Evidence map›Paper›PMID 9335612›Full record

ArticleGenetics1997

Two dominant mutations in the mouse fused gene are the result of transposon insertions.

T J Vasicek, L Zeng, X J Guan, T Zhang, F Costantini, S M Tilghman

Abstract read
In one paragraph

Article in Genetics, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

58 citing papers in PubMed, 169 citations in OpenAlex.

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  10. Aryl Hydrocarbon Receptor: From Homeostasis to Tumor Progression.Frontiers in cell and developmental biology · 2022
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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

6 authors at 3 institutions in 1 country.

T J VasicekHoward Hughes Medical Institute, Princeton University, New Jersey 08544, USA.
L Zeng
X J Guan
T Zhang
F Costantini
S M Tilghman
Columbia University · USHoward Hughes Medical Institute · USPrinceton University · US

Funding

ROLE OF THE C-RET RECEPTOR TYROSINE KINASE IN KIDNEY DEVELOPMENTP01DK046934 · NIDDK · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI AL-AWQATI, QAIS · 1993 to 1998
–
NIDDK NIH HHS DK-46934
6 · The paper itself

Abstract

The mouse Fused locus encodes a protein that has been implicated in the regulation of embryonic axis formation. The protein, which has been named Axin to distinguish it from the product of the unrelated Drosophila melanogaster gene fused, contains regions of similarity to the RGS (regulators of G-protein signaling) family of proteins as well as to dishevelled, a protein that acts downstream of Wingless in D. melanogaster. Loss-of-function mutations at Fused lead to lethality between days 8 and 10 of gestation. Three dominant mutations result in a kinked tail in heterozygotes. Two of the dominant mutations, Fused and Knobbly, result from insertion of intracisternal A particle retrotransposons into the gene. The insertion in Fused, within the sixth intron, creates a gene that produces wild-type transcripts as well as mutant transcripts that initiate at both the authentic promoter and the 3'-most long terminal repeat of the insertion. Knobbly, an insertion of the retrotransposon into exon 7, precludes the production of wild-type protein. Thus the Fused homozygote is viable whereas Knobbly is a recessive embryonic lethal. In both mutants the dominant kink-tailed phenotype is likely to result from the synthesis of similar amino-terminal fragments of Axin protein that would contain the RGS domain, but lack the dishevelled domain.

Indexed as

Genes, DominantMutationRepressor ProteinsRetroelementsAnimalsAxin ProteinBase SequenceDNAHomozygoteMiceProteinsRNA, MessengerTranscription, GeneticAxin ProteinDNAProteinsRepressor ProteinsRetroelementsRNA, Messenger

Identifiers

PMID9335612
PMCPMC1208197
OpenAlexW2102788951

What OpenQuestion holds

Textmetadata
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.