List of works - Takeshi Usui

A 22-year-old woman with hypocalcemia and clinical features of albright hereditary osteodystrophy diagnosed with sporadic pseudohypoparathyroidism type Ib using a methylation-specific multiplex ligation-dependent probe amplification assay.

scientific article published on May 2014

A Novel Missense Mutation of the MEN1 Gene in a Patient with Multiple Endocrine Neoplasia Type 1 with Glucagonoma and Obesity.

scientific article published in October 2015

A family of RTHβ with p.R316C mutation presenting occasional syndrome of inappropriate secretion of TSH.

scientific article published on 12 December 2014

A large functioning parathyroid cyst in a patient with multiple endocrine neoplasia type 1

scientific article published on 02 February 2013

A male case of nonclassical 21-hydroxylase deficiency first manifested in his sixties with adrenocortical incidentaloma.

scientific article published on 7 March 2008

A novel GATA3 nonsense mutation in a newly diagnosed adult patient of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome.

scientific article

A novel loss-of-function mutation of GATA3 (p.R299Q) in a Japanese family with Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) syndrome.

scientific article published on 30 October 2015

A rare CYP 21 mutation (p.E431K) induced deactivation of CYP 21A2 and resulted in congenital adrenal hyperplasia

scientific article published on 15 October 2014

A subtype prediction score for primary aldosteronism.

scientific article

ARMC5 Alterations in Primary Macronodular Adrenal Hyperplasia (PMAH) and the Clinical State of Variant Carriers

scientific article published on 23 July 2019

Aberrant expression of thyroid hormone receptor beta isoform may cause inappropriate secretion of TSH in a TSH-secreting pituitary adenoma.

scientific article

Adiponectin in anorexia nervosa and bulimia nervosa.

scientific article published in April 2004

Challenging Differential Diagnosis of Hypergastremia and Hyperglucagonemia with Chronic Renal Failure: Report of a Case with Multiple Endocrine Neoplasia Type 1

scientific article

Chronic kidney disease score for predicting postoperative masked renal insufficiency in patients with primary aldosteronism

scientific article published on 12 June 2014

Chronic primary adrenal insufficiency after unilateral adrenonephrectomy: A case report

scientific article published in December 2017

Clinical and molecular features of a TSH-secreting pituitary microadenoma.

scientific article published on January 2005

Confirmatory Testing in Primary Aldosteronism

scientific article published on 14 March 2012

Cyclic AMP-responsive region of the human proopiomelanocortin (POMC) gene

scientific article published on 01 March 1989

Do differences in risk factors explain the lower rates of coronary heart disease in Japanese versus U.S. women?

scientific article published on 28 September 2013

Effects of food deprivation and high fat diet on immunoreactive dynorphin A(1-8) levels in brain regions of Zucker rats.

scientific article

Effects of lifestyle intervention on weight and metabolic parameters in patients with impaired glucose tolerance related to beta-3 adrenergic receptor gene polymorphism Trp64Arg(C/T): Results from the Japan Diabetes Prevention Program

scientific article published on 29 October 2015

Effects of natural S‐equol supplements on overweight or obesity and metabolic syndrome in the Japanese, based on sex and equol status ⬇️

scientific article published on March 1, 2013

Effects of recombinant human interleukin-1 alpha, -1 beta, 2 and 6 on ACTH synthesis and release in the mouse pituitary tumour cell line AtT-20

scientific article published on 01 July 1989

Effects of sex, age and BMI on screening tests for impaired glucose tolerance.

scientific article published in May 2004

Equol producers can have low leptin levels among prediabetic and diabetic females.

scientific article

Expression of adrenocorticotropin-releasing hormone precursor gene in placenta and other nonhypothalamic tissues in man

scientific article published on 01 September 1988

Expression of prostaglandin E receptor EP4 subtype in rat adrenal zona glomerulosa: involvement in aldosterone release

scientific article published on 01 August 2000

Familial congenital choanal atresia with GATA3 associated hypoparathyroidism-deafness-renal dysplasia syndrome unidentified on auditory brainstem response

scientific article published on 02 November 2018

Functional analysis of the cell-specific enhancer in the human proopiomelanocortin gene by beta-galactosidase histochemical staining.

