Asako Doi

发表

Des-acyl ghrelin protects microvascular endothelial cells from oxidative stress-induced apoptosis through sirtuin 1 signaling pathway.

M. Nishi, H. Furuta, Takeshi Shimada, 2014, Metabolism: clinical and experimental.

Uncoupling protein 2 promoter polymorphism -866G/A affects peripheral nerve dysfunction in Japanese type 2 diabetic patients.

K. Nanjo, M. Nishi, H. Furuta, 2006, Diabetes care.

Regulation of AMP-activated Protein Kinase Signaling by AFF4 Protein, Member of AF4 (ALL1-fused Gene from Chromosome 4) Family of Transcription Factors, in Hypothalamic Neurons*

H. Furuta, Asako Doi, T. Akamizu, 2012, The Journal of Biological Chemistry.

IA-2β, but not IA-2, is induced by ghrelin and inhibits glucose-stimulated insulin secretion

K. Nanjo, M. Nishi, H. Furuta, 2006 .

MSH6/2 and PD-L1 Expressions Are Associated with Tumor Growth and Invasiveness in Silent Pituitary Adenoma Subtypes

S. Yamada, H. Furuta, Asako Doi, 2020, International journal of molecular sciences.

Atypical pituitary adenoma with MEN1 somatic mutation associated with abnormalities of DNA mismatch repair genes; MLH1 germline mutation and MSH6 somatic mutation.

M. Nishi, S. Yamada, H. Furuta, 2017, Endocrine journal.

The influence of thyroid autoimmunity on pregnancy outcome in infertile women: a prospective study.

M. Nishi, Asako Doi, H. Ariyasu, 2020, Endocrine journal.

IA-2beta, but not IA-2, is induced by ghrelin and inhibits glucose-stimulated insulin secretion.

K. Nanjo, M. Nishi, H. Furuta, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Expression of unfolded protein response markers in the pheochromocytoma with Waardenburg syndrome: a case report

M. Nishi, K. Yoshiura, H. Furuta, 2020, BMC Endocrine Disorders.

A functional variant in the human betacellulin gene promoter is associated with type 2 diabetes.

T. Sanke, K. Nanjo, M. Nishi, 2005, Diabetes.

Extracellular superoxide dismutase gene polymorphism is associated with insulin resistance and the susceptibility to type 2 diabetes.

T. Sanke, K. Nanjo, M. Nishi, 2006, Diabetes research and clinical practice.

Pro198Leu missense polymorphism of the glutathione peroxidase 1 gene might be a common genetic predisposition of distal symmetric polyneuropathy and macrovascular disease in Japanese type 2 diabetic patients

K. Nanjo, M. Nishi, H. Furuta, 2011, Journal of diabetes investigation.

Subcellular localization of glucose transporter 4 in the hypothalamic arcuate nucleus of ob/ob mice under basal conditions

K. Nanjo, Asako Doi, E. Senba, 2005, Brain Research.

PAX4 mutations in Thais with maturity onset diabetes of the young.

K. Nanjo, M. Nishi, H. Furuta, 2007, The Journal of clinical endocrinology and metabolism.

BRIEF REPORT PAX4 Mutations in Thais with Maturity Onset Diabetes of the Young

K. Nanjo, M. Nishi, H. Furuta, 2007 .

Differential role of GPR142 in tryptophan-mediated enhancement of insulin secretion in obese and lean mice

Asako Doi, H. Ariyasu, T. Akamizu, 2018, PloS one.

Autosomal Dominant Hypocalcemia With Atypical Urine Findings Accompanied by Novel CaSR Gene Mutation and VitD Deficiency

M. Nishi, H. Furuta, Asako Doi, 2020, Journal of the Endocrine Society.

SUMO4 Met55Val polymorphism is associated with coronary heart disease in Japanese type 2 diabetes individuals.

T. Sanke, K. Nanjo, M. Nishi, 2009, Diabetes research and clinical practice.

Identification of a variant associated with early‐onset diabetes in the intron of the insulin gene with exome sequencing

M. Nishi, K. Yoshiura, H. Furuta, 2018, Journal of diabetes investigation.

Ghrelin inhibits insulin secretion through the AMPK–UCP2 pathway in β cells

K. Nanjo, M. Nishi, H. Furuta, 2010, FEBS letters.

A family in which people with a heterozygous ABCC8 gene mutation (p.Lys1385Gln) have progressed from hyperinsulinemic hypoglycemia to hyperglycemia

M. Nishi, H. Furuta, Asako Doi, 2020, Journal of diabetes.

Ferulic acid prevents pathological and functional abnormalities of the kidney in Otsuka Long-Evans Tokushima Fatty diabetic rats.

