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Gastrointestinal Physiology and Diseases

Overview of attention for book
Cover of 'Gastrointestinal Physiology and Diseases'

Table of Contents

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    Book Overview
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    Chapter 1 CRISPR/Cas9-Mediated Genome Editing of Mouse Small Intestinal Organoids.
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    Chapter 2 Lentivirus-Based Stable Gene Delivery into Intestinal Organoids.
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    Chapter 3 Co-culture of Gastric Organoids and Immortalized Stomach Mesenchymal Cells.
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    Chapter 4 An Air-Liquid Interface Culture System for 3D Organoid Culture of Diverse Primary Gastrointestinal Tissues.
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    Chapter 5 Organotypical Tissue Cultures from Fetal and Neonatal Murine Colon.
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    Chapter 6 Ussing Chamber Technique to Measure Intestinal Epithelial Permeability.
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    Chapter 7 HPLC-Based Metabolomic Analysis of Normal and Inflamed Gut.
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    Chapter 8 Gastrointestinal Physiology and Diseases
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    Chapter 9 Gastrointestinal Physiology and Diseases
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    Chapter 10 Gastrointestinal Physiology and Diseases
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    Chapter 11 Gastrointestinal Physiology and Diseases
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    Chapter 12 Label-Free Imaging of Eosinophilic Esophagitis Mouse Models Using Optical Coherence Tomography.
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    Chapter 13 Near-Infrared Fluorescence Endoscopy to Detect Dysplastic Lesions in the Mouse Colon.
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    Chapter 14 Visualization of Signaling Molecules During Neutrophil Recruitment in Transgenic Mice Expressing FRET Biosensors.
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    Chapter 15 In Vivo Myeloperoxidase Imaging and Flow Cytometry Analysis of Intestinal Myeloid Cells.
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    Chapter 16 Gastrointestinal Physiology and Diseases
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    Chapter 17 Gastrointestinal Physiology and Diseases
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    Chapter 18 Purification and Adoptive Transfer of Group 3 Gut Innate Lymphoid Cells.
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    Chapter 19 Immunotherapy with iTreg and nTreg Cells in a Murine Model of Inflammatory Bowel Disease.
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    Chapter 20 Gastrointestinal Physiology and Diseases
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    Chapter 21 Investigation of Host and Pathogen Contributions to Infectious Colitis Using the Citrobacter rodentium Mouse Model of Infection.
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    Chapter 22 Gastrointestinal Physiology and Diseases
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    Chapter 23 Oxazolone-Induced Colitis as a Model of Th2 Immune Responses in the Intestinal Mucosa.
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    Chapter 24 The Mongolian Gerbil: A Robust Model of Helicobacter pylori-Induced Gastric Inflammation and Cancer.
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    Chapter 25 A Rapid Screenable Assay for Compounds That Protect Against Intestinal Injury in Zebrafish Larva.
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    Chapter 26 AOM/DSS Model of Colitis-Associated Cancer.
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    Chapter 27 Characterization of Colorectal Cancer Development in Apc (min/+) Mice.
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    Chapter 28 Modeling Murine Gastric Metaplasia Through Tamoxifen-Induced Acute Parietal Cell Loss.
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    Chapter 29 The Hamster Buccal Pouch Model of Oral Carcinogenesis.
Attention for Chapter 17: Gastrointestinal Physiology and Diseases
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Chapter title
Gastrointestinal Physiology and Diseases
Chapter number 17
Book title
Gastrointestinal Physiology and Diseases
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3603-8_17
Pubmed ID
Book ISBNs
978-1-4939-3601-4, 978-1-4939-3603-8
Authors

Takemura, Naoki, Uematsu, Satoshi, Naoki Takemura, Satoshi Uematsu

Editors

Andrei I. Ivanov

Abstract

Dendritic cells (DCs) are the most professional antigen-presenting cells that are indispensable for the initiation of adaptive immune responses. DCs are heterogeneous in terms of their origin, anatomical location, cell-surface markers, and functions. Previous studies have demonstrated that there exist several groups of DCs in the lamina propria (LPDC) of gastrointestinal tract, which collectively contribute to the maintenance of gut homeostasis through the regulation of the balance between active immunity and tolerance. However, although intestinal LPDCs are attractive research target for understanding the immunological mechanisms in the gut, isolation of the LPDCs is complicated and technically difficult for unskilled people. Therefore, establishment of the method to isolate intestinal LPDCs is a major obstacle in this research. Here, we describe the methods that we have established for the isolation of primary DCs from the LP of mouse small intestine. Our isolation method provides high yield of viable LP leukocytes (LPLs) including DCs. Combination with FACS sorting allows for the selective isolation of CD103(+)CD8α(+) DCs and CD103(+)CD8α(-) DCs from the LPLs. Furthermore, isolated LPDCs can be subjected to immunological assays, such as measurement of cytokine productions following stimulation of Toll-like receptors. Thus, our methods would be useful for studying the functions of LPDCs of mouse small intestine.

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X Demographics

The data shown below were collected from the profiles of 2 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 7 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 7 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 3 43%
Student > Postgraduate 1 14%
Unknown 3 43%
Readers by discipline Count As %
Agricultural and Biological Sciences 2 29%
Immunology and Microbiology 2 29%
Unknown 3 43%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 03 June 2016.
All research outputs
#14,853,520
of 22,875,477 outputs
Outputs from Methods in molecular biology
#4,700
of 13,131 outputs
Outputs of similar age
#218,996
of 393,698 outputs
Outputs of similar age from Methods in molecular biology
#468
of 1,471 outputs
Altmetric has tracked 22,875,477 research outputs across all sources so far. This one is in the 33rd percentile – i.e., 33% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,131 research outputs from this source. They receive a mean Attention Score of 3.4. This one has gotten more attention than average, scoring higher than 59% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 393,698 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 41st percentile – i.e., 41% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 1,471 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 63% of its contemporaries.