scientific article published on July 1994

Gene expression of the human prostaglandin E receptor EP4 subtype: differential regulation in monocytoid and lymphoid lineage cells by phorbol ester

scientific article

Genetic analysis of two Japanese patients with non-classical 21-hydroxylase deficiency.

scientific article published in May 2009

Genetic and epigenetic states of the GNAS complex in pseudohypoparathyroidism type Ib using methylation-specific multiplex ligation-dependent probe amplification assay.

scientific article

Ghrelin strongly stimulates growth hormone release in humans

scientific article published on 01 December 2000

H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency

scientific article published on October 2009

Histopathological diagnosis of primary aldosteronism using CYP11B2 immunohistochemistry.

scientific article published on 26 February 2013

Identification of a novel human thyroid hormone receptor beta isoform as a transcriptional modulator

scientific article

Image in endocrinology. Pheochromocytoma with subclinical Cushing's syndrome caused by corticomedullary mixed tumor of the adrenal gland.

scientific article

Immunoreactive corticotropin-releasing hormone levels in discrete hypothalamic nuclei of genetically obese Zucker rats

scientific article published on 01 September 1993

Importance of the Average Glucose Level and Estimated Glycated Hemoglobin in a Diabetic Patient with Hereditary Hemolytic Anemia and Liver Cirrhosis.

scientific article published on 8 December 2017

In Silico Analysis Identification of a Novel Germ-Line VHL Mutation in a Patient of Malignant Pheochromocytoma.

scientific article published in June 2014

Inheritance of an autosomal recessive disorder, Gitelman's syndrome, across two generations in one family

scientific article published on 01 June 2011

Isolation of Drosophila CREB-B: a novel CRE-binding protein.

scientific article published on September 1993

Lack of ACTH and androgen receptor expression in a giant adrenal myelolipoma associated with 21-hydroxylase deficiency.

scientific article published in January 2008

Leptin-to-adiponectin ratio as a potential atherogenic index in obese type 2 diabetic patients

scientific article published on 01 October 2004

Lipid profiles in the untreated patients with Hashimoto thyroiditis and the effects of thyroxine treatment on subclinical hypothyroidism with Hashimoto thyroiditis.

scientific article published on 22 December 2009

Lung squamous cell carcinoma associated with hypoparathyroidism with sensorineural deafness and renal dysplasia syndrome: a case report.

scientific article

Molecular cloning and expression of rat prostaglandin E receptor EP2 subtype.

scientific article published on May 1994

Molecular cloning of human prostacyclin receptor cDNA and its gene expression in the cardiovascular system.

scientific article

Molecular mechanism of the inhibitory effect of aldosterone on endothelial NO synthase activity.

scientific article

Mutation analysis of Gsalpha, adrenocorticotropin receptor and p53 genes in Japanese patients with adrenocortical neoplasms: including a case of Gsalpha mutation

scientific article published on 01 August 2000

Novel AVPR2 mutation causing partial nephrogenic diabetes insipidus in a Japanese family

scientific article published on 01 May 2016

P53 gene mutation in an atypical corticotroph adenoma with Cushing's disease

scientific article published on 02 September 2008

PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus

scientific article published on 14 March 2016

Pheochromocytoma complicated by cyanotic congenital heart disease: a case report

scientific article published on 28 April 2016

Prevention of type 2 diabetes in a primary healthcare setting: three-year results of lifestyle intervention in Japanese subjects with impaired glucose tolerance

scientific article

Primary hyperparathyroidism due to atypical vertically long cystic adenoma.

scientific article

Prostaglandin-dependent in vitro stimulation of adrenocortical steroidogenesis by interleukins

scientific article published on 01 January 1991

R27X nonsense mutation of the SDHB gene in a patient with sporadic malignant paraganglioma.

