Evidence map›Paper›PMID 8834240›Full record

ArticleHuman genetics1996

Identification and characterization of three genes and two pseudogenes on chromosome 13.

M de Fatima Bonaldo, P Jelenc, L Su, L Lawton, M T Yu, D Warburton, M B Soares

Abstract read
PubMed Publisher
In one paragraph

Article in Human genetics, 1996. 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
–field-weighted citation impact, top 96% 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, 4 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

7 authors at 2 institutions in 1 country.

M de Fatima BonaldoDepartment of Psychiatry, Columbia University, New York, NY 10032, USA.
P Jelenc
L Su
L Lawton
M T Yu
D Warburton
M B Soares
Columbia University · USNew York Psychoanalytic Society and Institute · US

Funding

PHYSICAL MAPPING OF HUMAN CHROMOSOME 13P01HG000861 · NHGRI · COLUMBIA UNIV NEW YORK MORNINGSIDE · 1993 to 1995
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SUBTRACTIVE CLONING OF CDNAS DELETED IN THE 13Q SYNDROMER55HD028422 · NICHD · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI SOARES, MARCELO BENTO · 1991 to 1991
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BIOMEDICAL RESEARCH SUPPORTS07RR005395 · NCRR · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI PARDES, HERBERT · 1985 to 1991
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NCRR NIH HHS S07 RR05395-30NHGRI NIH HHS P01 HG00861NICHD NIH HHS 1R55HD28422
6 · The paper itself

Abstract

A study was conducted on the feasibility of isolating genes and pseudogenes that map to chromosome 13 by a hybridization-based approach using a 13-specific library and pools of repeat-free cDNA clones. Five pairs of cDNA and chromosome 13 genomic clones were identified and characterized. Partial or full-length sequence was derived from all cDNAs, and database searches were performed for putative gene identification. Partial sequence was also obtained from the chromosome 13 genomic clones for comparison with those of the hybridizing cDNAs. As a result of these analyses we identified three genes, a putative homologue of a porcine mRNA encoding an unidentified hepatic protein, a putative homologue of a yeast integral membrane protein, and a gene for a translationally controlled tumor protein, and two processed pseudogenes, ribosomal proteins L23a and S3a. The latter was formerly identified as the v-fos transformation effector gene, Fte-1, and recently cited as a possible candidate for the BRCA2 gene on chromosome 13. All genes and pseudogenes were localized to cytogenetic bands by in situ hybridization of metaphase chromosomes with probes derived from the chromosome 13 genomic clones.

Indexed as

Amino Acid SequenceBase SequenceChromosomes, Human, Pair 13HumansMolecular Sequence DataPolymerase Chain ReactionPseudogenesRepetitive Sequences, Nucleic AcidSequence Homology, Amino AcidSequence Homology, Nucleic Acid

Identifiers

PMID8834240
OpenAlexW1964524451

What OpenQuestion holds

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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.