Evidence map›Paper›PMID 10613844›Full record

ArticleGenome research1999

Perfect conserved linkage across the entire mouse chromosome 10 region homologous to human chromosome 21.

T Wiltshire, M Pletcher, S E Cole, M Villanueva, B Birren, J Lehoczky, K Dewar, R H Reeves

Abstract read
In one paragraph

Article in Genome research, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Review
  2. A comprehensive mouse IBD database for the efficient localization of quantitative trait loci.Mammalian genome : official journal of the International Mammalian Genome Society · 2006
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Current awareness.Yeast (Chichester, England) · 2000
    Article
  8. Review
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

8 authors.

T WiltshireDepartment of Physiology, Johns Hopkins School of Medicine, Baltimore, Maryland 21205, USA.
M Pletcher
S E Cole
M Villanueva
B Birren
J Lehoczky
K Dewar
R H Reeves

Funding

UTILIZATION OF TRANSGENICS IN THE STUDY OF DOWN SYNDROMEP01HD024605 · NICHD · JOHNS HOPKINS UNIVERSITY · PI REEVES, ROGER H · 1989 to 2004
$8.2M
GENETIC, PHYSICAL AND COMPARATIVE MAPPING IN MUSR01HG000405 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI REEVES, ROGER H · 1991 to 1999
–
NHGRI NIH HHS HG00405NICHD NIH HHS HD24605NICHD NIH HHS P01 HD024605
6 · The paper itself

Abstract

The distal end of human Chromosome (HSA) 21 from PDXK to the telomere shows perfect conserved linkage with mouse Chromosome (MMU) 10. This region is bounded on the proximal side by a segment of homology to HSA22q11.2, and on the distal side by a region of homology with HSA19p13.1. A high-resolution PAC-based physical map is described that spans 2.8 Mb, including the entire 2.1 Mb from Pdxk to Prmt2 corresponding to HSA21. Thirty-four expressed sequences are mapped, three of which were not mapped previously in any species and nine more that are mapped in mouse for the first time. These genes confirm and extend the conserved linkage between MMU10 and HSA21. The ordered PACs and dense STS map provide a clone resource for biological experiments, for rapid and accurate mapping, and for genomic sequencing. The new genes identified here may be involved in Down syndrome (DS) or in several genetic diseases that map to this conserved region of HSA21.

Indexed as

Chromosome MappingChromosomes, Human, Pair 21Genetic LinkageAnimalsBacteriophage P1Base SequenceContig MappingHumansMicePhysical Chromosome Mapping

Identifiers

PMID10613844
PMCPMC311004

What OpenQuestion holds

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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.