scientific article published on 5 May 2009

Rebound hypersecretion of GH following octreotide withdrawal due to liver dysfunction in an acromegalic patient

scientific article published on 01 October 2000

Resistance to dopamine agonists in prolactinoma is correlated with reduction of dopamine D2 receptor long isoform mRNA levels

scientific article published on 29 November 2011

Salivary cortisol levels are associated with outcomes of weight reduction therapy in obese Japanese patients.

scientific article published on 25 August 2011

Serum levels of IgG and IgG4 in Hashimoto thyroiditis.

scientific article published on 22 May 2013

Short-term effects of β-adrenergic antagonists and methimazole in new-onset thyrotoxicosis caused by Graves' disease.

scientific article

Shortened saline infusion test for subtype prediction in primary aldosteronism

scientific article published on 01 May 2015

Stomach is a major source of circulating ghrelin, and feeding state determines plasma ghrelin-like immunoreactivity levels in humans.

scientific article

Structural organization and chromosomal assignment of the human prostacyclin receptor gene.

scientific article

Successful treatment of Cushing's disease caused by ectopic intracavernous microadenoma

scientific article published on 01 September 2011

Suppressed levels of growth hormone and insulin-like growth factor-1 during successful pregnancy in persistent acromegaly

scientific article published on 01 April 2010

Tension pneumocephalus after administration of two 0.25 mg cabergoline tablets in MEN1-related macroprolactinoma

scientific article published on 07 June 2013

The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome

scientific article

The impact of equol-producing status in modifying the effect of soya isoflavones on risk factors for CHD: a systematic review of randomised controlled trials

scientific article

The incidence of gestational hyperthyroidism and postpartum thyroiditis in treated patients with Graves' disease

scientific article published on 01 August 2007

The phytochemical lindleyin, isolated from Rhei rhizoma, mediates hormonal effects through estrogen receptors

scientific article published on 01 November 2002

The retinoid X receptor binding to the thyroid hormone receptor: relationship with cofactor binding and transcriptional activity.

scientific article

Three novel mutations in Japanese patients with 21-hydroxylase deficiency.

scientific article

Thyroid Storm with Heart Failure Treated with a Short-acting Beta-adrenoreceptor Blocker, Landiolol Hydrochloride

scientific article published on 01 July 2015

Thyroid hormone action is disrupted by bisphenol A as an antagonist.

scientific article published in November 2002

Toxic thyroid adenoma presenting as hypokalemic periodic paralysis

scientific article published on 02 October 2007

Two rare TSH receptor amino acid substitutions in toxic thyroid adenomas.

scientific article

Two rare cases of familial (mother and daughter) adrenocorticotropic hormone-independent Cushing's syndrome due to adrenal adenoma, as well as the asynchronous development of another contralateral adrenal adenoma in the mother

scientific article published on 01 May 2014

Two-site immunoradiometric assay for adrenocorticotrophin: a cautionary study about the reactivity to its precursor molecules

scientific article published on 01 February 1989

Unusual Proliferative Glomerulonephritis in a Patient Diagnosed to Have Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome with a Novel Mutation in the GATA3 Gene.

scientific article published on June 2017

Vanishing pituitary gland on MR imaging.

scientific article published on 15 January 2010

[A case of malignant lymphoma presenting with pleuropericardial effusion]

scientific article published on 01 April 1989

[A case of thyrotropin-, growth hormone-, and prolactin-secreting pituitary adenoma with a remarkable response to long-acting somatostatin analogue (SMS201-995)]

scientific article published on 01 November 1989

[The cutting-edge of medicine; diagnosis and treatment of malignant pheochromocytoma]

scientific article published on 01 August 2012

¹⁸F-FDG-PET-positive adrenal tumour

scientific article

List of works by Takeshi Usui

A 22-year-old woman with hypocalcemia and clinical features of albright hereditary osteodystrophy diagnosed with sporadic pseudohypoparathyroidism type Ib using a methylation-specific multiplex ligation-dependent probe amplification assay.

A Novel Missense Mutation of the MEN1 Gene in a Patient with Multiple Endocrine Neoplasia Type 1 with Glucagonoma and Obesity.

