Evidence map›Paper›PMID 16847751›Full record

ArticleCellular & molecular biology letters2006

The identification and characterization of a testis-specific cDNA during spermatogenesis.

Ying Chen, Jiarui Hu, Ping Song, Wuming Gong

Abstract read
In one paragraph

Article in Cellular & molecular biology letters, 2006. 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
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.

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

4 authors.

Ying ChenLaboratory of Molecular Genetics and Developmental Biology, College of Life Science, Wuhan University, Wuhan, China.
Jiarui Hu
Ping Song
Wuming Gong

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using bioinformatics and experimental validation, we obtained a cDNA (named srsf) which was exclusively expressed in the mouse testes. RT-PCR analysis showed that srsf mRNA was not expressed in the gonad during the sex determination period or during embryogenesis. In developing mouse testis, srsf expression was first detected on post-natal day 10, reached its highest level on day 23, and then reduced to and remained at a moderate level throughout adulthood. In situ hybridization analysis demonstrated that srsf mRNA was expressed in pachytene spermatocytes and round spermatids in the testes. The predicted protein contains one RNA-binding domain (RBD) and a serine-arginine rich domain (RS), which are characterized by some splicing factors of SR family members. These findings indicate that srsf may play a role during spermatogenesis.

Indexed as

Amino Acid SequenceAnimalsBase SequenceDNA, ComplementaryFemaleMaleMiceMice, Inbred BALB CMolecular Sequence DataRNA-Binding ProteinsRNA SplicingRNA Splicing FactorsSpermatogenesisTestisDNA, ComplementaryGm6687 protein, mouseRNA-Binding ProteinsRNA Splicing Factors

Identifiers

PMID16847751
PMCPMC6275928

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.