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Iodine and tri-iodo-thyronine reduce the incidence of type 1 diabetes mellitus in the autoimmune prone BB rats

https://doi.org/10.1080/08916930802438774
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/clin.1993.1169openalex-snapshot
An Excess of Dietary Iodine Accelerates the Development of a Thyroid-Associated Lymphoid Tissue in Autoimmune Prone BB Rats
inferredcites →https://doi.org/10.1007/bf00404999openalex-snapshot
Insulin treatment prevents diabetes mellitus but not thyroiditis in RT6-depleted diabetes resistant BB/Wor rats
inferredcites →https://doi.org/10.1007/bf00703140openalex-snapshot
Reduction of diabetes incidence of BB Wistar rats by early prophylactic insulin treatment of diabetes-prone animals
inferredcites →https://doi.org/10.1007/s00125-002-0842-5openalex-snapshot
Thyroxine induces pancreatic beta-cell apoptosis in rats
inferredcites →https://doi.org/10.1007/s00125-004-1507-3openalex-snapshot
Insulin resistance is a risk factor for progression to Type 1 diabetes
inferredcites →https://doi.org/10.1016/0140-6736(90)90004-oopenalex-snapshot
Prevention of diabetes mellitus in BB rats by neonatal stimulation of β cells
inferredcites →https://doi.org/10.1016/s1568-9972(03)00080-6openalex-snapshot
The etiology of autoimmune diabetes and thyroiditis: evidence for common genetic susceptibility
inferredcites →https://doi.org/10.1034/j.1600-0463.2002.100502.xopenalex-snapshot
Postnatal development of β‐cells in rats
inferredcites →https://doi.org/10.1038/9442openalex-snapshot
The NOD mouse model of type 1 diabetes: As good as it gets?
inferredcites →https://doi.org/10.1084/jem.164.4.1145openalex-snapshot
Prevention of diabetes in BioBreeding/Worcester rats with monoclonal antibodies that recognize T lymphocytes or natural killer cells.
inferredcites →https://doi.org/10.1111/j.1365-2818.1987.tb02837.xopenalex-snapshot
The efficiency of systematic sampling in stereology and its prediction*
inferredcites →https://doi.org/10.1111/j.1699-0463.1991.tb01289.xopenalex-snapshot
Reduction of diabetes incidence in NOD mice by neonatal glucose treatment
inferredcites →https://doi.org/10.1159/000234689openalex-snapshot
The Effect of Thyroxine on Spontaneous Thyroiditis in BB/W Rats
inferredcites →https://doi.org/10.1196/annals.1288.060openalex-snapshot
Multicenter Prevention Trial of Slowly Progressive Type 1 Diabetes with Small Dose of Insulin (the Tokyo Study)
inferredcites →https://doi.org/10.1210/edrv-5-3-411openalex-snapshot
Thyroid Hormones, Gonadal and Adrenocortical Steroids and the Function of the Islets of Langerhans
inferredcites →https://doi.org/10.1210/en.136.12.5731openalex-snapshot
Genetics of the BB rat: association of autoimmune disorders (diabetes, insulitis, and thyroiditis) with lymphopenia and major histocompatibility complex class II
inferredcites →https://doi.org/10.1210/en.138.4.1736openalex-snapshot
Apoptosis Participates in the Remodeling of the Endocrine Pancreas in the Neonatal Rat
inferredcites →https://doi.org/10.1210/endo-103-5-1546openalex-snapshot
Insulin Secretion and the Morphological and Metabolic Characteristics of Pancreatic Islets of Hyperthyroid ob/ob Mice*
inferredcites →https://doi.org/10.1210/endo-97-5-1321openalex-snapshot
Development of the Hypothalamic-Pituitary-Thyroid Axis in the Neonatal Rat
inferredcites →https://doi.org/10.1210/endo-99-1-125openalex-snapshot
Thyroid Function and Insulin Secretion from the Perfused Pancreas in the Rat
inferredcites →https://doi.org/10.1210/jcem.84.4.5598openalex-snapshot
Effects of Thyroid Hormones on Apoptotic Cell Death of Human Lymphocytes1
inferredcites →https://doi.org/10.1530/eje.0.1510375openalex-snapshot
Neonatal stimulation of the thyroid gland with iodine or suppression during adolescence with triiodothyronine changes the prevalence of autoimmune thyroiditis in BB rats
inferredcites →https://doi.org/10.1530/eje.1.01951openalex-snapshot
The effects of thyroid hormones on circulating markers of cell-mediated immune response, as studied in patients with differentiated thyroid carcinoma before and during thyroxine withdrawal
inferredcites →https://doi.org/10.1677/joe.0.1790245openalex-snapshot
The postnatal growth of the beta-cell mass in pigs
inferredcites →https://doi.org/10.1677/joe.1.06137openalex-snapshot
Integrative study of hypothalamus–pituitary–thyroid–immune system interaction: thyroid hormone-mediated modulation of lymphocyte activity through the protein kinase C signaling pathway
inferredcites →https://doi.org/10.2337/diab.29.9.673openalex-snapshot
Development of Insulin Release by Fetal Rat Pancreas In Vitro: Effects of Glucose, Amino Acids, and Theophylline
inferredcites →https://doi.org/10.2337/diab.30.12.1058openalex-snapshot
Lymphocytic Thyroiditis and Diabetes in the BB/W Rat: A New Model of Autoimmune Endocrinopathy
inferredcites →https://doi.org/10.2337/diab.37.3.286openalex-snapshot
Maturation of Insulin Response to Glucose During Human Fetal and Neonatal Development: Studies with Perifusion of Pancreatic Isletlike Cell Clusters
inferredcites →https://doi.org/10.2337/diab.38.10.1211openalex-snapshot
Interaction of β-Cell Activity and IL-1 Concentration and Exposure Time in Isolated Rat Islets of Langerhans
inferredcites →https://doi.org/10.2337/diab.39.8.933openalex-snapshot
Insulitis and Diabetes in NOD Mice Reduced by Prophylactic Insulin Therapy
inferredcites →https://doi.org/10.2337/diabetes.49.8.1341openalex-snapshot
Linear correlation between beta-cell mass and body weight throughout the lifespan in Lewis rats: role of beta-cell hyperplasia and hypertrophy.
