Evidence map›Paper›PMID 28395326›Full record

ReviewBiology of reproduction2017

Signaling mechanisms in mammalian sperm motility.

Maria João Freitas, Srinivasan Vijayaraghavan, Margarida Fardilha

Abstract readReview
In one paragraph

Review in Biology of reproduction, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 1 pooled it
–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

84 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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24 more citing papers are in PubMed but not listed here.

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

3 authors.

Maria João FreitasLaboratory of Signal Transduction, Institute for Research in Biomedicine, Medical Sciences Department, University of Aveiro, Campus Universitário de Santiago, Aveiro, Portugal.
Srinivasan VijayaraghavanDepartment of Biological Sciences, Kent State University, Kent, Ohio, USA.
Margarida FardilhaLaboratory of Signal Transduction, Institute for Research in Biomedicine, Medical Sciences Department, University of Aveiro, Campus Universitário de Santiago, Aveiro, Portugal.

Funding

Protein Phosphatase Action in Mammalian Spermatogenesis and Sperm FunctionR15HD068971 · NICHD · KENT STATE UNIVERSITY · PI VIJAYARAGHAVAN, SRINIVASAN · 2012 to 2012
$422k
NICHD NIH HHS R15 HD068971
6 · The paper itself

Abstract

The goal of sperm is to fertilize the oocyte. To achieve that purpose, it must acquire motility in the epididymis and hyperactivated motility in the female reproductive tract. Motility is only achieved when the sperm presents a fully functional flagellum, is capable of producing energy to fuel the movement, and suffers epididymal maturation and capacitation. Since sperm is a transcriptionally silent cell, motility depends on the activation and/or inhibitions of key signaling pathways. This review describes and discusses the main signaling pathways involved in primary and hyperactivated motility, as well as the bioenergetic mechanisms necessary to produce energy to fuel sperm motility. Although the complete human sperm motility process is far from being fully known, we believe that in the upcoming decades extensive progress will be made. Understanding the signaling pathways behind sperm motility can help pinpoint the cause of male infertility and uncover targets for male contraception.

Indexed as

Sperm MotilityGlycolysisHumansMaleOxidative PhosphorylationSignal TransductionSpermatozoaSperm Tailepididymisfemale reproductive systemphosphorylationsignaling pathwayssperm motility

Identifiers

PMID28395326
PMCPMC13397030

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.