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MSH6/2 and PD-L1 Expressions Are Associated with Tumor Growth and Invasiveness in Silent Pituitary Adenoma Subtypes.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 8, p. 2831, doi. 10.3390/ijms21082831
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- Article
Isolated ACTH deficiency following immunization with the BNT162b2 SARS-CoV-2 vaccine: a case report.
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- BMC Endocrine Disorders, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12902-022-01095-3
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- Article
Hypopituitarism and cranial nerve involvement mimicking Tolosa-Hunt syndrome as the initially presenting feature of diffuse large B-cell lymphoma: a case report.
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- BMC Endocrine Disorders, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12902-022-00973-0
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- Article
Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association.
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- Journal of Human Genetics, 2009, v. 54, n. 4, p. 236, doi. 10.1038/jhg.2009.17
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- Article
Association of TCF7L2 polymorphisms with susceptibility to type 2 diabetes in 4,087 Japanese subjects.
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- Journal of Human Genetics, 2008, v. 53, n. 2, p. 174, doi. 10.1007/s10038-007-0231-5
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- Article
Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.
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- Nature Genetics, 2008, v. 40, n. 9, p. 1092, doi. 10.1038/ng.207
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- Article
Oncostatin M is a potential agent for the treatment of obesity and related metabolic disorders: a study in mice.
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- Diabetologia, 2015, v. 58, n. 8, p. 1868, doi. 10.1007/s00125-015-3613-9
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- Article
Early detection of euglycemic ketoacidosis during thoracic surgery associated with empagliflozin in a patient with type 2 diabetes: A case report.
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- Journal of Diabetes Investigation, 2021, v. 12, n. 4, p. 664, doi. 10.1111/jdi.13365
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- Article
Bilateral atrophy of the extensor digitorum brevis muscle might be a useful sign for diagnosing diabetic polyneuropathy in Japanese men who do not sit in the traditional "seiza" style.
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- Journal of Diabetes Investigation, 2021, v. 12, n. 3, p. 398, doi. 10.1111/jdi.13367
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- Article
Nicotinic acetylcholine receptor signaling regulates inositol‐requiring enzyme 1α activation to protect β‐cells against terminal unfolded protein response under irremediable endoplasmic reticulum stress.
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- Journal of Diabetes Investigation, 2020, v. 11, n. 4, p. 801, doi. 10.1111/jdi.13211
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- Article
Identification of a compound heterozygous inactivating ABCC8 gene mutation responsible for young‐onset diabetes with exome sequencing.
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- Journal of Diabetes Investigation, 2020, v. 11, n. 2, p. 333, doi. 10.1111/jdi.13138
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- Article
Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6‐year clinical course.
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- Journal of Diabetes Investigation, 2020, v. 11, n. 2, p. 502, doi. 10.1111/jdi.13127
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- Article
Clinical polyneuropathy does not increase with prediabetes or metabolic syndrome in the Japanese general population.
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- Journal of Diabetes Investigation, 2019, v. 10, n. 6, p. 1565, doi. 10.1111/jdi.13058
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- Article
Identification of a variant associated with early‐onset diabetes in the intron of the insulin gene with exome sequencing.
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- Journal of Diabetes Investigation, 2019, v. 10, n. 4, p. 947, doi. 10.1111/jdi.12974
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- Article
Difference in normal limit values of nerve conduction parameters between Westerners and Japanese people might need to be considered when diagnosing diabetic polyneuropathy using a Point‐of‐Care Sural Nerve Conduction Device (NC‐stat®/DPNCheck™)
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- Journal of Diabetes Investigation, 2018, v. 9, n. 5, p. 1173, doi. 10.1111/jdi.12818
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- Article
Familial Young-Onset Diabetes, Pre-Diabetes and Cardiovascular Disease Are Associated with Genetic Variants of <i>DACH1</i> in Chinese.
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- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0084770
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- Article
Genetic Associations of Type 2 Diabetes with Islet Amyloid Polypeptide Processing and Degrading Pathways in Asian Populations.
