Evidence map›Paper›PMID 11714728›Full record

ArticleThe Journal of cell biology2001

NAPO as a novel marker for apoptosis.

B S Sayan, G Ince, A E Sayan, M Ozturk

Abstract read
In one paragraph

Article in The Journal of cell biology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Differential control of TAp73 and DeltaNp73 protein stability by the ring finger ubiquitin ligase PIR2.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

B S SayanDepartment of Molecular Biology, Bilkent University, 06533 Ankara, Turkey.
G Ince
A E Sayan
M Ozturk

Funding

TUMOR SUPPRESSOR P53 GENE IN VIRAL HEPATOCARCINOMAR01CA054567 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI ISSELBACHER, KURT J · 1991 to 1994
–
NCI NIH HHS CA-54567
6 · The paper itself

Abstract

Apoptosis or programmed cell death plays a pivotal role in embryonic development and maintenance of homeostasis. It is also involved in the etiology of pathophysiological conditions such as cancer, neurodegenerative, autoimmune, infectious, and heart diseases. Consequently, the study of apoptosis is now at center of both basic and clinical research applications. Therefore, sensitive and simple apoptosis detection techniques are required. Here we describe a monoclonal antibody-defined novel antigen, namely NAPO (negative in apoptosis), which is specifically lost during apoptosis. The anti-NAPO antibody recognizes two nuclear polypeptides of 60 and 70 kD. The antigen is maintained in quiescent and senescent cells, as well as in different phases of the cell cycle, including mitosis. Thus, immunodetection of NAPO antigen provides a specific, sensitive, and easy method for differential identification of apoptotic and nonapoptotic cells.

Indexed as

ApoptosisAnimalsAntibodies, MonoclonalAntigensCell CycleCell LineCell NucleusCellular SenescenceCulture Media, Serum-FreeHumansIn Situ Nick-End LabelingMiceMicroscopy, FluorescenceNuclear ProteinsPrecipitin TestsTumor Cells, CulturedAntibodies, MonoclonalAntigensCulture Media, Serum-FreeNuclear Proteins

Identifiers

PMID11714728
PMCPMC2150886

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.