A family of RTHβ with p.R316C mutation presenting occasional syndrome of inappropriate secretion of TSH.

A large functioning parathyroid cyst in a patient with multiple endocrine neoplasia type 1

A male case of nonclassical 21-hydroxylase deficiency first manifested in his sixties with adrenocortical incidentaloma.

A novel GATA3 nonsense mutation in a newly diagnosed adult patient of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome.

A novel loss-of-function mutation of GATA3 (p.R299Q) in a Japanese family with Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) syndrome.

A rare CYP 21 mutation (p.E431K) induced deactivation of CYP 21A2 and resulted in congenital adrenal hyperplasia

A subtype prediction score for primary aldosteronism.

ARMC5 Alterations in Primary Macronodular Adrenal Hyperplasia (PMAH) and the Clinical State of Variant Carriers

Aberrant expression of thyroid hormone receptor beta isoform may cause inappropriate secretion of TSH in a TSH-secreting pituitary adenoma.

Adiponectin in anorexia nervosa and bulimia nervosa.

Challenging Differential Diagnosis of Hypergastremia and Hyperglucagonemia with Chronic Renal Failure: Report of a Case with Multiple Endocrine Neoplasia Type 1

Chronic kidney disease score for predicting postoperative masked renal insufficiency in patients with primary aldosteronism

Chronic primary adrenal insufficiency after unilateral adrenonephrectomy: A case report

Clinical and molecular features of a TSH-secreting pituitary microadenoma.

Confirmatory Testing in Primary Aldosteronism

Cyclic AMP-responsive region of the human proopiomelanocortin (POMC) gene

Do differences in risk factors explain the lower rates of coronary heart disease in Japanese versus U.S. women?

Effects of food deprivation and high fat diet on immunoreactive dynorphin A(1-8) levels in brain regions of Zucker rats.

Effects of lifestyle intervention on weight and metabolic parameters in patients with impaired glucose tolerance related to beta-3 adrenergic receptor gene polymorphism Trp64Arg(C/T): Results from the Japan Diabetes Prevention Program

Effects of natural S‐equol supplements on overweight or obesity and metabolic syndrome in the Japanese, based on sex and equol status ⬇️

Effects of recombinant human interleukin-1 alpha, -1 beta, 2 and 6 on ACTH synthesis and release in the mouse pituitary tumour cell line AtT-20

Effects of sex, age and BMI on screening tests for impaired glucose tolerance.

Equol producers can have low leptin levels among prediabetic and diabetic females.

Expression of adrenocorticotropin-releasing hormone precursor gene in placenta and other nonhypothalamic tissues in man

Expression of prostaglandin E receptor EP4 subtype in rat adrenal zona glomerulosa: involvement in aldosterone release

Familial congenital choanal atresia with GATA3 associated hypoparathyroidism-deafness-renal dysplasia syndrome unidentified on auditory brainstem response

Functional analysis of the cell-specific enhancer in the human proopiomelanocortin gene by beta-galactosidase histochemical staining.

Gene expression of the human prostaglandin E receptor EP4 subtype: differential regulation in monocytoid and lymphoid lineage cells by phorbol ester

Genetic analysis of two Japanese patients with non-classical 21-hydroxylase deficiency.

Genetic and epigenetic states of the GNAS complex in pseudohypoparathyroidism type Ib using methylation-specific multiplex ligation-dependent probe amplification assay.

Ghrelin strongly stimulates growth hormone release in humans

H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency

Histopathological diagnosis of primary aldosteronism using CYP11B2 immunohistochemistry.

Identification of a novel human thyroid hormone receptor beta isoform as a transcriptional modulator

Image in endocrinology. Pheochromocytoma with subclinical Cushing's syndrome caused by corticomedullary mixed tumor of the adrenal gland.

Immunoreactive corticotropin-releasing hormone levels in discrete hypothalamic nuclei of genetically obese Zucker rats

Importance of the Average Glucose Level and Estimated Glycated Hemoglobin in a Diabetic Patient with Hereditary Hemolytic Anemia and Liver Cirrhosis.