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- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0062378
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- Article
Polymorphisms in the IDE-KIF11-HHEX gene locus are reproducibly associated with type 2 diabetes in a Japanese population.
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- 2008
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- Publication type:
- journal article
PAX4 mutations in Thais with maturity onset diabetes of the young.
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- 2007
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- Publication type:
- journal article
Nonsense and Missense Mutations in the Human Hepatocyte Nuclear Factor-1β Gene (TCF2) and Their Relation to Type 2 Diabetes in Japanese.
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- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 8, p. 3859, doi. 10.1210/jcem.87.8.8776
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- Article
A polymorphic marker in the leptin gene associated with Japanese morbid obesity.
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- Journal of Molecular Medicine, 2000, v. 78, n. 9, p. 516, doi. 10.1007/s001090000143
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- Article
Autosomal Dominant Hypocalcemia With Atypical Urine Findings Accompanied by Novel CaSR Gene Mutation and VitD Deficiency.
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- Journal of the Endocrine Society, 2021, v. 5, n. 3, p. 1, doi. 10.1210/jendso/bvaa190
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- Article
Effect of SARS-CoV-2 BNT162b2 mRNA vaccine on thyroid autoimmunity: A twelve-month follow-up study.
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- Frontiers in Endocrinology, 2023, p. 1, doi. 10.3389/fendo.2023.1058007
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- Publication type:
- Article
Profiling of Unfolded Protein Response Markers and Effect of IRE1α-specific Inhibitor in Pituitary Neuroendocrine Tumor.
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- Endocrinology, 2024, v. 165, n. 4, p. 1, doi. 10.1210/endocr/bqae008
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- Article
Uncoupling Protein 2 Promoter Polymorphism -866G/A Affects Peripheral Nerve Dysfunction in Japanese Type 2 Diabetic Patients.
- Published in:
- Diabetes Care, 2006, v. 29, n. 4, p. 888, doi. 10.2337/diacare.29.04.06.dc05-1984
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- Publication type:
- Article
Negative pressure suction during blood sampling may reduce the difference in self-monitoring of blood glucose results between fingertip pricking and forearm pricking.
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- 2004
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- Publication type:
- journal article
Expression of unfolded protein response markers in the pheochromocytoma with Waardenburg syndrome: a case report.
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- BMC Endocrine Disorders, 2020, v. 20, n. 1, p. 1, doi. 10.1186/s12902-020-00574-9
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- Publication type:
- Article
A novel mutation, Ser159Pro in the NeuroD1/BETA2 gene contributes to the development of diabetes in a Chinese potential MODY family.
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- Molecular & Cellular Biochemistry, 2007, v. 303, n. 1/2, p. 115, doi. 10.1007/s11010-007-9463-0
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- Article
Kir6.2 E23 K polymorphism is related to secondary failure of sulfonylureas in non-obese patients with type 2 diabetes.
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- Journal of Diabetes Investigation, 2013, v. 4, n. 5, p. 445, doi. 10.1111/jdi.12070
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- Article
Clinical and functional characterization of the Pro1198 Leu ABCC8 gene mutation associated with permanent neonatal diabetes mellitus.
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- Journal of Diabetes Investigation, 2013, v. 4, n. 3, p. 269, doi. 10.1111/jdi.12049
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- Article
Increased arterial stiffness is closely associated with hyperglycemia and improved by glycemic control in diabetic patients.
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- Journal of Diabetes Investigation, 2013, v. 4, n. 1, p. 82, doi. 10.1111/j.2040-1124.2012.00229.x
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- Article
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.
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- Journal of Diabetes Investigation, 2011, v. 2, n. 6, p. 474, doi. 10.1111/j.2040-1124.2011.00127.x
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- Article
Numbness and paresthesia in bilateral toes and soles, and disproportional sweating restricted to face and trunk are suitable symptoms useful for the diagnosis of diabetic symmetric polyneuropathy.
