Evidence map›Paper›PMID 9258683›Full record

ArticleGenetics1997

Genetic studies of the mouse mutations mahogany and mahoganoid.

K A Miller, T M Gunn, M M Carrasquillo, M L Lamoreux, D B Galbraith, G S Barsh

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 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

31 citing papers in PubMed, 121 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. MC1R: Front and Center in the Bright Side of Dark Eumelanin and DNA Repair.International journal of molecular sciences · 2018
    Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Attractin gene deficiency contributes to testis vacuolization and sperm dysfunction in male mice.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2009
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Disruption of the RIIbeta subunit of PKA reverses the obesity syndrome of Agouti lethal yellow mice.Proceedings of the National Academy of Sciences of the United States of America · 2008
    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

6 authors at 4 institutions in 1 country.

K A MillerDepartment of Pediatrics, Stanford University School of Medicine, California 94305-5428, USA.
T M Gunn
M M Carrasquillo
M L Lamoreux
D B Galbraith
G S Barsh
Stanford University · USTrinity College · USHoward Hughes Medical Institute · USTexas A&M University · US

Funding

PATHOGENESIS OF OCULAR ALBINISMR01EY010223 · NEI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ORLOW, SETH J. · 1994 to 2005
$1.9M
NEI NIH HHS EY-10223NIDDK NIH HHS DK-28506
6 · The paper itself

Abstract

The mouse mutations mahogany (mg) and mahoganoid (md) are negative modifiers of the Agouti coat color gene, which encodes a paracrine signaling molecule that induces a swithc in melanin synthesis from eumelanin to pheomelanin. Animals mutant for md or mg synthesize very little or no pheomelanin depending on Agouti gene background. The Agouti protein is normally expressed in the skin and acts as an antagonist of the melanocyte receptor for alpha-MSH (Mc1r); however, ectopic expression of Agouti causes obesity, possibly by antagonizing melanocortin receptors expressed in the brain. To investigate where md and mg lie in a genetic pathway with regard to Agouti and Mc1r signaling, we determined the effects of these mutations in animals that carried either a loss-of-function Mc1r mutation (recessive yellow, Mc1re) or a gain-of-function Agouti mutation (lethal yellow, Ay). We found that the Mc1re mutation suppressed the effects of md and mg, but that md and mg suppressed the effects of Ay on both coat color and obesity. Plasma levels of alpha-MSH and of ACTH were unaffected by md or mg. These results suggest that md and mg interfere directly with Agouti signaling, possibly at the level of protein production or receptor regulation.

Indexed as

Intercellular Signaling Peptides and ProteinsMutationAdrenocorticotropic HormoneAgouti Signaling Proteinalpha-MSHAnimalsCrosses, GeneticFemaleHair ColorMaleMelaninsMiceMice, Inbred C3HMice, Inbred C57BLMice, Mutant StrainsObesityAdrenocorticotropic HormoneAgouti Signaling Proteinalpha-MSHa protein, mouseeumelaninIntercellular Signaling Peptides and ProteinsMelaninspheomelaninProteinsReceptors, CorticotropinReceptors, Melanocortin

Identifiers

PMID9258683
PMCPMC1208084
OpenAlexW2161121343

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.