inferredcites →https://doi.org/10.2337/diacare.27.9.2191openalex-snapshot
Temporary Preservation of β-Cell Function by Diazoxide Treatment in Childhood Type 1 Diabetes
inferredcites →https://doi.org/10.3109/08916939108997149openalex-snapshot
The Functional State of the Beta Cells in the Pathogenesis of Insulin-Dependent Diabetes Mellitus
inferredcites →https://doi.org/10.3109/08916939209083127openalex-snapshot
Anti-Diabetogenic Effect of Fusidic Acid in Diabetes Prone Bb Rats
inferredcites →https://doi.org/10.3181/00379727-187-42677openalex-snapshot
Developmental Changes in Rat Thyroid Responsiveness to Thyrotropin Administered by the Subcutaneous and Peroral Route
inferredcites →https://doi.org/10.4049/jimmunol.164.1.152openalex-snapshot
Effects of T3Rα1 and T3Rα2 Gene Deletion on T and B Lymphocyte Development

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4006015openalex-extracted
Preventive Effect of Molecular Iodine Supplement in Pancreatic Alterations Related to Hypothyroidism in Female Rabbits
inferred← citeshttps://doi.org/10.1002/mnfr.201100299openalex-snapshot
Excess dietary iodine differentially affects thyroid gene expression in diabetes, thyroiditis‐prone versus ‐resistant BioBreeding (BB) rats
inferred← citeshttps://doi.org/10.1007/s00210-023-02802-0openalex-snapshot
Current advancement in the preclinical models used for the assessment of diabetic neuropathy
inferred← citeshttps://doi.org/10.1007/s13238-014-0123-3openalex-snapshot
Recent progress in studies of factors that elicit pancreatic β-cell expansion
inferred← citeshttps://doi.org/10.1016/j.expneurol.2017.03.004openalex-snapshot
Diabetic aggravation of stroke and animal models
inferred← citeshttps://doi.org/10.1016/j.jtemb.2019.07.005openalex-snapshot
Selenium and iodine in diabetes mellitus with a focus on the interplay and speciation of the elements
inferred← citeshttps://doi.org/10.1017/s1751731112001073openalex-snapshot
Effect of dietary iodine on thyroid hormones and energy blood metabolites in lactating goats
inferred← citeshttps://doi.org/10.1111/j.1476-5381.2012.01911.xopenalex-snapshot
The use of animal models in diabetes research
inferred← citeshttps://doi.org/10.1155/2015/208947openalex-snapshot
Can Exposure to Environmental Chemicals Increase the Risk of Diabetes Type 1 Development?
inferred← citeshttps://doi.org/10.1155/2016/9051426openalex-snapshot
Experimental Diabetes Mellitus in Different Animal Models
inferred← citeshttps://doi.org/10.1186/s42826-021-00101-4openalex-snapshot
Experimental animal models for diabetes and its related complications—a review
inferred← citeshttps://doi.org/10.2174/0115748855348225241125084653openalex-snapshot
Diabetic Animal Models: A Prospective Futuristics Outlook
inferred← citeshttps://doi.org/10.2174/1871530319666190626143832openalex-snapshot
Future Perspective of Diabetic Animal Models
inferred← citeshttps://doi.org/10.3390/ijms241914903openalex-snapshot
Preventive Effect of Molecular Iodine in Pancreatic Disorders from Hypothyroid Rabbits
inferred← citeshttps://doi.org/10.3390/life16050864openalex-snapshot
Trace Elements in the Pancreas: From Physiological Homeostasis to the Pathogenesis of Diabetes, Pancreatitis, and Cancer—A Review
inferred← citeshttps://doi.org/10.3390/molecules25235630openalex-snapshot
Minerals in Pregnancy and Their Impact on Child Growth and Development
inferred← citeshttps://doi.org/10.3390/nu14030715openalex-snapshot
Molecular Iodine Supplement Prevents Streptozotocin-Induced Pancreatic Alterations in Mice
inferred← citeshttps://doi.org/10.3892/mmr.2012.895openalex-snapshot
Establishment of inducible cAMP early repressor transgenic fibroblasts in a porcine model of human type 1 diabetes mellitus
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