Evidence map›Paper›PMID 23960722›Full record

ArticleSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society2010

Separation of biological proteins by liquid chromatography.

Imran Ali, Hassan Y Aboul-Enein, Prashant Singh, Rakesh Singh, Bhavtosh Sharma

Open access · hybridAbstract read
In one paragraph

Article in Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Precision medicine and metabolic syndrome.ARYA atherosclerosis · 2022
    Review
  3. Finding a Needle in a Haystack: Proteomics in Heart Failure.JACC. Basic to translational science · 2020
    Review
  4. Article
  5. 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

5 authors at 2 institutions in 2 countries.

Imran AliDepartment of Chemistry, Jamia Millia Islamia (Central University), New Delhi 110 025, India.
Hassan Y Aboul-Enein
Prashant Singh
Rakesh Singh
Bhavtosh Sharma
Jamia Millia Islamia · INNational Research Centre · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

After the success of human genome project, proteome is a new emerging field of biochemistry as it provides the knowledge of enzymes (proteins) interactions with different body organs and medicines administrated into human body. Therefore, the study of proteomics is very important for the development of new and effective drugs to control many lethal diseases. In proteomics study, analyses of proteome is essential and significant from the pathological point of views, i.e., in several serious diseases such as cancer, Alzheimer's disease and aging, heart diseases and also for plant biology. The separation and identification of proteomics is a challenging job due to their complex structures and closely related physico-chemical behaviors. However, the recent advances in liquid chromatography make this job easy. Various kinds of liquid chromatography, along with different detectors and optimization strategies, have been discussed in this article. Besides, attempts have been made to include chirality concept in proteomics for understanding mechanism and medication of various disease controlled by different body proteins.

Indexed as

2D-nano LC, two-dimensional nano liquid chromatography quadrupoleACN, acetonitrileAIEC, anion exchange chromatographyCEC, capillary electro-chromatographyChiralityCIEF, capillary isoelectric focusingCSF, cerebrospinal fluidEC, electro-chromatographyESI-LC–MS, electrospray ionization liquid chromatography–mass spectrometryFA, formic acidFLP, FMRF amide-like peptideFT-ICR-MS, ion cyclotron resonance-mass spectrometryGeneGPI-APs, glycosylphosphadylinositol anchored proteinsGSH, glutathione stimulating hormoneGSTs, glutathione-S-transferase isoenzymeHFBA, heptafluorobutyric acidHPLC, high performance liquid chromatographyICAT, isotope coded affinity tagIEF-SEC, isoelectrofocussing size-exclusion chromatographyIMCD, inner medullary collecting ductLC-dual ESI, liquid chromatography dual electrospray ionization-Fourier transformLC–MS, liquid chromatography–mass spectrometryLC-Q-TOF, liquid chromatography-quadrupole time-of-flight tandem massLiquid chromatographyMALDI-TOF, matrix-assisted laser desorption/ionization-time-of flightMFGM, milk fat globule membranesMMA, mass measurement accuracyMPC, mesenchymal progenitor cellMS/MS, spectrometryNano detectionNLFs, Nasal lavage fluidsNLP, neuropeptide like proteinPC2, prohormone convertase-2PreparationProteomicsPS II, photosystem IIQ-TOFMS/MS, time-of-flight tandem-mass spectrometryRPLC, reversed phase liquid chromatographySCX, strong cation exchangeSEC, size-exclusion chromatographyTFA, trifluoroacetic acidTIC, total ion currentTRAF, tumor necrosis factor receptor

Identifiers

PMID23960722
PMCPMC3730981
OpenAlexW2029082013

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.