Evidence map›Paper›PMID 8535064›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society1995

Mouse chromosome-specific painting probes generated from microdissected chromosomes.

M C Liechty, B K Hall, J M Scalzi, L M Davis, W J Caspary, J C Hozier

Abstract read
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In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

0 citing papers in PubMed, 13 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 institutions in 1 country.

M C LiechtyApplied Genetics Laboratories, Inc, Melbourne, Florida 32901, USA.
B K Hall
J M Scalzi
L M Davis
W J Caspary
J C Hozier
Applied Genetics Laboratories · USNational Institute of Environmental Health Sciences · US

Funding

SEQUENCE ANALYSIS OF TK AND HPRT GENE MUTATIONSN43ES021002 · NIEHS · APPLIED GENETICS LABORATORIES, INC. · PI LIECHTY, MELISSA C · 1992 to 1992
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MOUSE CHROMOSOME-SPECIFIC PAINTING PROBESR43GM050114 · NIGMS · APPLIED GENETICS LABORATORIES, INC. · PI LIECHTY, MELISSA C · 1993 to 1993
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NIEHS NIH HHS N43-ES-21002NIGMS NIH HHS IR43GM50114-01
6 · The paper itself

Abstract

Using degenerate primer amplification of chromosomes microdissected from banded cytogenetic preparations, we constructed both whole chromosome painting probes for mouse Chromosomes (Chrs) 1, 2, 3, and 11 and a centromere probe that strongly paints most mouse centromeres. We also amplified a Robertsonian translocation chromosome microdissected from unstained preparations to construct a painting probe for Chrs 9 and 19. The chromosome probes uniformly painted the respective chromosomes of origin. We demonstrated the utility of the Chr 11 probe in aberration analysis by staining mutants that we had previously identified as containing a Chr 11 translocation, and in some mutant cell lines we observed chromosome rearrangements not previously detected in stained cytogenetic preparations. The technology of microdissection and amplification applies to all mouse chromosomes or to specific subchromosomal regions and will be useful in mouse genetics, in aberration analysis, and for chromosome identification.

Indexed as

DNA ProbesIn Situ Hybridization, FluorescenceAnimalsBase SequenceCentromereDiploidyDNA PrimersGenetic MarkersMaleMiceMice, Inbred C57BLMolecular Sequence DataMutationDNA PrimersDNA ProbesGenetic Markers

Identifiers

PMID8535064
OpenAlexW2019265853

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.