondrial DNA variant associated with left ventricular hypertrophy in diabetes

Biochemical and biophysical research communications, 2003-12, Vol.312 (3), p.858-864

2003

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A Case of Diabetic Amyotrophy Associated with 3243 Mitochondrial tRNA(leu; UUR) Mutation and Successful Therapy with Coenzyme Q10

ENDOCRINE JOURNAL, 1995, Vol.42 (2), p.141-145

1995

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Inactive Aldehyde Dehydrogenase 2 Worsens Glycemic Control in Patients With Type 2 Diabetes Mellitus Who Drink Low to Moderate Amounts of Alcohol

Alcoholism, clinical and experimental research, 2000-04, Vol.24 (4), p.5S-11S

2000

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Influence of ALDH2 Genotype on Peripheral Neuropathy in Non-Insulin-Dependent Diabetes Mellitus

Journal of the Japan Diabetes Society, 1998/02/28, Vol.41(2), pp.119-125

1998

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A review of the effectiveness of motivational interviewing interventions (MI) in the field of occupational health

RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: a study of the Japanese Childhood AML Cooperative Study Group

Preferential release of newly synthesized insulin assessed by a multi-label reporter system using pancreatic β-cell line MIN6

WT1 mutation in pediatric patients with acute myeloid leukemia: a report from the Japanese Childhood AML Cooperative Study Group

Immunohistochemical Analysis of IA-2 Family of Protein Tyrosine Phosphatases in Rat Gastrointestinal Endocrine Cells

Dynamic behavior and alkyne insertion reactions of alkenyl- and thiolate-bridged diiron carbonyl complexes

CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML)

THE METABOLIC SYNDROME FROM THE VIEW POINT OF PUBLIC HEALTH: WITH SPECIAL REFERENCE TO NONALCOHOLIC FATTY LIVER DISEASE

Preferential Release of Newly Synthesized Insulin Assessed by a Multi-Label Reporter System Using Pancreatic [beta]-Cell Line MIN6

Down-regulation of endogenous Wt1 expression by sry transgene in the murine embryonic mesonephros-derived M15 cell line

ASSOCIATION OF CHANGE IN THE TYPE OF JOB WITH PREVALENCE OF COMPONENTS OF THE METABOLIC SYNDROME—SPECIAL REFERENCE TO JOB STRESS

Design of Hammerhead Ribozymes that Cleave Murine Sry mRNA In Vitro and In Vivo

CHANGE OF COMPONENTS OF THE METABOLIC SYNDROME IN A WORKERS’ HEALTH CHECKUP AFTER FIVE YEARS —RELATION WITH ELEVATED LIVER ENZYMES, GENE POLYMORPHISMS FOR ALDH 2, β3-AR AND LIFESTYLE

NUP98-NSD1 Fusion Gene Is Strongly Associated with a Poor Prognosis in Pediatric Acute Myeloid Leukemia: A Study of the Japanese Childhood AML99 Cooperative Study Group

A case of diabetic amyotrophy associated with 3243 mitochondrial tRNA(leu; UUR) mutation and successful therapy with coenzyme Q10

Aldehyde dehydrogenase 2 and β3-Adrenergic receptor gene polymorphisms: Their association with elevated liver enzymes and metabolic syndrome

Diet therapy and physical exercise for diabetes

ALDH 2 Gene Mutation and Glycemic Control in Type-2 Diabetes

Mitochondrial tRNALeu(UUR) Mutation at Position 3243 and Symptomatic Polyneuropathy in Type 2 Diabetes

Clinical Effects of Metformin in Patients with Nonobese Type 2 Diabetes

Mitochondrial tRNA(Leu(UUR)) mutation at position 3243 and symptomatic polyneuropathy in type 2 diabetes

A mitochondrial DNA variant associated with left ventricular hypertrophy in diabetes

A Case of Diabetic Amyotrophy Associated with 3243 Mitochondrial tRNA(leu; UUR) Mutation and Successful Therapy with Coenzyme Q10

Inactive Aldehyde Dehydrogenase 2 Worsens Glycemic Control in Patients With Type 2 Diabetes Mellitus Who Drink Low to Moderate Amounts of Alcohol

Influence of ALDH2 Genotype on Peripheral Neuropathy in Non-Insulin-Dependent Diabetes Mellitus

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