Evidence map›Paper›PMID 25472048›Full record

ReviewReproduction, fertility, and development2014

Gamete derivation from embryonic stem cells, induced pluripotent stem cells or somatic cell nuclear transfer-derived embryonic stem cells: state of the art.

Charles A Easley, Calvin R Simerly, Gerald Schatten

Abstract readReview
In one paragraph

Review in Reproduction, fertility, and development, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Cryobanking European Mink (International journal of molecular sciences · 2022
    Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. 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

3 authors.

Charles A EasleyLaboratory of Translational Cell Biology, Department of Cell Biology, Emory University School of Medicine, 615 Michael Street, Atlanta, GA 30322, USA.
Calvin R SimerlyDepartment of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA 15108, USA.
Gerald SchattenDepartment of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA 15108, USA.

Funding

Frontiers in Alzheimer's and Aging Research (FrA2R)R25AG043365 · NIA · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI GERALD SCHATTEN · 2012 to 2026
$5.8M
Frontiers in Stem Cells in Cancer(FriSC2)R25CA163168 · NCI · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI SCHATTEN, GERALD · 2011 to 2020
$3.1M
Frontiers in Human Embryonic Stem CellsT15HL074353 · NHLBI · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI SCHATTEN, GERALD · 2003 to 2008
$1.0M
Rehabilitative and Regenerative Medicine for Minority Health & Health DisparitiesT15HD072833 · NICHD · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI SCHATTEN, GERALD · 2012 to 2014
$390k
NCI NIH HHS R25 CA163168NHLBI NIH HHS T15 HL074353NIA NIH HHS R25 AG043365NICHD NIH HHS T15 HD072833
6 · The paper itself

Abstract

Generating gametes from pluripotent stem cells (PSCs) has many scientific justifications and several biomedical rationales. Here, we consider several strategies for deriving gametes from PSCs from mice and primates (human and non-human) and their anticipated strengths, challenges and limitations. Although the 'Weismann barrier', which separates the mortal somatic cell lineages from the potentially immortal germline, has long existed, breakthroughs first in mice and now in humans are artificially creating germ cells from somatic cells. Spermatozoa with full reproductive viability establishing multiple generations of seemingly normal offspring have been reported in mice and, in humans, haploid spermatids with correct parent-of-origin imprints have been obtained. Similar progress with making oocytes has been published using mouse PSCs differentiated in vitro into primordial germ cells, which are then cultured after xenografting reconstructed artificial ovaries. Progress in making human oocytes artificially is proving challenging. The usefulness of these artificial gametes, from assessing environmental exposure toxicity to optimising medical treatments to prevent negative off-target effects on fertility, may prove invaluable, as may basic discoveries on the fundamental mechanisms of gametogenesis.

Indexed as

Nuclear Transfer TechniquesAnimalsCell DifferentiationEmbryonic Stem CellsGerm CellsHumansInduced Pluripotent Stem CellsIn Vitro TechniquesMicePrimates

Identifiers

PMID25472048
PMCPMC4346179

What OpenQuestion holds

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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.