Evidence map›Paper›PMID 7931087›Full record

ArticleThe Journal of experimental medicine1994

Use of recombinant congenic and congenic strains of NOD mice to identify a new insulin-dependent diabetes resistance gene.

D V Serreze, M Prochazka, P C Reifsnyder, M M Bridgett, E H Leiter

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 144 citations in OpenAlex.

  1. Advancing Animal Models of Human Type 1 Diabetes.Cold Spring Harbor perspectives in medicine · 2024
    Review
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  14. Genetic and Pharmacologic Models for Type 1 Diabetes.Current protocols in mouse biology · 2013
    Article
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  16. Article
  17. Review
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  19. Article
  20. Cutting edge: genetic characterization of IFN-producing killer dendritic cells.Journal of immunology (Baltimore, Md. : 1950) · 2009
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

D V SerrezeJackson Laboratory, Bar Harbor, Maine 04609.
M Prochazka
P C Reifsnyder
M M Bridgett
E H Leiter
Jackson Laboratory · US

Funding

Diabetogenic Role of MHC Class I Alleles in NOD MiceR01DK046266 · NIDDK · JACKSON LABORATORY · PI SERREZE, DAVID V · 2000 to 2018
$7.2M
GENETICS &PATHOGENESIS OF NON-OBESE DIABETIC (NOD) MICER01DK036175 · NIDDK · JACKSON LABORATORY · PI LEITER, EDWARD H · 1986 to 2005
$2.1M
PATHOGENESIS OF AUTOIMMUNE DIABETES IN MICER01DK027722 · NIDDK · JACKSON LABORATORY · PI LEITER, EDWARD H · 1986 to 2004
$902k
PATHOGENESIS OF AUTOIMMUNE DIABETES IN MICER37DK027722 · NIDDK · JACKSON LABORATORY · PI LEITER, EDWARD H · 1994 to 2001
$677k
DIABETOGENIC ROLE OF H-2G7 CLASS I ALLELES IN NOD MICER29DK046266 · NIDDK · JACKSON LABORATORY · PI SERREZE, DAVID V. · 1993 to 1998
–
NIDDK NIH HHS DK-27722NIDDK NIH HHS DK-36175NIDDK NIH HHS DK-46266
6 · The paper itself

Abstract

Insulin-dependent diabetes mellitus (IDDM) in NOD/Lt mice represents a complex polygenic disease. NOR/Lt is a recombinant congenic strain (RCS) in which limited regions of the NOD/Lt genome have been replaced by genome from the C57BL/KsJ strain. NOR mice are insulitis resistant and diabetes free despite genetic identity with NOD at numerous chromosomal regions containing previously described insulin-dependent diabetes (Idd) genes, including the strongly diabetogenic H2g7 major histocompatibility complex (MHC) haplotype. The present study revealed BKs-derived genome on segments of chromosomes (Chr) 1, 2, 4, 5, 7, 11, 12, and 18, approximating 11.6% of the total NOR genome analyzed. (NOD x NOR)F2 segregation analysis was employed to identify chromosomal regions in NOR containing Idd resistance alleles. IDDM developed in 33% (10/30) of F1 females, and 29.3% (36/123) of F2 females aged to 1 yr. A previously unrecognized diabetes resistance locus (designated Idd13r) strongly protective in homozygous state was identified on NOR Chr 2 in linkage with the Il1 alpha structural gene. The existence of this locus was confirmed by construction of a NOD stock congenic for NOR-derived markers on Chr 2. Our analysis shows the utility of RCS and congenic stocks for the identification and isolation of non-MHC genes with strong antidiabetogenic functions.

Indexed as

AllelesAnimalsBase SequenceChromosome MappingDiabetes Mellitus, Type 1FemaleHumansMaleMiceMice, Inbred NODMolecular Sequence DataRecombination, Genetic

Identifiers

PMID7931087
PMCPMC2191696
OpenAlexW2042615532

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Registered trials

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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.