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Type-1 Diabetes

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Cover of 'Type-1 Diabetes'

Table of Contents

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    Book Overview
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    Chapter 286 Methylation Analysis in Distinct Immune Cell Subsets in Type 1 Diabetes.
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    Chapter 287 Histology of Type 1 Diabetes Pancreas.
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    Chapter 288 Fluorescence In Situ Hybridization with Concomitant Immunofluorescence in Human Pancreas.
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    Chapter 289 Type 1 Diabetes: Current Perspectives.
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    Chapter 290 Laser Capture and Single Cell Genotyping from Frozen Tissue Sections.
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    Chapter 291 Pancreatic Beta Cell Survival and Signaling Pathways: Effects of Type 1 Diabetes-Associated Genetic Variants.
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    Chapter 292 Islet Autoantibody Analysis: Radioimmunoassays.
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    Chapter 293 Tracking Immunological Responses of Islet Antigen-Specific T Cells in the Nonobese Diabetic (NOD) Mouse Model of Type 1 Diabetes.
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    Chapter 294 Adoptive Transfer of Autoimmune Diabetes Using Immunodeficient Nonobese Diabetic (NOD) Mice.
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    Chapter 295 Identification of Islet Antigen-Specific CD8 T Cells Using MHCI-Peptide Tetramer Reagents in the Non Obese Diabetic (NOD) Mouse Model of Type 1 Diabetes.
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    Chapter 296 Islet Autoantibody Detection by Electrochemiluminescence (ECL) Assay.
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    Chapter 307 Type 1 Diabetes High-Risk HLA Class II Determination by Polymerase Chain Reaction Sequence-Specific Primers.
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    Chapter 330 Detection of C-Peptide in Urine as a Measure of Ongoing Beta Cell Function
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    Chapter 331 The Gut Microbiome in the NOD Mouse
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    Chapter 339 Molecular Methods and Protein Synthesis for Definition of Autoantibody Epitopes.
Attention for Chapter 294: Adoptive Transfer of Autoimmune Diabetes Using Immunodeficient Nonobese Diabetic (NOD) Mice.
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Chapter title
Adoptive Transfer of Autoimmune Diabetes Using Immunodeficient Nonobese Diabetic (NOD) Mice.
Chapter number 294
Book title
Type-1 Diabetes
Published in
Methods in molecular biology, January 2016
DOI 10.1007/7651_2015_294
Pubmed ID
Book ISBNs
978-1-4939-3641-0, 978-1-4939-3643-4
Authors

Evy De Leenheer, F. Susan Wong

Editors

Kathleen M. Gillespie

Abstract

Studying Type 1 Diabetes (T1D) in the nonobese diabetic (NOD) mouse model can be cumbersome as onset of disease does not usually occur naturally prior to the age of 12-14 weeks and is often restricted to female mice. Furthermore, the onset of disease occurs at random, which makes studying T1D in statistically meaningful cohorts of NOD mice a challenge. Transfer models of T1D into immunodeficient mice, such as NOD SCID mice, allows the study of potential therapeutic interventions in larger cohorts of animals, over shorter periods of time. In this chapter we discuss the adoptive transfer of diabetes into immunodeficient mice on the NOD genetic background that are generally available to the research community.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 8 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 8 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 2 25%
Student > Ph. D. Student 2 25%
Student > Bachelor 1 13%
Researcher 1 13%
Student > Postgraduate 1 13%
Other 0 0%
Unknown 1 13%
Readers by discipline Count As %
Immunology and Microbiology 3 38%
Agricultural and Biological Sciences 2 25%
Chemistry 1 13%
Engineering 1 13%
Unknown 1 13%