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- Journal of Diabetes Investigation, 2011, v. 2, n. 6, p. 464, doi. 10.1111/j.2040-1124.2011.00124.x
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- Publication type:
- Article
Effect of anti-oxidants, Ricetrienol and α-tocopherol, on adipocytokine abnormalities and fatty liver in Otsuka Long-Evans Tokushima Fatty diabetic rats.
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- Journal of Diabetes Investigation, 2011, v. 2, n. 3, p. 186, doi. 10.1111/j.2040-1124.2010.00090.x
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- Article
A family in which people with a heterozygous ABCC8 gene mutation (p.Lys1385Gln) have progressed from hyperinsulinemic hypoglycemia to hyperglycemia.
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- Journal of Diabetes, 2020, v. 12, n. 1, p. 21, doi. 10.1111/1753-0407.12990
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- Publication type:
- Article
Pro198Leu Missense Polymorphism of Glutathione Peroxidase 1 Gene Affects Impaired Vibratory Perception in Toe and the Painful Leg Cramp in Japanese Type 2 Diabetic Patients.
- Published in:
- Diabetes, 2007, v. 56, p. A610
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- Publication type:
- Article
Common Variant in the Transcription Factor7-Like2 (TCF7L2) Gene Is Associated with Impaired Insulin Secretion in Japanese Type 2 Diabetic Patients.
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- Diabetes, 2007, v. 56, p. A297
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- Article
Increased Fluctuations in Blood Glucose and Systolic Blood Pressure Are Risk Factors of the Diabetic Retinopathy.
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- Diabetes, 2007, v. 56, p. A218
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- Publication type:
- Article
Association Studies of Variants in the Genes Involved in Pancreatic β-Cell Function in Type 2 Diabetes in Japanese Subjects.
- Published in:
- Diabetes, 2006, v. 55, n. 8, p. 2379, doi. 10.2337/db05-1203
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- Article
A functional variant in the human betacellulin gene promoter is associated with type 2 diabetes.
- Published in:
- 2005
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- Publication type:
- journal article
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.
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- 2004
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- Publication type:
- journal article
Uncoupling protein 2 promoter polymorphism -866G/A affects its expression in beta-cells and modulates clinical profiles of Japanese type 2 diabetic patients.
- Published in:
- 2004
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- Publication type:
- journal article
A missense mutation of Pax4 gene (R121W) is associated with type 2 diabetes in Japanese.
- Published in:
- 2001
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- Publication type:
- journal article
Nonsense mutation of islet-1 gene (Q310X) found in a type 2 diabetic patient with a strong family history.
- Published in:
- 2000
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- Publication type:
- journal article
Brief Genetics Report: Beta-cell transcription factors and diabetes no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3beta gene (HNF3B) in Japanese patients with m...
- Published in:
- Diabetes, 2000, v. 49, n. 2, p. 302, doi. 10.2337/diabetes.49.2.302
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- Publication type:
- Article
Beta-cell transcription factors and diabetes.
- Published in:
- Diabetes, 1998, v. 47, n. 8, p. 1356, doi. 10.2337/diabetes.47.8.1356
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- Article
Organization and partial sequence of the hepatocyte nuclear factor-4 alpha/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY.
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- 1997
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- Publication type:
- journal article
An approach for identifying simple sequence repeat DNA polymorphisms near cloned cDNAs and genes. Linkage studies of the islet amyloid polypeptide/amylin and liver glycogen synthase genes and NIDDM.
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- 1996
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- Publication type:
- journal article
Association of the prohormone convertase 2 gene (PCSK2) on chromosome 20 with NIDDM in Japanese subjects.
- Published in:
- 1995
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- Publication type:
- journal article
Elevated Serum Immunoglobulin G4 Levels in Patients with Graves' Disease and Their Clinical Implications.
- Published in:
- Thyroid, 2014, v. 24, n. 4, p. 736, doi. 10.1089/thy.2013.0448
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- Publication type:
- Article