Evidence map›Paper›PMID 31248780›Full record

ArticleImmunity2019

Defining Genetic Variation in Widely Used Congenic and Backcrossed Mouse Models Reveals Varied Regulation of Genes Important for Immune Responses.

Danielle A Chisolm, Wayne Cheng, Shelby A Colburn, Aaron Silva-Sanchez, Selene Meza-Perez, Troy D Randall, Amy S Weinmann

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  5. Proceedings of the National Academy of Sciences of the United States of America · 2025
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  16. Generation of Bone Marrow Chimeras.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  17. Genetic Strategies to Study T Cell Development.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  18. Article
  19. Impaired Intracellular CaInternational journal of molecular sciences · 2022
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Danielle A ChisolmDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Wayne ChengDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Shelby A ColburnDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Aaron Silva-SanchezDepartment of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Selene Meza-PerezDepartment of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Troy D RandallDepartment of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Amy S WeinmannDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA. Electronic address: weinmann@uab.edu.
University of Alabama at Birmingham · US

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Virus-induced Cell Fate Decisions in Anti-Viral ImmunityU19AI109962 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI RANDALL, TROY D · 2014 to 2018
$11.6M
Molecular characterization of the role for T-bet and Bcl-6 in immune cell metabolism and differentiationR01AI061061 · NIAID · UNIVERSITY OF WASHINGTON · PI WEINMANN, AMY SUSAN · 2004 to 2025
$7.0M
Role of microbiota in therapy to ovarian cancerR01CA216234 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI RANDALL, TROY D · 2017 to 2021
$2.1M
Molecular characterization of the role for metabolites in immune cell differentiationR56AI061061 · NIAID · UNIVERSITY OF WASHINGTON · PI WEINMANN, AMY SUSAN · 2009 to 2021
$672k
NCI NIH HHS P30 CA013148NCI NIH HHS R01 CA216234NIAID NIH HHS R01 AI061061NIAID NIH HHS R56 AI061061NIAID NIH HHS U19 AI109962
6 · The paper itself

Abstract

Genetic variation influences how the genome is interpreted in individuals and in mouse strains used to model immune responses. We developed approaches to utilize next-generation sequencing datasets to identify sequence variation in genes and enhancer elements in congenic and backcross mouse models. We defined genetic variation in the widely used B6-CD45.2 and B6.SJL-CD45.1 congenic model, identifying substantial differences in SJL genetic content retained in B6.SJL-CD45.1 strains on the basis of the vendor source of the mice. Genes encoding PD-1, CD62L, Bcl-2, cathepsin E, and Cxcr4 were within SJL genetic content in at least one vendor source of B6.SJL-CD45.1 mice. SJL genetic content affected enhancer elements, gene regulation, protein expression, and amino acid content in CD4

Indexed as

AnimalsCathepsin ECommerceEnhancer Elements, GeneticGene Expression RegulationGenetic BackgroundGenetic VariationGerminal CenterHigh-Throughput Nucleotide SequencingImmunityInbreedingLeukocyte Common AntigensMiceMice, CongenicMice, Inbred C57BLModels, AnimalCathepsin ECXCR4 protein, humanLeukocyte Common AntigensPtprc protein, mouseReceptors, CXCR4CD45.1CD8(+) T cellsCxcr4ERVgerm-freeLy5.1Rgs16T-betTfhTh1

Identifiers

PMID31248780
PMCPMC6883924
OpenAlexW2950139277

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.