Evidence map›Paper›PMID 42732522›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Freeze-Drying and Room Temperature Preservation of Mammalian Sperm.

Sayaka Wakayama, Daiyu Ito, Teruhiko Wakayama

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. 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

3 authors.

Sayaka WakayamaAdvanced Biotechnology Center, University of Yamanashi, Yamanashi, Japan.
Daiyu ItoFaculty of Life and Environmental Sciences, University of Yamanashi, Yamanashi, Japan.
Teruhiko WakayamaAdvanced Biotechnology Center, University of Yamanashi, Yamanashi, Japan. twakayama@yamanashi.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Freeze-drying technology enables the safe preservation of genetic resources at room temperature, even in situations where liquid nitrogen cannot be replenished following a major disaster. In addition, genetic resource storage becomes easier, and international transport becomes possible at low cost. In addition, freeze-drying has been found to confer resistance to high temperatures and radiation, and research into the safe and permanent preservation of genetic resources outside the Earth is now underway. It has also become possible to generate cloned individuals from freeze-dried somatic cells, enabling the recovery and preservation of genetic resources even from infertile animals. However, the birth rate using freeze-dried sperm is significantly lower than that achieved with fresh sperm, and long-term storage has not yet been demonstrated. Therefore, this technology has not yet gained reliability and has not been put into practical use, although these issues are being addressed by the latest research. This chapter first provides an overview of current sperm freeze-drying methods, followed by a detailed freeze-drying protocol.

Indexed as

CryopreservationSemen PreservationSpermatozoaAnimalsFreeze DryingHumansMaleMammalsSperm Injections, IntracytoplasmicTemperatureCloneFreeze-dryingGenetic resourcesICSIPreservationRoom temperatureSpermatozoa

Identifiers

PMID42732522

What OpenQuestion holds

Textmetadata
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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.