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Gene expression of the human prostaglandin E receptor EP4 subtype: differential regulation in monocytoid and lymphoid lineage cells by phorbol esterThe impact of equol-producing status in modifying the effect of soya isoflavones on risk factors for CHD: a systematic review of randomised controlled trialsIdentification of a novel human thyroid hormone receptor beta isoform as a transcriptional modulator.Prevention of type 2 diabetes in a primary healthcare setting: three-year results of lifestyle intervention in Japanese subjects with impaired glucose toleranceAberrant expression of thyroid hormone receptor beta isoform may cause inappropriate secretion of TSH in a TSH-secreting pituitary adenoma.Challenging Differential Diagnosis of Hypergastremia and Hyperglucagonemia with Chronic Renal Failure: Report of a Case with Multiple Endocrine Neoplasia Type 1Stomach is a major source of circulating ghrelin, and feeding state determines plasma ghrelin-like immunoreactivity levels in humans.Short-term effects of β-adrenergic antagonists and methimazole in new-onset thyrotoxicosis caused by Graves' disease.Structural organization and chromosomal assignment of the human prostacyclin receptor gene.Molecular cloning of human prostacyclin receptor cDNA and its gene expression in the cardiovascular system.Primary hyperparathyroidism due to atypical vertically long cystic adenoma.¹⁸F-FDG-PET-positive adrenal tumourA novel loss-of-function mutation of GATA3 (p.R299Q) in a Japanese family with Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) syndrome.The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome.Molecular cloning and expression of rat prostaglandin E receptor EP2 subtype.Isolation of Drosophila CREB-B: a novel CRE-binding protein.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.Pheochromocytoma complicated by cyanotic congenital heart disease: a case reportH62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase DeficiencyTension pneumocephalus after administration of two 0.25 mg cabergoline tablets in MEN1-related macroprolactinomaDo differences in risk factors explain the lower rates of coronary heart disease in Japanese versus U.S. women?A subtype prediction score for primary aldosteronism.The retinoid X receptor binding to the thyroid hormone receptor: relationship with cofactor binding and transcriptional activity.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.Functional analysis of the cell-specific enhancer in the human proopiomelanocortin gene by beta-galactosidase histochemical staining.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.Clinical and molecular features of a TSH-secreting pituitary microadenoma.Two rare TSH receptor amino acid substitutions in toxic thyroid adenomas.Lipid profiles in the untreated patients with Hashimoto thyroiditis and the effects of thyroxine treatment on subclinical hypothyroidism with Hashimoto thyroiditis.Thyroid hormone action is disrupted by bisphenol A as an antagonist.Equol producers can have low leptin levels among prediabetic and diabetic females.Effects of sex, age and BMI on screening tests for impaired glucose tolerance.Adiponectin in anorexia nervosa and bulimia nervosa.A novel GATA3 nonsense mutation in a newly diagnosed adult patient of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome.R27X nonsense mutation of the SDHB gene in a patient with sporadic malignant paraganglioma.Lack of ACTH and androgen receptor expression in a giant adrenal myelolipoma associated with 21-hydroxylase deficiency.A male case of nonclassical 21-hydroxylase deficiency first manifested in his sixties with adrenocortical incidentaloma.Salivary cortisol levels are associated with outcomes of weight reduction therapy in obese Japanese patients.Genetic analysis of two Japanese patients with non-classical 21-hydroxylase deficiency.Effects of food deprivation and high fat diet on immunoreactive dynorphin A(1-8) levels in brain regions of Zucker rats.
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Takeshi Usui
@ast
Takeshi Usui
@en
Takeshi Usui
@es
Takeshi Usui
@nl
type
label
Takeshi Usui
@ast
Takeshi Usui
@en
Takeshi Usui
@es
Takeshi Usui
@nl
prefLabel
Takeshi Usui
@ast
Takeshi Usui
@en
Takeshi Usui
@es
Takeshi Usui
@nl
P108
P1153
P106
P1153
10540848000
55348566400
57193299904
P31
P496
0000-0002-8301-6766