Lista de obras - Takeshi Usui - Dominio Público Uruguay

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.

artículo científico publicado en 2014

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

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

artículo científico publicado en 2013

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

artículo científico publicado en 2008

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

artículo científico publicado en 2013

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

A subtype prediction score for primary aldosteronism.

artículo científico publicado en 2014

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.

artículo científico publicado en 2011

Adiponectin in anorexia nervosa and bulimia nervosa.

artículo científico publicado en 2004

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

artículo científico publicado en 2017

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

artículo científico publicado en 2014

Chronic primary adrenal insufficiency after unilateral adrenonephrectomy: A case report

artículo científico publicado en 2017

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

artículo científico publicado en 2005

Confirmatory Testing in Primary Aldosteronism

artículo científico publicado en 2012

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

artículo científico publicado en 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.

artículo científico publicado en 1987

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

artículo científico publicado en 2015

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

artículo científico publicado el 1 de marzo de 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

artículo científico publicado en 1989

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

artículo científico publicado en 2004

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

artículo científico publicado en 2014

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

artículo científico publicado en 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

artículo científico publicado en 2018

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

artículo científico publicado en 1994

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

artículo científico publicado en 1996

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

artículo científico publicado en 2009

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

artículo científico publicado en 2013

Ghrelin strongly stimulates growth hormone release in humans

artículo científico publicado en 2000

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

artículo científico publicado en 2009

Histopathological diagnosis of primary aldosteronism using CYP11B2 immunohistochemistry.

artículo científico publicado en 2013

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

artículo científico publicado en 2010

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

artículo científico publicado en 2009

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

artículo científico publicado en 1993

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

artículo científico publicado en 2017

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

artículo científico publicado en 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.

artículo científico publicado en 1993

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

artículo científico publicado en 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.

artículo científico publicado en 2009

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

artículo científico publicado en 2018

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

artículo científico publicado en 1994

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

artículo científico publicado en 1994

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

artículo científico publicado en 2006

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

artículo científico publicado en 2000

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

artículo científico publicado en 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

artículo científico publicado en 2016

Pheochromocytoma complicated by cyanotic congenital heart disease: a case report

artículo científico publicado en 2016

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

artículo científico publicado en 2011

Primary hyperparathyroidism due to atypical vertically long cystic adenoma.

artículo científico publicado en 2014

Prostaglandin-dependent in vitro stimulation of adrenocortical steroidogenesis by interleukins

artículo científico publicado en 1991

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

artículo científico publicado en 2009

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

artículo científico publicado en 2000

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

artículo científico publicado en 2011

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

artículo científico publicado en 2011

Serum levels of IgG and IgG4 in Hashimoto thyroiditis.

artículo científico publicado en 2013

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

artículo científico publicado en 2012

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.

artículo científico publicado en 2001

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

artículo científico publicado en 1995

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

artículo científico publicado en 2010

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

artículo científico publicado en 2013

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

artículo científico publicado en 2015

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

artículo científico publicado en 2016

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

artículo científico publicado en 2007

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

artículo científico publicado en 2002

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

artículo científico publicado en 2009

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

artículo científico publicado en 2003

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

artículo científico publicado en 2015

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

artículo científico publicado en 2002

Toxic thyroid adenoma presenting as hypokalemic periodic paralysis

artículo científico publicado en 2007

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

artículo científico publicado en 2011

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

artículo científico publicado en 2014

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

artículo científico publicado en 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.

artículo científico publicado en 2017

Vanishing pituitary gland on MR imaging.

artículo científico publicado en 2010

[A case of malignant lymphoma presenting with pleuropericardial effusion]

artículo científico publicado en 1989

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

artículo científico publicado en 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

artículo científico publicado en 2015

Lista de obras de 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.