K. Nanjo, M. Nishi, H. Furuta, 2008, Diabetes research and clinical practice.

Functional variants in the glutathione peroxidase-1 (GPx-1) gene are associated with increased intima-media thickness of carotid arteries and risk of macrovascular diseases in japanese type 2 diabetic patients.

T. Sanke, K. Nanjo, M. Nishi, 2004, Diabetes.

Effect of SARS-CoV-2 BNT162b2 mRNA vaccine on thyroid autoimmunity: A twelve-month follow-up study

M. Nishi, H. Furuta, Asako Doi, 2023, Frontiers in Endocrinology.

Effect of anti‐oxidants, Ricetrienol and α‐tocopherol, on adipocytokine abnormalities and fatty liver in Otsuka Long‐Evans Tokushima Fatty diabetic rats

K. Nanjo, M. Nishi, H. Furuta, 2010, Journal of diabetes investigation.

Elevated serum immunoglobulin G4 levels in patients with Graves' disease and their clinical implications.

M. Nishi, H. Furuta, Asako Doi, 2014, Thyroid : official journal of the American Thyroid Association.

Clinical and functional characterization of the Pro1198Leu ABCC8 gene mutation associated with permanent neonatal diabetes mellitus

K. Nanjo, M. Nishi, H. Furuta, 2013, Journal of diabetes investigation.

Hypersecretion of ACTH and PRL from pituitary adenoma in MEN1, adequately managed by medical therapy

M. Nishi, H. Furuta, Asako Doi, 2017, Endocrinology, diabetes & metabolism case reports.

False-positive staining of thyroglobulin distinguished from mixed medullary and follicular thyroid carcinoma by duplex in situ hybridization.

Asako Doi, H. Ariyasu, T. Akamizu, 2020, Endocrine journal.

Reduced Expression of Mismatch Repair Genes MSH6/MSH2 Directly Promotes Pituitary Tumor Growth via the ATR–Chk1 Pathway

M. Nishi, S. Yamada, H. Furuta, 2018, The Journal of clinical endocrinology and metabolism.

Imbalanced Expression of IGF2 and PCSK4 Is Associated With Overproduction of Big IGF2 in SFT With NICTH: A Pilot Study

S. Tsujii, Shintaro Okamura, Asako Doi, 2018, The Journal of clinical endocrinology and metabolism.

Distribution of serum immunoglobulin G4 levels in Hashimoto's thyroiditis and clinical features of Hashimoto's thyroiditis with elevated serum immunoglobulin G4 levels.

M. Nishi, H. Furuta, Asako Doi, 2015, Endocrine journal.

Clinicopathological features of Riedel's thyroiditis associated with IgG4-related disease in Japan.

M. Nishi, M. Hirokawa, Asako Doi, 2015, Endocrine journal.

Regulation of Ghrelin Signaling by a Leptin-induced Gene, Negative Regulatory Element-binding Protein, in the Hypothalamic Neurons*

K. Nanjo, H. Furuta, Asako Doi, 2010, The Journal of Biological Chemistry.

Polymorphisms in the IDE-KIF11-HHEX gene locus are reproducibly associated with type 2 diabetes in a Japanese population.

T. Sanke, K. Nanjo, M. Nishi, 2008, The Journal of clinical endocrinology and metabolism.

Thyroid function, glycemic control, and diabetic nephropathy in patients with type 2 diabetes over 24 months: prospective observational study

M. Nishi, H. Furuta, Asako Doi, 2023, BMC Endocrine Disorders.

Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6‐year clinical course

M. Nishi, H. Furuta, Asako Doi, 2019, Journal of diabetes investigation.

Identification of a compound heterozygous inactivating ABCC8 gene mutation responsible for young‐onset diabetes with exome sequencing

M. Nishi, H. Furuta, Asako Doi, 2019, Journal of diabetes investigation.