Evidence map›Paper›PMID 40208525›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Initiating Separate Cultures of Keratinocytes and Melanocytes from a Single Biopsy.

Karel Ferland, Henri De Koninck, Bettina Cattier, Sergio Cortez Ghio, Danielle Larouche, Lucie Germain

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Karel Ferland *Centre de recherche en organogénèse expérimentale de l'Université Laval / LOEX, Centre de recherche du CHU de Québec-Université Laval, Axe médecine régénératrice, and Département de Chirurgie, Faculté de Médecine, Université Laval, Québec, QC, Canada.
Henri De Koninck *Centre de recherche en organogénèse expérimentale de l'Université Laval / LOEX, Centre de recherche du CHU de Québec-Université Laval, Axe médecine régénératrice, and Département de Chirurgie, Faculté de Médecine, Université Laval, Québec, QC, Canada.
Bettina CattierCentre de recherche en organogénèse expérimentale de l'Université Laval / LOEX, Centre de recherche du CHU de Québec-Université Laval, Axe médecine régénératrice, and Département de Chirurgie, Faculté de Médecine, Université Laval, Québec, QC, Canada.
Sergio Cortez GhioCentre de recherche en organogénèse expérimentale de l'Université Laval / LOEX, Centre de recherche du CHU de Québec-Université Laval, Axe médecine régénératrice, and Département de Chirurgie, Faculté de Médecine, Université Laval, Québec, QC, Canada.
Danielle LaroucheCentre de recherche en organogénèse expérimentale de l'Université Laval / LOEX, Centre de recherche du CHU de Québec-Université Laval, Axe médecine régénératrice, and Département de Chirurgie, Faculté de Médecine, Université Laval, Québec, QC, Canada.
Lucie GermainCentre de recherche en organogénèse expérimentale de l'Université Laval / LOEX, Centre de recherche du CHU de Québec-Université Laval, Axe médecine régénératrice, and Département de Chirurgie, Faculté de Médecine, Université Laval, Québec, QC, Canada. lucie.germain@fmed.ulaval.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A significant stride in enhancing the care for extensively burned patients has been made through the cultivation of autologous keratinocytes, resulting in the formation of cohesive epithelial tissue sheets. Beyond clinical applications, both keratinocyte and melanocyte cultures play vital roles in investigating diverse cellular and molecular mechanisms underlying various skin pathologies. In epithelial cell culture, preserving stem cells is crucial, necessitating dependable methods and optimal conditions. Well-cultured keratinocytes typically exhibit consistent cuboid morphology and maintain proliferative capacity over numerous passages. In contrast, melanocyte culture requires specialized additives to stimulate growth, sustain differentiation, and ensure purity. This chapter provides a comprehensive guide to the materials and techniques essential for efficient keratinocyte culture for clinical purposes and melanocyte culture for research endeavors. Covered aspects include tissue sampling and transportation, isolation, routine culture, subculture, and cryopreservation.

Indexed as

Cell Culture TechniquesKeratinocytesMelanocytesBiopsyCell DifferentiationCell ProliferationCells, CulturedCell SeparationCryopreservationHumansCell therapyCultured epithelial autograftEpidermisEpitheliumKeratinocyteMelanocyteRegenerative medicineTissue engineeringWound healing

Identifiers

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.