In Silico Analysis Identification of a Novel Germ-Line VHL Mutation in a Patient of Malignant Pheochromocytoma.

Inheritance of an autosomal recessive disorder, Gitelman's syndrome, across two generations in one family

Isolation of Drosophila CREB-B: a novel CRE-binding protein.

Lack of ACTH and androgen receptor expression in a giant adrenal myelolipoma associated with 21-hydroxylase deficiency.

Leptin-to-adiponectin ratio as a potential atherogenic index in obese type 2 diabetic patients

Lipid profiles in the untreated patients with Hashimoto thyroiditis and the effects of thyroxine treatment on subclinical hypothyroidism with Hashimoto thyroiditis.

Lung squamous cell carcinoma associated with hypoparathyroidism with sensorineural deafness and renal dysplasia syndrome: a case report.

Molecular cloning and expression of rat prostaglandin E receptor EP2 subtype.

Molecular cloning of human prostacyclin receptor cDNA and its gene expression in the cardiovascular system.

Molecular mechanism of the inhibitory effect of aldosterone on endothelial NO synthase activity.

Mutation analysis of Gsalpha, adrenocorticotropin receptor and p53 genes in Japanese patients with adrenocortical neoplasms: including a case of Gsalpha mutation

Novel AVPR2 mutation causing partial nephrogenic diabetes insipidus in a Japanese family

P53 gene mutation in an atypical corticotroph adenoma with Cushing's disease

PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus

Pheochromocytoma complicated by cyanotic congenital heart disease: a case report

Prevention of type 2 diabetes in a primary healthcare setting: three-year results of lifestyle intervention in Japanese subjects with impaired glucose tolerance

Primary hyperparathyroidism due to atypical vertically long cystic adenoma.

Prostaglandin-dependent in vitro stimulation of adrenocortical steroidogenesis by interleukins

R27X nonsense mutation of the SDHB gene in a patient with sporadic malignant paraganglioma.

Rebound hypersecretion of GH following octreotide withdrawal due to liver dysfunction in an acromegalic patient

Resistance to dopamine agonists in prolactinoma is correlated with reduction of dopamine D2 receptor long isoform mRNA levels

Salivary cortisol levels are associated with outcomes of weight reduction therapy in obese Japanese patients.

Serum levels of IgG and IgG4 in Hashimoto thyroiditis.

Short-term effects of β-adrenergic antagonists and methimazole in new-onset thyrotoxicosis caused by Graves' disease.

Shortened saline infusion test for subtype prediction in primary aldosteronism

Stomach is a major source of circulating ghrelin, and feeding state determines plasma ghrelin-like immunoreactivity levels in humans.

Structural organization and chromosomal assignment of the human prostacyclin receptor gene.

Successful treatment of Cushing's disease caused by ectopic intracavernous microadenoma

Suppressed levels of growth hormone and insulin-like growth factor-1 during successful pregnancy in persistent acromegaly

Tension pneumocephalus after administration of two 0.25 mg cabergoline tablets in MEN1-related macroprolactinoma

The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome

The impact of equol-producing status in modifying the effect of soya isoflavones on risk factors for CHD: a systematic review of randomised controlled trials

The incidence of gestational hyperthyroidism and postpartum thyroiditis in treated patients with Graves' disease

The phytochemical lindleyin, isolated from Rhei rhizoma, mediates hormonal effects through estrogen receptors

The retinoid X receptor binding to the thyroid hormone receptor: relationship with cofactor binding and transcriptional activity.

Three novel mutations in Japanese patients with 21-hydroxylase deficiency.

Thyroid Storm with Heart Failure Treated with a Short-acting Beta-adrenoreceptor Blocker, Landiolol Hydrochloride

Thyroid hormone action is disrupted by bisphenol A as an antagonist.

Toxic thyroid adenoma presenting as hypokalemic periodic paralysis

Two rare TSH receptor amino acid substitutions in toxic thyroid adenomas.