Evidence map›Paper›PMID 3478706›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1987

Isolation and characterization of cDNA clones for human erythrocyte beta-spectrin.

J T Prchal, B J Morley, S H Yoon, T L Coetzer, J Palek, J G Conboy, Y W Kan

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1987. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

10 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
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  7. Article
  8. Human chromosome 8.Journal of medical genetics · 1988
    Review
  9. Chromosomal location of three spectrin genes: relationship to the inherited hemolytic anemias of mouse and man.Proceedings of the National Academy of Sciences of the United States of America · 1988
    Article
  10. 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

7 authors at 1 institution in 1 country.

J T PrchalDepartment of Opthalmology, University of Alabama, Birmingham 35294.
B J Morley
S H Yoon
T L Coetzer
J Palek
J G Conboy
Y W Kan
University of Alabama at Birmingham · US

Funding

ABNORMAL HEMOGLOBIN SYNTHESIS--MECHANISMS AND DETECTIONR01DK016666 · NIDDK · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI KAN, YUET W · 1994 to 2005
$1.7M
ABNORMAL HEMOGLOBIN SYNTHESIS--MECHANISMS AND DETECTIONR37DK016666 · NIDDK · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI KAN, YUET W · 1986 to 2001
$1.2M
STRUCTURAL AND FUNCTIONAL STUDIES OF BAND 4.2P01HL037462 · NHLBI · ST. ELIZABETH'S MEDICAL CENTER OF BOSTON · PI LIU, SHIH-CHUN D · 1987 to 1996
–
NHLBI NIH HHS HL-37462NIDDK NIH HHS DK-16666PHS HHS 525095
6 · The paper itself

Abstract

Spectrin is an important structural component of the membrane skeleton that underlies and supports the erythrocyte plasma membrane. It is composed of nonidentical alpha (Mr 240,000) and beta (Mr 220,000) subunits, each of which contains multiple homologous 106-amino acid segments. We report here the isolation and characterization of a human erythroid-specific beta-spectrin cDNA clone that encodes parts of the beta-9 through beta-12 repeat segments. This cDNA was used as a hybridization probe to assign the beta-spectrin gene to human chromosome 14 and to begin molecular analysis of the gene and its mRNA transcripts. RNA transfer blot analysis showed that the reticulocyte beta-spectrin mRNA is 7.8 kilobases in length. Southern blot analysis of genomic DNA revealed the presence of restriction fragment length polymorphisms (RFLPs) within the beta-spectrin gene locus. The isolation of human spectrin cDNA probes and the identification of closely linked RFLPs will facilitate analysis of mutant spectrin genes causing congenital hemolytic anemias associated with quantitative and qualitative spectrin abnormalities.

Indexed as

Cloning, MolecularGenesAmino Acid SequenceBase SequenceDNAErythrocyte MembraneHumansMacromolecular SubstancesMolecular Sequence DataMolecular WeightSpectrinDNAMacromolecular SubstancesSpectrin

Identifiers

PMID3478706
PMCPMC299317
OpenAlexW2053802543

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.