Evidence map›Paper›PMID 17591928›Full record

ArticleThe Journal of molecular diagnostics : JMD2007

Layered peptide array for multiplex immunohistochemistry.

Gallya Gannot, Michael A Tangrea, Heidi S Erickson, Peter A Pinto, Stephen M Hewitt, Rodrigo F Chuaqui, John W Gillespie, Michael R Emmert-Buck

Abstract readComparative StudyEvaluation Study
In one paragraph

Article in The Journal of molecular diagnostics : JMD, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. 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.

Gallya GannotPathogenetics Unit, Advanced Technology Center, Laboratory of Pathology and Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892-4605, USA.
Michael A Tangrea
Heidi S Erickson
Peter A Pinto
Stephen M Hewitt
Rodrigo F Chuaqui
John W Gillespie
Michael R Emmert-Buck

Funding

Technology DevelopmentZIABC010729 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI EMMERT-BUCK, MICHAEL · 2009 to 2014
$2.5M
Technology DevelopmentZ01BC010729 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI EMMERT-BUCK, MICHAEL R · 2006 to 2008
$1.3M
Tissue Microarray Design of Genetic Screening ProductZ01SC010364 · SC · CLINICAL SCIENCES · PI KLEINER, DAVID E · 2000 to 2007
$932k
Intramural NIH HHS
6 · The paper itself

Abstract

Layered peptide array is a new methodology for multiplex molecular measurements from two-dimensional life science platforms. The technology can be used in several different configurations depending on the needs of the investigator. Described here is an indirect layered peptide array (iLPA) that is capable of measuring proteins on a solid surface, such as target antigens on a tissue section. A prototype iLPA system was developed and subsequently examined for reproducibility and specificity and then compared with standard immunohistochemistry. Semiquantitative, multiplex proteomic analysis of histological sections was achieved with up to 20 membranes. The experimental variability was 18%. Overall, the data suggest that iLPA technology will be a relatively simple and inexpensive method for molecular measurements from tissue sections.

Indexed as

Brain NeoplasmsBreast NeoplasmsCarcinomaColonic NeoplasmsFeasibility StudiesFemaleGene Expression Regulation, NeoplasticHumansImmunohistochemistryLung NeoplasmsLymphomaMaleMelanomaModels, BiologicalNeurilemmomaOvarian NeoplasmsPeptide Fragments

Identifiers

PMID17591928
PMCPMC1899424

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.